U.S. patent application number 12/566886 was filed with the patent office on 2010-08-12 for obesity controlling method.
This patent application is currently assigned to Temple University-Of the Commonwealth System of Higher Education. Invention is credited to Larry S. Miller.
Application Number | 20100204673 12/566886 |
Document ID | / |
Family ID | 22840162 |
Filed Date | 2010-08-12 |
United States Patent
Application |
20100204673 |
Kind Code |
A1 |
Miller; Larry S. |
August 12, 2010 |
OBESITY CONTROLLING METHOD
Abstract
A method of controlling obesity by injecting bio-compatible
bulking material into the pyloric sphincter area of the stomach.
The injection of this material bulks the pyloric sphincter,
retarding stomach emptying and producing a feeling of satiation in
the patient. The method may be supplemental and augmented by
inducing flacid paralysis of the stomach by injecting botulinum
toxin into the muscle tissue of the antrum or fundus of the
stomach.
Inventors: |
Miller; Larry S.; (Bala
Cynwyd, PA) |
Correspondence
Address: |
DRINKER BIDDLE & REATH;ATTN: INTELLECTUAL PROPERTY GROUP
ONE LOGAN SQUARE, SUITE 2000
PHILADELPHIA
PA
19103-6996
US
|
Assignee: |
Temple University-Of the
Commonwealth System of Higher Education
Philadelphia
PA
|
Family ID: |
22840162 |
Appl. No.: |
12/566886 |
Filed: |
September 25, 2009 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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11478560 |
Jun 29, 2006 |
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12566886 |
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10343668 |
Aug 13, 2003 |
7608578 |
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PCT/US01/24971 |
Aug 9, 2001 |
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11478560 |
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60224324 |
Aug 11, 2000 |
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Current U.S.
Class: |
604/500 |
Current CPC
Class: |
A61K 38/39 20130101;
A61P 3/04 20180101; A61K 31/715 20130101; A61F 5/0079 20130101 |
Class at
Publication: |
604/500 |
International
Class: |
A61M 31/00 20060101
A61M031/00 |
Claims
1. A method for treating obesity in a body of a patient having a
mouth and a gastrointestinal tract extending through a stomach and
a pyloric sphincter formed by a wall comprising passing an
implant-forming material through the mouth and down the
gastrointestinal tract to the vicinity of the pyloric sphincter and
forming at least one implant in the wall in the vicinity of the
pyloric sphincter from the implant-forming material to retard
emptying of the stomach.
2. The method of claim 1 wherein the wall has a muscle layer, the
at least one implant being formed in the muscle layer of the
wall.
3. The method of claim 1 wherein the passing step includes the step
of introducing an endoscope through the mouth and into the
gastrointestinal tract and passing the implant-forming material
through the endoscope.
4. The method of claim 3 wherein the forming step includes the step
of injecting the implant-forming material into the wall.
5. A method for treating obesity in a body of a patient having a
mouth and a gastrointestinal tract extending through a stomach
formed by a wall comprising passing an implant-forming material
through the mouth and down the gastrointestinal tract to the
stomach and forming at least one implant in the wall of the stomach
from the implant-forming material to provoke longer periods of
satiety.
6. The method of claim 5 wherein the wall has a muscle layer, the
at least one implant being formed in the muscle layer of the
wall.
7. The method of claim 5 wherein the passing step includes the step
of introducing an endoscope through the mouth and into the
gastrointestinal tract and passing the implant-forming material
through the endoscope.
8. The method of claim 7 wherein the forming step includes the step
of injecting the implant-forming material into the wall.
9. A method for treating obesity in a body of a patient having a
gastrointestinal tract extending through a stomach and a pyloric
sphincter formed by a wall comprising the step of forming at least
one implant in the wall in the vicinity of the pyloric sphincter to
retard emptying of the stomach.
10. The method of claim 9 wherein the wall has a muscle layer, the
at least one implant being formed in the muscle layer of the
wall.
11. A method for treating obesity in a body of a patient having a
gastrointestinal tract extending through a stomach formed by a
wall, comprising the step of introducing a solution into the wall
of the stomach to form at least one implant in the wall so as to
provoke longer periods of satiety.
12. The method of claim 11 wherein the wall has a muscle layer, the
at least one implant being formed in the muscle layer of the
wall.
13. A method for treating morbid obesity in a body of a mammal
having a mouth and a gastrointestinal tract extending through a
stomach and a pyloric sphincter formed by a wall comprising passing
an implant-forming material through the mouth and down the
gastrointestinal tract to the vicinity of the pyloric sphincter and
forming at least one implant in the wall in the vicinity of the
pyloric sphincter from the implant-forming material to inhibit
emptying of the stomach.
14. The method of claim 13 wherein the wall has a muscle layer, the
at least one implant being formed in the muscle layer of the
wall.
15. The method of claim 13 wherein the passing step includes the
step of introducing a catheter through the mouth and into the
gastrointestinal tract and passing the implant-forming material
through the catheter.
16. The method of claim 15 wherein the forming step includes the
step of injecting the implant-forming material into the wall.
17. A method for treating morbid obesity in a body of a mammal
having a mouth and a gastrointestinal tract extending through a
stomach formed by a wall comprising passing an implant-forming
material through the mouth and down the gastrointestinal tract to
the stomach and forming at least one implant in the wall of the
stomach from the implant-forming material to provoke longer periods
of satiety.
18. The method of claim 17 wherein the wall has a muscle layer, the
at least one implant being formed in the muscle layer of the
wall.
19. The method of claim 17 wherein the passing step includes the
step of introducing a catheter through the mouth and into the
gastrointestinal tract and passing the implant-forming material
through the catheter.
20. The method of claim 19 wherein the forming step includes the
step of injecting the implant-forming material into the wall.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 11/478,560 filed Jun. 29, 2006, which is a
continuation of U.S. patent application Ser. No. 10/343,668 filed
Aug. 13, 2003, which is a National Phase Application of
International Patent Application No. PCT/US01/24971 filed Aug. 9,
2001, which claims the benefit of U.S. Provisional Application No.
60/224,324 filed Aug. 11, 2000.
[0002] The present invention relates to a method of controlling
obesity by injecting bio-compatible bulking material into the
pyloric sphincter area of the stomach. The injection of this
material bulks the pyloric sphincter, retarding stomach emptying
and producing a feeling of satiation in the patient.
BACKGROUND OF THE INVENTION
[0003] Obesity is one of the major causes of heart disease, lipid
abnormalities, hypertension and osteoarthritis. Treatment of
obesity has the potential to lower the risk of all of these
diseases as well as improve the condition of patients who already
suffer from such illnesses. In addition, it is well known that a
large percentage of Americans and Europeans are considered to be
obese based on height and weight ratios issued by the World Health
Organization (WHO). These numbers in conjunction with the dangerous
diseases affiliated with or caused by obesity indicate that there
is a substantial need for effective treatment.
[0004] Current weight reduction programs usually include
administration of systemic medications, which suppress the appetite
or reduce the fat and/or sugar uptake of the digest track. However,
systemic medications often display side effects some of which may
be severe. Dietary changes that reduce caloric intake are also
prescribed for the treatment of obesity, but such treatment
requires rigorous compliance by the patient for effectiveness and
is often ineffective as a result of non-compliance. In addition,
surgery, which bypasses a portion of the stomach and/or the small
intestine, is also used in the treatment of obesity. Surgical
methods, however, are highly invasive and subject a patient to all
the possible risks involved with major surgery including
infection.
[0005] Safe and effective treatment is a long felt need in the
treatment of obesity. Because of complications and/or
ineffectiveness associated with current treatments a minimally
invasive, effective treatment is preferred and is provided by the
method of this invention.
BRIEF SUMMARY OF THE INVENTION
[0006] The present invention provides a minimally invasive method
for controlling obesity comprising injecting a bio-compatible
bulking material submucosally or intramuscularly into the pyloric
area of the stomach in an amount sufficient to cause the lumen of
pylorus to narrow and slow gastric emptying.
DETAILED DESCRIPTION OF THE INVENTION
[0007] The entire disclosure of U.S. patent application Ser. No.
11/478,560 filed Jun. 29, 2006 and Ser. No. 10/343,668 filed Aug.
13, 2003 and U.S. Provisional Application No. 60/224,324 filed Aug.
11, 2000 are expressly incorporated by reference herein.
[0008] The invention is a method of treating obesity in which
gastric emptying is slowed by narrowing the pyloric sphincter or
pylorus. The invention comprises injecting a bio-compatible bulking
material into the pyloric area of the stomach, preferably either
submucosally or intramuscularly. By narrowing the pyloric region of
the stomach, the stomach will fill more quickly and empty more
slowly as a patient eats. The clinical effect of this treatment
will be to increase the time the patient feels satiated after
eating, therefore decreasing the need and desire to eat and
reducing the caloric intake of the patient.
[0009] The pylorus can be caused to narrow by the injection of a
bio-compatible bulking material into the mucosal or muscular area
around the pylorus. Such an injection can be accomplished by a two
step process wherein an endoscopy is performed to locate the
pylorus and a needle is placed through the biopsy channel of the
endoscope in order to inject the bulking material. Such an
injection will increase the bulk of the pylorus and thus narrow the
gastric outlet from the stomach to the start of the small
intestines.
[0010] The bio-compatible bulking materials suitable for the
present invention include collagen, fibrin and elastin as well as
other naturally occurring and synthetically derived bio-compatible
polymers. Certain polymers such as collagen or fibrin glue have
been demonstrated to be well tolerated when injected into lumen in
humans. In addition, such materials are commercially available. For
instance, collagen may be purchased from FribroGen, Inc., Cohesion
Technologies, Inc., Hydromer, Inc., and Bard, Inc., and fibrin glue
may be purchased from Abbott Laboratories, Inc. Various other
similar products for injection include, but are not limited to,
Contigen.RTM.. (Contigen is a registered trademark of the Collagen
Corporation and is a protein composition for medical implants for
relief of urinary tract disorders), Zyderm.RTM.. (Zyderm is a
registered trademark of the Collagen Corporation and is a protein
composition for dermal implantation), Zyplast.RTM.. (Zyplast is a
registered trademark of the Collagen Corporation and is a collagen
implant used for soft tissue augmentation), rh collagen,
Dermalogen.RTM.. (Dermalogen is a registered trademark of
Collagenesis, Inc. and is injectable human tissue for treating
wrinkles and scars), Autologen.RTM.. (Autologen is a registered
trademark of Autogenesis Technologies, Inc. and is processed
collagen for implantation), and autologous fat.
[0011] Collagen for use in the present invention can be from
several sources including porcine, bovine, or human. It can be
either fibrillar or nonfibrillar. Collagen can be administered in
aqueous solution form or in the denatured state as gelatin. In
addition, it can be administered in either a crosslinked or a
non-crosslinked form.
[0012] Although collagen is preferred as the bio-compatible bulking
material to be injected into the pyloric muscle, other materials
can be used. For instance, Teflon paste, synthetic polymeric
hydrogels, glycoaminoglycans, proteoglycans, silicone
microimplants, Durasphere.RTM.. (Durasphere is a registered
trademark of Advanced UroScience, Inc. and consists of
biocompatible, implantable microspheres for local tissue
augmentation), and microbeads suspended in biological fluid
lubricants such as dextran have been demonstrated to be tolerated
when injected into human lumen.
[0013] The amount of bio-compatible bulking material injected into
the pyloric area of the stomach will be dependent of a variety of
factors. For instance, the size of the individual, the severity of
the individual's obesity, and the shape and distension of the
pylorus will all be determinative in calculating the amount of
bulking material injected. It is estimated that the opening of the
pyloric sphincter can be reduced at least 10% and up to 90% by the
instant invention.
[0014] The injection of collagen or fibrin glue into the pylorus is
expected to last for 3 to 12 months. If the body absorbs the
bio-compatible bulking material, it can be re-injected by a repeat
of the method described. If the narrowing of the pylorus is found
to be too great, the opening can be increased by the use of a
balloon, which can be inserted into the pylorus and inflated to
increase the opening. This flexibility in adjusting the pyloric
opening to accommodate specific patent requirements provides a
unique advantage over present surgical procedures.
[0015] While the injection of the bulking bio-compatible bulking
material into the pyloric area will control obesity, the invention
may encompass additional support procedures. For instance, the
pyloric area can also be narrowed by intentionally scarring the
pyloric area with either a laser or a thermal device. In such an
embodiment of the invention, a laser or heating device could be
placed through the biopsy channel of the endoscope and used to
cauterize an area of the pylorus. In addition, in another
embodiment of the invention, a sewing device could be placed
through the biopsy channel of the endoscope and used to sew the
pylorus and narrow the opening of the pyloric sphincter.
[0016] In yet another embodiment of the invention, gastric emptying
can be further delayed by inducing a flaccid paralysis of the of
the stomach. Botulinum toxin will cause a paralysis of the stomach
if it is strategically injected into either the muscles of the
fundus or the antrum of the stomach. Paralyzing the stomach in this
way will prolong satiety by further delaying gastric emptying. The
effects of botulinum toxin is expected to last for a period of 9 to
18 months.
* * * * *