U.S. patent application number 11/868551 was filed with the patent office on 2009-02-05 for methods for removal of lipids from fluids.
This patent application is currently assigned to Lipid Sciences, Inc.. Invention is credited to David C. Bomberger, Pablo E. Garcia, Eric Hegwer, Thomas P. Low, Ripudaman Malhotra.
Application Number | 20090032468 11/868551 |
Document ID | / |
Family ID | 34682437 |
Filed Date | 2009-02-05 |
United States Patent
Application |
20090032468 |
Kind Code |
A1 |
Bomberger; David C. ; et
al. |
February 5, 2009 |
Methods for Removal of Lipids from Fluids
Abstract
This invention is directed to systems and methods for removing
lipids from a fluid, such as plasma, or from lipid-containing
organisms. These systems contact a fluid with an extraction
solvent, which causes the lipids in the fluid to separate from the
fluid or causes lipids in the lipid-containing organisms to
separate from the lipid-containing organism, using at least one
hollow fiber contactor. The separated lipids are removed from the
fluid. The extraction solvent is removed from the fluid or at least
reduced to a level below a particular threshold enabling the fluid
to be administered to a patient without the patient experiencing
undesirable consequences. Once the fluid has been processed, the
fluid may be administered to a patient who donated the fluid, to a
different patient, or be stored.
Inventors: |
Bomberger; David C.;
(Belmont, CA) ; Garcia; Pablo E.; (Redwood City,
CA) ; Hegwer; Eric; (Menlo Park, CA) ; Low;
Thomas P.; (Belmont, CA) ; Malhotra; Ripudaman;
(San Carlos, CA) |
Correspondence
Address: |
JOHN S. PRATT, ESQ;KILPATRICK STOCKTON, LLP
1100 PEACHTREE STREET
ATLANTA
GA
30309
US
|
Assignee: |
Lipid Sciences, Inc.
Pleasanton
CA
|
Family ID: |
34682437 |
Appl. No.: |
11/868551 |
Filed: |
October 8, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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11589376 |
Oct 30, 2006 |
7297262 |
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11868551 |
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11221617 |
Sep 8, 2005 |
7166223 |
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11589376 |
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11059064 |
Feb 16, 2005 |
6991727 |
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11221617 |
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10178773 |
Jun 21, 2002 |
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11059064 |
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60301112 |
Jun 25, 2001 |
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60301108 |
Jun 25, 2001 |
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60300927 |
Jun 25, 2001 |
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60301109 |
Jun 25, 2001 |
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60387281 |
Jun 7, 2002 |
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Current U.S.
Class: |
210/645 ;
210/634 |
Current CPC
Class: |
A61M 2202/206 20130101;
B01D 61/362 20130101; B01D 11/043 20130101; A61M 1/3472 20130101;
A61M 1/3486 20140204; A61M 1/3616 20140204; A61M 1/3693 20130101;
A61M 1/34 20130101; A61M 1/3468 20140204; A61M 1/342 20130101; A61M
2202/0456 20130101; A61M 1/3482 20140204; A61M 2202/203 20130101;
B01D 11/0492 20130101; A61M 1/3403 20140204; B01D 61/246 20130101;
B01D 2313/50 20130101; A61M 1/3496 20130101; A61M 1/341 20140204;
B01D 63/02 20130101; A61M 1/3603 20140204; B01D 63/046 20130101;
A61M 2202/08 20130101; A61M 2205/3368 20130101; B01D 11/043
20130101; B01D 11/0492 20130101 |
Class at
Publication: |
210/645 ;
210/634 |
International
Class: |
B01D 11/04 20060101
B01D011/04 |
Claims
1-17. (canceled)
18. A method for removing lipids from a fluid containing lipids or
lipid-containing organisms, comprising: contacting the fluid with a
first extraction solvent in a first device and forming a first
mixture comprising the fluid and the first extraction solvent,
wherein at least a portion of the lipids dissolve in the first
extraction solvent; removing at least a portion of the first
extraction solvent from the first mixture by contacting the first
mixture with a second extraction solvent in a second device, which
forms a second mixture comprising the first extraction solvent, the
second extraction solvent and the fluid; and removing at least a
portion of the second extraction solvent from the second mixture
using a third device.
19. The method of claim 18, wherein the first device is a hollow
fiber contactor.
20. The method of claim 18, wherein the second device is a hollow
fiber contactor.
21. The method of claim 18, wherein the third device is a hollow
fiber contactor.
22. The method of claim 18, further comprising: providing at least
one solvent sensing device to detect the presence of the first
extraction solvent in the second mixture and to detect the presence
of the second extraction solvent in the second mixture after
removing at least a portion of the second extraction solvent from
the second mixture.
23. The method of claim 18, wherein removing at least a portion of
the second extraction solvent from the second mixture using a third
device comprises passing the second mixture through a final phase
subsystem comprising a hollow fiber contactor.
24. The method of claim 23, wherein the final phase subsystem is a
recirculating subsystem and the method further comprises using a
sensor to determine when sufficient amounts of the first and second
extraction solvents have been removed from the second mixture as
the second mixture passes through the recirculating subsystem.
25. The method of claim 18, wherein removing at least a portion of
the second extraction solvent from the second mixture using a third
device comprises contacting the second mixture with a gas.
26. The method of claim 25, further comprising circulating the gas
through a gas filtering loop comprising a carbon bed to remove the
first and the second extraction solvents from the gas.
27. The method of claim 18, further comprising: providing a first
pump disposed between the first extraction solvent source and the
first device that transfers the first extraction solvent to the
first device; and providing a second pump disposed between the
second extraction solvent source and the second device that
transfers the second extraction solvent to the second device.
Description
RELATED APPLICATIONS
[0001] This application claims the benefit of the filing dates of
U.S. Provisional Patent Application No. 60/301,112, filed Jun. 25,
2001; U.S. Provisional Patent Application No. 60/301,108, filed
Jun. 25, 2001; U.S. Provisional Patent Application No. 60/300,927,
filed Jun. 25, 2001; U.S. Provisional Patent Application No.
60/301,109, filed Jun. 25, 2001; U.S. Provisional Patent
Application No. 60/346,094, filed Jan. 2, 2002; and U.S.
Provisional Patent Application No. TBD, filed Jun. 7, 2002, all of
which are incorporated by reference herein.
FIELD OF THE INVENTION
[0002] The present invention relates to systems and methods for the
removal of lipids from fluids, especially plasma, or from
lipid-containing organisms, or both, using solvent extraction. The
delipidated fluid may be administered to an animal or human for
therapeutic use such as treatment of arteriosclerosis and
atherosclerotic vascular diseases, removal of excess fat within an
animal or human, and reduction of infectivity of lipid-containing
organisms.
BACKGROUND OF THE INVENTION
Hyperlipidemia and Arteriosclerosis
[0003] Cardiovascular, cerebrovascular, and peripheral vascular
diseases are responsible for a significant number of deaths
annually in many industrialized countries. One of the most common
pathological processes underlying these diseases is
arteriosclerosis. Arteriosclerosis is characterized by lesions,
which begin as localized fatty thickenings in the inner aspects of
blood vessels supplying blood to the heart, brain, and other organs
and tissues throughout the body. Over time, these atherosclerotic
lesions may ulcerate, exposing fatty plaque deposits that may break
away and embolize within the circulation. Atherosclerotic lesions
obstruct the lumens of the affected blood vessels and often reduce
the blood flow within the blood vessels, which may result in
ischemia of the tissue supplied by the blood vessel. Embolization
of atherosclerotic plaques may produce acute obstruction and
ischemia in distal blood vessels. Such ischemia, whether prolonged
or acute, may result in a heart attack or stroke from which the
patient may or may not recover. Similar ischemia in an artery
supplying an extremity may result in gangrene requiring amputation
of the extremity.
[0004] For some time, the medical community has recognized the
relationship between arteriosclerosis and levels of dietary lipid,
serum cholesterol, and serum triglycerides within a patient's blood
stream. Many epidemiological studies have been conducted revealing
that the amount of serum cholesterol within a patient's blood is a
significant predictor of coronary disease. Similarly, the medical
community has recognized the relationship between hyperlipidemia
and insulin resistance, which can lead to diabetes mellitus.
Further, hyperlipidemia and arteriosclerosis have been identified
as being related to other major health problems, such as obesity
and hypertension.
[0005] Hyperlipidemia may be treated by changing a patient's diet.
However, use of a patient's diet as a primary mode of therapy
requires a major effort on the part of patients, physicians,
nutritionists, dietitians, and other health care professionals and
thus undesirably taxes the resources of health professionals.
Another negative aspect of this therapy is that its success does
not rest exclusively on diet. Rather, success of dietary therapy
depends upon a combination of social, psychological, economic, and
behavioral factors. Thus, therapy based only on correcting flaws
within a patient's diet is not always successful.
[0006] In instances when dietary modification has been
unsuccessful, drug therapy has been used as an alternative. Such
therapy has included use of commercially available hypolipidemic
drugs administered alone or in combination with other therapies as
a supplement to dietary control. Hypolipidemic drugs have had
varying degrees of success in reducing blood lipid; however, none
of the hypolipidemic drugs successfully treats all types of
hyperlipidemia. While some hypolipidemic drugs have been fairly
successful, the medical community has not found any conclusive
evidence that hypolipidemic drugs cause regression of
atherosclerosis. In addition, all hypolipidemic drugs have
undesirable side effects. As a result of the lack of success of
dietary control, drug therapy and other therapies, atherosclerosis
remains a major cause of death in many parts of the world.
[0007] To combat this disturbing fact, a relatively new therapy has
been used to reduce the amount of lipid in patients for whom drug
and diet therapies were not sufficiently effective. This therapy,
referred to as plasmapheresis therapy or plasma exchange therapy,
involves replacing a patient's plasma with donor plasma or more
usually a plasma protein fraction. While having been fairly
successful, this treatment has resulted in complications due to
introduction of foreign proteins and transmission of infectious
diseases. Further, plasma exchange undesirably removes many plasma
proteins, such as very low-density lipoprotein (VLDL), low-density
lipoprotein (LDL), and high-density lipoprotein (HDL).
[0008] HDL is secreted from both the liver and the intestine as
nascent, disk-shaped particles that contain cholesterol and
phospholipids. HDL is believed to play a role in reverse
cholesterol transport, which is the process by which excess
cholesterol is removed from tissues and transported to the liver
for reuse or disposal in the bile. Therefore, removal of HDL from
plasma is not desirable.
[0009] Other apheresis techniques exist that can remove LDL from
plasma. These techniques include absorption of LDL in
heparin-agarose beads (affinity chromatography), the use of
immobilized LDL-antibodies, cascade filtration absorption to
immobilize dextran sulphate, and LDL precipitation at low pH in the
presence of heparin. Each method removes LDL but not HDL.
[0010] LDL apheresis, however, has disadvantages. For instance,
significant amounts of plasma proteins in addition to LDL are
removed during apheresis. In addition, LDL apheresis must be
performed frequently, such as weekly, to obtain a sustained
reduction in LDL-cholesterol. Furthermore, LDL removal may be
counterproductive because low LDL levels in a patients blood may
result in increased cellular cholesterol synthesis. Thus, removal
of LDL from a patient's blood may have negative side effects.
[0011] Yet another method of achieving a reduction in plasma
cholesterol in homozygous familial hypercholesterolemia,
heterozygous familial hypercholesterolemia and patients with
acquired hyperlipidemia is an extracorporeal lipid elimination
process, referred to as cholesterol apheresis. In cholesterol
apheresis, blood is withdrawn from a patient, the plasma is
separated from the blood, and the plasma is mixed with a solvent
mixture. The solvent mixture extracts lipids from the plasma.
Thereafter, the delipidated plasma is recombined with the patient's
blood cells and returned to the patient.
[0012] More specifically, lipid apheresis results in the removal of
fats from plasma or serum. However, unlike LDL apheresis, the
proteins (apolipoproteins) that transport lipids remain soluble in
the treated plasma or serum. Thus, the apolipoproteins of VLDL, LDL
and HDL are present in the treated plasma or serum. These
apolipoproteins, in particular apolipoprotein A1 from the
delipidated HDL in the plasma or serum, are responsible for the
mobilization of unwanted lipids or toxins, such as excessive
amounts of deposited lipids including cholesterol in arteries,
plaques, and excessive amounts of triglycerides, adipose tissue,
and fat soluble toxins present in adipose tissue. These excessive
amounts of lipids or toxins are transferred to the plasma or serum,
and then bound to the newly assembled apolipoproteins. Application
of another lipid apheresis procedure successively removes these
unwanted lipids or toxins from the plasma and thus the body. The
main advantage of this procedure is that LDL and HDL are not
removed from the plasma. Instead, only cholesterol, some
phospholipid and a considerable amount of triglycerides are
removed.
[0013] While lipid apheresis has the potential to overcome the
shortcomings of dietary control, drug therapy and other apheresis
techniques, existing apparatuses and methods for lipid apheresis do
not provide a sufficiently rapid and safe process. Thus, a need
exists for systems, apparatuses and methods capable of conducting
lipid apheresis more quickly than accomplished with conventional
equipment and methods.
[0014] Unfortunately, existing lipid apheresis systems suffer from
a number of disadvantages that limit their ability to be used in
clinical applications, such as in doctors' offices and other
medical facilities. One disadvantage is the explosive nature of the
solvents used to delipidate this plasma. If used in a continuous
system, these solvents are in close proximity to patients and
medical staff. Thus, it would be advantageous to limit this
exposure; however, this hazard is clearly present for the duration
of the delipidation process, which usually runs for several
hours.
[0015] Another disadvantage is the difficulty in removing a
sufficient amount of solvents from the delipidated plasma in order
for the delipidated plasma to be safely returned to a patient. In
addition, patients are subjected to an increased chance of
prolonged exposure to solvents in a continuous system. Furthermore,
current techniques do not provide for sequential multi-washes
because the volume of blood necessary for continuous processing
using conventional equipment requires removal of an amount of blood
that would harm the patient. In other words, conventional equipment
does not allow for automated continuous removal, processing and
return of plasma to a patient in a manner that does not negatively
impact total blood volume of the patient. While the long-term
toxicity of various extraction solvents is not known, especially
when present in the bloodstream, clinicians know that some solvents
may cross the blood-brain barrier. Furthermore, external contact
with solvents is known to cause clinical symptoms, such as
irritation of mucous membranes, contact dermatitis, headaches,
dizziness and drowsiness. Therefore, conventional equipment for
lipid apheresis is not adequate to conduct continuous processing of
a patient's blood.
Infectious Disease
[0016] While the medical community has struggled to develop cures
for hyperlipidemia and arteriosclerosis, it has likewise struggled
in its battle against infectious diseases. Infectious diseases are
a major cause of suffering and death throughout the world.
Infectious disease of varied etiology affects billions of animals
and humans each year and inflicts an enormous economic burden on
society. Many infectious organisms contain lipid as a major
component of the membrane that surrounds them. Three major classes
of organisms that produce infectious disease and contain lipid in
their cell wall or envelope include bacteria, viruses, and
protozoa. Numerous bacteria and viruses that affect animals and
humans cause extreme suffering, morbidity and mortality. Many
bacteria and viruses travel throughout the body in fluids, such as
blood, and some reside in plasma. These and other infectious agents
may be found in other fluids, such as peritoneal fluid, lymphatic
fluid, pleural fluid, pericardial fluid, cerebrospinal fluid, and
in various fluids of the reproductive system. Disease can be caused
at any site bathed by these fluids. Other bacteria and viruses
reside primarily in different organ systems or in specific tissues,
where they proliferate and enter the circulatory system to gain
access to other tissues and organs.
[0017] Infectious agents, such as viruses, affect billions of
people annually. Recent epidemics include the disease commonly
known as acquired immune deficiency syndrome (AIDS), which is
believed to be caused by the human immunodeficiency virus (HIV).
This virus is rapidly spreading throughout the world and is
prevalent in various sub-populations, including individuals who
receive blood transfusions, individuals who use needles
contaminated with the disease, and individuals who contact infected
fluids. This disease is also widespread in certain countries.
Currently, no known cure exists.
[0018] It has long been recognized that a simple, reliable and
economically efficient method for reducing the infectivity of the
HIV virus is needed to decrease transmission of the disease.
Additionally, a method of treating fluids of infected individuals
is needed to decrease transmission of the virus to others in
contact with these fluids. Furthermore, a method of treating blood
given to blood banks is needed to decrease transmission of the
virus to individuals receiving transfusions. Moreover, an apparatus
and method are needed for decreasing the viral load of an
individual or an animal by treating the plasma of that individual
and returning the treated plasma to the individual such that the
viral load in the plasma is decreased.
[0019] Other major viral infections that affect animals and humans
include, but are not limited to meningitis, cytomegalovirus, and
hepatitis in its various forms. While some forms of hepatitis may
be treated with drugs, other forms have not been successfully
treated in the past.
[0020] At the present time, most anti-viral therapies focus on
preventing or inhibiting viral replication by manipulating the
initial attachment of the virus to the T4 lymphocyte or macrophage,
the transcription of viral RNA to viral DNA and the assembly of new
virus during reproduction. Such a focus has created major
difficulty with existing treatments, especially with regard to HIV.
Specifically, the high mutation rate of the HIV virus often renders
treatments ineffective shortly after application. In addition, many
different strains of HIV have already become or are becoming
resistant to anti-viral drug therapy. Furthermore, during
anti-viral therapy, resistant strains of the virus may evolve.
Finally, many common therapies for HIV infection involve several
undesirable side effects and require patients to ingest numerous
pills daily. Unfortunately, many individuals are afflicted with
multiple infections caused by more than one infectious agent, such
as HIV, hepatitis and tuberculosis. Such individuals require even
more aggressive and expensive drugs to counteract disease
progression. Such drugs may cause numerous side effects as well as
multi-drug resistance. Therefore, an effective method and apparatus
is needed that does not rely on drugs for combating infections
organisms found in fluids. Such a method should reduce the
infectivity of infectious organisms.
[0021] Thus, a need exists to overcome the deficiencies of
conventional systems and methods for removing lipids from fluids,
such as plasma or serum, and for removing lipids from infectious
organisms contained in a fluid. Furthermore, a need exists for an
apparatus and method to perform delipidation rapidly, either in a
continuous or discontinuous manner of operation. A need further
exists for such an apparatus and process to perform safely and
reliably, and to produce delipidated fluid having residual plasma
solvent levels meeting acceptable standards. In addition, a need
exists for an apparatus having minimal physical connection between
a patient and the lipid apheresis process. Furthermore, a need
exists for an economical medical apparatus that is sterile and made
of a disposable construction for a single use application. Finally,
a need exists for such an apparatus and process to be automated,
thereby requiring minimal operator intervention during the course
of normal operation.
SUMMARY OF THE INVENTION
[0022] This invention is directed to systems and methods for
removing lipids from a liquid, and more particularly, this
invention is directed to the removal of lipids from plasma or from
lipid-containing organisms using devices employing multiple
solvents. Specifically, the system is adapted to remove lipids from
a fluid after passing through the system only once.
[0023] According to one embodiment, the system for removal of
lipids from fluids or from lipid-containing organisms, or both,
typically includes three subsystems, which may include, but are not
limited to, an initial phase subsystem, an intermediate phase
subsystem, and a final phase subsystem. The initial phase subsystem
is composed in part of a fluid source, a first extraction solvent
source, and a device, such as a hollow fiber contactor (HFC), for
combining the biological source and the first extraction
solvent.
[0024] The HFC is composed of a generally hollow cylindrical body,
referred to as the shell, having a plurality of hollow fibers that
are positioned in the body generally parallel to a longitudinal
axis of the body. Each hollow fiber has a length slightly shorter
than the length of the body of the HFC and has a very small
diameter. A HFC typically has about 3,000 to about 5,000 hollow
fibers positioned within its body, but may have as few as two or
three hollow fibers or greater than 5,000 hollow fibers. An HFC is
primarily defined by several characteristics: the type of membrane
material of the hollow fiber, the type and number of holes or pores
in the membrane of the hollow fiber, the size of the pores, and the
total effective surface area of the fibers or membrane. The HFC
also contains chambers at each end to feed a fluid or gas into the
hollow fibers at one end and receive the fluid or gas at the other
end of the hollow fibers. The HFC allows another fluid or gas to
flow around the outside of the hollow fibers in a region referred
to as a chamber or the shell side of the hollow fibers. The chamber
is formed by the interior surface of the shell forming the HFC and
the outside surfaces of the hollow fibers.
[0025] For purposes of this invention, the fluid containing lipids
or lipid-containing organisms flows through the lumens of the
hollow fibers while simultaneously, the first extraction solvent
flows through the chamber on the shell side of the hollow fibers,
or vice versa. The fluid is directed through the lumens of the
hollow fibers because the volume of the lumens is less than the
shell side of the lumens; therefore, keeping the volume fluids
withdrawn from a patient to a minimum. The first extraction
solvents permeate the hollow fibers and mix with the fluids within
the lumens of the hollow fibers. The first extraction solvent
produces a suspension of lipid particles in the first mixture that
is formed from a fluid and the first extraction solvent. The
solvent disrupts the lipid-protein structure and frees the lipid
particles, which are not very soluble in the fluid.
[0026] A substantial amount of lipid is removed from the fluid due
to a diffusion gradient established between the high concentration
of lipid in the fluid in the hollow fibers and the zero or low
concentration of lipid in the extraction solvent located on the
shell side of the hollow fibers. The lipids dissolve in the
solvents, diffuse through the membranes forming the hollow fibers,
and are carried away by the extraction solvent in the shell. Some
of the lipids may also attach to the surface of the hollow fibers.
Further, some lipid particles may be removed with a filter
positioned between the initial phase subsystem and the final phase
subsystem. The concentration of lipids in the fluid after passing
through the first phase subsystem is less than the initial
concentration of lipids in the fluid prior to starting the process.
The first phase subsystem forms a first mixture of fluid containing
lipids or lipid containing organisms, or both, and first extraction
solvent. The first extraction solvent contained in the HFC on the
shell side of the hollow fibers in the first subsystem is removed
and may be discarded as waste. After passing through the first
phase subsystem, the fluid is immediately passed to the
intermediate phase subsystem.
[0027] In the intermediate phase subsystem, the first mixture
received from the initial phase subsystem is sent through at least
one HFC. The HFC may be similar or different than the HFC used in
the initial phase subsystem. More specifically, the mixture is sent
through the hollow fibers of the HFC and contacted with a second
separate extraction solvent that is contained in the HFC on the
shell side of the hollow fibers, or vice versa. The second
extraction solvent primarily removes a majority of the first
extraction solvent from the mixture of the fluid in a manner
similar to the removal process for lipid that occurs in the initial
phase subsystem. The second extraction solvent additionally removes
a portion of any residual lipids remaining in the fluid. After the
second extraction solvent has flowed through the HFC on the shell
side of the hollow fibers in the intermediate subsystem, the second
extraction solvent is deposited in an extraction solvent waste
receptacle. After leaving the intermediate phase subsystem, the
fluid contains a fraction of the original lipids, a fraction of the
first extraction solvent, and a minimal amount of the second
extraction solvent. Once the mixture of the fluid containing the
first and second extraction solvents has passed through the
intermediate phase subsystem, the mixture is transferred to the
final phase subsystem.
[0028] The final phase subsystem may be composed of a once-through
system, a recirculating system, or another system for removing
solvents. The once-through system and the recirculating system are
similar in design but have different configurations. Generally in
either system, the fluid passes through at least one HFC where it
is exposed to a gas to remove at least a portion of any remaining
solvents. The volatile solvent in the fluid evaporates into the gas
stream. In another embodiment, the gas may be replaced with mineral
oil. Removal of these solvents is accomplished by passing the
mixture through the hollow fibers of the HFC while the gas is
passed through the HFC on the shell side of the hollow fibers as
many times as necessary to remove the solvents. The gas removes the
solvents and is passed through a gas filter loop, which may be
composed of a carbon bed, a pump, at least one pressure regulator,
and at least one filter, for removing the solvents from the gas. In
other embodiments, the carbon bed may be replaced by one or more
filters, condensers or cold traps, or catalytic combusters to
remove the solvent vapors from the gas before it is recycled
through the HFC. At this point, the fluid can be safely returned to
the donor, stored, or transferred to another patient to be
administered for therapeutic purposes. If the recirculating final
phase subsystem is used, the fluid must be sent through the system
multiple times before the solvent level is reduced to a safe level
in the fluid. A sensor may be used to determine when sufficient
amounts of solvents have been removed from the fluid.
[0029] In an alternative embodiment, any one of the subsystems
described above, or any combination of these subsystems, may be
replaced by a subsystem having at least two HFCs in parallel. This
parallel subsystem allows a fluid, or a mixture of a fluid and an
extraction solvent, to flow through the hollow fibers of at least
one first HFC while a second HFC is not used. This parallel
subsystem includes sensors for detecting lipids and is coupled to a
control system that redirects the flow from the first HFC to the
second HFC when it detects the presence of lipids above a
predetermined threshold. Once the flow has been changed, the first
HFC can be washed, replaced, receive a reverse flow, or be
reoriented. This parallel subsystem enables the delipidation system
to have the capacity to run the fluid or mixture through an
operable HFC at all times. In yet another alternative embodiment, a
single HFC may be used to accomplish all three steps of this
delipidation process.
[0030] An advantage of this invention is that fluids containing
lipids and lipid containing organisms can be delipidated in a time
efficient manner because the fluid need only travel once through
the system.
[0031] Another advantage of this invention is that fluid can be
processed in a continuous manner and returned to a patient without
requiring withdrawal of an unacceptable amount of blood from the
patient.
[0032] Yet another advantage of this invention is that the system
uses HFCs to complete all aspects of the process, thereby
minimizing the number of moving parts within the system and the
likelihood of failure resulting from moving parts.
[0033] Still another advantage of this invention is that by
removing lipids from lipid-containing organisms, the infectivity of
those organisms is reduced as well.
[0034] These and other features and advantages of the present
invention will become apparent after review of the following
drawings and detailed description of the disclosed embodiments.
BRIEF DESCRIPTION OF THE DRAWINGS
[0035] The accompanying drawings, which are incorporated in and
form a part of the specification, illustrate preferred embodiments
of the present invention and, together with the description,
disclose the principles of the invention.
[0036] FIG. 1 is a block diagram of an embodiment of this
invention.
[0037] FIG. 2 is a schematic diagram of an embodiment of this
invention showing an initial phase subsystem, an intermediate phase
subsystem, and a final phase subsystem, wherein the final phase
subsystem is a once-through final phase subsystem.
[0038] FIG. 3 is a schematic diagram of an embodiment of this
invention showing a recirculating final phase subsystem.
[0039] FIG. 4 is a perspective view of a HFC with a partial cut
away section.
[0040] FIG. 5 is cross-sectional view of a portion of a hollow
fiber of a HFC, according to another aspect of the present
invention.
[0041] FIG. 6 depicts an alternative configuration of HFCs in the
subsystems.
DETAILED DESCRIPTION OF THE INVENTION
[0042] This invention relates to systems, apparatus and methods
useful for delipidation of fluids in animals, including humans. In
a preferred embodiment, the fluid is plasma; however, the fluid can
be composed of other materials, as described below. This system and
apparatus can treat arteriosclerosis and atherosclerotic vascular
diseases, and remove lipid from lipid-containing organisms or
infectious agents circulating within the blood of animals and
humans, thereby rendering these organisms less infective.
I. DEFINITIONS AND SOLVENTS
A. Definitions
[0043] The term "fluid" is defined as fluids from animals or humans
that contain lipids, fluids from culturing tissues and cells that
contain lipids, fluids mixed with lipid-containing cells, and
fluids mixed with lipid-containing organisms. For purposes of this
invention, delipidation of fluids include delipidation of cells and
organisms in a fluid. Fluids include, but are not limited to:
biological fluids, such as, blood, plasma, serum, lymphatic fluid,
cerebrospinal fluid, peritoneal fluid, pleural fluid, pericardial
fluid; various fluids of the reproductive system including, but not
limited to, semen, ejaculatory fluids, follicular fluid and
amniotic fluid; cell culture reagents such as normal sera, fetal
calf serum or serum derived from any animal or human; and
immunological reagents, such as various preparations of antibodies
and cytokines, from culturing tissues and cells, fluids mixed with
lipid-containing cells, and fluids containing a lipid-containing
organisms, such as a saline solution containing lipid-containing
organisms.
[0044] The term "hollow fiber contactor" (HFC) is defined as being
any conventional HFC or other HFC. Typically, HFCs have an outer
body, referred to as a shell and forming a chamber, for containing
a plurality of hollow fibers positioned generally parallel to a
longitudinal axis of the shell. The hollow fibers are generally
cylindrical tubes having small diameters formed by a permeable
membrane having pores that allow certain materials to pass through
the membrane. The HFC is designed to allow a first material to pass
through the lumens of the hollow fibers and a second material to
pass through the HFC on the shell side of the hollow fibers. The
first material may pass from the lumens of the hollow fibers,
through the pores of the hollow fibers and into the second material
on the shell side of the hollow fibers, or vice versa. The ability
for the materials to pass through the pores of the hollow fibers is
predicated on numerous factors, such as pore size, pressure, flow
rate, solubility, and others.
[0045] The term "lipid" is defined as any one or more of a group of
fats or fat-like substances occurring in humans or animals. The
fats or fat-like substances are characterized by their insolubility
in water and solubility in organic solvents. The term "lipid" is
known to those of ordinary skill in the art and includes, but is
not limited to, complex lipid, simple lipid, triglycerides, fatty
acids, glycerophospholipids (phospholipids), true fats such as
esters of fatty acids, glycerol, cerebrosides, waxes, and sterols
such as cholesterol and ergosterol.
[0046] The term "lipid" is also defined as including
lipid-containing organisms or lipid-containing infectious agents.
Lipid-containing infectious agents are defined as any organism or
agent containing lipids. Such lipids may be found, for example, in
a bacterial cell wall or viral envelope. Lipid-containing organisms
include, but are not limited to, eukaroyotic and prokaryotic
organisms, bacteria, viruses, protozoa, mold, fungi, and other
lipid-containing parasites.
[0047] The term "infectious organism" means any lipid-containing
infectious organism capable of causing infection. Some infectious
organisms include bacteria, viruses, protozoa, parasites, fungi and
mold. Some bacteria which may be treated with the method of this
invention include, but are not limited to, the following:
Staphylococcus; Streptococcus, including S. pyogenes; Enterococci,
Bacillus, including Bacillus anthracis, and Lactobacillus;
Listeria; Corynebacterium diphtheriae; Gardnerella including G.
vaginalis; Nocardia; Streptomyces; Thermoactinomyces vulgaris;
Treponema; Camplyobacter; Pseudomonas including P. aeruginosa;
Legionella; Neisseria including N. gonorrhoeae and N. meningitides;
Flavobacterium including F. meningosepticum and F. odoratum;
Brucella; Bordetella including B. pertussis and B. bronchiseptica;
Escherichia including E. coli; Klebsiella; Enterobacter; Serratia
including S. marcescens and S. liquefaciens; Edwardsiella; Proteus
including P. mirabilis and P. vulgaris; Streptobacillus;
Rickettsiaceae including R. rickettsii; Chlamydia including C.
psittaci and C. trachomatis; Mycobacterium including M.
tuberculosis, M. intracellulare, M. fortuitum, M. laprae, M. avium,
M. bovis, M africanum, M. kansasii, M. intracellulare, and M.
lepraemurium; and Nocardia, and any other bacteria containing lipid
in their membranes.
[0048] Viral infectious organisms which may be inactivated by the
above system include, but are not limited to, the lipid-containing
viruses of the following genuses: Alphavirus (alphaviruses),
Rubivurus (rubella virus), Flavivirus (Flaviviruses), Pestivirus
(mucosal disease viruses), (unnamed, hepatitis C virus),
Coronavirus, (Coronaviruses), Torovirus, (toroviruses), Arteivirus,
(arteriviruses), Paramyxovirus, (Paramyxoviruses), Rubulavirus
(rubulavriuses), Morbillivirus (morbillivuruses), Pneumovirinae
(the pneumoviruses), Pneumovirus (pneumoviruses), Vesiculovirus
(vesiculoviruses), Lyssavirus (lyssaviruses), Ephemerovirus
(ephemeroviruses), Cytorhabdovirus (plant rhabdovirus group A),
Nucleorhabdovirus (plant rhabdovirus group B), Filovirus
(filoviruses), Influenzavirus A, B (influenza A and B viruses),
Influenza virus C (influenza C virus), (unnamed, Thogoto-like
viruses), Bunyavirus (bunyaviruses), Phlebovirus (phleboviruses),
Nairovirus (nairoviruses), Hantavirus (hantaviruses), Tospovirus
(tospoviruses), Arenavirus (arenaviruses), unnamed mammalian type B
retroviruses, unnamed, mammalian and reptilian type C retroviruses,
unnamed type D retroviruses, Lentivirus (lentiviruses), Spumavirus
(spumaviruses), Orthohepadnavirus (hepadnaviruses of mammals),
Avihepadnavirus (hepadnaviruses of birds), Simplexvirus
(simplexviruses), Varicellovirus (varicelloviruses),
Betaherpesvirinae (the cytomegaloviruses), Cytomegalovirus
(cytomegaloviruses), Muromegalovirus (murine cytomegaloviruses),
Roseolovirus (human herpes virus 6), Gammaherpesvirinae (the
lymphocyte-associated herpes viruses), Lymphocryptovirus
(Epstein-Bar-like viruses), Rhadinovirus (saimiri-ateles-like
herpes viruses), Orthopoxvirus (orthopoxviruses), Parapoxvirus
(parapoxviruses), Avipoxvirus (fowlpox viruses), Capripoxvirus
(sheeppoxlike viruses), Leporipoxvirus (myxomaviruses), Suipoxvirus
(swine-pox viruses), Molluscipoxvirus (molluscum contagiosum
viruses), Yatapoxvirus (yabapox and tanapox viruses), Unnamed,
African swine fever-like viruses, Iridovirus (small iridescent
insect viruses), Ranavirus (front iridoviruses), Lymphocystivirus
(lymphocystis viruses of fish), Togaviridae, Flaviviridae,
Coronaviridae, Enabdoviridae, Filoviridae, Paramyxoviridae,
Orthomyxoviridae, Bunyaviridae, Arenaviridae, Retroviridae,
Hepadnaviridae, Herpesviridae, Poxviridae, and any other
lipid-containing virus.
[0049] These viruses include the following human and animal
pathogens: Ross River virus, fever virus, dengue viruses, Murray
Valley encephalitis virus, tick-borne encephalitis viruses
(including European and far eastern tick-borne encephalitis
viruses, human coronaviruses 229-E and OC43 and others (causing the
common cold, upper respiratory tract infection, probably pneumonia
and possibly gastroenteritis), human parainfluenza viruses 1 and 3,
mumps virus, human parainfluenza viruses 2, 4a and 4b, measles
virus, human respiratory syncytial virus, rabies virus, Marburg
virus, Ebola virus, influenza A viruses and influenza B viruses,
Arenaviruss: lymphocytic choriomeningitis (LCM) virus; Lassa virus,
human immunodeficiency viruses 1 and 2, or any other
immunodeficiency virus, hepatitis A virus, hepatitis B virus,
hepatitis C virus, Subfamily: human herpes viruses 1 and 2, herpes
virus B, Epstein-Barr virus), (smallpox) virus, cowpox virus,
molluscum contagiosum virus.
[0050] All protozoa containing lipid, especially in their plasma
membranes, are included within the scope of the present invention.
Protozoa that may be inactivated by the system and apparatus of the
present invention include, but are not limited to, the following
lipid-containing protozoa: Trypanosoma brucei, Trypanosoma
gambiense, Trypanosoma cruzi, Leishmania donovani, Leishmania
vianni, Leishmania tropica, Giardia lamblia, Giardia intestinalis,
Trichomonas vaginalis, Entamoeba histolytica, Entamoeba coli,
Entamoeba hartmanni Naegleria species, Acanthamoeba species,
Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae,
Plasmodium ovale, Toxoplasma gondii, Cryptosporidium parvum,
Cryptosporidium muris, Isospora belli, Cyclospora cayetansis,
Balantidium species, Babesia bovis, Babesia, microti, Babesia
divergens, Encephalitozoon intestinalis, Pleistophora species,
Nosema ocularum, Vittaforma corneae, Septata intestinalis,
Enterocytozoon, Dientamoeba fragilis, Blastocystis species,
Sarcocystis species, Pneumocystis carinii, Microsporidium
africanum, Microsporidium ceylonensis, Eimeria acervulina, Eimeria
maxima, Eimeria tenella and Neospora caninum and any other
lipid-containing protozoa. It is to be understood that the present
invention is not limited to the protozoa provided in the list
above.
[0051] A preferred protozoa treated with the method of the present
invention is Coccidia, which includes Isospora species,
Cryptosporidium species, Cyclospora species, Toxoplasma species,
Sarcocystis species, Neospora species, and Eimeria species. These
coccidian parasites cause intestinal disease, lymphadenopathy,
encephalitis, myocarditis, and pneumonitis.
[0052] The terms "protozoal infection" or "infectious disease" mean
diseases caused by protozoal infectious organisms. The diseases
include, but are not limited to, African sleeping sickness, Chagas'
disease, Leishmaniasis, Giardiasis, Trichomoniasis, amebiasis,
primary amebic encephalitis, granulomatous amebic encephalitis,
malaria, Toxoplasmosis, Cryptosporidiosis, Isosporiasis,
Cyclosporiasis, Balantidiasis, Babesiosis, microsporidiosis,
Dientamoeba fragilis infection, Blastocystis hominis infection,
Sarcosporidiosis, pneumonia, and coccidiosis. A preferred protozoal
infection treated with the method of the present invention is
Coccidiosis, which is caused by Isospora species, Cryptosporidium
species, Cyclospora species, Toxoplasma species, Sarcocystis
species, Neospora species, and Eimeria species. These coccidian
parasites cause human intestinal disease, lymphadenopathy,
encephalitis, myocarditis, and pneumonitis. These coccidian
parasites also cause disease in animals, including cattle, dogs,
cats, and birds. Avians, and chickens, turkeys and quail in
particular, are affected by Coccidiosis, especially by Eimeria
species such as E. acervulina, E. maxima, E. necatrix, E. bruneti,
E. mitis, E. praecox and E. tenella.
[0053] The term "continuous" refers to the process of delipidating
a fluid, such as plasma, while the animal or human remains
connected to an apparatus for delipidating the fluid. Additionally,
"continuous" refers to the internal processes of the lipid removal
system, wherein the fluid continually flows within the lipid
removal system from subsystem to subsystem.
[0054] The term "batch" refers to the process of delipidating a
fluid, such as plasma, without returning or passing the delipidated
fluid directly to the animal or human during the delipidation
process. Rather, the delipidated fluid is stored. Additionally,
"batch" refers to the internal process of the lipid removal
machine, wherein the fluid does not continually flow within the
lipid removal system from subsystem to subsystem.
[0055] The term "delipidation" refers to the process of removing at
least a portion of a total concentration of lipids from a fluid or
from a lipid-containing organism.
[0056] The term "first extraction solvent" is defined as one or
more solvents used in the initial stage subsystem for extracting
lipids from a fluid containing lipids or from lipid-containing
organisms. The first extraction solvent enters the fluid and
remains in the fluid until removed by other subsystems. Suitable
extraction solvents include solvents that extract or dissolve
lipids, including, but not limited to, alcohols, phenols,
hydrocarbons, amines, ethers, esters, halohydrocarbons,
halocarbons, and combinations thereof. Preferred first extraction
solvents are combinations of alcohols and ethers, which include,
but are not limited to, n-butanol, di-isopropyl ether or isopropyl
ether, which are both referred to as (DiPE), diethyl ether (DEE),
sevoflourane, perfluorocyclohexanes, trifluoroethane, isoflurane,
cyclofaorohexanol and combinations thereof.
[0057] The term "second extraction solvent" is defined as one or
more solvents that facilitate removal of at least a portion of the
first extraction solvent. Suitable second extraction solvents
include any solvent that facilitates removal of the first
extraction solvent mixed with or exposed to the fluid containing
lipids or lipid-containing organisms, or both. Second extraction
solvents include any solvent that facilitates removal of the first
extraction solvent including, but not limited to, ethers, alcohols,
phenols, hydrocarbons, amines, esters, halohydrocarbons,
halocarbons, and combinations thereof. Preferred second extraction
solvents include an ether, such as diethyl ether, which facilitates
removal of lower order alcohols, such as n-butanol, from the
fluid.
[0058] The term "patient" refers to animals and humans, which may
be either a fluid source or a recipient of delipidated fluid or
delipidated organisms.
B. Solvents
[0059] Numerous organic solvents may be used in the method of this
invention for removal of lipid from fluids and from
lipid-containing organisms, especially infectious organisms,
provided that the solvents or combinations thereof are effective in
solubilizing lipids. Suitable solvents comprise mixtures of
hydrocarbons, ethers, alcohols, phenols, esters, halohydrocarbons,
halocarbons and amines. Other solvents which may be used with this
invention include amines and mixtures of amines. Preferred solvents
are combinations of alcohols and ethers. Another preferred solvent
comprises an ether or combinations of ethers. It is preferred that
the solvent or combination of solvents has a relatively low boiling
point to facilitate removal of the solvent via a combination of
vacuum and possibly heat applications.
[0060] Examples of suitable amines for use in removal of lipids
from lipid-containing organisms are those which are substantially
water immiscible. Typical amines are aliphatic amines having a
carbon chain of at least 6 carbon atoms. A non-limiting example of
such an amine is C.sub.6H.sub.13NH.sub.2. Another suitable amine is
perfluorotributyl amine.
[0061] The alcohols which are preferred for use in this invention,
when used alone, include those alcohols that are not appreciably
miscible with plasma or other fluids. Such alcohols include, but
are not limited to, straight chain and branched chain alcohols,
including pentanols, hexanols, heptanols, octanols, and alcohols
containing higher numbers of carbons. Halogenated alcohols may be
employed, including, but not limited to, heptafluoro-butanol.
[0062] When alcohols are used in combination with another solvent,
for example, an ether, a hydrocarbon, an amine, or a combination
thereof, C.sub.1-C.sub.8 containing alcohols may be used. Preferred
alcohols for use in combination with another solvent include
C.sub.4-C.sub.8 containing alcohols. Accordingly, preferred
alcohols are butanols, pentanols, hexanols, such as 1-hexanol,
heptanols, octanols, and ethanols, and iso forms thereof.
Particularly preferred are the butanols (1-butanol and 2-butanol).
As stated above, the most preferred alcohol is the C.sub.4 alcohol,
butanol. The specific choice of alcohol will depend on the second
solvent employed. In a preferred embodiment, lower alcohols are
combined with lower ethers.
[0063] Ethers, used alone, or in combination with other solvents,
preferably alcohols, are another preferred solvent for use in the
method of the present invention. Particularly preferred ethers are
the C.sub.4-C.sub.8 containing-ethers, including but not limited
to, diethyl ether, and propyl ethers, including, but not limited
to, di-isopropyl ether. Asymmetrical ethers and halogenated ethers
may also be employed. Also useful in the present invention are
combinations of ethers, such as di-isopropyl ether and diethyl
ether. When ethers and alcohols are used in combination as a first
solvent for contacting the fluid containing lipids or
lipid-containing organisms, or both, any combination of alcohol and
ether may be used provided the combination is effective to
partially or completely remove lipids from the fluid or the
lipid-containing organism.
[0064] In one embodiment, lipids are removed from the viral
envelope or bacterial cell wall of the infectious organism, which
reduces the infectivity of the virus or bacteria. When alcohols and
ether are combined as a first extraction solvent for removing
lipids from a fluid containing lipids or lipid-containing
organisms, or both, preferred ratios of alcohol to ether in this
solvent are about 0.01%-60% alcohol to about 40%-99.99% of ether,
with a preferred ratio of about 10%-50% of alcohol with about
50%-90% of ether, with a most preferred ratio of about 20%-45%
alcohol and about 55%-80% ether. An especially preferred
combination of alcohol and ether is the combination of butanol and
di-isopropyl ether. Another especially preferred combination of
alcohol and ether is the combination of butanol with diethyl
ether.
[0065] When butanol and di-isopropyl ether are combined as a first
extraction solvent for removing lipids from a fluid containing
lipids or from lipid-containing organisms, or both, contained in a
fluid, preferred ratios of butanol to di-isopropyl ether in this
solvent are about 0.01%-60% butanol to about 40%-99.99% of
di-isopropyl ether, with a preferred ratio of about 10%-50% of
butanol with about 50%-90% of di-isopropyl ether, with a most
preferred ratio of about 20%-45% butanol and about 55%-80%
di-isopropyl ether. The most preferred ratio of butanol and
di-isopropyl ether is about 40% butanol and about 60% di-isopropyl
ether.
[0066] When butanol is used in combination with diethyl ether in a
first extraction solvent, preferred ratios of butanol to diethyl
ether in this combination are about 0.01%-60% butanol to about
40%-99.99% diethyl ether, with a preferred ratio of about 10%-50%
butanol with about 50%-90% diethyl ether, with a most preferred
ratio of about 20%-45% butanol and about 55%-80% diethyl ether. The
most preferred ratio of butanol and diethyl ether in a first
solvent is about 40% butanol and about 60% diethyl ether.
[0067] Hydrocarbons in their liquid form dissolve compounds of low
polarity such as the lipids in fluids and lipids found in membranes
of organisms. Hydrocarbons which are liquid at about 37.degree. C.
are effective in disrupting a lipid membrane of an infectious
organism. Accordingly, hydrocarbons comprise any substantially
water immiscible hydrocarbon which is liquid at about 37.degree. C.
Suitable hydrocarbons include, but are not limited to, the
following: C.sub.5 to C.sub.20 aliphatic hydrocarbons such as
petroleum ether, hexane, heptane, and octane; haloaliphatic
hydrocarbons such as chloroform, trifluoroethane,
1,1,2-trichloro-1,2,2-trifluoroethane, 1,1,1-trichloroethane,
trichloroethylene, tetrachloroethylene dichloromethane and carbon
tetrachloride; thioaliphatic hydrocarbons; perfluorocarbons, such
as perfluorocyclohexane, perfluorohexane,
perfluoromethylcyclohexane, and perfluorodimethylcyclohexane;
fluoroethers such as sevoflurane; each of which may be linear,
branched or cyclic, saturated or unsaturated; aromatic hydrocarbons
such as benzene; alkylarenes such as toluene, haloarenes,
haloalkylarenes and thioarenes. Other suitable solvents may also
include: saturated or unsaturated heterocyclic compounds such as
water insoluble derivatives of pyridine and aliphatic, thio or halo
derivatives thereof; and perfluorooctyl bromide. Another suitable
solvent is perfluorodecalin.
II. OVERVIEW
[0068] For purposes of explanation, the removal of lipids from
plasma, termed delipidation, is discussed in detail. However, this
is not meant to limit the application of the invention solely to
delipidation of plasma. Rather, the same principles and process
apply to other fluids and to removal of lipids from
lipid-containing organisms. The delipidation system 10 of this
invention receives fluid from a patient, or other source, removes
lipids contained within the fluid, and returns the delipidated
fluid to the patient, or other source. The delipidation system of
this invention may be used as a continuous system, by returning
fluid to a patient immediately after lipids have been removed, or
as a batch system by removing lipids from the fluid without
immediately returning the fluids to the patient.
[0069] In one embodiment of this invention, as shown in FIG. 1, the
invention may be used to delipidate plasma. For instance, whole
blood is drawn from a patient using conventional procedures and
subjected to a conventional plasma separation process. Such
cellular separation systems include, but are not limited to,
apheresis and plasmapheresis systems, such as SPECTRA and TRIMA
manufactured by Cobe BCT, Gambro BCT, Lakewood, Colo.;
AUTOPHERESIS-C manufactured by Baxter Healthcare Corporation,
Deerfield, Ill.; or AS104 manufactured by Fresenius, Berlin,
Germany. In another embodiment, blood is combined with an
anticoagulant, such as sodium citrate, and centrifuged at forces
approximately equal to 2,000 times gravity. The red blood cells are
then aspirated from the plasma. This plasma separation process
returns the blood cells to the patient and collects the plasma. The
plasma, or lipid-containing organisms therein, are then subjected
to the lipid removal process of this invention, which is described
in detail below.
[0070] In general, the delipidation method includes multiple phases
including, but not limited to, an initial phase, an intermediate
phase, and a final phase. The initial phase removes lipids from a
fluid, for example plasma, or from at least one lipid-containing
organism, using a first extraction solvent. The intermediate phase
completes the delipidation process and removes at least a portion
of the first extraction solvent, as well as residual lipids, from
the fluid using a second extraction solvent. The final phase
removes the remainder of the first extraction solvent and the
majority of the second extraction solvent from the fluid using an
inert gas, such as air, or mineral oil, so that the delipidated
fluid can be administered to a patient. The delipidated plasma is
then in a condition to be returned to the patient or stored for
administration to another patient for therapeutic applications.
III. THE DELIPIDATION SYSTEM
[0071] The delipidation system 10 is composed of at least three
phases for delipidating a fluid containing lipids or
lipid-containing organisms, or both, which include an initial
phase, an intermediate phase, and a final phase. As is illustrated
in FIG. 2, the initial phase may be carried out using an initial
phase subsystem 11 composed of a first extraction solvent source
12, an extraction solvent waste receptacle 13, a fluid source 14,
and at least one hollow fiber contactor (HFC) 16. The intermediate
phase may be carried out using intermediate phase subsystem 29,
which may include at least one HFC, and in one embodiment, may
include three HFCs 34, 36 and 38, for completing the delipidation
process and removing at least a portion of the first extraction
solvent. The final phase may be carried out using final phase
subsystem 47, which may be composed of either a once-through final
phase subsystem 41 or a recirculating final phase subsystem 43
shown in FIG. 3, both of which are composed of at least one
HFC.
[0072] The number of HFCs used in each subsystem may be dictated by
the amount of lipids desired to be removed. The number and size of
the HFCs are a function of the flow rate of fluids or gases within
the hollow fibers and in the chamber formed by the shell of the HFC
and the outside surfaces of the hollow fibers, the porosity of the
hollow fibers, and the amount of surface area of the hollow fiber.
Adjusting one of these factors requires the other factors be
changed in order to yield the same output at the same rate.
Additionally, patients having a higher initial starting level of
lipids may require greater surface area of hollow fibers to be used
to obtain therapeutic effects.
A. Initial Phase Subsystem
[0073] Initial phase subsystem 11 is used to at least partially
delipidate a fluid. In one embodiment, a substantial amount of the
lipid may be removed from a fluid within initial phase subsystem 11
using at least one HFC 16 and a first extraction solvent. Initial
phase subsystem 11 may include two or more HFCs 16 coupled in
series or parallel, or any combination thereof, such as the
configuration shown as final phase subsystem 43 and 41 in FIGS. 2
and 3. As shown in FIG. 2 and in more detail in FIGS. 4 and 5, HFC
16 has a generally cylindrical body that contains a plurality of
hollow fibers 20, which typically number between about 3,000 and
about 5,000, and a chamber 22 formed by the inside surface of the
cylindrical exterior wall of HFC 16, referred to as the shell side
of the membranes. Each hollow fiber 20 is a cylindrical tube formed
from a membrane having a small diameter, such as between about 0.2
millimeters and about 1.0 millimeters, and pores 28 sized to allow
gases and liquids to pass through hollow fiber 20. Hollow fibers 20
are positioned in a HFC so that their longitudinal axes are
generally parallel to the longitudinal axis of the HFC. Pores 28
need only be large enough to allow the first and second extraction
solvents to diffuse through pores 28 into the plasma and for the
lipids to diffuse through pores 28 and into the solvents or attach
to the inside surfaces of hollow fibers 20 or pores 28. Pores 28
may have a diameter within the range of between about 5 kilodaltons
and about 500 kilodaltons or between about 3 nanometers and about
300 nanometers. Varying the size of pores 28 can allow either more
or less materials to pass through pores 28.
[0074] While not being bound by the following statements, the
following discussion is a possible explanation of the operation of
the system at the pores 28 of the hollow fibers 20. The hollow
fibers 20 may be formed of either hydrophobic or hydrophilic
materials. If hollow fibers 20 formed from a hydrophobic material
are used, the solvent fills pores 28, and an interface forms
between the solvent in pores 28 and the fluid that remains in the
lumens. The solvent diffuses across the interface into the fluid,
but there is minimal, if any, mixing of the fluid and the solvent.
Thus, there exists very little possibility of an emulsion forming.
The lipids that may have been solubilized by the action of the
solvents diffuse into the solvent in the pores 28 at the interface.
The lipids continue to diffuse through pores 28 until the lipids
are swept away by the solvent flowing through HFC 16 on the shell
side of the lumens. If a hydrophilic material is used to form
hollow fibers 20, pores 28 fill with fluid, and the solvent does
not fill pores 28. The lipids then diffuse through pores 28.
[0075] The preferred material is a hydrophobic material because the
highest transport rate is achieved when pores 28 are filled with
the material having the highest solubility for the material desired
to be passed through pores 28. In this case, lipids are more
soluble in the solvents described above than in the fluid. Thus, a
hydrophobic material is preferred.
[0076] The flow rate of the fluid and first extraction solvent
dictates the required amount of permeable surface area on hollow
fibers 20. For instance, the slower the flow rate, the smaller the
surface area required, and conversely, the faster the flow rate,
the larger the surface area required. This is dictated by a mass
transport formula. The formula below illustrates the situation for
a soluble gas:
Q 1 ( C i n - C out ) = K 1 A m .DELTA. C l m = K l A m ( C i n - P
out H ) - ( C out - P i n H ) ln C i n - P out H C out - P out H
##EQU00001##
where C.sub.out represents the liquid phase concentration (output),
C.sub.in represent the liquid phase id concentration (input),
K.sub.1 represents the overall mass transport coefficient, A.sub.m
represents the total membrane contact area, Q.sub.1 represents the
liquid flow rate, H represents the Henry's Law coefficient and P
represents the gas phase partial pressure. If P.sub.in and
P.sub.out are small in magnitude and/or H is large, the terms P and
H are negligible. In this case, the first equation simplifies
to:
C out = C i n ln ( - K l A m Q 1 ) . ##EQU00002##
Examples of commercially available HFCs are the CELGARD mini model
no. G471, G476, G478, or G495 available from CelGard, Charlotte,
N.C., and the Spectrum MINIKROS model no. M21S-600-01N, available
from Spectrum Laboratories, Inc., Rancho Dominguez, Calif.
[0077] The first extraction solvent source 12 may be any device or
system capable of the supplying a first extraction solvent to
system 10. First extraction solvent source 12 is coupled to chamber
22 of HFC 16 using conduit 18, which can be formed from pipe,
tubing, or other such devices. The first extraction solvent may be
feed to chamber 22 via gravity, pump 15, or other such means. Pump
15 is coupled to conduit 18 between first extraction solvent source
12 and HFC 16 for pumping the first extraction solvent from first
extraction source 12 to HFC 16. In one embodiment, pump 15 is a
peristaltic pump, such as MASTERFLEX L/S model number 07523-40
available from Cole Parmer Instrument Company, Vernon Hills, Ill.,
or other pumps not having vanes that contact the fluid being
pumped.
[0078] In one embodiment, initial phase subsystem 11 includes an
extraction solvent waste receptacle 13 that is coupled to HFC 16
using conduit 25 for containing the first extraction solvent after
it has passed from first extraction solvent source 12 through HFC
16. First extraction solvent source 12 and extraction solvent waste
receptacle 13 may be composed of a tank, a flask, or other devices
known to those skilled in the art for containing solvents.
[0079] Fluid source 14 is coupled to HFC 16 using conduit 27. Fluid
source 14 may be composed of a tank, a flask, a plasmapheresis bag,
and other devices known to those skilled in the art for containing
a fluid. In one embodiment, a pump 17 is coupled to conduit 27
between fluid source 14 and HFC 16 for transferring fluid from
fluid source 14 to HFC 16. Pump 17 can be a peristaltic pump, such
as MASTERFLEX L/S model number 07523-40 available from Cole Parmer
Instrument Company, Vernon Hills, Ill., or other pumps not having
vanes that contact the fluid being pumped. A valve 19 can be
located between fluid source 14 and HFC 16, and, more specifically,
between fluid source 14 and pump 17 for controlling the release of
fluids from fluid source 14. Valve 19 can be composed of, but is
not limited to, pinch, globe, ball, gate, or other conventional
valves.
[0080] A saline fluid source 21 is coupled to HFC 16 using conduit
27 for containing a saline fluid and may be composed of a tank,
sealed bag, flask or other similar device for containing fluids.
Release of the saline fluid can be controlled using a valve 23 that
may be similar or identical to valve 19.
B. Intermediate Phase Subsystem
[0081] System 10 further includes an intermediate phase subsystem
29 for completing the delipidation process and for removing a
significant portion of the first extraction solvent from the
mixture of fluid and first extraction solvent. This is accomplished
by using at least one HFC to introduce a second extraction solvent
to the mixture of the fluid and the first extraction solvent. In
embodiments having two or more HFCs, the HFCs may be coupled
together in series or in parallel, as shown in final phase
subsystems 43 and 47 in FIGS. 2 and 3. In one embodiment,
intermediate phase subsystem 29 includes three HFCs 34, 36, and 38,
which each have generally the same integral components as HFC 16
and are coupled together in series. Three HFCs are used to obtain
the proper amount of membrane surface area using commonly available
conventional HFCs. The amount of surface area needed is determined
using the mass transport formula described above. In one
embodiment, the total permeable membrane surface area contained
within the HFCs is about 3.3 square meters and is designed to be
used with a flow rate of fluid of about 20 milliliters per minute
and to reduce n-butanol, which was introduced in initial phase
subsystem 11, from a concentration of approximately 40,000 parts
per million (ppm) to about 0 ppm when washed with DiPE flowing at
40 milliliter per minute. However, the amount of surface area may
vary depending on the factors set forth above. The plurality of
hollow fibers 35, 37 and 39 of HFCs 34, 36 and 38 are coupled
together using conduit 40, which can be composed of flexible or
rigid pipe, tubing or other devices. Similarly, chambers 70, 72,
and 74 of HFCs 34, 36 and 38 are coupled together using conduit 42,
which can be composed of flexible or rigid pipe, tubing or other
devices. In addition, intermediate phase subsystem 29 includes a
second extraction solvent source 44, which is coupled to chamber 22
of HFC 38 through conduit 42.
[0082] In one embodiment, a pump 45 is coupled to conduit 42
between second extraction solvent source 44 and HFC 38 for
transferring the second extraction solvent from second extraction
solvent source 44 to HFC 38. Pump 45 can include, but is not
limited to, a peristaltic pump, such as MASTERFLEX L/S model number
07523-40 from Cole Parmer Instrument Company, Vernon Hills, Ill.,
or other pumps. Extraction solvent waste receptacle 13 is coupled
to chamber 22 of HFC 34 through conduit 42 to receive waste second
extraction solvent.
C. Final Phase Subsystem
[0083] System 10 also includes final phase subsystem 47 for
removing the first and second extraction solvents from the fluid so
that the fluid can be safely administered to the patient from which
the fluid was taken, to another patient for therapeutic
applications, placed in storage for later use, or for another
purpose. Final phase subsystem can be composed of at least two
embodiments. One embodiment is capable of removing substantially
all residual solvent from a fluid after passing the fluid through
the system only one time. This system is referred to as a
once-through final phase subsystem 41 and is shown schematically in
FIG. 2. Another embodiment requires that the fluid be recirculated
through a system multiple times to reduce the amount of residual
solvent in the fluid to a level that will allow the fluid to be
administered to a patient without the patient experiencing
undesirable effects. This system is referred to as a recirculating
final phase subsystem 43 and is shown schematically in FIG. 3.
[0084] 1. Once-Through Solvent Removal Subsystem
[0085] In the once-through embodiment, final phase subsystem 41 is
composed of at least one HFC 48. In one embodiment, final phase
subsystem 41 is composed of at least two HFCs 48 and 49, each
having the same general internal configuration as the HFCs
previously described. HFC 48 includes a plurality of hollow fibers
76 that are coupled to a pervaporation buffer source 30 through
conduit 50. Conduit 50 can be composed of flexible or rigid pipe,
tubing or other such devices known to those of ordinary skill in
the art. The plurality of hollow fibers 76 of HFC 48 are coupled to
the hollow fibers 78 of HFC 49 through conduit 51. Final phase
subsystem 41 may also include a delipidated fluid receptacle 66 for
collecting the delipidated fluid after it has passed through HFCs
48 and 49. Delipidated fluid receptacle 66 may be composed of a
flexible, sterile bag, a tank or other such device. In one
embodiment, delipidated fluid receptacle 66 can be coupled directly
to a patient for administering the delipidated fluid to the
patient. However, the delipidated fluid receptacle 66 is not
required to be coupled to a patient.
[0086] Final phase subsystem 41 also includes pervaporation buffer
source 30, which may be coupled to conduit 50 between HFC 38 and
HFC 48. Pervaporation buffer source 30 allows final phase subsystem
41 to be turned on or off using a valve. Pervaporation buffer
source 30 includes a sensor 31 for detecting levels of first
extraction solvents or second extraction solvents, or both, within
the fluid. In one embodiment, sensor 31 can be adapted to detect an
extraction solvent composed of n-butanol. In another embodiment,
three-way valve 32 is coupled to conduit 50 for diverting fluid
that sensor 31 has shown as containing a second solvent above a
particular threshold to intermediate phase subsystem 29 through
conduit 33.
[0087] Once-through final phase subsystem 41 includes a gas
filtering loop 52 for removing the first and second extraction
solvents from a gas used in the subsystem 41. In one embodiment,
gas filtering loop 52 can include, but is not limited to, a carbon
bed 54, a first filter 56, a second filter 58, a first pressure
regulator 60, a second pressure regulator 62 and a pump 64. These
elements may be coupled together using a conduit, a coupling or
other connection device. Suitable filters may have a lipophilic or
hydrophilic membranes. First and second filters 56 and 58 maybe
sterile filters for preventing contamination of the system if pump
64 is removed. Carbon bed 54 is coupled to HFCs 48 and 49 for
receiving gases having first and second extraction solvents. Carbon
bed 54 removes most of the first and second extraction solvents
from the gases being passed through the chambers 22 of HFCs 48 and
49. The remainder of the first and second extraction solvents are
removed using first and second filters 56 and 58. Gas filtering
loop 52 includes pump 64 for circulating the gases through the gas
filtering loop 52 and through HFCs 48 and 49. Pump 64 may include,
but is not limited to, a vacuum pump. Gas filtering loop 52
includes a vent 68 adapted to release the gas from loop 52 if
desired. In other embodiments, the concentration of solvents in the
gas loop may be reduced by using one or more filters, a condenser,
a cold trap, or a catalytic combustor, in place of, or in addition
to, the carbon bed.
[0088] HFCs 48 and 49 have been tested and successfully reduce
total concentrations of solvents, such as di-isopropyl ether and
di-ethyl ether, in water and plasmas, such as human and bovine
plasma, using different HFCs, pressures, and flow rates, as shown
in Table 1 below. Table 2 below shows the reduction in
concentrations of DiPE in water, bovine plasma and human plasma as
a function of time. HFCs 48 and 49 may have a total surface area of
permeable membrane formed by the hollow fibers between about 4,200
square centimeters and about 18,000 square centimeters, depending
on the type of HFC used. Further, the gas flow rate was varied
between about 2 liters per minute to about 10 liters per minute,
and the plasma flow rate was varied between about 10 mL per minute
to about 60 mL per minute. Operating the once-through final
subsystem 99 in this manner can reduce the initial concentrations
of solvents from between about 28,000 ppm and 9,000 ppm to By
between about 1327 ppm and about 0.99 ppm within between about 14
minutes and 30 minutes.
TABLE-US-00001 TABLE 1 Initial Lumen Pressure Pressure Volume DIPE
Final Module Flow rate Air Flow before HFC after HFC Carbon Treated
conc DIPE (Quantity) Orientation Phase (cc/min) (L/min) (psig)
(psig) (g) (L) ppm conc ppm Effect of Module Fresenius F6 (1) Horiz
H.sub.2O 20 9.3 0.44 -0.74 100 0.75 9045 1327 & F8 (1) Spectrum
Horiz H.sub.2O 20 ~9 -0.13 -1.01 100 0.75 9684 3 11200 cm.sup.2 (2)
Celgard (1) Vertical H.sub.2O 20 11 -0.2 -1.21 100 0.5 10518 0.99
Spectrum Horiz Human 20 9.2 0.91 -0.06 100 0.75 12200 6 11200
cm.sup.2 (2) Plasma Celgard (2) Vertical Human 20 10.1 -0.16 -1.3
150 0.25 27822 9 Effect of Flow Rate Spectrum Horiz H.sub.2O 18
0.71 -0.83 0.75 9055 18 11200 cm.sup.2 (2) Spectrum Horiz H.sub.2O
20 0.65 -0.88 0.75 8851 22 11200 cm.sup.2 (2) Spectrum Horiz
H.sub.2O 40 0.7 -0.85 0.75 10016 11 11200 cm.sup.2 (2) Spectrum
Horiz H.sub.2O 60 0.65 -0.82 100 0.75 10134 93 11200 cm.sup.2 (2)
Celgard (1) Vertical H.sub.2O 20 9.3 0.44 -0.2 100 0.75 7362 22
Celgard (1) Vertical H.sub.2O 40 9.2 0.44 -0.2 100 0.75 9366 193
Effects of Pressure Celgard (2) Vertical Human 20 9.7 0.11 -1.33
100 0.25 18782 ND Celgard (2) Vertical Human 20 9.2 -1.39 -2.93 100
0.25 15246 ND Celgard (2) Vertical Human 20 8.1 -2.79 -4.12 100
0.25 13144 ND Full Body Volume Celgard (2) Vertical Human 20 5.3
-1.1 -1.8 300 3100 9040 24
TABLE-US-00002 TABLE 2 DIPE concentrations [ppm] Time [min] Water
Bovine Human (Norm) 0 6782.094027 9473.974574 11351.10738 2
1716.182938 3012.065643 3868.491245 4 118.591244 485.1426701
636.1926821 6 16.36572648 102.9572692 125.8618995 8 5.364620368
36.33996072 60.440048 10 4.230662874 16.08489373 34.50180421 12
2.019251402 23.54890574 16.71332069 14 1.537721419 9.218693213
17.32898791 16 3.169227108 6.549024255 15.26858655
[0089] 2. Recirculating Solvent Removal Subsystem
[0090] In another embodiment as shown in FIG. 3, the final phase
subsystem may be composed of a recirculating final phase subsystem
43 requiring that a fluid be passed multiple times through the
subsystem before the residual extraction solvents have been removed
to an acceptable level. Recirculating final phase subsystem 43
differs from the once-through final phase subsystem 41 in that the
flow rate of the fluid in the recirculating final phase subsystem
43 is much faster than the flow rate of the fluid through the
once-through final phase subsystem 41. The controlling parameters
are residence time in the HFC, which is dictated by the flow rate,
and interior volume of the HFC.
[0091] Recirculating final phase subsystem 43 is similar in design
to the once-through final phase subsystem 41 described above.
Specifically, the recirculating final phase subsystem 43 includes a
re-circulating vessel 90 coupled to at least two HFCs 92 and 94 in
a parallel configuration. The export ports 97 and 99 of HFCs 92 and
94 are in turn coupled to an input port 93 of recirculating vessel
90. Recirculating vessel 90 also includes a port 95 for receiving
fluid from intermediate phase subsystem 29. Recirculating vessel 90
may be composed of a flexible, sterile bag, a tank or other such
device. Recirculating vessel 90 is coupled to pump 96 for
circulating a fluid through the subsystem 41. Valves 98 and 100 are
positioned to control the flow of fluid by either causing the fluid
to be recirculated around the system or to be released to output
buffer 102.
[0092] Recirculating final phase subsystem 43 includes a solvent
sensor 104 and a pressure sensor 106 for controlling the system. In
addition, the subsystem 43 includes gas filtering loop 52, which
includes a carbon bed 108, a first filter 110, a pump 112, and a
second filter 114 for removing extraction solvent from a gas used
in HFCs 92 and 94 in the same manner as described for the
once-through final subsystem 41. Suitable filters may have
lipophilic or hydrophilic membranes. First filter 110 and second
filter 114 provide a sterile barrier between pump 112 and gas
filtering loop 52 so that pump 112 may be removed from loop 52.
Recirculating final phase subsystem 43 also includes a scale 116
for weighing the contents of the output buffer 102, at least two
fluid level sensors 118 and 120, temperature sensors 122, 130 and
132, a fluid pressure detector 124, a current overload detector
126, an encoder 128, pressure sensors 134 and 136, a current
overload detector 138 and a vent 140.
[0093] The recirculating final phase subsystem 43 operates by
circulating a fluid containing lipids or lipid-containing organisms
through hollow fibers of HFCs 92 and 94 and recirculation vessel 90
while a gas or mineral oil is circulated through the shell sides of
HFCs 92 and 94, or vice versa. In other words, the gas can flow
through the hollow fibers, and the fluid can flow through the HFC
on the shell side of the hollow fibers. During this process,
solvents are removed from the fluid by passing through pores 28 of
the hollow fibers of HFCs 92 and 94. This process is repeated until
sensor 104 detects a solvent level lower than a predetermined
threshold, which may be, but is not limited to, about 10 parts per
million (ppm) for n-butanol. Then valve 98 is closed, and valve 100
is opened to direct the fluid to output buffer 102. During this
process, the gas that is used to remove the solvent from the fluid
is sent through the carbon bed 108 to remove the solvent from the
gas. The gas is processed in this manner while the fluid is
circulated through HFCs 92 and 94.
[0094] HFCs 92 and 94 have been tested and successfully reduce
total concentrations of solvents, such as di-isopropyl ether and
di-ethyl ether, in water and plasmas, such as human and bovine
plasma, as shown in Table 3 below. HFCs 92 and 94 may have a total
surface area of permeable membrane formed by the hollow fibers
between about 4,200 square centimeters and about 18,000 square
centimeters, depending on the type of HFC used. Further, the gas
flow rate was varied between about 2 liters per minute to about 14
liters per minute, and the plasma flow rate was varied between
about 9 mL per minute to about 900 mL per minute. Operating the
recirculating subsystem 43 in this manner can reduce the initial
concentrations of solvents, such as DiPE and DEE, from between
about 31,000 ppm and 9,400 ppm to between about 312 ppm and about 2
ppm within between about 14 minutes and 80 minutes.
TABLE-US-00003 TABLE 3 Lumen Solvent to be Shell Lumen Module
Initial Solvent Final Solvent Time Material Removed Material Shell
Flow Flow (Surface Area) Conc (ppm) Conc (ppm) recirculating Water
Diethyl Ether Air 7 L/min 220 Fresenius 31000 265 30 min F80A
(18000 cm2) Water Diisopropyl Air 12.3 L/min 750 Celgard 6782 2 14
min Ether (8400 cm2) Bovine Diisopropyl Air 12.3 L/min 750 Celgard
9473 7 16 min Plasma Ether (8400 cm2) Human Diisopropyl Air 12.3
L/min 750 Celgard 11351 15 16 min Plasma Ether (8400 cm2) Water
Diisopropyl Heavy 10 cc/min 4 cc/min Spectrum 4635 312 80 min Ether
Mineral Oil (8000 cm2)
D. Additional System Components
[0095] A solvent sensing device may be positioned within initial
phase subsystem 11, intermediate phase subsystem 29, or final phase
subsystem 47 to detect the presence of solvent in either the fluid
and/or in the gas used in final phase subsystem 47. The fluid may
be circulated through intermediate phase subsystem 29 until the
solvent sensing device indicates that the solvent has been
substantially removed, at which point the fluid can be used for
administration to the animal or human or collected for subsequent
therapeutic use.
[0096] Various types of solvent sensing devices may be used.
Preferably the sensors are capable of detecting very low levels of
solvent. One such sensor is capable of measuring differences in
infrared absorption spectra between solvents and plasma. Using
approaches known to those skilled in the art, several light sources
and detectors can be integrated into a non-contact optical sensor
that can be calibrated to measure the concentrations of one or all
of the solvents. Another useful sensor includes a resistive sensor,
such as model number TGS2620 or TGS822 available from Figaro USA
Inc., Glenview, Ill., that uses a resistance processor to detect
presence of very low levels of solid particles. Yet another type of
optical sensor includes one that determines or identifies molecules
comprising a solvent. Optionally, indirect measurement of solvent
level in the fluid could be performed by measuring the amount of
solvent in gas circulation loop 52. However, direct measurement is
more reliable, because an obstruction in filter(s) 56, 58 or other
flow impediment may falsely indicate that solvent has been
extracted from the gas, when the solvent has remained in the
fluid.
[0097] Suitable materials for use in any of the apparatus
components as described herein include materials that are
biocompatible, approved for medical applications that involve
contact with internal body fluids, and in compliance with U.S. PV1
or ISO 10993 standards. Further, the materials should not
substantially degrade during at least a single use, from for
instance, exposure to the solvents used in the present invention.
The materials should typically be sterilizable, preferably by
radiation or ethylene oxide (EtO) sterilization. Such suitable
materials should be capable of being formed into objects using
conventional processes, such as, but not limited to, extrusion,
injection molding and others. Materials meeting these requirements
include, but are not limited to, nylon, polypropylene,
polycarbonate, acrylic, polysulphone, polyvinylidene fluoride
(PVDF), fluoroelastomers such as VITON, available from DuPont Dow
Elastomers L.L.C., thermoplastic elastomers such as SANTOPRENE,
available from Monsanto, polyurethane, polyvinyl chloride (PVC),
polytetrafluoroethylene (PTFE), polyphenylene ether (PFE),
perfluoroalkoxy copolymer (PFA), which is available as TEFLON PFA
from E.I. du Pont de Nemours and Company, and combinations
thereof.
E. Alternative Embodiments
[0098] The embodiment described above is composed of three
subsystems, wherein each subsystem includes at least one HFC. In an
alternative embodiment, one or more of the subsystems can have at
least two HFCs positioned in a parallel configuration, as shown
schematically in FIG. 6. The parallel configuration allows a fluid
to be directed through the hollow fibers 148 or 150 of HFC 152 or
HFC 156. The configuration of HFC 152 and HFC 156 is not restricted
to a single HFC. Rather, HFC 152 and 156 may each be composed of a
plurality of HFCs connected in series. The parallel configuration
of HFCs shown in FIG. 6 can be substituted for initial phase
subsystem 11, intermediate phase subsystem 29, or final phase
subsystem 47, or any combination of these subsystems.
[0099] The parallel configuration allows a fluid to be routed
through a first side of the system until the HFC does not operate
at a predetermined level because, for instance, too much lipid has
attached to the inside surfaces of the hollow fibers. If this
occurs, the system is reconfigured using valves 166, 168, 172 and
174 to direct the fluid through a second side of the system. While
the fluid is flowing through the second side of the system, the at
least one HFC in the second side can be subjected to a wash or a
reverse flow, be reoriented or replaced.
[0100] The parallel configuration of the HFCs includes sensors 158
and 160 that are coupled to the lines leading to HFCs 152 and 156
to monitor the amount of lipid present in the flow coming from the
hollow fibers of the HFCs. The parallel subsystem also includes
valves 162, 164, 166 and 168 for controlling flow of a fluid.
Initially, valves 162 and 164 are open and valves 166 and 168 are
closed to direct a fluid through HFC 152, or vice versa. In
operation, a fluid or a mixture of a fluid and a solvent flows
through port 151 to hollow fibers 148 of HFC 152 until sensor 158
detects the presence of a lipid greater than a ft predetermined
threshold. Upon detection of a lipid above the threshold limit, the
fluid is routed through the hollow fibers 150 of HFC 156 by closing
valves 162 and 164 and opening valves 166 and 168. These valves may
be manually operated or operated with motors or other electrical or
automatic devices.
[0101] While a fluid is routed through HFC 156, HFC 152 may be
subjected to a wash in wash container 170 using valves 172 and 174
to remove lipid from the inside surfaces of the hollow fibers. For
instance, hexanes may be used to dissolve lipids that have attached
to surfaces of the hollow fibers. Alternatively, HFC 152 may be
replaced or reoriented so that the flow of fluid through the hollow
fibers is opposite the direction it flowed through previously. In
yet another alternative embodiment, the system can be configured so
that the flow of fluid through the hollow fibers 148 of HFC 152 can
be reversed without physically moving HFC 152. HFC 156 can also be
arranged in the same manners as described for HFC 152. Further, HFC
152 can be subjected to a wash in a wash container 176 using valves
178 and 180.
[0102] In yet another alternative embodiment, all three phases, the
initial, intermediate and final phases, of the delipidation process
may be completed using one or more HFCs in series or parallel, or
any combination thereof, such as shown in final phase subsystems 43
and 41 in FIGS. 2 and 3. In one embodiment, a single HFC may be
used to complete all three steps. Specifically, any of the HFCs
shown in the Figures, such as the HFC shown in FIG. 4, may be used
to complete the steps of mixing a fluid with a first extraction
solvent that forms a first mixture of the fluid and the first
extraction solvent, separating at least a portion of the first
extraction solvent from the mixture using a second extraction
solvent, which forms a second mixture of the fluid and the first
and second extraction solvents, and removing at least a portion of
the first and second extraction solvents from the second mixture to
yield a delipidated fluid capable of being administered to a
patient without the patient experiencing undesirable
consequences.
[0103] For instance, the HFC may be composed of the Celgard G478
HFC. The single HFC performs the first step of mixing a fluid and a
first extraction solvent. In one embodiment, this may be
accomplished by circulating a fluid through the lumens of hollow
fibers of an HFC while passing a mixture of 60% DiPE and 40%
n-butanol through the shell side of the lumens of the HFC for about
20 minutes, or vice versa. This process forms a first mixture of
fluid and first extraction solvent and separates lipids from the
fluid or lipid-containing organisms. The fluid is then circulated
through the lumens of the HFC for about 90 minutes while a second
extraction solvent, referred to as a wash and composed of about
100% DiPE, is circulated through the shell side of the lumens, or
vice versa. This process removes the n-butanol from the first
mixture and forms a second mixture including the fluid and the
first and second extraction solvent. The second mixture is then
circulated through the lumens of the HFC while ambient air is
passed through the HFC on the shell side of the lumens, or vice
versa, until the solvents have been removed from the now
delipidated fluid.
IV. DELIPIDATION PROCESS
[0104] The delipidation process begins by priming delipidation
system 10, as shown in FIG. 2, using a saline fluid stored within
saline fluid source 21. Other physiological fluids may be used;
however, saline is preferable because it is isotonic with plasma.
The saline fluid is inserted into delipidation system 10 in order
to limit the amount of water removed from the fluid during the
delipidation process, and to pre-wet the fibers of the HFCs. If the
saline solution is not used, an undesirable amount of water may be
extracted from the fluid. Once delipidation system 10 has been
primed, saline fluid source 21 is turned off and system 10 receives
fluids from fluid source 14. Fluid source 14 may store the fluids
for any length of time depending upon the requirements, such as
temperature, of the fluids. Optionally, fluid source 14 may be
temperature controlled within a range between about 4 degrees
Celsius and about 37 degrees Celsius. The fluid can be sent to HFC
16 through numerous ways, such as by using pump 17 or by allowing
the biological material to flow by gravity into the hollow fibers
20 of HFC 16. Alternatively, pumps may be positioned to pull fluid
through HFC 16 rather than pushing it through. As the fluid flows
through HFC 16, the first extraction solvent is sent from first
extraction solvent source 12 to chamber 22 of HFC 16. The first
extraction solvent may be sent to HFC 16 through numerous ways
similar to the methods of transporting the fluid, such as by using
pump 15 or gravity flow.
[0105] The first extraction solvent is delivered from first
extraction solvent source 12 to chamber 22 so that the first
extraction solvent flows within chamber 22 in the same direction
that the fluid flows through hollow fibers 20 of HFC 16.
Circulating the first extraction solvent and the fluid in this
manner causes the first extraction solvent to contact the fluid by
allowing the solvent to diffuse through pores 28 of hollow fiber 20
into the fluid and the lipid to diffuse across the pores 28 of
hollow fiber 20. In certain embodiments, a portion of the lipid
extracted from the fluid may attach to the inside surface of hollow
fibers 20. In another embodiment, first phase system 11 may be
configured so that the first extraction solvent is deposited within
chamber 22 of HFC 16 so that the first extraction solvent flows in
a direction that is generally opposite to the direction of flow of
the fluid. In one embodiment, the first extraction solvent is
composed of a mixture of DiPE and n-butanol. Specifically, the
mixture includes about 60% DiPE and about 40% n-butanol. However,
as described above, first extraction solvent is not limited to this
particular mixture and may be composed of mixtures formed by the
materials in the amounts listed above.
[0106] After the first extraction solvent has flowed through
chamber 22 of HFC 16, the first extraction solvent is deposited
within extraction solvent waste receptacle 13. The first mixture of
fluid and first extraction solvent flows from hollow fibers 20 to
intermediate phase subsystem 29, and more particularly, through
conduit 40, and into hollow fibers 35 of HFC 34. Intermediate phase
subsystem 29 operates similarly to initial phase subsystem 11.
[0107] Intermediate phase subsystem 29 continues the delipidation
process started within initial phase subsystem 11 and begins to
remove the first extraction solvent from the fluid. Particularly,
the first mixture of fluid and first extraction solvent flows
through hollow fibers 35, 37 and 39 of HFCs 34, 36 and 38. While
the mixture of first extraction solvent and fluid is located in the
lumens of hollow fibers 35, 37 and 39, the second extraction
solvent is transferred from second extraction solvent source 44 to
chamber 74 of HFC 38. The second extraction solvent may be
transferred to second extraction solvent source 44 using pump 45,
allowed to flow by gravity into HFC 38, or by another means.
Preferably, the second extraction fluid flows in a direction
generally opposite to the direction of flow of the mixture located
within hollow fibers 35, 37 and 39 of HFCs 34, 36 and 38, which is
also referred to as countercurrent flow. Thus, the second
extraction solvent flows first through HFC 38, then through HFC 36
and finally through HFC 34. However, in another embodiment, the
second extraction solvent can flow generally opposite to the
direction of the flow in the hollow fibers 35, 37 and 39 without
flowing through HFCs 38, 36 and 34 in this particular order, but in
another order. In yet another embodiment, the second extraction
fluid can flow within chambers 70, 72 and 74 of HFCs 34, 36 and 38
in the same general direction as the direction of flow of the
mixture in hollow fibers 35, 37 and 39 of HFCs 34, 36 and 38. As
described above, the second extraction solvent may include any
solvent that facilitates removal of the first extraction solvent.
In one embodiment, the second extraction solvent is composed of
DiPE.
[0108] While the mixture of the first extraction solvent and the
fluid is in HFCs 34, 36 and 38, the second extraction solvent
passes from chambers 70, 72, and 74 through hollow fibers 35, 37
and 39, thereby enabling the second extraction solvent to contact
the first mixture of fluid and the first extraction solvent. After
the second extraction solvent passes through HFCs 34, 36 and 38,
the second extraction solvent is deposited within extraction
solvent receptacle 13. The second extraction solvent removes at
least a portion of the first extraction solvent and remaining
lipids from the mixture. At least a portion of the first extraction
solvent and remaining lipids pass across membrane 20 through pores
28. However, a portion of the second extraction solvent passes
across membrane 20 through pores 28 into the mixture of the first
extraction solvent and the fluid, thereby forming a second mixture.
Further, in certain embodiments, a portion of the remaining lipids
may attach to the inside surface of hollow fibers 35, 37 and
39.
[0109] The second mixture of the fluid, the first extraction
solvent and the second extraction solvent is then sent to the final
phase subsystem 47 for extracting the first and second extraction
solvents from the mixture. In one embodiment where a once-through
extraction system 41 is used, the mixture of the fluid and the
first and second extraction solvents is sent from HFC 38 to hollow
fibers 76 of HFC 48 through conduit 50. While the mixture flows
into HFC 48, a gas is sent into chamber 80 of HFC 48 from gas
filtering loop 52. In one embodiment, the gas flows in a direction
generally opposite to the flow of mixture of the fluid and the
first and second extraction solvents in the plurality of hollow
fibers 76 and 78 of HFCs 48 and 49. However, this flow can be
reversed as described above. As the gas is circulated through
chambers 80 and 82 of HFCs 48 and 49, the gas fills the pores of
hollow fibers 76 and 78. If a volatile solvent is used as the first
extraction solvent, any gas capable of extracting the first
extraction solvent from the delipidated plasma may be used such as,
but not limited to, air, nitrogen or other inert gases.
[0110] The first and second extraction solvents are removed from
the fluid as the gas fills pores 28 of the hollow fiber 20. The
solvent diffuses through the pores 28 of the hollow fiber 20 and
dissolves into the gas flowing around the fibers in chamber 22. In
other words, the solvent volatilizes at hollow fiber 20. The
solvent is typically highly soluble in the gas, meaning that
resistance to solvent transfer is most significant at the inside
wall of the hollow fiber 20. Typically, resistance to solvent
transfer is a mathematical function of fluid velocity in hollow
fiber 20 raised to the one third power. Many factors may be
adjusted so that the fluid does not weep through fiber membrane 20,
and the gas does not push through pores 28 to form a droplet phase
in the fluid. Specifically, the surface chemistry and surface
tension are controlled by adjusting properties of hollow fiber 20
such as pressure, temperature, fluid flow rate, material, and the
like. Alternatively, these properties can be adjusted so that the
fluid enters pores 28 rather than the gas. Preferably, the fibers
are hydrophobic and prevent the plasma from flowing through the
pores. Advantageously, hydrophobic fibers provide a more robust
membrane, and the differential pressure across the wall of the
fiber is not as critical. Alternatively, the fibers may be
hydrophilic, as described above. During this process, the first and
second extraction solvents diffuse into the gas, and the gas
containing these solvents is carried from chambers 80 and 82 to gas
filtering loop 52.
[0111] If the once-through final phase subsystem 41 is used, the
second mixture of fluid and solvents is sent through the at least
one HFC only one time. However, if the final phase subsystem is a
recirculating final phase subsystem 43, the second mixture of fluid
and solvents is required to be circulated multiple times through
the system 43 before the solvent kg level within the delipidated
fluid is reduced to a level enabling the delipidated fluid to be
safely administered to a patient. Sensor 104 is used to detect the
presence of a solvent to determine whether the final phase is
complete.
[0112] In gas filtering loop 52, the gas containing the first and
second extraction solvents is passed through carbon bed 54 to
remove a significant portion of the solvents. The gas then flows
through first filter 56 for removal of remaining first and second
extraction solvents located within the gas. The gas flows through
first pressure regulator 60, pump 64, and second pressure regulator
62. Any solvents are filtered out using second filter 58 before
sending the gas to HFCs 48 and 49. The gas can be vented through
vent 68 if desired. This process was described for gas filtering
loop 52 coupled to the once-through final phase subsystem 41.
However, this process is the same process used to clean the gas of
solvents in the recirculating final phase subsystem 43.
V. EXAMPLE
[0113] The delipidation process using an embodiment of this
invention begins by first priming delipidation system 10 with about
1 liter of saline solution stored within saline fluid source 21. In
addition, the shell side of the lumens of HFC 16 is primed with
DiPE and n-butanol, and the shell sides of HFCs 34, 36 and 38 are
primed with DiPE. Once primed, plasma is introduced to HFC 16 at a
flow rate of about 20 milliliters per minute, wherein the plasma
contacts a first extraction solvent composed of a premix mixture of
about 60 percent di-isopropyl ether (DiPE) and about 40 percent
n-butanol. The first extraction solvent flows through a HFC at a
rate of about 20 milliliters per minute and in the same general
direction as the plasma. The first extraction solvent and the
plasma contact each other, and the first extraction solvent removes
a substantial amount of lipids from the plasma. In one embodiment,
the initial phase subsystem removes up to about 80 percent of total
cholesterol and triglycerides and about 100 percent of HDL. HFC 16
has about 1.8 square meters of permeable surface area through which
the first extraction solvent can flow and a holdup capacity of 0.1
liter. Initial phase subsystem 11 removes lipids and produces a
first mixture of fluid and first extraction solvent.
[0114] The first mixture is then sent to HFC 34 in intermediate
phase subsystem 29 at a rate of about 20 milliliters per minute
where it is washed with a second extraction solvent composed of
DiPE flowing at a rate of 40 milliliters per minute generally
opposite to the direction of flow of the plasma in HFC 34.
Specifically, the second extraction solvent flows through chambers
70, 72 and 74 while the first mixture of the first extraction
solvent and plasma flows through the plurality of hollow fibers 35,
37 and 39 in a direction generally opposite to the second
extraction solvent. While in intermediate phase subsystem 29, the
plasma flows through HFCs 34, 36 and 38, which have a total
permeable surface area of hollow fibers of about 3.3 square meters.
These HFCs each have a holdup capacity of about 0.1 liter within
the hollow fibers, totaling about 0.3 liters for the intermediate
phase subsystem 29. Intermediate phase subsystem 29 produces a
second mixture composed of the fluid and the first and second
extraction solvents. In one embodiment, using the parameters listed
above, approximately 40,000 ppm of n-butanol, and 10,000 ppm of
DiPE is mixed in the plasma as the plasma enters intermediate phase
subsystem 29. The second extraction solvent comprising DiPE flowing
counter to the plasma at a rate of about 40 milliliter per minute
lowers the n-butanol concentration from about 40,000 ppm to about 0
ppm before the plasma leaves HFC 38. Having the second extraction
solvent flowing against the flow of plasma allows second extraction
solvent containing 0 ppm of n-butanol to contact the plasma having
little n-butanol just before it leaves HFC 38. Thus, the second
extraction solvent is able to extract the lower concentration of
n-butanol more easily using this configuration.
[0115] In one embodiment, the second mixture received from
intermediate phase subsystem 29 is then sent to a final phase
subsystem 47. The final phase subsystem may be either a
once-through final phase subsystem 41 or a recirculating final
phase subsystem 43. In the once-through final phase subsystem 41,
the mixture of fluid and solvents is sent through pervaporation
buffer source 30 where sensor 31 determines the amount of n-butanol
within plasma. If the plasma contains n-butanol, the plasma is
returned to HFC 34 through conduit 33. Otherwise, the delipidated
plasma is sent to HFCs 48 and 49 where the first and second
extraction solvents (DiPE and n-butanol) are removed by passing the
delipidated plasma mixture through the hollow fibers 76 and 78 of
HFCs 48 and 49 at a rate of between about 10 milliliters per minute
and about 60 milliliters per minute and passing air through the
chambers 80 and 82 of HFCs 48 and 49 at a flow rate varying between
about 2 liters per minute to about 10 liters per minute in a
direction generally opposite to the flow of the delipidated plasma
mixture. Typically, the HFCs 48 and 49 include hollow fibers made
of polysulfone and polypropylene fibers, such as those produced by
Celgard, Charlotte, N.C., Spectrum Laboratories, Inc., Rancho
Dominguez, Calif., and Fresenius, Berlin, Germany. HFCs 48 and 49
include a total surface area of permeable membrane formed by the
hollow fibers between about 4,200 square centimeters and about
18,000 square centimeters depending on the type of HFC used.
Operating the once-through final subsystem 41 in this manner can
reduce the initial concentrations of solvents from between about
28,000 ppm (parts per million) and 9,000 ppm to between about 1327
ppm and about 0.99 ppm in about 16 minutes.
[0116] If the recirculating final phase subsystem 43 is used, the
mixture of fluid and solvent is required to be sent through HFCs 92
and 94 multiple times to sufficiently reduce the level of solvents
in the fluid. Typically, the HFCs 92 and 94 in the recirculating
final phase subsystem 43 include polysulfone and polypropylene
fibers, such as those produced by Celgard, Charlotte, N.C.,
Spectrum Laboratories, Inc., Rancho Dominguez, Calif., and
Fresenius, Berlin, Germany. HFCs 92 and 94 each include a total
surface area of permeable membrane formed by the hollow fibers
between about 4,200 square centimeters and about 18,000 square
centimeters depending on the type of HFC used. Further, the typical
flow rate of gas on the shell side of the hollow fibers varies
between about 2 liters per minute to about 14 liters per minute,
and the flow rate of the fluid varies between about 9 milliliters
per minute to about 900 milliliters per minute. Operating the
recirculating final subsystem 43 in this manner can reduce the
initial concentrations of solvents from between about 31,000 ppm
and 6,700 ppm to between about 312 ppm and about 2 ppm within
between about 14 minutes and about 80 minutes, respectively.
[0117] The air is passed through gas filtering loop 52 to remove
the solvents. Specifically, the air is passed through carbon bed
54, first filter 56, first pressure regulator 60, pump 64 and
second pressure regulator 62. The air may be vented through vent 68
if desired. This system can process approximately 3.5 liters of
plasma in about 175 minutes. Once the delipidated plasma has passed
through HFCs 48 and 49, the delipidated plasma may be returned to a
patient or stored within delipidated fluid receptacle 66.
[0118] In one particular experiment, the amount of cholesterol was
reduced from 155 milligrams per deciliter to about 35 milligrams
per deciliter. Further, the amount of apolipoprotein B was reduced
from about 50 milligrams per deciliter to about 28 milligrams per
deciliter. However, the concentration of chloride ions and albumin
remained relatively unchanged throughout the treatment process.
F. Exemplary Embodiments
[0119] The embodiments described above may be manufactured so that
all components that come in contact with a fluid, containing lipids
or lipid-containing organisms, or both, during operation are
contained within a single module that may be disposable. To prevent
the spread of diseases and for other health reasons, the
delipidation system 10 should be cleaned after each use before
being used with a fluid from a different source. In one embodiment,
a module containing the devices described above is disposable,
which enables the system to be set up quickly after having been
used. Delipidation device 10 may be prepared for use with another
patient's fluid by simply removing a module and replacing it with a
sterile module that may have never been used or may have been
sterilized since a prior use.
G. Experimental Results
[0120] A system having an initial, intermediate, and final phase
subsystems was employed. The initial phase subsystem was composed
of three HFCs manufactured by Celgard. The W intermediate phase
subsystems was composed of three HFCs manufactured by Spectrum and
the final phase subsystem was composed of two HFCs manufactured by
Celgard. All HFCs were oriented in series. Plasma was applied to
the lumens of the HFCs. In the initial phase subsystem, the shell
side of the HFCs contained a mixture of 40% butanol and 60% DiPE
flowing in the same direction as the plasma flowing through the
lumens of the HFCs at a rate of about 20 ml/min.
[0121] In the intermediate phase subsystem, 100 percent DiPE flowed
through the HFCs on the shell side of the lumens at a rate of 40 ml
per minute in a countercurrent direction to the direction of flow
of the plasma through the lumens of the HFCs. In the final phase
subsystem, air flowed through the three HFCs on the shell side of
the lumens. Clinical chemistry data characterizing the parameters
in the effluent delipidated plasma were obtained using a Hitachi
911. Results indicated dramatic reductions in cholesterol,
triglycerides and HDL. Very little change or no change was observed
in electrolytes (Na, Cl, and K), calcium, phosphorous, protein,
albumin, globulin, phospholipids, creatinine, BUN, glucose, and
alkaline phosphatase.
[0122] While various embodiments of this invention have been set
forth above, these descriptions of the preferred embodiment are
given for purposes of illustration and explanation. Variations,
changes, modifications, and departures from the systems and methods
disclosed above may be adopted without departure from the spirit
and scope of this invention.
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