U.S. patent application number 09/794772 was filed with the patent office on 2002-08-29 for liquid chromatographic method and system.
This patent application is currently assigned to Isco, Inc.. Invention is credited to Blakley, Scott L., Davison, Dale A.
Application Number | 20020116988 09/794772 |
Document ID | / |
Family ID | 25163627 |
Filed Date | 2002-08-29 |
United States Patent
Application |
20020116988 |
Kind Code |
A1 |
Davison, Dale A ; et
al. |
August 29, 2002 |
LIQUID CHROMATOGRAPHIC METHOD AND SYSTEM
Abstract
To economically perform preparatory chromatography, a plurality
of pumps each having a corresponding one of a plurality of pistons
and a corresponding one of a plurality of cylinders are driven by
one motor to draw and pump solvent simultaneously into
corresponding columns. To form a gradient the pumps are connected
to two-way valves that are connected alternately to a first solvent
and a second solvent, whereby the time said valve is in a first
position controls the amount of solvent drawn from said first
reservoir into said pumps and the amount of time in said second
position controls the amount of said second solvent drawn into said
pumps and the solvent is mixed in the pumping systems. The
detectors are photodiodes mounted to light guides in the flow cells
that generate signals related to light absorbance and communicate
with a controller, whereby said controller receives signals
indicating solute between the light guides and causes collection of
solute.
Inventors: |
Davison, Dale A; (Greenwood,
NE) ; Blakley, Scott L.; (Omaha, NE) |
Correspondence
Address: |
Vincent L. Carney
P.O. Box 80836
Lincoln
NE
68501-0836
US
|
Assignee: |
Isco, Inc.
4700 Superior Street
Lincoln
NE
|
Family ID: |
25163627 |
Appl. No.: |
09/794772 |
Filed: |
February 27, 2001 |
Current U.S.
Class: |
73/61.55 ;
73/61.52 |
Current CPC
Class: |
G01N 2001/383 20130101;
G01N 30/466 20130101; G01N 2030/326 20130101; G01N 1/38 20130101;
G01N 35/1097 20130101; G01N 30/32 20130101; G01N 2030/324 20130101;
B01D 15/12 20130101; B01D 15/247 20130101; B01D 15/166
20130101 |
Class at
Publication: |
73/61.55 ;
73/61.52 |
International
Class: |
G01N 030/00 |
Claims
What is claimed is:
1. A multiple channel liquid chromatographic system comprising: at
least two syringe pumps; at least two sources of liquid; at least
one time-proportioning electronically controllable liquid gradient
switching valve; said switching valve being connected to switch
liquid flow from one or the other of said at least two sources of
liquid to an inlet of at least one of said at least two syringe
pumps; one of said at least two syringe pumps being used for each
one of the multiple channels; each of the said pumps having a
displacement of at least five milliliters, and said one of said
syringe pumps having a discharge outlet connected to a sample
injection device and thence to a chromatographic column.
2. A multiple channel liquid chromatographic system according to
claim 1 wherein said one of said at least two syringe pumps has a
piston and a cylinder; said pump having a refill flow rate at least
3 times faster than its delivery flow.
3. A multiple channel liquid chromatographic system in accordance
with claim 2 in which said at least one time-proportioning
electronically controllable liquid gradient switching valve is
arranged to produce consecutive pulses of liquid from at least one
of said at least two sources of liquid to a refill inlet at a fluid
velocity high enough to induce turbulent mixing in a space between
a head of said piston and that part of the cylinder not occluded by
the piston.
4. A multiple channel liquid chromatographic system in accordance
with claim 3 further including means for synchronizing the at least
one time-proportioning electronically controllable liquid gradient
switching valve with refill movement of said piston so that one
charge of each desired fluid at a desired volume proportion is
deposited in each pump and mixed to form at least one part of a
step of a stepped gradient.
5. A multiple channel liquid chromatographic system in accordance
with claim 3 further including: first means for shutting off fluid
flow between the said pump and the at least one time-proportioning
electronically controllable liquid gradient switching valve during
delivery; second means for synchronizing the at least one
time-proportioning electronically controllable liquid gradient
switching valve with refill movement of said piston so that one
charge of each desired fluid at a desired volume proportion is
deposited in each pump and mixed to form at least one part of a
step of a stepped gradient; and means for repeating the said first
and second means at consecutively different or same fluid
proportions to produce an entire stepped gradient.
6. A multiple channel liquid chromatographic system in accordance
with claim 5 wherein at least two equal charges of each of two
fluids are alternately delivered to an inlet of at least one of
said at least two syringe pumps; said two fluids being proportioned
in the at least one time-proportioning electronically controllable
liquid gradient switching valve during a refill stroke of said
piston and then delivered as a single step of a step gradient to
the rest of said system in the order of sample injection device,
chromatographic column, and fraction collector, said refill stroke
being sufficiently rapid to cause mixing in a cylinder of the
pump.
7. A multiple channel liquid chromatographic system in accordance
with claim 6 wherein said order includes an absorbance detector
between said chromatographic column and fraction collector.
8. A multiple channel liquid chromatographic system in accordance
with claim 6 having N channels wherein for the N channels there are
one of N time-proportioning electronically controllable liquid
gradient switching valves and N syringe pumps, all of which have
their pistons cycling together in synchronism and producing N
stepped gradients with one stroke of each pump corresponding to the
single step of each gradient.
9. A multiple channel liquid chromatographic system in accordance
with claim 8 wherein more than one consecutive, entire, synchronous
piston cycle correspond to a single step of the gradient.
10. A multiple channel liquid chromatographic system in accordance
with claim 9 wherein the stepped gradient is defined by the steps
of the gradient taken consecutively.
11. A multiple channel liquid chromatographic system in accordance
with claim 10 wherein each of said at least two syringe pumps
includes a piston and a cylinder; said multiple channel liquid
chromatographic system including a parallel moving frame attached
to at least two pistons, wherein movement of each of the pistons
with respect to a corresponding cylinder is carried out by the
parallel moving frame.
12. A multiple channel liquid chromatographic system in accordance
with claim 11 further including: a data system; a sample
concentration detector having an electrical output; said data
system including a recorder having an electrical recording output
connection; a fraction collector having a plurality of containers
and a timing cycle for depositing liquid in the containers; and the
data system being electrically connected to the electrical output
of said sample concentration detector and to the electrical
recording output connection wherein a container charge timing cycle
of the fraction collector is stopped during pump refill and
restarted and run during liquid delivery of the at least one of
said at least two syringe pumps.
13. A multiple channel liquid chromatographic system in accordance
with claim 12 further including a first mixing means and second
mixing means wherein the first mixing means resides in a fluid flow
path between the said at least one time-proportioning
electronically controllable liquid gradient switching valve and the
said at least one of said at least two syringe pumps inlet and the
second mixing means resides in the cylinder of the at least one of
said at least two syringe pumps downstream of the inlet of the at
least one time-proportioning electronically controllable liquid
gradient switching valve.
14. A multiple channel liquid chromatographic system in accordance
with claim 13 wherein the fluid flow path between the said at least
one time-proportioning electronically controllable liquid gradient
switching valve and the at least one of said at least two syringe
pumps inlet is a flow passageway sized to produce mixing in the
said passageway, which in combination with mixing in the pump
cylinder makes each step of the gradient sufficiently flat and
reproducible for a desired set of chromatographic separation
processes.
15. A multiple channel liquid chromatographic system in accordance
with claim 14 wherein the flow passageway has a volume less than
one-tenth that of a single charge, wherein the flow passageway has
a diameter of less than one-half the diameter of the pump cylinder;
said flow producing good axial mixing and poor transverse mixing on
a small scale charge and an outlet of said flow passageway
injecting into the pump cylinder where the flow becomes turbulent
flow thus enhancing transverse mixing and axial mixing on a large
scale.
16. A multiple channel liquid chromatographic system in accordance
with claim 14 wherein the flow passageway has a volume of at least
one-tenth that of a single charge; said flow producing good axial
mixing on a small scale and an outlet of said flow passageway
injecting into the pump cylinder where the flow undergoes enhanced
transverse mixing.
17. A multiple channel liquid chromatographic system in accordance
with claim 14 wherein the flow passageway has a volume of at least
one-tenth that of a single charge wherein the distance required for
further transverse mixing is small; said flow producing good axial
mixing and an outlet of said flow passageway injecting into the
larger diameter pump cylinder where the flow becomes turbulent and
undergoes transverse mixing and axial mixing.
18. A multiple channel liquid chromatographic system in accordance
with claim 1 in which said at least one time-proportioning
electronically controllable liquid gradient switching valve is
arranged to produce consecutive pulses of liquid from at least one
of said at least two sources of liquid to a refill inlet at a fluid
velocity high enough to induce turbulent mixing in a space between
a head of said piston and that part of the cylinder not occluded by
the piston.
19. A multiple channel liquid chromatographic system in accordance
with claim 18 further including means for synchronizing the at
least one time-proportioning electronically controllable liquid
gradient switching valve with refill movement of said piston so
that one charge of each desired fluid at a desired volume
proportion is deposited in each pump and mixed to form at least one
part of a step of a stepped gradient.
20. A multiple channel liquid chromatographic system in accordance
with claim 19 further including: first means for shuffing off fluid
flow between the said pump and said at least one time-proportioning
electronically controllable liquid gradient switching valve during
delivery; second means for synchronizing the at least one
time-proportioning electronically controllable liquid gradient
switching valve with refill movement of said piston so that one
charge of each desired fluid at a desired volume proportion is
deposited in each pump and mixed to form at least one part of a
step of a stepped gradient; and control means for repeating the
said first and second means at consecutively different or same
fluid proportions to produce an entire stepped gradient.
21. A multiple channel liquid chromatographic system in accordance
with claim 20 wherein at least two equal charges of each of two
fluids are alternately delivered to an inlet of at least one of
said at least two syringe pumps; said two fluids being mixed in the
at least one time-proportioning electronically controllable liquid
gradient switching valve during a rapid, energetic refill, and then
delivered as a single step of a step gradient to the rest of said
system in the order of sample injection device, chromatographic
column, and fraction collector.
22. A multiple channel liquid chromatographic system in accordance
with claim 21 wherein said order includes an absorbance detector
between said chromatographic column and fraction collector.
23. A multiple channel liquid chromatographic system in accordance
with claim 22 having N channels wherein for the N channels there
are one of N time-proportioning electronically controllable liquid
gradient switching valves and N syringe pumps, all of which have
their pistons cycling together in synchronism and producing N
stepped gradients with one stroke of each pump corresponding to the
single step of each gradient.
24. The multiple channel liquid chromatographic system in
accordance with claim 23 wherein more than one consecutive, entire,
synchronous piston cycle correspond to a single step of the
gradient.
25. A multiple channel liquid chromatographic system in accordance
with claim 24 wherein each step of the gradient taken consecutively
define the stepped gradient.
26. A multiple channel liquid chromatographic system in accordance
with claim 1 wherein each of said at least two syringe pumps
includes a piston and a cylinder; said multiple channel liquid
chromatographic system including a parallel moving frame attached
to at least two pistons, wherein movement of each of the pistons
with respect to a corresponding cylinder is carried out by the
parallel moving frame.
27. A multiple channel liquid chromatographic system in accordance
with claim 26 further including: a data system; a sample
concentration detector; a recorder; a fraction collector; said
fraction collector including a plurality of containers wherein the
data system is connected to an electrical output of said sample
concentration detector, the recording by the recorder of the data
system and the container charge timing of the fraction collector is
stopped during pump refill and restarted and run during liquid
delivery of the at least one of said at least two syringe
pumps.
28. A multiple channel liquid chromatographic system in accordance
with claim 27 further including a first mixing means and second
mixing means wherein the first mixing means resides in a fluid flow
path between the said at least one time-proportioning
electronically controllable liquid gradient switching valve and the
said at least one of said at least two syringe pumps inlet and the
second mixing means resides in the cylinder of the at least one of
said at least two syringe pumps downstream of the inlet of the at
least one time-proportioning electronically controllable liquid
gradient switching valve.
29. A multiple channel liquid chromatographic system in accordance
with claim 28 wherein the fluid flow path between the at least one
time-proportioning electronically controllable liquid gradient
switching valve and the at least one of said at least two syringe
pumps inlet is a tube or passage sized to produce flow in the said
fluid connection, and of length or volume enough to make each step
of the gradient sufficiently flat and reproducible for a desired
set of chromatographic separation processes.
30. A multiple channel liquid chromatographic system in accordance
with claim 29 wherein the flow passageway has a volume of at least
one-tenth that of a single charge; said flow producing good axial
mixing and poor transverse mixing and an outlet of the said flow
passageway injects liquid into the pump cylinder where it undergoes
enhanced transverse mixing and axial mixing.
31. A method of performing liquid chromatography comprising:
drawing at least first and second fluid solvent into a plurality of
pumps from at least a corresponding first and second source of
fluid; pumping said fluid from said plurality of pumps; said step
of pumping said fluid including the step of mixing said at least
first and second fluids in said pumps whereby a gradient is formed;
said step of mixing including the step of mixing said at least
first and second fluids prior to pumping said at least first and
second fluids from said pumps; said step of mixing further
including the step of drawing said first and second fluids through
at least one flow path, wherein the flow path is shaped to produce
good axial mixing and poor transverse mixing; and injecting said
fluids into a pump cylinder where it undergoes enhanced transverse
mixing and axial mixing.
32. The method of claim 31 wherein the enhanced mixing occurs
because the axially-mixed liquid entering the pump facilitates
further mixing because the distance required for further transverse
mixing is small.
33. A method according to claim 31 wherein the enhanced mixing
occurs because the tendency of some pairs of liquids not to mix at
their interfaces decreases because this interface is already
degraded at or before the outlet of flow means.
34. A liquid chromatographic system comprising: a plurality of
pumps each having a corresponding one of a plurality of pistons and
a corresponding one of a plurality of cylinders; at least one
motor; means connected to said at least one motor for driving at
least some of said plurality of pistons, wherein said at least one
motor includes one motor driving at least two pistons; at least
some of said plurality of cylinders being adapted to communicate
with a source of solvent, whereby at least some of said plurality
of pumps simultaneously pump a solvent driven by one motor; at
least one column; at least some of said plurality of pumps
communicating with said at least one column, whereby solvent may be
applied to said at least one column from said at least some of said
plurality of pumps; at least one flow detector communicating with
said at least one column, whereby effluent from said column may be
detected; and a controller communicating with said detector,
whereby effluent may be channeled to predetermined locations.
35. A liquid chromatographic system according to claim 34 wherein:
said at least one column is a plurality of columns; different ones
of said pumps communicating with corresponding ones of said
columns, whereby solvent may be applied to said columns; said at
least one flow detector is a plurality of flow detectors each
communicating with a different one of said columns, whereby
effluent from said columns may be detected; and said controller
communicating with said detectors, whereby effluent may be
channeled to predetermined locations.
36. A liquid chromatographic system comprising: a motor; a
plurality of pumps; said pumps being adapted to be connected to a
two-way valve; said two-way valve being adapted to be connected
alternately to a first solvent reservoir and a second solvent
reservoir, whereby the amount of time said valve is in a first
position controls the amount of solvent drawn from said first
reservoir into said pumps and the amount of time in a second
position controls the amount of solvent drawn from said second
reservoir into said pumps; means for injecting said solvent into
said pumps, whereby said solvent is further mixed in said pumps; a
plurality of columns; a plurality of detectors; each of said pumps
communicating with a different column and a different detector; and
each of said detectors communicating with a controller, whereby
said controller received signals indicating peaks.
37. A liquid chromatographic system in accordance with claim 36
wherein said plurality of pumps and said motor comprise a first
pumping system adapted to communicate with a first solvent; said
chromatographic system including a second pumping system having a
different plurality of pumps and different motor; said second
pumping system being adapted to communicate with a second solvent;
said first and second pumping systems communicating with a common
point, whereby a gradient may be formed of said first and second
solvents.
38. A liquid chromatographic system in accordance with claim 36
further including a fraction collector; said fraction collector
being connected to receive effluent from said columns.
39. A liquid chromatographic system in accordance with claim 36
further including a recorder; said recorder having a plurality of
channels adapted to record peaks from said plurality of
detectors.
40. A liquid chromatographic system in accordance with claim 34 in
which each of said pistons includes means for preventing damage as
said motor operates in the event of a jam.
41. A liquid chromatographic system in accordance with claim 40
further including: a drive plate; each of said pistons including a
corresponding one of a plurality of piston rods; a plurality of
springs; and a different one of each of said springs connecting a
corresponding one of said plurality of piston rods to said drive
plate, wherein said spring means release fluid pressure under a
predetermined load.
42. A liquid chromatographic system including: at least one pumping
system; said pumping system supplying solvent to at least one
detector; a light source; said light source applying light to said
at least one detector; a first light guide receiving light from
said light source and transmitting it to said at least one
detector; a second light guide positioned to receive light from
said first light guide and transmit it to a detector; and said
first and second light guides having their ends positioned within a
flow cell adjacent to each other so that light passes from an end
of said first light guide through solute in said flow cell and into
an end of the second light guide, whereby light is diminished
within said flow cell by absorbance by said solute.
43. A liquid chromatographic system according to claim 42 in which
said ends of said first and second light guides are spaced in the
region of 0.02 to 5 millimeters apart.
44. A liquid chromatographic system according to claim 42 in which
said light source includes: at least one lamp; means for focusing
light from said at least one lamp onto a diffraction grating; means
for focusing light from the diffraction grating onto an opening;
and at least some of a plurality of light guides having an end in
said opening whereby said at least some of said plurality of light
guides receive light from said diffraction grating.
45. A liquid chromatographic system in accordance with claim 42
including at least one column wherein: said at least one pumping
system comprises a plurality of pumps; said at least one column
comprising a plurality of columns, each of said plurality of
columns communicating with a different one of said plurality of
pumps; said at least one detector comprising a plurality of
detectors, each of said plurality of detectors communicating with a
different one of said plurality of columns, whereby each of said
detectors detects a signal; and said detectors including a
photodiode positioned against one end of said second light
guide.
46. A liquid chromatographic system in accordance with claim 42 in
which each of said light guides is in intimate contact with a
different photodiode.
47. A method of performing liquid chromatography comprising the
steps of: driving a plurality of pump pistons each being part of a
corresponding plurality of pumps with a single motor, wherein said
plurality of pumps pump solvent simultaneously and fill with
solvent simultaneously into at least one column; detecting solute
in the effluent from said at least one column; and channeling the
solute into at least one container.
48. A method in accordance with claim 47 wherein the step of:
driving a plurality of pump pistons includes the step of causing
solvent to flow from each of said plurality of pumps into
corresponding ones of a plurality of columns, wherein different
ones of said pumps communicate with corresponding ones of said
columns; said step of detecting solute including the step of
detecting solute in the effluent from said plurality of columns
wherein solute may be channeled to predetermined locations.
49. A method of performing liquid chromatography in accordance with
claim 47 comprising: drawing solvent into said plurality of pumps
and a corresponding plurality of twoway valves wherein each of said
two-way valves is connected alternately to a first solvent
reservoir and a second solvent reservoir, whereby the amount of
time said valve is in a first position controls the amount of
solvent drawn from said first reservoir into said pumps and the
amount of time in a second position controls the amount of solvent
drawn from said second reservoir into said pumps; mixing said
solvent in said pumps whereby a gradient is formed.
50. A method in accordance with claim 47 wherein said plurality of
pumps and said motor comprise a first pumping system which
communicates with a first solvent and; a second pumping system
having a different plurality of pumps and a different motor
communicates with a second solvent wherein; said first and second
pumping systems pump solvent to a common point, to form a gradient
of said first and second solvents.
51. A method in accordance with claim 49 further including the step
of collecting solute from at least one of said columns.
52. A method in accordance with claim 49 in which the step of
detecting includes the step of recording peaks from a plurality of
detectors.
53. A method in accordance with claim 47 wherein any of said
pistons is released from said motor if subjected to a load beyond a
predetermined load.
54. A method in accordance with claim 47 wherein a plurality of
piston rods is connected to a drive plate wherein pressure is
released under a predetermined load.
55. A method of performing chromatography comprising the steps of:
pumping solvent through at least one detector; transmitting light
through said at least one detector from a first light guide;
receiving light passing through solute from said first light guide
to a second light guide; and transmitting light received by said
second light guide to a detector wherein said first and second
light guides have their ends positioned within a flow cell adjacent
to each other so that light passes from an end of one light guide
through solute in said flow cell and into an end of the second
light guide, whereby light is diminished within said flow cell by
absorbance by said solute.
56. A method according to claim 55 in which said step of
transmitting light includes the substeps of: transmitting light
from at least one lamp; focusing light from said at least one lamp
onto a diffraction grating; and focusing light from the diffraction
grating onto an opening wherein at least some of a plurality of
light guides having an end in said opening whereby said at least
some of said plurality of light guides receive light from said
diffraction grating.
57. A method in accordance with claim 55 further including the step
of detecting light with photodiodes positioned against one end of
said second light guide.
58. A pumping system comprising: at least one pump having a
cylinder, a piston and a pump head with an outlet; at least one
inlet tube having first and second ends communicating with the
cylinder at one end and adapted to communicate with at least two
sources of fluid at the other end; said at least one inlet tube
having a diameter and length shaped for the flow; and drive means
for driving said piston with sufficient speed to cause turbulent
mixing in said cylinder, wherein fluid from said at least two
sources of fluid are mixed before being pumped from said
outlet.
59. A pumping system in accordance with claim 58 further including
an electronically controlled valve having an outlet and at least
two inlets communicating at said outlet with said second end of
said tube and at a first of said at least two inlets with one
source of fluid and at a second of said at least two inlets with a
second source of fluid whereby said at least one pump may pump a
mixture of fluids.
60. A pumping system in accordance with claim 59 further including
control means for switching said valve outlet from one of said at
least two inlets to the second of said at least two inlets at least
once during a refill stroke of said at least one pump.
61. A pumping system in accordance with claim 58 further including
at least one syringe pump wherein said at least one syringe pump
has a piston and a cylinder; said pump having a refill flow rate at
least 3 times faster than its delivery flow.
62. A pumping system in accordance with claim 61 in which at least
one time-proportioning electronically controllable liquid gradient
switching valve is arranged to produce consecutive pulses of liquid
from at least one of said sources of fluid to a refill inlet at a
fluid velocity high enough to induce turbulent mixing in a space
between a head of the said piston and that part of the cylinder not
occluded by the piston.
63. A pumping system in accordance with claim 62 wherein said at
least one pump includes a plurality of pumps, said pumping system
further including means for synchronizing the at least one
time-proportioning electronically controllable liquid gradient
switching valve with refill movement of the said piston so that one
charge of each desired fluid at a desired volume proportion is
deposited in each pump and mixed to form at least one part of a
step of a stepped gradient.
64. A pumping system in accordance with claim 63 further including:
first means for shutting off fluid flow between said pump and the
at least one time-proportioning electronically controllable liquid
gradient switching valve during delivery; second means for
synchronizing the at least one time-proportioning
electronically-controllable liquid gradient switching valve with
refill movement of said piston so that one charge of each desired
fluid at a desired volume proportion is deposited in each pump and
mixed to form at least one part of a step of a stepped gradient;
and means for repeating the said first and second means at
consecutively different or same fluid proportions to produce an
entire stepped gradient.
65. A pumping system in accordance with claim 64 wherein at least
two equal charges of each of two fluids are alternately delivered
to an inlet of said at least one syringe pump; said two fluids
being mixed in the at least one time-proportioning electronically
controllable liquid gradient switching valve during a refill stroke
of said piston, and then delivered as a single step of a step
gradient, said refill stroke being sufficiently rapid to cause
mixing in a cylinder of the pump.
66. A pumping system in accordance with claim 65 wherein more than
one consecutive, entire, synchronous piston cycle corresponds to a
single step of the gradient.
67. A pumping system in accordance with claim 66 wherein the
stepped gradient is defined by the steps of the gradient taken
consecutively.
68. A pumping system in accordance with claim 67 wherein said at
least one syringe pump includes a piston and a cylinder, said
multiple channel liquid chromatographic system including a parallel
moving frame attached to at least one piston, wherein the motion of
each of the pistons with respect to a corresponding cylinder is
carried out by the parallel moving frame.
69. A pumping system in accordance with claim 58 further including:
a data system; a sample concentration detector having an electrical
output; said data system including a recorder having an electrical
recording output connection; a fraction collector having a
plurality of containers and a timing cycle for depositing liquid in
the containers; and the data system being electrically connected to
the electrical output of said sample concentration detector and to
the electrical recording output connection wherein a container
charge timing cycle of the fraction collector is stopped during
pump refill and restarted and run during liquid delivery of the at
least one syringe pump.
70. A pumping system in accordance with claim 69 further including
a first mixing means and second mixing means wherein the first
mixing means resides in a fluid flow path between said at least one
time-proportioning electronically controllable liquid gradient
switching valve and said at least one syringe pump inlet and the
second mixing means resides in the cylinder of said at least one
syringe pump downstream of the inlet of the at least one
time-proportioning electronically controllable liquid gradient
switching valve.
71. A multiple channel liquid chromatographic system in accordance
with claim 70 wherein the fluid flow path between the said at least
one time-proportioning electronically controllable liquid gradient
switching valve and said at least one syringe pump inlet is a flow
passageway sized to produce mixing in the said fluid flow path, and
of length or volume enough to make each step of the gradient
sufficiently flat and reproducible for a desired set of
chromatographic separation processes.
72. A pumping system in accordance with claim 71 wherein the flow
passageway has a volume of at least one-tenth that of a single
charge, said flow producing good axial mixing and poor transverse
mixing and an outlet of said flow passageway injecting into the
pump cylinder where the flow undergoes enhanced transverse mixing
and axial mixing.
73. A pumping system in accordance with claim 58 wherein said at
least one pump includes at least two syringe pumps and at least two
equal charges of each of two fluids are alternately delivered to an
inlet of at least one of said at least two syringe pumps; said two
fluids being mixed in at least one time-proportioning
electronically controllable liquid gradient switching valve during
a refill stroke of said piston, and then delivered as a single step
of a step gradient, said refill stroke being sufficiently rapid to
cause mixing in a cylinder of the pump.
74. The pumping system of claim 73 wherein more than one
consecutive, entire, synchronous piston cycle correspond to a
single step of the gradient.
75. A pumping system in accordance with claim 74 wherein the
stepped gradient is defined by the steps of the gradient taken
consecutively.
76. A pumping system in accordance with claim 75 wherein each of
said at least two syringe pumps includes a piston and a cylinder,
said pumping system including a parallel moving frame attached to
at least two pistons, wherein movement of each of the pistons with
respect to a corresponding cylinder is carried out by the parallel
moving frame.
Description
BACKGROUND OF THE INVENTION
[0001] This invention relates to liquid chromatographic methods and
apparatuses.
[0002] Inexpensive liquid chromatographic apparatuses have been
developed and are in use, particularly for preparatory
chromatography where the emphasis is on quickly obtaining
relatively large samples at low cost. Such systems generally
include at least one solvent reservoir, a pump, a controller, a
chromatographic column, a collector and usually a detector.
Commonly, provision is made for a gradient to be developed and such
gradient systems require at least two solvent reservoirs and some
mechanism for mixing the solvent from each of the two reservoirs
together to form a gradient for application to the column.
[0003] The prior art apparatuses have a disadvantage in that they
are not as inexpensive as desired or require a longer period of
time than desired for the separation.
SUMMARY OF THE INVENTION
[0004] Accordingly, it is an object of the invention to provide a
novel chromatographic system and method.
[0005] It is a still further object of the invention to provide a
low-cost method of providing substantial amounts of solvent to a
chromatographic system.
[0006] It is a still further object of the invention to provide an
inexpensive gradient chromatographic system.
[0007] It is a still further object of the invention to provide a
low-cost detection system equipped to handle relatively large
amounts of solvent and separated materials.
[0008] In accordance with the above and further objects of the
invention, a chromatographic system includes a plurality of pumps,
all driven together by a single pump motor for drawing solvent from
solvent reservoirs, pumping the solvent through a plurality of
columns for separation of sample, pumping the solvent and solute
through a plurality of detectors for detecting solute and pumping
the solute into a fraction collector for collection. The solvent is
pulled from the reservoir through a plurality of outlets of a
manifold so that a plurality of flow streams may be pulled into the
corresponding plurality of pumps from one or more solvent
reservoirs. The pumps may each receive the combined output of a
plurality of different solvent reservoirs in controlled ratios, and
in the preferred embodiment, with multiple charges of each solvent
for each pump cycle to form a gradient and the different solvents
in the case of such a gradient are mixed in the path between a flow
inlet conduit to the pump and the pump outlet with the pump
cylinder and inlet tube being dimensioned to provide adequate
mixing during refill of the pump. The ratios of solvents are
controlled by a solenoid operated valve in the preferred
embodiment. Mixing in the pump cylinders is aided by a rapid refill
stroke pulling solvent into an off-center inlet port of the piston
pumps, causing turbulence.
[0009] With this arrangement, a single motor is able to drive a
multiplicity of pumps which together can supply a large amount of
solvent to a number of columns simultaneously. In the preferred
embodiment at least two different reservoirs pull solvents and
different gradients are applied to at least some columns. However,
embodiments in which the same solvent is applied to each column is
possible and a gradient may be applied to some columns and a single
solvent to others. In the event that the piston for one of the
pumps jams, pressure automatically is released, such as for example
with a fluid pressure release valve, so the pump drive can continue
to be driven by the single motor without damage or stalling. In one
embodiment, the gradient is formed without separate mixers and the
mixing is done in the pump and the inlet to the pump and/or other
equipment associated with the system.
[0010] An inexpensive detecting arrangement is utilized that
comprises a light source which focuses light from a central spot on
a lamp for stability and selects the frequency of light with a
diffraction grating, reflecting the selected light through a slot
and onto a plurality of light conductors. The selected light is
transmitted through the light conductors to flow cells. Each flow
cell has within it two light guides that are aligned and have a
space between them for some of the fluid from the chromatographic
column to flow. One of the light guides in each of the flow cells
receives light from a corresponding one of the light conductors and
transmits it to the other light guide through the effluent from the
column without intervening focusing means to provide light-guide to
light-guide communication in the flow cell through the fluid
passing in between the two light guides. The light that is not
absorbed in the flow cell is detected by photodiodes located
directly against the receiving light guides.
[0011] From the above description, it can be understood that, the
chromatographic system and chromatographic method of this invention
is low cost and yet provides substantial yield in a short time.
SUMMARY OF THE DRAWINGS
[0012] The above noted and other features of the invention will be
better understood from the following detailed description when
considered with reference to the accompanying drawings in
which:
[0013] FIG. 1 is a block diagram of a liquid chromatographic system
in accordance with an embodiment of the invention;
[0014] FIG. 2 is a simplified partly-schematic, partly-side
elevational view of solvent reservoirs, manifolds and a purge
system used in the embodiment of FIG. 1;
[0015] FIG. 3 is a block diagram of a pump array useful in the
embodiment of FIG. 1;
[0016] FIG. 4 is a simplified partly-schematic, partly-rear
elevational view of solvent reservoir manifold and purge system
connections used in the embodiment of FIG. 1;
[0017] FIG. 5 is an elevational sectional view of a pump array and
motor for driving the pistons for the pumps in the pump array
useful in the embodiment of FIG. 1;
[0018] FIG. 6 is a sectional view through lines 6-6 of FIG. 4;
[0019] FIGS. 7-12 are progressive schematic drawings of an on-off
valve, delayed coil and pump in six different positions of
operation:
[0020] (a) FIG. 7 being a first position at the start of a refill
stroke of the pump;
[0021] (b) FIG. 8 being a second position in the refill stroke of
the pump;
[0022] (c) FIG. 9 being a third position in the refill stroke of
the pump;
[0023] (d) FIG. 10 being a forth position in the refill stroke of
the pump;
[0024] (e) FIG. 11 being a fifth position in the refill stroke of
the pump; and
[0025] (f) FIG. 12 being a sixth position in the refill stroke of
the pump.
[0026] FIG. 13 is a block diagram of a column and detector array in
accordance with the embodiment of FIG. 1;
[0027] FIG. 14 is a schematic diagram of an array of light sources,
flow cells and sensors in accordance with an embodiment of the
invention;
[0028] FIG. 15 is a fractional enlarged view of a portion of FIG.
14 showing light inlets to flow cells in accordance with an
embodiment of the invention;
[0029] FIG. 16 is a block diagram illustrating the detection of
fluid in accordance with an embodiment of the invention.
[0030] FIG. 17 is fragmentary simplified enlarged view of a portion
of the embodiment of FIG. 16;
[0031] FIG. 18 is a schematic drawing showing a portion of the
optical system in accordance with an embodiment of the
invention;
[0032] FIG. 19 is a block diagram showing the interconnections
between portions of the preparatory chromatograph of an embodiment
of the invention;
[0033] FIG. 20 is a flow diagram of a portion of a program utilized
in an embodiment of the invention; and
[0034] FIG. 21 is a flow diagram illustrating the performance of
the embodiment of the invention.
DETAILED DESCRIPTION
[0035] In FIG. 1, there is shown a block diagram of a preparatory
liquid chromatographic system 10 having a pumping system 12, a
column and detector array 14, a collector system 16, a controller
18 and a purge system 20. The pumping system 12 supplies solvent to
the column and detector array 14 under the control of the
controller 18. The purge system 20 communicates with a pump array
34 to purge the pumps and the lines between the pumps and the
columns between chromatographic runs. The pump array 34 supplies
solvent to the column and detector array 14 from which effluent
flows into the collector system 16 under the control of the
controller 18. The controller 18 receives signals from detectors in
the column and detector array 14 indicating bands of solute and
activates the fraction collector system 16 accordingly in a manner
known in the art. One suitable fraction collection system is the
FOXY.RTM. 200 fraction collector available from Isco, Inc., 4700
Superior Street, Lincoln, Neb. 68504.
[0036] To supply solvent to the pump array 34, the pumping system
12 includes a plurality of solvent reservoirs and manifolds, a
first and second of which are indicated at 30 and 32 respectively,
a pump array 34 and a motor 36 which is driven under the control of
the controller 18 to operate the array of pumps 34 in a manner to
be described hereinafter. The controller 18 also controls the
valves in the pump array 34 to control the flow of solvent and the
formation of gradients as the motor actuates the pistons of the
reciprocating pumps in the pump array 34 simultaneously to pump
solvent from a plurality of pumps in the array and to draw solvent
from the solvent reservoirs and manifolds such as 30 and 32.
[0037] During this pumping process a pump piston may become jammed.
If a pump in the pump array 34 should become jammed, there is an
automatic release mechanism for releasing pressure from at least
that one pump to avoid damage. In the preferred embodiment, the
release mechanism is a fluid pressure release mechanism for that
pump set at a value above the rate pressure such as at 170 psi so
the motor 36 may continuously move the pistons up and down without
damage. Moreover, valves in the pump array 34 control the amount of
liquid, if any, and the proportions of liquids from different
reservoirs in the case of gradient operation that are drawn into
the pump and pumped from it. The manifolds communicate with the
reservoirs so that a plurality of each of the solvents such as the
first and second solvents in the solvent reservoir manifold 30 and
32 respectively can be drawn into the array of pumps 34 to permit
simultaneous operation of a number of pumps.
[0038] While in the preferred embodiment, an array of reciprocating
piston pumps are used, any type of pump is suitable whether
reciprocating or not and whether piston or not. A large number of
different pumps and pumping principles are known in the art and to
persons of ordinary skill in the art and any such known pump or
pumping principle may be adaptable to the invention disclosed
herein with routine engineering in most cases provided that one
motor drives a plurality of pumps. While two solvents are disclosed
in the embodiment of FIG. 1, only one solvent may be used or more
than two solvents. Because of the operation of a plurality of pumps
simultaneously driven by a single motor, efficiency and cost
reduction are obtained by this pumping mechanism.
[0039] To process the effluent, the collector system 16 includes a
fraction collector 40 to collect solute, a manifold 42 and a waste
depository 44 to handle waste from the manifold 42. One or more
fraction collectors communicate with a column and detector array 14
to receive the solute from the columns, either with a manifold or
not. A manifold may be used to combine solute from more than one
column and deposit them together in a single receptacle or each
column may deposit solute in its own receptacle or some of the
columns each may deposit solute in its own corresponding receptacle
and others may combine solute in the same receptacles. The manifold
42 communicates with the column and detector array 14 to channel
effluent from each column and deposit it in the waste depository
44. The fraction collector 40 may be any suitable fraction
collector such as that disclosed in U.S. Pat. No. 3,418,084 or the
above-identified FOXY fraction collector.
[0040] The column and detector array 14 includes a plurality of
particularly economical flow cells, a different one of the flow
cells communicating with each of the columns. The flow cells
include within them light guides positioned so that the effluent
flows between them and around them, the light guides being
sufficiently close to obtain suitable sensitivity at high light
absorbance for a preparatory operation as will be described
hereinafter and the total cross-sectional area of the flow path and
the total volume of flow being sufficient to permit bubbles, if
any, to flow around the light guides so as to avoid distorting the
detection of light.
[0041] In FIG. 2, there is shown a partly schematic and partly
elevational view of the first solvent reservoir and manifold 30,
the second solvent reservoir and manifold 32 and the purge system
20 illustrating the manner in which the manifolds are mounted in a
housing 160. The first solvent reservoir and manifold 30 includes a
first manifold 52 having one inlet and ten outlets 58A-58J, a
conduit 56 and a first solvent reservoir 50, which solvent
reservoir 50 holds a first solvent 54. The conduit 56 communicates
with the solvent 54 in the solvent reservoir 50 on one end and
communicates with the interior of the manifold 52 at its other end.
Each of the outlets 58A-58J of the manifold 52 communicate with the
interior of a different one of ten cylinders of the pumps (not
shown in FIG. 2) through appropriate valves. Similarly, the second
manifold 53 communicates with the second solvent 55 in the second
solvent reservoir 51 through a conduit 57. The manifold 53 has a
plurality of outlet conduits 59A-59J which communicate with the
interiors of a corresponding number of the pump cylinders through
appropriate valves as described in more detail hereinafter so that
the solvent from the reservoir 50 and the solvent from the
reservoir 51 may be mixed together in a proportion that is set in
accordance with the timing of the valves.
[0042] The purge manifold 96 communicates with a gas source 90
through a conduit 91 and a pressure regulator 92 and the three-way
valve 94 to maintain an appropriate pressure for purging the lines.
This manifold 96 has ten outlets 98A-98J each communicating with a
different one of the ten conduits connecting a corresponding one of
the corresponding pumps to a corresponding one of ten corresponding
columns to transmit gas back through the piston pumps to purge the
cylinders of the piston pumps and the conduits connecting the pumps
to the columns. Each of the conduits connected to the purge
connector arrangement lead to a corresponding pump in the pump
array 34 (FIG. 1) which in turn communicates with the corresponding
one of the columns in the column and detector array 14 (FIG. 1).
One such purge connector arrangement 76E is shown in FIG. 2
connected by a conduit 99E to the outlet 98E from the manifold 96
to purge the conduits 68E and 88E.
[0043] Between chromatographic runs, the pressurized gas source 90,
which is commonly a source of nitrogen gas, communicates through
the pressure regulator 92 and the three-way valve 94 with the
manifold 96 to provide purging fluid to each of the corresponding
outlets 98A-98J for each of the pump and column combinations
indicated by the T joints, one of which is shown at 80E.
[0044] With this arrangement, respective ones of the purge conduits
99A-99J (only 99E being shown in FIG. 2 connecting manifold outlet
98E to check valve 82E) are connected to apply air or nitrogen gas
or other purging substance to the respective ones of the T-joints
80A-80J (80E being shown in FIG. 2) to purge conduits 68A-68E (68E
being shown in FIG. 2) and 88A-88E (88E being shown in FIG. 2) and
their corresponding pumps through a corresponding one of the purge
connectors 76A-76J (76E being shown in FIG. 2). Each of the purge
connections, such as 76E, corresponds with a corresponding one of
the manifold purge outlets 98A-98J, the corresponding one of the
check valves 82A-82J and corresponding ones of the conduits
88A-88E. The check valves 82A-82J are arranged to prevent effluent
from the pumps from flowing back to the manifold 96 and the
electrically operated three way valve 94 permits selecting the time
for purging under the control of the controller 18 (FIG. 1). The
purge system 20 permits purging of the pumps as well as the lines
between the pumps and the column and detector array 14 and in the
column and detector array 14.
[0045] While in the preferred embodiment, the manifolds 52, 53 and
96 each have ten outlet conduits which communicate with ten pump
cylinders through appropriate valves as will be described
hereinafter, each could have more or less than ten outlets. Each of
the reservoirs is similar to the reservoir 30 and operates in a
similar manner to provide the same solvent from the same reservoir
to a plurality of pump cylinders for simultaneous pumping of the
solvent into a plurality of columns.
[0046] In FIG. 3, there is shown a schematic block diagram of a
pump array 34 having a plurality of piston pump systems 60A-60J,
the piston pump systems 60A-60E, being shown for illustration in
FIG. 3 although in the preferred embodiment there are ten such
pumps each arranged to communicate with corresponding ones of the
ten outlets from the manifold 52 and with corresponding ones of the
outlets from the manifold 53 to pump solvent from the reservoirs 50
and 51 (FIG. 2) into corresponding ones of the columns (not shown
in FIG. 3). In FIG. 3, four of the pump systems 60A-60D are shown
in block form and a fifth 60E is shown in greater detail with the
understanding that each of the ten pump systems are substantially
identical so that the explanation of the pump system 60E is an
adequate explanation for all of the pump systems.
[0047] Each of the pump systems communicates with a corresponding
one of the manifold outlets 58A-58J and 59A-59J to receive two
different solvents for the purpose of forming a gradient. They may
also communicate with a source of purge fluid as indicated by the
purge conduits 66A-66J. With this arrangement, each of the pumps
draws solvent into it from the solvent reservoirs 50 and 51 (FIG.
2). The solvent flows from the pumps through a corresponding one of
the outlets 68A-68J.
[0048] The pump system 60E includes the inlet conduit 58E from the
first solvent reservoir 50 and manifold 52 (FIG. 1 and 2), the
inlet conduit 59E from the second solvent reservoir 51 and manifold
53, a three-way solenoid valve 70E, a two-way solvent valve 72E, a
long flow conduit 73E, a reciprocating piston pump 74E, and a check
valve 78E. With this arrangement, the two different solvents from
conduit 58E and 59E are applied to the pump 74E through a common
point connecting the three-way solenoid valve 70E and the two-way
solvent valve 72E. In the preferred embodiment, two cycles of
solvent are applied for each stroke of the piston pump. The size of
the cylinder, the size of the flow conduit 73E, the speed of the
refill and delivery strokes of the piston are selected to ensure
mixing within the pump 74E and flow conduit 73E so as to pump a
formed gradient through the conduit 86E, through the check valve
78E and the outlet conduit 68E to the column and detector array 14
(FIG. 1). For this purpose the pump cylinders are in the range of
one inch to eight inches long. In the preferred embodiment, the
cylinders are 3.5 inches long.
[0049] To provide two injections or charges of solvent during a
refill portion of a pump cycle, the two-way
electronically-controlled solvent valve 72E opens once during each
piston refill stroke of the pump 74E and closes during the delivery
portion of the pump cycle. In the preferred embodiment, the valve
72E is a solenoid valve. To provide a gradient, the three-way
electronically-controlled proportioning valve 70E twice during each
refill stroke opens first to the first solvent reservoir 50 and
then to the second solvent reservoir 51 (FIG. 2) to provide both
solvents in two stages for better mixing. The proportion of the
time the valve 70E is open to the first solvent reservoir 50 and
then to the second solvent reservoir 51 determines the composition
of the mixture in the gradient. Both of the solenoid operated
valves 70E and 72E are under the control of the controller 18 to
which they are electrically connected. Between chromatographic
runs, the lines may be purged through the conduit 66E for air or
nitrogen, through the check valve 82E and through the T-joint 80E
which are connected in the preferred embodiment to the piston pump
74E and to the check valve 78E.
[0050] In FIG. 4, there is shown an elevational view of the
backside of the chromatographic system 10, simplified for purposes
of explanation including the pump array 34 with a plurality of
pumps 74A-74J (74F, 74E and 74D being shown in FIG. 4) with pistons
182E and 182F being driven by the carriage 174 as will be explained
more completely hereinafter. For convenience, three inlets to the
pumps 74F, 74E and 74D are shown, with 74E being at the opposite
side of the carriage 174 from 74F and 74E and 74D. The pumps 74F,
74E, and 74D are connected at their inlet ports to respective ones
of the flow conduits 73F, 73E and 73D respectively to receive fluid
from corresponding ones of the valves 70F, 70E, and 70D. The valves
70F, 70E and 70D are, in turn, connected to the valves 72F, 72E and
72D to receive solvent from respective ones of the valves 72F, 72E
and 72D connected to respective ones of the outlets of the manifold
52 and from respective ones of the outlets of the manifold 53 so
that the valves 72F, 72E and 72D combine the first and second
solvents and permit them to flow to corresponding ones of the
valves 70F, 70E and 70D. Similarly, the manifold 96 has its outlets
connected to corresponding ones of the check valves 82A-82J (82E
being shown in FIG. 4) and of corresponding ones of the T-joints
80A-80J (T-joint 80E being shown in FIG. 4) within the conduits 86E
and 68E (FIG. 3) and its inlet connected to a source of air or
nitrogen 91 through the pressure regulator 92 and valve 94 to
provide a purging flow of air or nitrogen between chromatographic
runs.
[0051] In FIG. 5, there is shown an elevational sectional view
taken through lines 5-5 of FIG. 6 of the pump array 34 including
pumps 74A-74J and the single motor 36 which is a Pittman Model GM
14901E161 available from Pittman Division of Penn Engineering,
having an address at 343 Godshall Drive, Harleysville, Pa.
19438-0003. The pump array includes a ball screw 172, a piston rod
drive plate 174, a ball nut assembly 176, and a cylinder retaining
plate 178. With this arrangement, the motor 36 drives the ball
screw 172 to pull the piston rod drive plate 174 upwardly and
pushes it downwardly as the ball screw assembly 172 is rotated by
the motor 36. The ball nut assembly 176 is rigidly attached to the
piston rod drive plate 174. As the piston moves, the pump cylinders
are held in place by the cylinder retaining plate 178 so that each
of the pumps pumps simultaneously.
[0052] In this view, only pump 74E and the pump 74J are shown, and
only the pump 74E will be described in detail with the
understanding that each of the pumps 74A-74J are substantially the
same. The pump 74E includes the piston rod 180E, the piston 182E,
the cylinder 184E, a piston plug 186E, an inlet 188E and an outlet
190E. With this arrangement, the piston rod 180E drives the piston
182E within the cylinder 184E. As the piston 182E is moved
downwardly, solvent is pulled through the inlet 188E in the piston
plug 186E at the top of the cylinder 184E and when the piston 182E
is moved upwardly, fluid is forced from the pump outlet 190E within
the plug 186E.
[0053] In the preferred embodiment, the pumps 74A-74J have a
cylinder displacement programmable for 5 to 18 ml and pump at
pumping rates between 5 to 50 ml/min. The valves 70A-70J twice each
refill cycle select: (1) an open position to first solvent 54 (FIG.
2) or a closed position in which no solvent flows for 100 percent
solvent 54; or (2) an open position for the first solvent followed
by an open position for the second solvent 55 for a mixture. These
values may vary and are selected so that a gradient can be formed
suitable for preparatory chromatography to obtain the desired
substance. With this arrangement, the time the valves are open
determines the respective amounts of the first and second solvents
that are injected in that time period so that both the first
solvent 54 and second solvent 55 are injected into the pump
cylinder 184E in selected amounts twice in each intake stroke of
the pump in which the piston plug 186E moves downwardly.
[0054] In the refill of a pump cycle portion, because of the length
of the flow paths in the cylinders and in the flow conduits
73D-73F, the cylinder length and the speed of the refill stroke,
the solvents are mixed to form substantially continuous steps of
stepped gradient (the gradient may proceed in steps but each step
from a pump cycle is substantially continuous) as the solvent is
pulled inwardly. For this purpose, the refill stroke of the piston
is at least 3 times faster than the delivery stroke to cause
turbulent flow in the cylinder during refill. The two-way valves
72D-72F permit fluid to flow into the cylinder 184E during a refill
stroke and close the cylinder 184E during a delivery stroke so that
the cylinder 184E receives a fixed amount of fluid which it pumps
outwardly. The stroke is controlled by the motor 36 and ball screw
172 under the control of the controller 18 (FIG. 1). This is
acceptable with preparatory chromatography because the demands on
the continuousness of the flow are not as great as in analytical
chromatography.
[0055] The motor 36 is mounted to the housing of the
chromatographic system by the mounting bracket 192 and coupled to
the ball screw 172 through the coupling 194 to rotate the screw rod
within the ball screw 172 and thus pull the drive plate 174
upwardly and downwardly. The drive plate 174 is guided in its path
by two guide rods 196 and 198 (FIG. 4).
[0056] In FIG. 6, there is shown a sectional view through lines 6-6
of FIGS. 4 and 5 showing the placement of the cylinders for the
pumps 74A-74J as held within the cylinder retaining plate 178. As
shown in this view, the ball screw 172 passes through the plate so
as to pull upwardly the piston drive plate 174 in a delivery stroke
and move downwardly the piston drive plate 174 in a pump cylinder
filling stroke. The guide rods 196 and 198 guide the drive plate
upwardly and downwardly.
[0057] In FIGS. 7-12 there is shown a developed view of the two way
valve 72E, the inlet tubing 73E, and the pump 74E showing six
different positions of the pump which result in mixing of solvents
A and B in the preferred embodiment to provide a gradient that is
suitable for preparatory chromatography. The diameter of the inlet
tubing 73E is selected so as to facilitate mixing of solvents A and
B which are inserted one after the other into the tubing 73E by
proportioning valve 70E to provide charges into the pump chamber.
The pump chamber is also sufficiently long to facilitate mixing. In
the preferred embodiment, the tubing 73E has a length of 35 inches
and should have a length of between 10 inches and 250 inches and a
narrow inner diameter, such as for example 0.085 inches. The
cylinder 160E is relatively long and narrow, being 3.6 inches long
with a diameter of 0.612 inches in the preferred embodiment. It
should have a length in the range of 3 to 8 inches and a ratio of
length to diameter of between 3 and 8 inches.
[0058] The cylinder 160E is shown in FIG. 7, the initial position,
against the head 168E in which blocks flow into the inlet 162E into
the tubing 73E and outflow from the outlet 164E. A short time
later, the piston 161E has been withdrawn causing fluid to flow
through the inlet 162E which is on one side of the cylinder 160E to
cause mixing as a circular current is formed such as in the eddy
current as shown in FIG. 8 at 166E. Still later, as shown in FIG.
9, further eddy currents occur in the pump chamber as the piston
continues to withdraw and as shown in FIG. 10 still further eddy
currents near the piston. The eddy currents result in mixing before
the pump stroke of the piston. In FIG. 12, the upward stroke is
beginning in position six and the downward stroke has ended so as
to move a relatively well mixed fluid out through the outlet.
[0059] In FIG. 13, there is shown a schematic diagram of a column
and detector array 14 having a plurality of columns and detectors 5
of which are indicated as 100A-100E, a corresponding plurality of
outlet conduits 68A-68E; a corresponding plurality of solute
outlets 110A-110E; a corresponding plurality of waste outlets
108A-108E from the manifold 42 and a fraction collector 40. In the
preferred embodiment, there are ten columns and detectors. For
illustration, the column and detectors 100A-100D are shown as a
general block whereas the column and detector 100E is shown in
greater detail with the understanding that the collector and
detectors 100A-100D are substantially the same. Moreover, while
five collectors and detectors are shown to correspond with the
example being used in this application, more or fewer could readily
be used and ten are used in the preferred embodiment.
[0060] The collector and detector 100E includes the injector system
102E, a column 104E, a detection system 106E, the waste outlet 108E
and the solute outlet 110E. With this arrangement, solvent, whether
a gradient or not, flows in the conduit 68E through the injector
102E, a column 104E, the flow cell 122E, where solute may be
detected and from there into the collection system 40 for the
collection of solute and the disposal of waste. The column 104E may
be any type of chromatographic column regardless of the mode of
operation and it is generally picked in accordance with the
separation of problem. In the preferred embodiment the column is
the REDISEP disposable column sold by Isco, Inc., 4700 Superior
Street, Lincoln, Neb. 68504. It is mounted to either receive a
sample injection manually from a syringe or automatically from the
injector 102E as well as receiving solvent on the outlet 68E. Its
outlet flows through the detection system 106E.
[0061] The detection system 106E includes a light source 142E, a
flow cell 122E, a detector 124E and a valve 126E for channeling
fluid either to the waste outlet 44 through conduit 108 or to the
collector on outlet 110E. The light source 142E hereinafter
referred to as the optical bench applies light from a source common
to each of the column and detector assemblies 100A-100E and applies
it through each of the corresponding ones of the flow cells
including the flow cell 122E and from there to the corresponding
detectors including the detector 124E. The signal received
indicates the effluent to be channeled to the collector and that to
be channeled to waste for the particular column and detector
system.
[0062] The injector system 102E includes a solid sample load
cartridge 101E and a four-way manual selective valve 103E for
controlling the selection of sample and injection into the column
104E. In the embodiment of FIG. 13, an individual injector system
(injector system 102E being shown in FIG. 13) is provided for each
of the column although the outlet from one injector could go to a
manifold to supply the same sample to a plurality of columns and/or
the outlet from one injection cartridge could go to a plurality of
injection valves if desired. Similarly, a single fraction collector
40 is shown but a plurality of such collectors could be used with
the individual valves connected to more than one collector. The
injector 102E includes the four-way valve 103E for alternately
injecting sample from the sample cartridge 101E and selecting the
solvent gradient from the outlet 68E from the pumping system. Thus
a sample may be injected and then with a turning of the manual
valve 103E the chromatographic run may be initiated. While a manual
four-way valve 103E is shown, automatic injector valves are also
available and may be utilized.
[0063] In FIG. 14, there is shown a diagrammatic view of an optical
bench 120 common to all of the flow cells 122A-122J and one
reference flow cell 122R, having a single stable illuminated spot
131, a diffraction grating system 132 and a multiple pickup system
134 for providing stable light to each of the flow cells 122A-122J
and the reference cells 122R. The illuminated spot 131 is the
bright spot of a deuterium lamp 130. With this arrangement, a
single small stable spot of light is transmitted onto the
diffraction grating system 132 which in turn supplies the light to
the multiple pickup system 134 for transmission through multiple
paths for the multiple light sources such as 142A-142J and 142R for
use by the corresponding detectors 124A-124J and 124R and flow
cells 122A-122J and 122R in the system. The single light source 130
includes a suitable lamp 136, an aspherical condensing mirror 138,
a source aperture plate 150 and an aspherical focusing mirror
154.
[0064] The lamp 136, which in the preferred embodiment is a
deuterium lamp, transmits light from its central spot 131 to the
condensing mirror 138 which reflects the light through a small
aperture 152 in the aperture plate 150 to provide a narrow spot of
light to the focusing mirror 154 for reflection onto a diffraction
grating in the diffraction grating system 132. A suitable system of
this type is described in greater detail in U.S. Pat. No. 5,239,359
except that instead of including aperture stops to restrict the
light to a small flow cell opening, the light is focused onto a
slit 157 in an aperture plate 156 for multiple light guides
142A-142J and 142R to multiple flow cells 122A-122J and 122R. The
grating 132 reflects a stable line of light from the central spot
of a selected frequency through a slit 157 in an aperture plate 156
mounted to the collar or tubular member 175 within the multiple
pickup 134.
[0065] The aspherical condensing mirror 138 is used to focus an
image of the 1-mm diameter light source in the deuterium lamp 130
on the UV entrance slit at the monochromator light entrance. The
aspherical focusing mirror 154 produces a focused anastigmatic slit
image, at the wavelength selected by the diffraction grating 132,
on the slit-shaped entrance aperture of an 11-channel fiber optic
bundle. Each channel consist of one, single discrete UV-grade
quartz optical fiber of 400 .mu.m diameter. The fiber optic bundle
allows a single sample, low cost monochromator to be used for
multiple UV absorbance chromatographic detectors. This results in
cost savings in a parallel system.
[0066] The diffraction grating 132 is a plain grating with 1200
grooves per millimeter, and disperses the light from the lamp 136.
The angle between the diffraction grating 132 and the central light
beam coming from the aspherical focusing mirror 154 determines the
center wavelength of the light entering the multiple individual
optic fibers in the fiber optics bundle. The software controls an
encoded motor, which actuates the grating in the monochromator.
This allows the computer to control the detection wavelength used
by the system. This encoded motor precisely sets the angle between
the aspherical focusing mirror 154 and diffraction grating 132 by
moving an arm to which the diffraction grating 132 is attached. The
diffraction grating 132 swings on an arm to keep the monochromator
focused throughout the wavelength range.
[0067] The light travels through the respective optic fibers in the
fiber optic bundle. Each optic fiber is coupled to a flow cell,
which is the light exit of the monochromator. A total of eleven
individual optical fibers are organized in a nested linear array in
the light inlet and fiber optic bundle to maximize the amount of
light to each individual optical fiber and minimize the difference
in light level and wavelength between them. Ten of the optical
fibers are coupled to flow cells, which pass light through the
chromatographic flow stream and then to measuring detectors. The
reference fibers (eleventh fiber) is near the center of the linear
array to minimize flicker noise from the deuterium lamp 130.
[0068] The multiple pickup 134 includes the aperture plate 156, the
optical fibers 142A-142J and 142R positioned along the slit 157 so
that the narrow slot of light is applied to them. The optical
fibers transmit the light to corresponding ones of the flow cells
122A-122J and 122R with each of the flow cells including a
corresponding light guide described hereinafter that transmits the
light to a matching light guide in the flow cell. The matching
light guide receives the light after it has passed through the
effluent and transmits it to photodetectors.
[0069] In FIG. 15 there is shown a plan view of the aperture plate
156 having a central elongated opening or slit 157 within a tubular
member 175. The central elongated opening 157 has within it
aperture stops 176R, 176A-176J each receiving a corresponding one
of the light guides 142R, 142A-142J for a reference light source
and light sources 142A142J. This provides substantially equal
intensity light sources to each of the flow cells 122R, 122A-122J
to provide a reference 122R and ten measuring flow cells. In this
manner, a stable source of light is reflected onto multiple light
guides 142R, 142A-142J for use by the multiple detectors and flow
cells of the system. The multiple light guides are a fiber optics
bundle.
[0070] In FIG. 16, there is shown a block diagram of the flow cells
122A-122E, the detectors 124A-124E and the controller 18
interconnected to illustrate some aspects of the invention that are
applicable to the flow cells 122R, 122A-122J and detectors
124R,124A-124J. As best shown in FIG. 16, the flow cell 122E
includes a first light guide 143E, a second light guide 140E and
the flow path 148E for effluent through the flow cell 122E. As
shown in this view, the two light guides 143E and 140E are
positioned adjacent to each other and in close proximity with the
flow path 148E extending around it with sufficient volume to permit
bubbles to pass around the space between the light guides 143E and
140E rather than blocking the path in the light guides. The light
guide 143E is in communication at one end with the light guide 140E
with the fluid in the flow cell 122E and at its opposite end with a
photodiode detector 124E to detect light absorbance within the flow
path 148E. This signal is applied with appropriate buffering to the
controller 18.
[0071] The controller 18 includes interalia an absorbance monitor
144, a recorder 146 and a microprocessor 147. The absorbance
monitor 144 receives light from the detectors 124A-124E indicating
the light that is absorbed and applies it to the microprocessor 147
which converts it to a logarithmic current. The recorder 146 may be
utilized to record the bands of effluent but because the
application of this chromatographic system is principally
preparatory the recorder 146 will be unnecessary for most
applications. The microprocessor 147 may be an Intel 80C196KC
available from Intel Corporation, 1501 S. Mopac Expressway, Suite
400, Austin, Tex. 78746.
[0072] In FIG. 17 there is shown an enlarged, fragmentary
perspective view of the flow cell 122E. The distance between the
end of the light guide 143E and the end of the light guide 140E in
the flow path 148E is approximately 0.1 mm (millimeters) in the
preferred embodiment and should be in the range of 0.02 mm to 5 mm.
It must be close enough to pass light between the two ends without
excessive refraction or attenuation to prevent detection and far
enough to provide a measure of absorbance sufficient to indicate
the solute.
[0073] In FIG. 18, there is shown a block diagram of a flow cell
122E and the reference flow cell 122R (dry cell with no fluid for
reference purposes) connected to a calibration system to establish
an absorbance signal, adjusted to provide a zero baseline. As best
shown if FIG. 18, the flow cell 122E has within it a light guide
143E, which in the preferred embodiment is a quartz rod, on one
side and on the other side another quartz rod 140E positioned with
its end close to the end of the quartz rod 143E to provide a short
space between them for the flow of fluid 148E in the flow path 148
and a large area around them for the flow of the liquid and any
bubbles that may be in it. The quartz rod 143E abuts or nearly
abuts the end of the light conductor 142E to receive light for
transmission through the fluid 148E and into the light conductor
142E. Similarly, the flow cell 122R has the light conductor 142R
abutting a quartz rod 143R which is inside the flow cell 122R and
closely adjacent to the end of another quartz rod 140R for
receiving light transmitted by the quartz rod 143R.
[0074] The light transmitted by the quartz rods 140E and 140R is
converted to an electrical signal by the photodiode 191E and 191R
respectively. This signal is conducted through the circuits 181E
and 181R respectively transmitting it for absorbance in the fluid
148R to the circuit 181. The space between light conductors and the
quartz light guide and between the photodiode and light guide is as
short as possible to permit focusing in the case of different
diameters. If the same diameter, they would touch but are separated
slightly to permit the light from the small diameter to expand to
the larger diameter or vice versa.
[0075] To receive and correct the signal from the flow cell such as
122E with respect to the reference 148R, the circuit 181 includes
the signal receiving circuits 181E and 181R to receive and process
the signal from the flow cells such as the flow cell 122E with
respect to the reference signal from the reference flow cell 122R.
The signal receiving circuit 181E includes a photodiode detector
191E, and amplifier 192E and analog-to-digital converter 194E and a
logarithmic conversion circuit 196E.
[0076] The photodiode detector 191E abuts the quartz rod 140E to
convert the absorbance signal from the fluid 148E to an electrical
signal, which is amplified in the amplifier 192E and converted to a
digital signal. The digital signal is converted to a logarithmic
signal of the received signal in the converter 196E by a standard
digital conversion in the microprocessor and transmitted to one
side of a reference signal subtracter. Similarly, the signal
receiving circuit 181R includes a photodiode detector 191R for
receiving the reference signal from the reference flow cell 148R
and converting it to an electric signal.
[0077] The electric signal is amplified by an amplifier 192R
connected to the photodiode detector 191R and transmitted to the
analog-to-digital converter 194R which in turn transmits a digital
signal representing absorbance to the logarithmic of the received
signal in the converter 196E by a standard digital conversion in
the microprocessor and transmitted to one side of a reference
signal subtracter. The reference signal subtracter subtracts the
reference signal from the reference flow cell 122R from the
absorbance signal from the flow cell 122E, resulting in a signal
representing the absorbance which is transmitted to a reference
off-set circuit 184. The reference off-set circuit 184 transmits a
signal to a signal zero control circuit 186 that by subtracting a
baseline constant in a manner known in the art and transmits the
corrected absorbance signal through the conductor 188. In the
preferred embodiment, there is a reference cell of the ten
measuring flow cells and the necessary calculations are performed
in a microprocessor.
[0078] The flow cells 122R and 122A-122J have a very short
pathlength for the light, which allows very concentrated samples to
be monitored. This short pathlength is accomplished by inserting 2
millimeter diameter UV quartz rod light guides 143R, 143A-143J and
140R, 140A-140J into each of the corresponding ones of the flow
streams 148R, 148A-148J with a very small gap between each pair of
two rods (typically 0.1 mm). This allows a very short effective
pathlength for the light, while also allowing unrestricted flow to
the fluid around the quartz rods. The light guides 143R and 140R
and light source from an optical fiber 142R is coupled to a blank
(dry) flow cell 122R, which passes light to a reference detector
191R. The reference detector signal is used for background optical
noise and drift subtraction on the remaining detector channels. For
purposes of best noise and drift reduction, the optical fiber used
for the reference is not one of the four outermost fibers in the
nested array.
[0079] The measuring and reference photodiode signals are amplified
with linear amplifiers 192R, 192A-192J (192E and 192R being shown
in FIG. 18). This signal is converted to a digital information with
analog-to-digital converters 194R, 194A-194J (194E and 194R being
shown in FIG. 18). These digital signals are converted to
logarithms in the converters 196R, 196A-196J (196E and 196R being
shown in FIG. 18). Now the reference signal can be subtracted to
compensate for lamp energy variations in the reference signal
subtracter 182. Next the baseline offset value is subtracted in the
off-set circuit 184. This zeroes out almost all absorbance due to
optical imbalance, including that of refractive index (thermal)
gradients in the clean solvent flowing through the system. The
baseline offset value is determined at the beginning of the
separation. The signal at the start of the separation does not
contain any solutes. The signal is stored and subtracted from the
signal for the duration of the separation. This results in the
correct absorbance signal. Both analog and digital methods of
accomplishing these signal conditioning tasks are well known in the
art.
[0080] Current state of the art in optical fiber technology results
in fibers that have a varying susceptibility to transmission
degradation (solarization) in the UV spectrum. It is also desirable
to leave the UV lamp on to improve lamp thermal stability and hence
detection stability. To satisfy these conflicting requirements, the
diffraction grating is programmed to focus visible light on the
fiber optics bundle at all times except when an actual separation
is occurring. It is also possible to move the grating to the far UV
(below 100 nm) where the energy output of the lamp is negligible.
This reduces the amount of time the fibers are exposed to UV
thereby reducing solarization, greatly increasing the life of the
optical fibers while allowing the lamp to remain on between
separations.
[0081] In FIG. 19, there is shown in block diagram having the
fraction collector diverter valves 214, the flow cell and detector
array 124, the controller 18, the pressure transducer 218 and the
valve array 212 for the pumping system. This block diagram
illustrates the connections between the controller 18, the pump
drive motor 36, the fraction collector diverter valves 214, the
flow cell and detector array 124, and the inlet purge and mixing
valves 212. As shown in FIG. 19, the controller 18 includes inter
alia functional components: the pump controller 200 and the valve
and detector controller 201. The valve array 212 includes the pump
mixing valves 70, the inlet valves 72 and the purge valve 94.
[0082] As shown in FIG. 19, the pump controller 200 is connected to
the series pump drive 36 and a pressure transducer 218 in a
feed-back arrangement such as that described in U.S. Pat. No.
5,360,320, the disclosure of which is incorporated herein by
reference. Specifically, the feed-back circuit disclosed in
connection with FIGS. 8 and 9 in columns 11,12,13 and 14 of U.S.
Pat. No. 5,360,320 for controlling the pump disclosed in FIG. 4 of
that patent is utilized here. The pump controller 200 also
interacts with the valve and detector controller 201 to control the
flow cell and detector array 124 and the fraction collector
diverter valves 214 for the fraction collector 40 (FIG. 13). The
valve and detector controller 201 supplies signals to control the
mixing valves 70A-70J shown collectively at 70, the inlet valves
72A-72J shown collectively at 72 and the purge valve 94 of the
valve array 212. With this arrangement, the detection of bands to
be collected controls the fraction collector valves to channel the
collection into appropriate containers.
[0083] In FIGS. 20 and 21, there is shown a block diagram
illustrating the operation of the controller 18 under software
control having a series of programed steps 230 for initiating the
pump fill cycle as shown in FIG. 20 and a series of steps 232 for
forming a gradient in the pump as shown in FIG. 21. The series of
steps 230 for initiating pump refill operation includes a start
step 234, a clear-registers step 236 for percentage B solvent and
total volume, a step 238 to move forward in gradient time until one
milliliter is delivered except for the percentage found in
percentage solvent B register and the percentage B solvent array
and adding one milliliter to total volume, the step 240 of deciding
if total volume is equal to the refill stroke or the end of the
gradient, the step 242 of adding the percentage B solvent array
together and dividing the two together to get the average
percentage of B solvent to total solvent for the stroke and
calculating the pumps position for switching three-way valves and
the step 244 for turning on the two-way valve to open the path to
the fluid from the three-way valve and putting the pump into the
refill mode and start refilling. These steps proceed in succession
as listed above.
[0084] As shown by the decision step 240, if the total volume is
equal to the refill stroke or the end of the gradient, the step 240
goes to step 242 to add all percentage B solvent array values
together and divide by total volume to get the average of B solvent
to total solvent for the stroke and calculating the pumps position
for switching the three-way valves. If the decision is no at
decision step 240 then step 238 is repeated to move the pistons in
the pump array forward in gradient time until one milliliter is
delivered except for the percentage found in the percentage of B
solvent to total solvent array and adding one milliliter to total
volume.
[0085] When the pump is in the refill mode at the end of step 244
and refilling has started as shown at position 246 (FIGS. 20 and
21), the program proceeds to step 248 (FIG. 22). Step 248 is a
decision step deciding if the pumps position is equal to the
position for switching to the A solvent. If it is then the program
proceeds to step 250 to switch the three-way valve to solvent A and
then returns to position 246. If the decision at step 248 in no,
then the program proceeds to step 252 to decide if the pumps
position is equal to the position for switching to the B solvent.
If the decision is yes, then the program proceeds to step 254 to
switch the three-way valve to solvent B and from there back to
position 246. If the decision is no, then the step proceeds to
decision step 256 to decide if the pump is full or the pump equal
to the total volume. If the decision is no, then the program
proceeds to step 246. If the decision at step 256 is yes, then the
program proceeds to step 258 to turn off the two-way valve after
which the program ends as shown at step 260.
[0086] In operation, a plurality of simple syringe pumps are driven
by the same motor to draw solvent simultaneously and pump the
solvent simultaneously through a corresponding plurality of columns
for separation and through a plurality of detectors for detecting
solute and channeling it into a fraction collector for automatic
collection. The solvent is pulled from one or more manifolds so
that a plurality of flow streams may be pulled into the
corresponding plurality of pumps from one or more solvent
reservoirs to form a gradient. In the case of gradient elution, a
valve opens to pull a first solvent into the cylinder and then
switches to pull in a second solvent. In the preferred embodiment,
when forming a gradient, the pump receives two cycles of flow from
two reservoirs so that a valve will cause solvent to flow from a
first reservoir into the pump cylinder and then, except at the
starting point of the gradient, from a second cylinder to pull a
first charge of solvent and repeats with the identical amount from
the first cylinder and the second cylinder to form a second charge
of solvent.
[0087] The solvents are pulled through a flow passageway that is
less than one-tenth the volume of a charge. The flow is mostly in
the transitional stage between laminar flow and bulk or turbulent
flow in the passageway. The passageway has a diameter less than
onehalf of the diameter of a pump cylinder. The force and rate is
enough to cause turbulent mixing in the cylinder of the pump. In
this manner, the gradient is mixed within the pump cylinder so that
a first mixture is pumped from several pumps together into
corresponding columns. If there is an interface between liquids, it
is degraded. It is pumped when the motor moves all of the pistons
of the syringe pumps upwardly. This process is repeated but the
gradient may gradually change so that in a series of steps, a
gradient is supplied. The flow through the passageway produces good
axial mixing and poor transverse mixing of flow on a small scale
and the turbulent flow caused in the pump cylinder enhances
transverse mixing and axial mixing on a larger scale. Larger scale
in this specification means one charge into the cylinder has
approximately one-tenth to one-half of the pump volume and small
scale means one-eighth to one-hundredth pump volume--full
displacement being taken as pump volume (18 ml in the preferred
embodiment). Between these values the quality of the mixing is
proportionately enhanced.
[0088] While simply designed syringe pumps are used in the
preferred embodiment, any other kind of pump may be used. Moreover,
only one cycle of flow of liquids into a pump may be used or
several may be used. Similarly, it is not necessary for two cycles
of the same mixture to be injected into a pump during each filling
of the cylinder but more cycles or one cycle can be used as
programmed. While in the preferred embodiment, a single motor
drives all of the pistons, more than one array of pumps can be
utilized with a motor driving a first plurality and a different
motor driving a second plurality.
[0089] The columns are simple separation columns and one column is
dedicated to each pump. After flowing through the column, the
liquid flows into inexpensively constructed detectors in which
light is applied through light guides into the flow cell and
received by a light guide from the flow cell. Photodetector diodes
are mounted directly against the ends of the receiving light guides
to receive electrical signals just outside of the flow cell. The
spacing of the light guides is such as to provide adequate
detection for preparatory chromatograph and the flow cell is large
enough so that while it detects absorbance of fluid flowing between
the light guides, other fluid flows around the light guides so that
if bubbles are formed in the flow cell, they will pass around the
guides. The light guides are sufficiently close together so as to
not receive large bubbles but to receive a substantial amount of
light passed between the two light guides and be able to determine
the amount of solute from the light that is absorbed.
[0090] A single lamp provides light which is applied to a
condensing mirror from a central spot on the lamp and applied
through an aperture plate to a focusing mirror which focuses on a
diffraction grating positioned to select an appropriate frequency
of light which is stable in a line applied to a slot. The plurality
of light conductors to be applied to detectors are positioned along
the narrow slot to receive stable light of substantially equal
intensity for transmission to the detectors. The detected light is
applied to a typical absorbance monitor which controls a fraction
collector to collect the preparatory fractions. With this
arrangement, since a large number of separations is being performed
simultaneously, a substantial amount of solute can be obtained in a
short time.
[0091] Although a preferred embodiment of the invention has been
described with some particularity, it is to be understood that the
invention may be practiced other than as specifically described.
Accordingly, it is to be understood that, within the scope of the
appended claims, the invention may be practiced other than as
specifically described.
* * * * *