U.S. patent application number 10/323810 was filed with the patent office on 2003-10-30 for hydrogel-forming sustained-release preparation.
This patent application is currently assigned to YAMANOUCHI PHARMACEUTICAL CO., LTD.. Invention is credited to Fukui, Muneo, Nakashima, Hiroshi, Okada, Akira, Sako, Kazuhiro, Sawada, Toyohiro.
Application Number | 20030203024 10/323810 |
Document ID | / |
Family ID | 26490061 |
Filed Date | 2003-10-30 |
United States Patent
Application |
20030203024 |
Kind Code |
A1 |
Sako, Kazuhiro ; et
al. |
October 30, 2003 |
Hydrogel-forming sustained-release preparation
Abstract
The invention provides a hydrogel-type sustained-release
preparation comprising (1) at least one drug, (2) an additive which
insures a penetration of water into the core of the preparation and
(3) a hydrogel-forming polymer, wherein said preparation is capable
of undergoing substantially complete gelation during its stay in
the upper digestive tract such as stomach and small intestine and
is capable of releasing the drug in the lower digestive tract
including colon. By the preparation of the invention, the drug is
efficiently released and absorbed even in the colon so that a
steady and sustained release effect can be achieved.
Inventors: |
Sako, Kazuhiro; (Shizuoka,
JP) ; Nakashima, Hiroshi; (Shizuoka, JP) ;
Sawada, Toyohiro; (Shizuoka, JP) ; Okada, Akira;
(Shizuoka, JP) ; Fukui, Muneo; (Shizuoka,
JP) |
Correspondence
Address: |
SUGHRUE MION, PLLC
2100 Pennsylvania Avenue, NW
Washington
DC
20037-3213
US
|
Assignee: |
YAMANOUCHI PHARMACEUTICAL CO.,
LTD.
|
Family ID: |
26490061 |
Appl. No.: |
10/323810 |
Filed: |
December 20, 2002 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10323810 |
Dec 20, 2002 |
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09702880 |
Nov 1, 2000 |
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09702880 |
Nov 1, 2000 |
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08403752 |
Mar 20, 1995 |
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6436441 |
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08403752 |
Mar 20, 1995 |
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PCT/JP93/01297 |
Sep 10, 1993 |
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Current U.S.
Class: |
424/468 |
Current CPC
Class: |
A61K 9/2054 20130101;
A61K 9/2031 20130101; A61K 9/2018 20130101 |
Class at
Publication: |
424/468 |
International
Class: |
A61K 009/22 |
Foreign Application Data
Date |
Code |
Application Number |
Sep 18, 1992 |
JP |
HEI-4-274979 |
Jun 8, 1993 |
JP |
HEI-5-165263 |
Claims
1. A hydrogel-type sustained-release preparation comprising (1) at
least one drug, (2) an additive which insures a penetration of
water into the core of the preparation and (3) a hydrogel-forming
polymer, wherein said preparation is capable of undergoing
substantially complete gelation during its stay in the upper
digestive tract including stomach and small intestine and is
capable of releasing the drug in the lower digestive tract
including colon.
2. The hydrogel-type sustained-release preparation according to
claim 1, wherein said additive which insures a penetration of water
into the core of the preparation is at least one additive having a
solubility that the volume of water required for dissolving 1 gram
of said additive is not more than 5 ml.
3. The hydrogel-type sustained-release preparation according to
claim 2, wherein said additive which insures a penetration of water
into the core of the preparation is at least one additive having a
solubility that the volume of water required for dissolving 1 gram
of said additive is not more than 4 ml.
4. The hydrogel-type sustained-release preparation according to
claim 1, wherein said hydrogel-forming polymer is either a polymer
having an average molecular weight of not less than 2,000,000 or a
polymer having a viscosity of not less than 1000 cps as measured at
1% concentration in water at 25.degree. C., or a mixture of two or
more of these polymers.
5. The hydrogel-type sustained-release preparation according to
claim 1 or 4, wherein said hydrogel-forming polymer includes at
least one polyethylene oxide.
6. The hydrogel-type sustained-release preparation according to any
one of claims 1 to 5, which comprises (1) at least one drug in an
amount of not more than 85% by weight based on the total
preparation, (2) an additive which insures a penetration of water
into the core of the preparation in an amount of from 5 to 80% by
weight based on the total preparation, and (3) a hydrogel-forming
polymer in an amount of from 10 to 95% by weight based on the total
preparation.
7. The hydrogel-type sustained-release preparation according to any
one of claims 1 to 6, which comprises (1) at least one drug in an
amount of not more than 80% by weight based on the total
preparation, (2) an additive which insures a penetration of water
into the core of the preparation in an amount of from 5 to 60% by
weight based on the total preparation, and (3) a hydrogel-forming
polymer in an amount of from 15 to 90% by weight based on the total
preparation.
8. The hydrogel-type sustained-release preparation according to any
one of claims 1 to 7, wherein said drug is nicardipine
hydrochloride.
Description
TECHNICAL FIELD
[0001] The present invention relates to a sustained-release
preparation capable of releasing a drug for a prolonged period of
time. More particularly, the invention relates to a hydrogel-type
sustained-release preparation capable of satisfactorily releasing a
drug not only in the upper digestive tract but also in the lower
digestive tract, particularly in the colon.
BACKGROUND ART
[0002] A variety of hydrogel-type preparations have heretofore been
proposed for realizing sustained release of drugs. For example,
JP-A-62-120315 discloses a preparation obtained by
compression-molding a drug, a hydrogel-forming water-soluble
polymer and an enteric coating base (the term "JP-A" as used herein
means an "unexamined published Japanese patent application").
JP-A-63-215620 discloses a hydrogel-type preparation which
comprises a core comprising a drug and a water-soluble polymer and
an outer layer comprising a water-soluble polymer as a base.
JP-B-40-2053 discloses a sustained-release preparation etc.
comprising a mixture of a drug and a high polymer of ethylene oxide
and, as an optional component, a hydrophilic substance etc. (the
term "JP-B" as used herein means an "examined Japanese patent
publication").
[0003] However, all of these preparations are designed to release a
drug continuously while the administered preparation is still
retained in the upper digestive tract, typically in the stomach and
small intestine, and are not intended to provide for a release of
the drug in the lower digestive tract, typically in the colon,
where little water is available. Thus, for any sustained-release
preparation designed to release a drug for absorption during its
descent down in the digestive tract, the extent of drug release and
absorption in the upper digestive tract has a major influence on
the bioavailability of the drug. However, it is generally believed
that the release of the drug in the colon can hardly be expected
because of the paucity of water and the influence of spodogenous
contents etc. and actually, little research has been undertaken on
drug release in colon (Pharm. Tech. Japan 8 (1), (1992), 41).
[0004] Furthermore, the biological half-life of a drug per se is
also an important factor in the design of sustained-release
preparations. It has been generally considered difficult to design
a preparation providing for dramatic sustained release for a drug
having a short half-life period (The Pharmaceuticals Monthly 25
(11), (1983), 29).
DISCLOSURE OF INVENTION
[0005] As a result of extensive studies on the sustained-release of
a drug, the inventors of the present invention discovered that the
release of a drug in the colon, which is low in water content, can
be achieved by providing a preparation adapted to absorb water into
its core to undergo substantially complete gelation during its stay
in the upper digestive tract such as stomach and small intestine,
and then move in the form of the gel down to the lower digestive
tract. The present invention was achieved based on the above
finding.
[0006] Thus, the present invention relates to a hydrogel-type
sustained-release preparation comprising (1) at least one drug, (2)
an additive providing for a penetration of water into the core of
the preparation, and (3) a hydrogel-forming polymer, which
preparation undergoes a substantially complete gelation during its
stay in the upper digestive tract such as stomach and small
intestine and is capable of releasing a drug in the colon.
[0007] The term "substantially complete gelation" of the
preparation as used in this specification refers to the state in
which not less than about 70%, preferably not less than about 80%,
of the preparation is gelled.
[0008] Since even the colon can be utilized as a site of
absorption, the sustained-release preparation of the present
invention prolongs the absorption period of the drug to a
remarkable extent and, hence, insures a steady blood level of the
drug. Thus, the preparation of the present invention absorbs water
during its stay in the upper digestive tract to undergo a
substantially complete gelation and then moves down into the lower
digestive tract with its surface being constantly eroded, and
maintains drug release by further erosion in the lower digestive
tract, with the result that a sustained and sufficient absorption
of the drug is achieved even in the colon where little water is
available.
[0009] The sustained-release preparation of the present invention
is described in further detail hereinafter.
[0010] The drug or drugs which can be used in the preparation
according to the present invention are not particularly limited in
kind, provided that they are used for sustained-release system.
[0011] Thus, representative examples of the drugs include
antiinflammatory, antipyretic, anticonvulsant and/or analgesic
agents such as indomethacin, diclofenac, diclofenac Na, codeine,
ibuprofen, phenylbutazone, oxyphenbutazone, mepirizol, aspirin,
ethenzamide, acetaminophen, aminopyrine, phenacetin, scopolamine
butylbromide, morphine, etomidoline, pentazocine, fenoprofen
calcium, etc; tuberculostats such as isoniazid, ethambutol
hydrochloride, etc.; cardiocirculatory system drugs such as
isosorbide dinitrate, nitroglycerin, nifedipine, barnidipine
hydrochloride, nicardipine hydrochloride, dipyridamole, amrinone,
indenolol hydrochloride, hydralazine hydrochloride, methyldopa,
furosemide, spironolactone, guanethidine nitrate, reserpine,
amosulalol hydrochloride, etc.; antipsychotic agents such as
chlorpromazine hydrochloride, amitriptyline hydrochloride,
nemonapride, haloperidol, moperone hydrochloride, perphenazine,
diazepam, lorazepam, chlordiazepoxide, etc.; antihistaminic agents
such as chlorpheniramine maleate, diphenhydramine hydrochloride,
etc.; vitamins such as thiamine nitrate, tocopherol acetate,
cycothiamine, pyridoxal phosphate, cobamamide, ascorbic acid,
nicotinamide, etc.; antigout agents such as allopurinol,
colchicine, probenecid, etc.; hypnotic sedatives such as
amobarbital, bromovalerylurea, midazolam, chloral hydrate, etc.;
antineoplastic agents such as fluorouracil, carmofur, aclarubicin
hydrochloride, cyclophosphamide, thiotepa, etc.; anticongestants
such as phenylpropanolamine, ephedrine, etc.; antidiabetics such as
acetohexamide, insulin, tolbutamide, etc.; diuretics such as
hydrochlorothiazide, polythiazide, triamterene, etc.;
bronchodilators such as aminophylline, formoterol fumarate,
theophylline, etc; antitussives such as codeine phosphate,
noscapine, dimemorfan phosphate, dextromethorphan, etc;
antiarrhythmic agents such as quinidine nitrate, digitoxin,
propafenone hydrochloride, procainamide, etc.; surface anesthetics
such as ethyl aminobenzoate, lidocaine, dibucaine hydrochloride,
etc.; antiepileptics such as phenytoin, ethosuximide, primidone,
etc.; synthetic adrenocortical steroids such as hydrocortisone,
prednisolone, triamcinolone, betamethasone, etc.; digestive system
drugs such as famotidine, ranitidine hydrochloride, cimetidine,
sucralfate, sulpiride, teprenone, plaunotol, etc.; central nervous
system drugs such as indeloxazine, idebenone, tiapride
hydrochloride, bifemelane hydrochloride, calcium hopantenate, etc;
hyperlipemia treating agents such as pravastatin sodium etc.; and
antibiotics such as ampicillin phthalidyl hydrochloride, cefotetan,
josamycin and so on. A typical drug among the above drugs is
nicardipine hydrochloride. Drugs having short biological half-lives
can also be utilized. The amount of the drug may be any of
pharmaceutically effective amount, but is usually below 85 wight %,
and preferably below 80 weight % based on the total weight of the
preparation.
[0012] In order that these drugs may be readily absorbed in the
colon which is low in water content, it is preferable to improve
their solubilities in advance. Known techniques for improving the
solubility of a drug which can be applied to hydrogel preparation
can be employed. Among such techniques (solubilizing treatment) can
be mentioned the method comprising adding a surfactant (e.g.
polyoxyethylene-hydrogenated castor oils, polyoxy-ethylene-sorbitan
higher fatty acid esters, polyoxyethylene polyoxypropylene glycols,
sucrose fatty acid esters, etc.) and the method comprising
preparing a solid dispersion of the drug and a solubilizer such as
a polymer (e.g., a water-soluble polymer such as
hydroxypropylmethylcellulose (HPMC), polyvinylpyrrolidone (PVP),
polyethylene glycol (PEG), etc. or an enteric polymer such as
carboxymethylethylcellulose (CMEC), hydroxypropylmethylcellulose
phthalate (HPMCP), methyl methacrylate-methacrylic acid copolymer
(Eudragit L and S; the trade name of Rhom & Haas Co.), etc.).
When the drug is a basic substance, the method comprising adding an
organic acid such as citric acid, tartaric acid or the like can be
employed. If necessary, the method involving the formation of a
soluble salt or the method comprising forming a clathrate using
cyclodextrin or the like can also be employed. These procedures for
solubilization can be modified as necessary according to the
particular drug.
[0013] ["Recent Manufacturing Pharmacy Technique and its
Application I", Isamu Utsumi et al., Medicinal Journal, 157-159
(1983); and "Pharmacy Monograph No. 1, Bioavailability", Tsuneji
Nagai et al., Softscience Co., 78-82 (1988)]
[0014] Among these methods, the method comprising preparing a solid
dispersion of the drug and a solubilizer is particularly preferred
(cf. JP-A-56-49314 and French Patent 2460667).
[0015] The additive for allowing water to penetrate into the core
of the preparation according to the present invention (this
additive for insuring a penetration of water into the preparation
core will hereinafter be referred to as "hydrophilic base") is such
that the amount of water required to dissolve 1 g of the
hydrophilic base is not more than 5 ml and preferably not more than
4 ml at the temperature of 20.+-.5.degree. C. The higher the
solubility of the hydrophilic base in water, the more effective is
the base in allowing water into the core of the preparation. The
hydrophilic base includes, inter alia, highly hydrophilic polymers
such as polyethylene glycol (PEG; e.g. PEG400, PEG1500, PEG4000,
PEG6000 and PEG20000, produced by Nippon Oils and Fats Co.) and
polyvinylpyrrolidone (PVP; e.g. PVP K30, the trade name of BASF),
sugar alcohols such as D-sorbitol, xylitol, etc., sugars such as
sucrose, anhydrous maltose, D-fructose, dextran (e.g. dextran 40),
glucose, etc., surfactants such as polyoxyethylene-hydrogenated
castor oil (HCO; e.g. Cremophor RH40 produced by BASF, HCO-40 and
HCO-60 produced by Nikko Chemicals Co.),
polyoxyethylene-polyoxypropylene glycol (e.g. Pluronic F68 produced
by Asahi Denka Kogyo K.K.), polyoxyethylene-sorbitan high molecular
fatty acid ester (Tween; e.g. Tween 80 produced by Kanto Kagaku
K.K.), etc.; salts such as sodium chloride, magnesium chloride,
etc.; organic acids such as citric acid, tartaric acid, etc.; amino
acids such as glycine, .beta.-alanine, lysine hydrochloride, etc.;
and amino sugars such as meglumine.
[0016] Preferred ones are PEG6000, PVP, D-sorbitol, etc.
[0017] The proportion of such hydrophilic base depends on the
characteristics of the drug (solubility, therapeutic efficacy,
etc.) and content of the drug, solubility of the hydrophilic base
itself, characteristics of the hydrogel-forming polymer used, the
patient's condition at the time of administration and other
factors. However, the proportion may preferably be a sufficient
level to achieve a substantially complete gelation during the stay
of the preparation in the upper digestive tract. The preparation
stays in the upper digestive tract in a different period depending
on the species and the individual but in about 2 hours after
administration in the case of dogs and in about 4 to 5 hours after
administration in the case of human (Br. J. clin. Pharmac, (1988)
26, 435-443). For administration to human, the proportion may
preferably be a sufficient level to achieve a substantially
complete gelation in about 4 to 5 hours after administration. The
proportion of the hydrophilic base is, therefore, generally about
5-80% by weight and preferably about 5-60% by weight based on the
total weight of the preparation.
[0018] When the content of the hydrophilic base is too small, the
necessary gelation into the core of the preparation does not
proceed so that the release of the drug in the colon becomes
insufficient. On the other hand, when the content of the
hydrophilic base is excessive, the gelation proceeds in a shorter
time but the resulting gel becomes so fragile that the release of
the drug is too fast, thus failing to insure a sufficient sustained
release. Moreover, because the amount of the base is large, the
product becomes bulky.
[0019] The hydrogel-forming polymer mentioned above should have the
physical characteristics, inclusive of viscosity in the gelled
state, which permit the preparation of the present invention to
retain its shape more or less during its travel down to the lower
digestive tract, namely the colon, by withstanding the contractile
forces of the digestive tract associated with the digestion of
food.
[0020] The hydrogel-forming polymer which can be used in the
preparation of the present invention is preferably a polymer
showing a high viscosity on gelation. For example, a polymer
showing a viscosity of not less than 1000 cps in 1% aqueous
solution (at 25.degree. C.) is particularly preferred.
[0021] The properties of the polymer depend on its molecular
weight. The hydrogel-forming polymer which can be used in the
present invention is preferably a substance of comparatively high
molecular weight, viz. a polymer having an average molecular weight
of not less than 2.times.10.sup.6 and more preferably not less than
4.times.10.sup.6.
[0022] Among such polymers are polyethylene oxide (PEO) having a
molecular weight of not less than 2.times.10.sup.6 [e.g., Polyox
WSR-303 (average mol. wt.: 7.times.10.sup.6; viscosity: 7500-10000
cps, 1% in H.sub.2O, 25.degree. C.), Polyox WSR Coagulant (average
mol. wt.: 5.times.10.sup.6; viscosity: 5500-7500 cps, under the
same condition above), Polyox WSR-301 (average mol. wt.:
4.times.10.sup.6; viscosity: 1650-5500 cps, under the same
condition above), Polyox WSR-N-60K (average mol. wt.:
2.times.10.sup.6; viscosity: 2000-4000 cps, 2% in H.sub.2O,
25.degree. C.), all of which are trade names of Union Carbide Co.];
hydroxypropylmethylcellulose (HPMC) [e.g., Metolose 90SH100000
(viscosity: 4100-5600 cps., 1% in H.sub.2O, 20.degree. C.),
Metolose 90SH50000 (viscosity: 2900-3900 cps, under the same
condition above), Metolose 90SH30000 (viscosity: 25000-35000 cps,
2% in H.sub.2O, 20.degree. C.), all of which are trade names of
Shin-Etsu Chemicals Co.]; sodium carboxymethylcellulose (CMC-Na)
[e.g., Sanlose F-150MC (average mol. wt.: 2.times.10.sup.5;
viscosity: 1200-1800 cps, 1% in H.sub.2O, 25.degree. C.), Sanlose
F-1000MC (average mol. wt.: 42.times.10.sup.4; viscosity:
8000-12000 cps, under the same condition above), Sanlose F-300MC
(average mol. wt.: 3.times.10.sup.5; viscosity: 2500-3000 cps,
under the same condition above), all of which are trade names of
Nippon Seishi Co., Ltd.]; hydroxyethylcellulose (HEC) [e.g., HEC
Daicel SE850 (average mol. wt.: 148.times.10.sup.4; viscosity:
2400-3000 cps, 1% in H.sub.2O, 25.degree. C.), HEC Daicel SE900
(average mol. wt.: 156.times.10.sup.4; viscosity: 4000-5000 cps,
under the same condition above), all of which are trade names of
Daicel Chemical Industries]; carboxyvinyl polymers [e.g., Carbopol
940 (average mol. wt.: ca. 25.times.10.sup.5; B.F. Goodrich
Chemical Co.) and so on.
[0023] The preferred is a PEO having an average molecular weight of
not less than 2.times.10.sup.6. Where a continuous release of the
drug over a long time, for example more than 12 hours, is required,
a polymer having a higher molecular weight, preferably an average
molecular weight of not less than 4.times.10.sup.6, or a higher
viscosity, preferably a viscosity of not less than 3000 cps at a
concentration of 1% in water at 25.degree. C., is preferable.
[0024] The above hydrogel-forming polymer may be used singly, or
two or more kind(s) of the above hydrogel-forming polymers in
mixture may be used. Or, the mixture of two or more kinds of any
polymers, which mixture has characteristics suitable for the
present invention, may be suitably used for the present
invention.
[0025] In order to insure a release of the drug in the human colon,
it is necessary that a portion of the preparation having undergone
gelation still remain in the colon even as late as at least 6-8
hours, preferably at least 12 hours, after administration.
[0026] In order to provide a hydrogel-type preparation having such
properties, although it depends on the volume of the preparation,
the kind of polymer and the properties and amount of the drug and
of the additive for insuring a penetration of water into the
preparation core, it is generally preferable that the preparation
contains 10-95 weight % (preferably, 15-90 weight %) of the
hydrogel-forming polymer based upon the preparation weighing less
than 600 mg, and one preparation contains not less than 70 mg per
preparation and preferably not less than 100 mg per preparation of
the hydrogel-forming polymer. If the amount of this polymer is less
than the above-mentioned level, the preparation will not tolerate
erosion in the digestive tract for a sufficiently long time and a
sufficient sustained release may not be achieved.
[0027] Regarding the types and proportions of the hydrophilic base
and hydrogel-forming polymer (the latter is hereinafter referred to
as hydrogel-forming base), their usefulness has been established by
the following experiments. Experimental Example (Types and
Proportions of Hydrophilic Base and Hydrogel-Forming Base)
[0028] (1) The Time Course of Gelation Velocity of the
Hydrogel-type Sustained-release Preparation According to the
Present Invention
[0029] Sample
[0030] 100 parts by weight of hydrogel-forming base Polyox WSR-303
(referred to as POLYOX303 hereinafter) blended with 150 parts by
weight of hydrophilic base PEG6000 was mixed in a mortar. The mixed
composition was compression-molded using an oil press at a
compression pressure of 1 ton/punch to provide tablets each
measuring 8.0 mm in diameter and weighing 200 mg.
[0031] Gelation Test
[0032] Using The Pharmacopeia of Japan XII (referred to "JP"
hereinafter) Disintegration Test Fluid 2, a gelation test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. Sample tablets were taken out at
predetermined intervals, the gel layer was removed and the diameter
(D obs) of the portion not forming a gel was measured. From this D
obs value, the gelation index (G) was calculated (Table 1, FIG. 1
and Equation 1).
[0033] The "gelation index" as used herein represents the
percentage of the portion of the tablet which has undergone
gelation. The method of calculating the gelation index is not
particularly limited but the following calculation method may be
mentioned as an example.
[0034] Thus, the test tablet is moistened for a predetermined time,
the volume (or weight) of the portion not forming a gel is then
measured and the result is subtracted from the volume (or weight)
of the tablet before the beginning of the test.
[0035] To be specific, the gel layer of the tablet moistened for a
predetermined time is removed, the diameter (or thickness) of the
portion not forming a gel is then measured and the gelation index
is calculated by means of Equation 1. The gelation index may also
be calculated by means of Equation 2 given hereinafter.
[0036] As an alternative which takes advantage of the difference in
strength between the gel layer and non-gel portion, the diameter
(or thickness) under a predetermined pressure is assumed to be the
diameter (or thickness) of the portion not forming a gel and the
gelation index is calculated from Equation 1.
1TABLE 1 Results of Gelation Test Testing Time D obs G (h) (mm) (%)
0 8.0 .+-. 0.0 0 0.5 6.8 .+-. 0.03 37.9 .+-. 0.7 1.0 5.8 .+-. 0.2
61.1 .+-. 1.8 2.0 4.0 .+-. 0.05 87.9 .+-. 0.4 3.0 2.0 .+-. 0.0 98.4
.+-. 0.0 4.0 0.0 100 5.0 0.0 100 (n = 3, Mean .+-. S.E.)
[0037] 1 Gelation Index ( G , % ) = ( 1 - ( D obs ) 3 ( D ini ) )
.times. 100 Equation 1 D obs : The diameter of the portion not
gelled after initiation of test D ini : The diameter of the
preparation before initiation of test
[0038] Results
[0039] The hydrogel tablet containing PEG6000 as a hydrophilic base
underwent gelation with its core diameter diminishing progressively
at a substantially constant rate. Two hours after the initiation of
the test, the hydrogel tablet substantially went through gelation
(not less than 80%).
[0040] (2) Content of Hydrophilic Base
[0041] Samples
[0042] One-hundred parts by weight of the hydrogel-forming base
POLYOX303 blended with a varying proportion, from 0 to 150 parts by
weight, of the hydrophilic base PEG6000 was mixed in a mortar and
compression-molded using an oil press at a compression pressure of
1 ton/punch to provide tablets each measuring 8.0 mm in diameter
and weighing 200 mg.
[0043] Gelation Test
[0044] Using JP Disintegration Test Fluid No. 2, the gelation test
was performed by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. The tablets were taken out at predetermined
intervals, the gel layer was stripped off and the diameter (D obs)
of the portion not forming a gel was measured. From the D obs
value, the gelation index (G) was calculated (Table 2 and FIG.
2).
2TABLE 2 Results of Gelation Test Blending Ratio G (%)
POLYOX303:PEG6000 2 h 4 h 100:0 29.7 .+-. 2.9 50.5 .+-. 1.4 100:5
44.2 .+-. 5.2 78.0 .+-. 2.1 100:10 52.3 .+-. 2.5 83.9 .+-. 0.5
100:15 84.6 .+-. 0.5 91.2 .+-. 2.0 100:25 84.6 .+-. 0.6 N.T. 100:50
85.2 .+-. 0.6 N.T. 100:100 87.1 .+-. 0.2 N.T. 100:150 87.9 .+-. 0.4
100.0 .+-. 0.0 N.T.: Not Tested (n = 3, Mean .+-. S.E.)
[0045] Results
[0046] It was found that the inclusion of 15 parts by weight (13.0%
of tablet weight) of the hydrophilic base PEG6000 resulted in not
less than 80% gelation in 2 hours. It was also found that the
inclusion of 10 parts by weight (9.1% of tablet weight) of the
hydrophilic base PEG6000 resulted in not less than 80% gelation in
4 hours.
[0047] (3) Screening of Hydrophilic Bases
[0048] Samples
[0049] One-hundred parts by weight of the hydrogel-forming base
POLYOX303 blended with 100 parts by weight of each test hydrophilic
base was mixed in a mortar and compression-molded using an oil
press at a compression pressure of 1 ton/punch to provide tablets
each measuring 8.0 mm in diameter and weighing 200 mg.
[0050] Gelation Test
[0051] Using JP Disintegration Test Fluid No. 2, the gelation test
was performed by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. The tablets were taken out at 2 hours after
initiation of the test and the gel layer was stripped off and the
diameter (D obs) of the portioned not forming a gel was measured.
From the D obs value, the gelation index (G) was calculated (Table
3 and FIG. 3).
3TABLE 3 Influence of Solubility of Various Additives on Gelation
Index Additive Solubility** G (%) No additive 29.7 .+-. 2.9 Lactose
8 ml 24.4 .+-. 1.9 D-Mannitol 6 ml 26.8 .+-. 1.9 Inositol 6 ml 42.0
.+-. 1.5 Glycine 4 ml 80.9 .+-. 0.7 PEG20000 4 ml 86.2 .+-. 0.3
Pluronic F68* 4 ml 95.1 .+-. 0.4 PVP K30 2 ml 82.2 .+-. 2.5 Dextran
40 2 ml 85.9 .+-. 1.0 Meglumine 2 ml 93.4 .+-. 0.8 Dextrose
Anhydrous 2 ml 94.2 .+-. 1.5 Lysine-HCl 2 ml 95.1 .+-. 1.3
.beta.-Alanine 2 ml 99.3 .+-. 0.2 PEG6000 1 ml 87.1 .+-. 0.2 Citric
acid 1 ml 93.2 .+-. 0.3 Maltose Anhydrous 1 ml 93.7 .+-. 0.7
Xylitol 1 ml 94.0 .+-. 1.4 Sucrose 1 ml 94.2 .+-. 1.1 D-Sorbitol 1
ml 97.0 .+-. 0.4 D-Fructose 1 ml 100
*Polyoxyethylene[160]polyoxypropylen- e[30]glycol (n = 3, Mean .+-.
S.E.) **Volume of water required for dissolving 1 gram measured in
accordance with the method for solubility measurement in JP (25
.+-. 5.degree. C.)
[0052] Results
[0053] When D-mannitol and lactose, which require more than 6 ml of
water and 8 ml of water for dissolution of 1 g, were respectively
added, the systems showed gelation indices comparable to the index
of the system using POLYOX303 alone, indicating that these
additives are less effective in causing gelation to proceed into
the core of the tablet.
[0054] It was found that as the hydrophilic base providing for not
less than 80% gelation in 2 hours, highly soluble bases (which
require not more than 5 ml, preferably not more than 4 ml, of water
for dissolution of 1 gram) such as glycine, PVP K30, PEG6000 and
D-sorbitol are suitable.
[0055] (4) Studies on Hydrogel-Forming Base
[0056] Using acetaminophen and nicardipine hydrochloride (Pd) as
model drugs, the proportion and molecular weight of a
hydrogel-forming base which are necessary for the sustained-release
preparation were investigated.
[0057] I. Study of Optimum Proportion
[0058] The relationship between the proportion of a
hydrogel-forming base and the pattern of dissolution was
investigated.
[0059] 1. Acetaminophen
4 TABLE 4 Formula (mg) Acetaminophen 50 50 50 50 50 PEG6000 50 50
50 50 50 POLYOX303 40 50 100 150 300 Weight (mg) 140 150 200 250
400 Diameter (mm) 6.5 7.0 8.0 8.5 9.5
[0060] The components mentioned in Table 4 in the indicated
proportions were mixed in a mortar, respectively, and each
composition was compression-molded using an oil press at a
compression pressure of 1 ton/punch to provide tablets (each
containing 50 mg of acetaminophen).
[0061] 2. Nicardipine Hydrochloride (Pd)
[0062] In a mixture of water and methanol (1:9) were dissolved 1
part by weight of Pd, 0.2 part by weight of HCO-60 and 0.4 part by
weight of hydroxypropylmethylcellulose (TC-5E, produced by
Shin-Etsu Chemical Co.) and the solution was spray-dried using a
spray dryer to provide Spray-dried Product 1.
5TABLE 5 Formula (mg) Spray-Dried 128 128 128 128 128 128 128
Product PEG6000 32 32 32 32 32 32 32 POLYOX303 64 96 120 160 200
240 320.9 Weight (mg) 224 256 280 320 360 400 460 Diameter (mm) 8.5
8.5 8.5 9.0 9.0 9.5 10.0
[0063] The component materials mentioned in Table 5 in the
indicated proportions were respectively mixed in a mortar and each
composition was compression-molded using an oil press at a
compression pressure of 1 ton/punch to provide tablets (each
containing 80 mg of Pd).
[0064] Dissolution Test
[0065] Using JP Disintegration Test Fluid 1 or 2, the dissolution
test was carried out by JP Dissolution Test Method 2 (paddle
method) using the acetaminophen and nicardipine hydrochloride (Pd)
tablets as models. Sampling was performed at predetermined
intervals and the amount of the drug in each sample was determined
by the UV method (FIGS. 4 and 5).
[0066] Results
[0067] It was found that the rate of dissolution could be
controlled by varying the proportion of the hydrogel-forming base
POLYOX303. It was also found that when 50 mg of acetaminophen was
used as the principal agent and not less than 100 mg (50% of tablet
weight) of POLYOX303 was added, a sustained release of the drug
lasting for not less than 12 hours was realized even under vigorous
agitation (paddle speed 200 rpm, pH 6.8). Similarly, when 80 mg of
Pd was used as the principal agent, the inclusion of not less than
96 mg (37.5% of tablet weight) of POLYOX303 insured a sustained
release lasting for not less than 12 hours even under vigorous
agitation (paddle speed 200 rpm, pH 1.2).
[0068] The optimum proportion of the hydrogel-forming base depends
on the types and amounts of the drug and hydrophilic base and the
desired dissolution rate, among other factors, but it was found
that the larger was the proportion of the hydrogel-forming base,
the greater was the sustainment of release. It was also found that
when a sustained release lasting for not less than 12 hours is
desired, it is necessary to include not less than about 70 mg,
preferably not less than 100 mg, of the hydrogel-forming base per
tablet.
[0069] II. Study of Relationship between Molecular Weight of
Hydrogel-Forming Base and Duration of Release
[0070] 1. Acetaminophen
6TABLE 6 Formula (Parts by Weight) Acetaminophen 50 PEG6000 50
Polyethylene Oxide (PEO) 250
[0071] As the polyethylene oxide (PEO), those species having
average molecular weights of 9.times.10.sup.5, 1.times.10.sup.6,
2.times.10.sup.6, 4.times.10.sup.6, 5.times.10.sup.6 and
7.times.10.sup.6 were used. In each case, the component materials
were mixed in a mortar and compression-molded using an oil press at
a compression pressure of 1 ton/punch to provide tablets each
measuring 9.0 mm in diameter and weighing 350 mg.
[0072] 2. Nicardipine Hydrochloride (Pd)
[0073] In a mixture of water and methanol (1:9) were dissolved 1
part by weight of Pd, 0.4 part by weight of HCO-40 and 0.8 part by
weight of hydroxypropylmethylcellulose (TC-5E, produced by
Shin-Etsu Chemical Co.) and the solution was spray-dried using a
spray dryer to provide Spray-dried Product 2.
7TABLE 7 Tablet Formula (Parts by Weight) Spray-Dried Product 2 178
PEG6000 48 Polyethylene Oxide (PEO) 344
[0074] As the polyethylene oxide (PEO), those species having
average molecular weights of 9.times.10.sup.5, 1.times.10.sup.6,
2.times.10.sup.6, 4.times.10.sup.6, 5.times.10.sup.6 and
7.times.10.sup.6 were used. In each case, the component materials
were mixed in a mortar and compression-molded using an oil press at
a compression pressure of 1 ton/punch to provide tablets each
measuring 11.0 mm in diameter and weighing 568 mg (containing 80 mg
of Pd).
[0075] Release Test
[0076] The acetaminophen- and nicardipine-containing preparations
were tested in the same manner as the dissolution test carried out
in I. Study of the Optimal Proportion (FIGS. 6 and 7).
[0077] Results
[0078] The rate of dissolution varied with different average
molecular weights of hydrogel-forming base polyethylene oxide
(PEO). When 50 mg of acetaminophen was used as the principal agent,
the use of PEO with an average molecular weight of not less than
4.times.10.sup.6 resulted in a sustained release lasting for not
less than 12 hours under vigorous agitation (paddle speed 200 rpm,
pH 6.8).
[0079] Similarly, when 80 mg of Pd was used as the principal agent,
the use of PEO with an average molecular weight of not less than
2.times.10.sup.6 enabled a sustained release lasting for not less
than 12 hours.
[0080] (5) Verification of In Vivo Gelation
[0081] Samples
[0082] The hydrogel-forming base (POLYOX303) and the hydrophilic
base (PEG6000, PVP K30, or D-sorbitol) in the ratios indicated
below were respectively mixed in a mortar and each mixture was
compression-molded using an oil press at a compression pressure of
1 ton/punch to provide tablets each measuring 8.0 mm in diameter
and weighing 200 mg.
[0083] POLYOX303:PEG6000=100:10, 25, 50, 100
[0084] POLYOX303:PVP K30=100:10, 25, 100
[0085] POLYOX303:D-sorbitol=100:10, 25, 100
[0086] Autopsy Test in Dogs
[0087] Male beagle dogs (Dogs A and B) fasted for about 20 hours
were respectively dosed orally with each test preparation, together
with 30 ml of water. Two hours later, the animals were anesthetized
with pentobarbital Na and, after bleeding, the abdomen was opened.
The tablet was recovered from the digestive tract and the D obs
value was determined. From this D obs value, the gelation index (G)
was calculated (Table 8).
8TABLE 8 Autopsy Test Data in Dogs Sample Administered Position of
Autopsy Data In Vitro Dog (POLYOX303 100:) Recovery D obs (mm) G
(%) G (%) A PEG6000 10 Colon 6.8 38.6 52.3 PEG6000 25 Colon 2.8
95.7 84.6 PEG6000 50 Colon N.D. 100 85.2 PEG6000 100 Colon N.D. 100
87.1 PVP K30 100 Colon N.D. 100 82.2 D-Sorbitol 100 Colon N.D. 100
97.0 B PEG6000 10 Stomach 3.2 93.6 52.3 PEG6000 25 Stomach 2.9 95.2
84.6 PVP K30 10 Stomach 2.5 96.9 -- PVP K30 25 Stomach 2.9 95.2 --
D-Sorbitol 10 Stomach 2.3 97.6 -- D-Sorbitol 25 Stomach 2.9 95.2 --
N.D. Not Detected
[0088] Results
[0089] In Dog A, the tablets had already been transported to the
colon by 2 hours after administration and the upper digestive tract
residence time was less than 2 hours. In contrast, all the tablets
except the one containing 10 parts of PEG6000 had already undergone
not less than 80% gelation, generally in agreement with in vitro
data.
[0090] In Dog B, the tablets remained in the stomach at 2 hours
after administration and all the tablets had undergone more than
80% gelation.
[0091] The above results indicated that hydrogel tablets containing
a hydrophilic base providing for not less than 80% gelation in
vitro (PVP K30, PEG6000 and D-sorbitol) in appropriate amounts are
ready to gel due to penetration of water into the tablet core even
in vivo.
[0092] If necessary, the preparation of the present invention may
include appropriate other pharmaceutically acceptable additives
such as vehicles (e.g., lactose, mannitol, potato starch, wheat
starch, rice starch, corn starch, and crystalline cellulose),
binders (e.g., hydroxylpropylmethylcellulose,
hydroxypropylcellulose, methylcellulose, and gum arabic), swelling
agents (e.g., carboxymethylcellulose, carboxymethylcellulose
calcium, and cross-linking carboxymethylcellulose sodium),
lubricants (e.g., stearic acid, calcium stearate, magnesium
stearate, talc, magnesium meta-silicate aluminate, calcium hydrogen
phosphate, and anhydrous calcium hydrogen phosphate), fluidizers
(e.g., hydrous silica, light anhydrous silicic acid, and dried
aluminum hydroxide gel), colorants (e.g., yellow iron sesquioxide
and iron sesquioxide), surfactants (e.g., sodium lauryl sulfate,
sucrose fatty acid ester), coating agents (e.g., zein,
hydroxypropylmethylcellulose, and hydroxypropylcellulose), aromas
(e.g., l-menthol, peppermint oil, and fennel oil), preservatives
(e.g., sodium sorbate, potassium sorbate, methyl p-benzoate, and
ethyl p-benzoate), etc.
[0093] The preparation of the present invention is a solid
preparation having a certain shape and hydrogel-forming ability,
and can be manufactured by the conventional processes utilized for
the production of hydrogel preparations. Typical processes are the
compression tabletting comprising blending the drug, hydrophilic
base and hydrogel-forming polymer, if necessary with the addition
of other additives, and compression-molding the resulting
composition; the capsule compression filling; the extrusion molding
comprising fusing a mixture and setting the fused mixture; and the
injection molding, etc. Thereafter, any coating treatment such as
sugar coating and film coating may be applied or filing into
capsules may be carried out.
[0094] Solubilization, if performed, of the drug for use in the
preparation of the invention can be carried out prior to the
above-described manufacturing process. The hydrophilic base
according to the present invention may double as said solubilizer
in the case that solubilization is carried out. For example, the
preparation of the present invention can be manufactured by a
process comprising blending the drug, previously solubilized using
the hydrophilic base and, if necessary, a different additive, with
the hydrogel-forming polymer and, if necessary, other additives,
and compression-molding the resulting composition.
[0095] If required, the sustained-release preparation of the
present invention may have a immediate-release portion. For
example, the preparation of the present invention may be provided
with such a immediate-release part by way of coating.
[0096] Depending on the intended use, the product of the invention
can be provided in the form of a dry coated tablet. For example,
when a high blood concentration at a definite time after
administration is desired, the core tablet is manufactured
according to a formulation providing for rapid drug release (with
an increased amount of the drug, a reduced amount of the
hydrogel-forming base, and/or an increased amount of the
hydrophilic base) and, then, the outer layer is formed using a
formulation providing for retarded release (with a reduced amount
of the drug, an increased amount of the hydrogel-forming base
and/or a reduced amount of the hydrophilic base) so that the rate
of drug release may be accelerated after a predetermined time.
BRIEF DESCRIPTION OF THE DRAWINGS
[0097] FIG. 1 shows the results of a gelation test with a
PEG6000-containing hydrogel-type sustained-release preparation;
[0098] FIG. 2 shows the results of a gelation test with
preparations varying in PEG6000 content;
[0099] FIG. 3 shows the gelation indices of various hydrophilic
bases after 2 hours;
[0100] FIG. 4 shows the relationship between the amount of
POLYOX303 and the pattern of release (drug: acetaminophen);
[0101] FIG. 5 shows the relationship between the amount of
POLYOX303 and the pattern of release (drug: nicardipine
hydrochloride);
[0102] FIG. 6 shows the relationship between the molecular weight
of PEO and the pattern of release (drug: acetaminophen);
[0103] FIG. 7 shows the relationship between the molecular weight
of PEO and the pattern of release (drug: nicardipine
hydrochloride);
[0104] FIG. 8 shows the results of the dissolution test (paddle
method) using the tablets according to Example 1 and Comparative
Example 1;
[0105] FIG. 9 shows the results of the gelation test using the
tablets according to Example 1 and Comparative Example 1;
[0106] FIG. 10 shows the time courses of plasma drug concentration
in dogs for the tablets according to Example 1 and Comparative
Example 1;
[0107] FIG. 11 shows a comparison between the dissolution test data
and the absorption pattern determined by the deconvolution method
for the tablet according to Comparative Example 1;
[0108] FIG. 12 shows a comparison between the dissolution test data
and the absorption pattern determined by the deconvolution method
for the tablet according to Example 1;
[0109] FIG. 13 shows the time courses of plasma drug concentration
in dogs for the tablets according to Example 2 and Comparative
Example 2;
[0110] FIG. 14 shows the results of the dissolution test (paddle
method) using the tablets according to Example 3 (SR) and
Comparative Example 3 (SR);
[0111] FIG. 15 shows the time courses of plasma drug concentration
in dogs for the tablets according to Example 3 and Comparative
Example 3;
[0112] FIG. 16 shows the results of the dissolution test (paddle
method) using the tablets according to Examples 4 and 5;
[0113] FIG. 17 shows the results of the dissolution test (paddle
method) using the tablets according to Examples 6, 7 and 10;
[0114] FIG. 18 shows the results of the dissolution test (paddle
method) using the tablets according to Example 12 and Comparative
Example 4;
[0115] FIG. 19 shows the time courses of plasma drug concentration
in dogs for the tablets according to Example 12 and Comparative
Example 4.
BEST MODE FOR WORKING THE INVENTION
[0116] The following examples are intended to describe the
preparation of the present invention in further detail and should
by no means be interpreted as limiting the scope of the
invention.
EXAMPLE 1
[0117]
9 AAP 100 (Parts by weight) PEG6000 400 POLYOX303 300
[0118] Acetaminophen (AAP) and PEG6000 were melted at 80.degree.
C., then cooled to solidify, and pulverized. The pulverizate and
POLYOX303 were mixed in a mortar and the resulting composition was
compression-molded using an oil press at a compression pressure of
1 ton/punch to provide tablets each measuring 9 mm in diameter and
weighing 400 mg (AAP content: 50 mg).
Comparative Example 1
[0119]
10 AAP 100 (Parts by weight) POLYOX303 200
[0120] AAP and POLYOX303 were mixed in a mortar and the resulting
mixture was compression-molded using an oil press at a compression
pressure of 1 ton/punch to provide tablets each measuring 8.5 mm in
diameter and weighing 300 mg (AAP content: 100 mg).
[0121] Using the tablets according to Example 1 and Comparative
Example 1, the following tests were carried out.
[0122] (1) Dissolution Test 1
[0123] Using JP Disintegration Test Fluid 2, a dissolution test was
carried out by JP Dissolution Test Method 2 (paddle method).
Sampling was carried out at predetermined intervals and AAP in each
sample solution was assayed by the UV method (Table 9 and FIG.
8).
11TABLE 9 Results of In Vitro Dissolution Test (%) (JP Test Fluid
2, Paddle Method, 200 rpm) Time (h) 0.0 0.5 1.0 2.0 3.0 4.0 6.0 8.0
10.0 12.0 Com- 0.0 9.4 15.7 25.8 34.7 42.8 56.5 68.3 78.4 86.4 par-
ative Ex- am- ple 1 Ex- 0.0 8.8 13.2 21.8 32.4 39.1 55.3 69.2 81.9
92.1 am- ple 1
[0124] (2) Gelation Test
[0125] Using JP Disintegration Test Fluid 2, a gelation test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. The tablets were taken out at predetermined
intervals and the diameter (D obs) of the portion not forming a gel
was measured. From the D obs values thus found, the gelation index
(G) was calculated (Table 10 and FIG. 9)
12TABLE 10 Results of Gelation Test Testing Time D obs G
Preparation (h) (mm) (%) Comparative 0 8.5 -- Example 1 2 7.8 .+-.
0.2 21.5 .+-. 7.6 4 7.5 .+-. 0.1 30.0 .+-. 2.5 6 6.7 .+-. 0.1 50.4
.+-. 3.0 Example 1 0 9.0 -- 2 5.6 .+-. 0.03 76.2 .+-. 0.3 4 3.1
.+-. 0.01 96.0 .+-. 0.1 6 0 .+-. 0.00 100.0 .+-. 0 (n = 3, Mean
.+-. S.E.)
[0126] (3) Dosing Test in Dogs 1
[0127] Male beagle dogs (n=4) fasted for about 20 hours were dosed
orally with the preparation of Example 1.times.2 tablets (AAP: 100
mg) or the preparation of Comparative Example 1 (AAP: 100 mg),
together with 30 ml of water. Blood sampling was carried out at
predetermined intervals and the plasma concentration of the drug
was determined by the HPLC/UV method (Table 11 and FIG. 10). The
absorption rate was calculated by the deconvolution method using
the plasma concentration data generated by intravenous
administration of 100 mg of AAP in water as the weighing function.
The absorption rate at 24 hours after administration of the
preparation of Example was taken as 100 (Table 12).
13TABLE 11 Pharmacokinetic Parameters AUC 0-24 C max T max MRT
Preparation (ng .multidot. h/ml) (ng/ml) (h) (h) Comparative 1469.7
.+-. 537.5 343.7 .+-. 21.7 1.3 .+-. 0.3 4.0 .+-. 1.2 Example 1
Example 1 2702.8 .+-. 151.5 349.9 .+-. 36.1 1.5 .+-. 0.3 7.0 .+-.
0.3 (n = 4, Mean .+-. S.E.)
[0128]
14TABLE 12 Absorption Rate (%) after Oral Administration of Tablet
to Dogs Time (h) 0.0 0.5 1.0 2.0 3.0 4.0 6.0 8.0 10.0 12.0 24.0
Comparative 0.0 8.1 18.7 27.2 33.3 37.8 45.9 50.3 53.1 55.4 58.8
Example 1 Example 1 0.0 7.5 14.3 31.0 39.1 45.9 60.2 75.5 87.4 95.6
100.0
[0129] Results
[0130] In the in vitro dissolution test, Comparative Example 1 and
Example 1 were almost identical in the pattern of dissolution (FIG.
8 and Table 9) but were markedly different from each other in water
penetration rate (relation index) (FIG. 9 and Table 10). When these
preparations were administered orally to dogs, the plasma drug
concentration after administration of the preparation of Example 1
was definitely well sustained as compared with the preparation of
Comparative Example 1 (FIG. 10). Moreover, both the area under the
plasma concentration-time curve (AUC) and the mean residence time
(MRT) of the preparation of Comparative Example 1 were fairly
divergent, presumably because of individual difference in transport
rate in the digestive tract (Table 11). In contrast, both the AUC
and MRT of the preparation of Example 1 were not much varying,
suggesting that this preparation was sparingly influenced by the
transport rate in the digestive tract. The absorption time was also
extended, with the result that despite the substantial parity of
maximum plasma concentration (C max) between the preparation of
Example 1 and that of Comparative Example 1, the AUC after
administration of the preparation of Example 1 was approximately
1.8 times as large.
[0131] The absorption pattern determined by the deconvolution
method was compared with the corresponding dissolution test data.
In the case of the preparation of Comparative Example 1, the
absorption of the drug during the first 2 hours after
administration, when the administered preparation was still in the
upper digestive tract, was comparable to the in vitro dissolution
data. However, the absorption after 2 hours was considerably
decreased (FIG. 11 and Table 12). The upper digestive tract
residence time of the preparation in fasted dogs is about 2 hours
and it is, therefore, clear that the drug was not well released and
absorbed in the lower digestive tract. In contrast, after
administration of the preparation of Example 1, the pattern of
absorption was comparable to the in vitro dissolution data. It is,
therefore, evident that the drug was released and absorbed in the
lower digestive tract as efficiently as in the upper digestive
tract (FIG. 12 and Table 12).
[0132] (4) Autopsy Test in Dogs
[0133] Three male beagle dogs fasted for about 20 hours were used.
Two, 4 and 6 hours before autopsy, each test preparation was
administered orally together with 30 ml of water. In autopsy, the
animals were bled to death under pentobarbital Na anesthesia, the
abdomen was opened, and the location of the preparation in the
digestive tract was determined (Table 13). The small intestine was
divided into 5 segments, which were designated as Small Int. 1, 2,
3, 4 and 5, reckoning from the uppermost segment.
[0134] Results
15TABLE 13 Location in Digestive Tract Dog No. 2 Hr 4 Hr 6 Hr
Comparative 1 Colon Colon Colon Example 1 2 Stomach Colon Colon 3
Small Int. 5 Colon Colon Example 1 1 Colon Colon Colon 2 Stomach
Colon Colon 3 Small Int. 5 Colon Colon
[0135] It is clear that the preparation of Comparative Example 1,
which had a low gelation index, and the preparation of Example 1,
the gelation index of which had been increased by the addition of
hydrophilic base, were substantially identical in the in vivo
transport rate in digestive tract. At 2 hours after administration,
both preparations were still in the stomach in one dog each but
were already in Small Int. 5 and colon in the remaining dogs. It
was, thus, confirmed that the upper digestive tract residence time
of the preparation was approximately 2 hours in fasted dogs in
agreement with the findings heretofore reported. However, the high
blood concentration after 2 hours following administration of the
preparation of Example 1 indicated that the drug was released
efficiently from this preparation and absorbed notwithstanding the
fact that the preparation was present in the lower digestive
tract.
Example 2
[0136]
16 Pd 160 (Parts by weight) HCO-60 80 TC-5E 160 PEG6000 400
POLYOX303 240
[0137] Nicardipine hydrochloride (Pd), HCO-60, TC-5E and PEG6000
were dissolved in a solvent mixture (dichloromethane-methanol) and
the solution was spray-dried using a spray dryer. This dry
preparation was mixed with POLYOX303 in a mortar and the resulting
composition was compression-molded using an oil press at a
compression pressure of 1 ton/punch to provide tablets each
measuring 9.0 mm in diameter and weighing 346.7 mg (Pd content:
53.3 mg).
Comparative Example 2
[0138]
17 Pd 130 (Parts by weight) Tween 80 26 Sustained-Release (SR)
Component CMEC 130 POLYOX303 57.2 Pd 30 Immediate-Release (QR)
Component TC-5E 15
[0139] In a solvent mixture (dichloromethane-methanol) were
dissolved nicardipine hydrochloride (Pd), Tween 80 and CMEC and the
solution was spray-dried using a spray dryer. The dried mixture was
blended with POLYOX303 and the resulting composition was
compression-molded using an oil press at a compression pressure of
0.8 ton/punch to provide tablets (SR) each measuring 8.0 mm in
diameter and weighing 171.6 mg (Pd content: 65 mg). Separately, Pd
and TC-5E were dissolved in a solvent mixture
(dichloromethane-methanol) and using a Hi-Coater, this
immediate-release component (QR; Pd: 15 mg) was coated on the SR
(Pd: 65 mg) component to provide tablets of Comparative Example 2
each weighing 194.1 mg (Pd: 80 mg).
[0140] Using the tablets of Example 2 and Comparative Example 2,
the following tests were carried out.
[0141] (1) Dissolution Test
[0142] Using JP Disintegration Test Fluid 1, a dissolution test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 200 rpm. Sampling was carried out at predetermined
intervals and the Pd in each sample solution was determined by the
UV method (Table 14).
18TABLE 14 Results of Dissolution Test Time (h) 1.0 2.0 3.0 4.0 5.0
6.0 8.0 10.0 12.0 Comparative 11.9 29.4 46.4 61.9 74.4 82.1 92.1
97.7 100.0 Example 2 (SR) Example 2 14.0 28.7 45.1 60.5 73.1 82.2
94.3 99.8 99.3
[0143] (2) Gelation Test
[0144] Using JP Disintegration Test Fluid 1, a gelation test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. After a testing time of 2 hours, the
tablets were taken out and the diameter (D obs) of the portion not
forming a gel was measured. From the D obs value thus found, the
gelation index (G) was calculated (Table 15).
19TABLE 15 Results of Gelation Test Testing Time D obs G
Preparation (h) (mm) (%) Comparative 0 8.0 -- Example 2 (SR) 2
Unchanged 0 Example 2 0 9.0 2 5.4 .+-. 0.02 76.2 .+-. 0.3 (n = 3,
Mean .+-. S.E.)
[0145] (3) Dosage Test in Dogs
[0146] Male beagle dogs (n=6) fasted for about 20 hours were orally
dosed with the preparation of Example 2.times.3 tablets (Pd: 160
mg) or the preparation of Comparative Example 2.times.2 tablets
(Pd: 160 mg), together with 30 ml of water. Blood sampling was
performed at predetermined intervals and the plasma concentration
of the drug was determined by the HPLC/UV method (Table 16 and FIG.
13).
20TABLE 16 Pharmacokinetic Parameters AUC C max T max Preparation
(ng .multidot. h/ml) (ng/ml) (h) Example 2 375.7 .+-. 89.3 52.9
.+-. 15.5 7.3 .+-. 3.5 (Pd: 160 mg) Comparative 125.0 .+-. 31.8
53.6 .+-. 12.5 1.3 .+-. 0.2 Example 2 (Pd: 160 mg) (n = 6, Mean
.+-. S.E.)
[0147] Results
[0148] In the in vitro dissolution test, the preparation of
Comparative Example 2 (SR) and that of Example 2 were substantially
identical in the pattern of dissolution (Table 14) but differed
from each other significantly in the rate of water penetration
(gelation index) (Table 15). When these preparations were orally
administered to dogs, the preparation of Example 2 showed a
definitely sustained plasma drug concentration as compared with the
preparation of Comparative Example 2. With respect to the
preparation of Comparative Example 2, the plasma concentration of
the drug decreased significantly after 2 hours when the
administered preparation entered into the lower digestive tract,
indicating that the drug was hardly released or absorbed in the
lower digestive tract. In contrast, in the case that the
preparation of Example 2 was administered, the plasma concentration
was well maintained even after 2 hours when the preparation was
moved into the lower digestive tract, indicating that the drug was
effectively released and absorbed in the lower digestive tract.
Furthermore, although the preparation of Example 2 showed a C max
value comparable to that following administration of the
preparation of Comparative Example 2, the former preparation gave
an AUC value approximately 3-fold as large due to the prolonged
absorption period.
EXAMPLE 3
[0149]
21 Pd 65 (Parts by weight) Tween 80 13 Sustained-Release (SR)
Component CMEC 65 PEG6000 65 POLYOX303 65 Pd 15 Immediate-Release
(QR) Component
[0150] Nicardipine hydrochloride (Pd), Tween 80 and CMEC were
dissolved in a solvent mixture (dichloromethane-methanol) and the
solution was spray-dried using a spray dryer. The dried mixture was
blended with PEG6000 and POLYOX303 and the resulting composition
was compression-molded using an oil press at a compression pressure
of 1.0 ton/punch to provide tablets (SR) each measuring 8.5 mm in
diameter and weighing 273 mg (QR; Pd content: 65 mg). For use as
the immediate-release (QR) component, tablets each containing 15 mg
of Pd were separately prepared.
Comparative Example 3
[0151]
22 Pd 65 (Parts by weight) Tween 80 13 Sustained-Release (SR)
Component CMEC 65 POLYOX303 28.6 Pd 15 Immediate-Release (QR)
Component TC-5E 7.5
[0152] Nicardipine hydrochloride (Pd), Tween 80 and CMEC were
dissolved in a solvent mixture (dichloromethane-methanol) and the
solution was spray-dried using a spray dryer. The dried mixture was
blended with POLYOX303 and the resulting composition was
compression-molded using an oil press at a compression pressure of
0.8 ton/punch to provide tablets (SR) each measuring 8.0 mm in
diameter and weighing 171.6 mg (Pd content: 65 mg). Separately, Pd
and TC-5E were dissolved in a solvent mixture
(dichloromethane-methanol) and using a Hi-Coater, this
immediate-release component (QR; Pd content: 15 mg) was coated on
the SR component (Pd content: 65 mg) to provide tablets each
weighing 194.1 mg (Pd: 80 mg).
[0153] (1) Dissolution Test
[0154] Using JP Disintegration Test Fluid 2, a dissolution test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 200 rpm. Sampling was carried out at predetermined
intervals and Pd in each sample solution was assayed by the UV
method.
[0155] The results of the above dissolution test using the
preparation of Comparative Example 3 (SR) and that of Example 3
(SR) are shown in FIG. 14.
[0156] (2) Gelation Test
[0157] Using JP Disintegration Test Fluid 1, a dissolution test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. After 2 hours, the tablets were taken out,
the gel layer was removed and the weight (W obs) of the portion not
forming a gel was determined. From the W obs value, the gelation
index (G) was calculated by means of Equation 2 given below (Table
17).
23TABLE 17 Results of Gelation Test (n = 3, Mean .+-. S.E.) Testing
Time W obs G Preparation (h) (g) (%) Comparative 0 0.167 -- Example
3 (SR) 2 0.153 .+-. 0.0 8.2 .+-. 1.4 Example 3 0 0.276 -- (SR) 2
0.055 .+-. 0.4 79.6 .+-. 0.4
[0158] 2 G ( % ) = ( 1 - ( W obs ) ( W ini ) .times. 100 W obs :
The residual weight after removal of the gel layer after initiation
of test W ini : The weight of the tablet before initiation of test
Equation 2
[0159] (3) Dosage Test in Dogs
[0160] Male beagle dogs (n=6) fasted for about 20 hours were orally
dosed with two tablets each of the preparation of Example 3 SR and
QR (Pd: 160 mg) or 2 tablets of the preparation of Comparative
Example 3 (Pd: 160 mg), together with 30 ml of water. Blood
sampling was performed at predetermined intervals and the plasma
concentration of the drug was determined by the HPLC/UV method
(FIG. 15 and Table 18).
24TABLE 18 Pharmacokinetic Parameters (n = 6, Mean .+-. S.E.) AUC
0-24 C max T max MRT Preparation (ng .multidot. h/ml) (ng/ml) (h)
(h) Comparative 125.0 .+-. 31.8 53.6 .+-. 12.5 1.3 .+-. 0.2 2.4
.+-. 0.4 Example 3 Example 3 547.1 .+-. 180.4 81.6 .+-. 14.8 3.9
.+-. 1.1 6.3 .+-. 1.0
[0161] (4) Autopsy Test in Dogs
[0162] Three male beagle dogs fasted for about 20 hours were used.
Two, 4 and 6 hours before autopsy, each test preparation was
administered orally together with 30 ml of water. In autopsy, the
animals were bled to death under pentobarbital Na anesthesia, the
abdomen was opened, and the location of the tablet in the digestive
tract was determined (Table 19). The small intestine was divided
into 5 segments, which were designated as Small Int. 1, 2, 3, 4 and
5, reckoning from the uppermost segment.
25TABLE 19 Location in Digestive Tract (Small Intestine was Divided
into 5 Segments) Dog No. 2 Hr 4 Hr 6 Hr Comparative 4 Colon Colon
Colon Example 3 5 Colon Colon Colon 6 Small Int. 1 Colon Colon
Example 3 4 Small Int. 5 Colon Colon 5 Colon Colon Colon 6 Small
Int. 1 Colon Colon
[0163] Results
[0164] In the in vitro dissolution test, the preparation of
Comparative Example 3 (SR) and that of Example 3 (SR) were
substantially identical in the pattern of dissolution (Table 14)
but differed considerably from each other in the gelation index
(Table 17). Autopsy revealed substantially the same transport rate
in the digestive tract for the preparation of Example 3 and that of
Comparative Example 3 (Table 19). When these preparations were
administered orally to dogs, the time course of plasma drug
concentration after administration of the preparation of Example 3
was definitely better sustained as compared with the preparation of
Comparative Example 3. With respect to the preparation of
Comparative Example 3, the plasma concentration decreased
remarkably after 2 hours when the administered preparation was
moved into the lower digestive tract, indicating that the drug was
hardly released and absorbed in the lower digestive tract. In
contrast, with respect to the preparation of Example 3, the plasma
drug concentration was well sustained even after 2 hours when the
administered preparation was moved into the lower digestive tract,
indicating that the drug was effectively released and absorbed even
in the lower digestive tract (FIG. 15). Moreover, although the C
max after administration of the preparation of Example 3 was not
much different from that after administration of the preparation of
Comparative Example 3, the former preparation gave an AUC value
about 4.4 times as large due to the prolonged absorption period
(Table 18).
EXAMPLE 4
[0165]
26 Pd 80 (mg) PVP K30 32 HCO-60 16 POLYOX303 240 Lubricant 4
[0166] Nicardipine hydrochloride (Pd), PVP K30 and HCO-60 were
dissolved in methanol. Using a fluidized-bed granulator, this
solution was sprayed over POLYOX303 to provide granules. To the
granules was added the lubricant and the resulting composition was
mixed and then compression-molded to provide tablets each measuring
9.5 mm in diameter and weighing 372 mg (Pd content: 80 mg).
EXAMPLE 5
[0167]
27 Pd 80 (mg) TC-5E 32 HCO-60 16 PEG6000 32 POLYOX303 240 Lubricant
8 Fluidizer 4
[0168] Nicardipine hydrochloride (Pd), TC-5E and HCO-60 were
dissolved in water-methanol (1:9) and the solution was spray-dried.
To the dried mixture were added POLYOX303 and 4 mg equivalent of
lubricant and the mixture was dry-granulated. To the granules were
added 4 mg equivalent of lubricant as well as fluidizer and the
resulting composition was mixed and compression-molded to provide
tablets each measuring 9.5 mm in diameter and weighing 412 mg (Pd
content: 80 mg).
EXAMPLE 6
[0169]
28 Pd 80 (mg) TC-5E 32 HCO-60 32 PEG6000 32 POLYOX303 384 Lubricant
11.2 Fluidizer 5.6
[0170] Nicardipine hydrochloride (Pd), TC-5E, HCO-60 and PEG6000
were dissolved in water-methanol (1:9) and the solution was
spray-dried. To this dried preparation were added POLYOX303 and 5.6
mg equivalent of lubricant and the mixture was dry-granulated. To
the granules thus prepared were added 5.6 mg equivalent of
lubricant as well as fluidizer and the resulting composition was
mixed and compression-molded to provide tablets each measuring 11
mm in diameter and weighing 576.8 mg (Pd content: 80 mg).
EXAMPLE 7
[0171]
29 Pd 80 (mg) TC-5E 64 Tween 80 32 PEG6000 32 POLYOX303 360
Lubricant 11.4 Fluidizer 5.7
[0172] Nicardipine hydrochloride (Pd), TC-5E and Tween 80 were
dissolved in water-methanol (1:9) and the solution was spray-dried.
To this dried preparation were added PEG6000, POLYOX303 and 5.7 mg
equivalent of the lubricant and the mixture was dry-granulated. To
the granules thus prepared were added 5.7 mg of lubricant as well
as fluidizer and the resulting composition was mixed and
compression-molded to provide tablets each measuring 11 mm in
diameter and weighing 585.1 mg (Pd content: 80 mg).
EXAMPLE 8
[0173] Pd and TC-5E were dissolved in water-methanol (1:9) and
using a Hi-Coater, the immediate-release component (Pd: 20 mg) was
coated on the tablets of Example 7 (Pd: 80 mg) to provide tablets
each weighing 625.1 mg (Pd: 100 mg).
EXAMPLE 9
[0174] Pd and HPC-SL were dissolved in methanol and using a
Hi-Coater, the immediate-release component (Pd: 20 mg) was coated
on the tablets of Example 7 (Pd: 80 mg) to provide tablets each
weighing 625.1 mg (Pd: 100 mg).
EXAMPLE 10
[0175]
30 Pd 80 (mg) TC-5E 64 HCO-40 32 PEG6000 48 POLYOX303 344 Lubricant
11.4 Fluidizer 5.7
[0176] Pd, TC-5E and HCO-40 were dissolved in water-methanol (1:9)
and the solution was spray-dried. To this dried preparation were
added PEG6000, POLYOX303 and 5.7 mg equivalent of lubricant and the
mixture was dry-granulated. To the granules thus prepared were
added 5.7 mg equivalent of lubricant as well as fluidizer and the
resulting composition was mixed and compression-molded to provide
tables each measuring 11 mm in diameter and weighing 585.1 mg (Pd
content: 80 mg).
EXAMPLE 11
[0177]
31 Pd 100 (mg) TC-5E 80 HCO-40 40 PEG6000 48 POLYOX303 300
Lubricant 11.4 Fluidizer 5.7
[0178] Pd, TC-5E and HCO-40 were dissolved in water-methanol (1:9)
and the solution was spray-dried. To this dried preparation were
added PEG6000, POLYOX303 and 5.7 mg equivalent of lubricant and the
mixture was dry-granulated. To the granules were added 5.7 mg
equivalent of lubricant as well as fluidizer and the resulting
composition was mixed and compression-molded to provide tablets
each measuring 11 mm in diameter and weighing 585.1 mg (Pd content:
100 mg).
[0179] (1) Dissolution Test
[0180] Using JP Disintegration Test Fluid 1, a dissolution test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 200 rpm. Sampling was carried out at predetermined
intervals and Pd in each sample solution was assayed by the UV
method.
[0181] The results of dissolution tests for preparations of
Examples 4 and 5 are shown in FIG. 16.
[0182] The results of dissolution tests for preparations of Example
6, Example 7 and Example 10 are shown in FIG. 17.
[0183] (2) Dosage Test in Dogs
[0184] Male beagle dogs (n=6) were orally dosed with 2 tablets of
the preparation of Example 5 or 2 tablets of the preparation of
Example 6 once a day for 4 consecutive days. Blood sampling was
carried out at predetermined intervals and the plasma concentration
of the drug was determined by the HPLC/UV method.
[0185] Results
[0186] Both of the preparations of Examples 5 and 6, in a
once-a-day administration, showed high C.sub.24 hr values (blood
concentrations at 24 hours after administration) and high
bioavailabilities.
EXAMPLE 12
[0187]
32 DF 37.5 (mg) PEG6000 37.5 POLYOX303 75.0
[0188] Diclofenac Na (DF), PEG6000 and POLYOX303 were mixed in a
mortar and using an oil press the composition was
compression-molded at a compression pressure of 1 ton/punch to
provide tables measuring 7 mm in diameter and weighing 150 mg (DF:
37.5 mg).
Comparative Example 4
[0189]
33 DF 37.5 (mg) POLYOX303 75.0
[0190] DF and POLYOX303 were mixed in a mortar and using an oil
press the mixture was compression-molded at a compression pressure
of 1 ton/punch to provide tablets each measuring 6.0 mm in diameter
and weighing 112.5 mg (DF content: 37.5 mg).
[0191] (1) Dissolution Test
[0192] Using JP Disintegration Test Fluid 2, a dissolution test was
carried out by JP Dissolution Test Method 2 (paddle method).
Sampling was carried out at predetermined intervals and DF in each
sample solution was assayed by the UV method (FIG. 18).
[0193] (2) Gelation Test
[0194] Using JP Disintegration Test Fluid 2, a gelation test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. The tablets were taken out at 2 hours
intervals and the diameter (D obs) of the portion not forming a gel
was measured. From the D obs value thus found, the gelation index
(G) was calculated (Table 20).
34TABLE 20 Results of Gelation Test (n = 3, Mean .+-. S.E.) Testing
Time G Preparation (h) (%) Example 12 2 88.2 .+-. 1.1 Comparative 2
37.0 .+-. 4.6 Example 4
[0195] (3) Dosage Test in Dogs
[0196] Male beagle dogs (n=5) fasted for about 20 hours were orally
dosed with the preparation of Example 12 (DF: 37.5 mg) or the
preparation of Comparative Example 4 (DF: 37.5 mg), together with
30 ml of water. Blood sampling was carried out at predetermined
intervals and the plasma concentration of the drug was determined
by the HPLC/UV method (Table 21 and FIG. 19).
35TABLE 21 Oral Dosage Test (in Fasting Condition) AUC 0-12 C max T
max Preparation (ng .multidot. h/ml) (ng/ml) (h) Comparative 5052
.+-. 1357 1188 .+-. 147 1.7 .+-. 0.6 Example 4 Example 12 8537 .+-.
1941 1381 .+-. 222 3.0 .+-. 1.3 (n = 5, Mean .+-. S.E.)
[0197] Results
[0198] In the in vitro dissolution test, the preparation of Example
12 and that of Comparative Example 4 were substantially identical
in the pattern of dissolution (FIG. 18) but differed considerably
from each other in the rate of water penetration (gelation index)
(Table 20). When these preparations were administered orally to
dogs, the preparation of Example 12 showed a definitely prolonged
blood concentration as compared with the preparation of Comparative
Example 4 (FIG. 19). Furthermore, in comparison with Comparative
Example 4, Example 12 gave an AUC value which was about 1.7 times
as large (Table 21). Thus, even for diclofenac Na which is an
acidic drug, it was confirmed that the application of the present
invention resulted in an efficient release and absorption of the
drug in the lower digestive tract as well.
EXAMPLE 13
[0199]
36 DF 75 (mg) PEG6000 75 POLYOX303 150
[0200] Diclofenac Na (DF), PEG6000 and POLYOX303 were mixed in a
mortar and using an oil press the composition was
compression-molded at a compression pressure of 1 ton/punch to
provide tablets each measuring 8.5 mm in diameter and weighing 300
mg (DF content: 75 mg).
EXAMPLE 14
[0201]
37 DF 75 (mg) PEG6000 75 POLYOX303 300
[0202] Diclofenac Na (DF), PEG6000 and POLYOX303 were mixed in a
mortar and using an oil press the composition was
compression-molded at a compression pressure of 1 ton/punch to
provide tablets each measuring 9.5 mm in diameter and weighing 450
mg (DF content: 75 mg).
EXAMPLE 15
[0203]
38 Famotidine 40 (mg) PEG6000 30 POLYOX303 150 Lubricant 2
[0204] Famotidine, PEG6000, POLYOX303 and lubricant were mixed and
compression-molded to provide tablets each measuring 8.0 mm in
diameter and weighing 222 mg (famotidine content: 40 mg).
EXAMPLE 16
[0205]
39 Barnidipine Hydrochloride 15 (mg) TC-5E 30 HCO-40 5 PEG20000 40
POLYOX303 207 Lubricant 3
[0206] Barnidipine hydrochloride, TC-5E and HCO-40 were dissolved
in water-methanol (1:9). Separately, PEG20000 and POLYOX303 were
mixed. Using a fluidized-bed granulator, the latter mixture was
sprayed with the above solution. The granules thus prepared were
dried, and after addition of lubricant, the composition was
compression-molded to provide tablets each measuring 9.0 mm in
diameter and 300 mg (barnidipine HCl content: 15 mg).
EXAMPLE 17
[0207]
40 Amosulalol Hydrochloride 40 (mg) Pluronic F68 40 POLYOX303 196
Lubricant 4
[0208] Amosulalol hydrochloride, Pluronic F68, POLYOX303 and
lubricant were mixed, pulverized and dry-granulated. The granules
were then compression-molded to provide tablets each measuring 8.5
mm in diameter and weighing 280 mg (amosulalol HCl content: 40
mg).
EXAMPLE 18
[0209]
41 Tamusulosin Hydrochloride 0.2 (mg) D-Sorbitol 17.8 Polyox WSR
N-60K 180 Lubricant 2
[0210] Tamusulosin hydrochloride, D-sorbitol and PEO (Polyox WSR
N-60K) were wet-granulated with ethanol and dried. To this dried
granules was added lubricant and the resulting composition was
mixed and then compression-molded to provide tablets each measuring
8 mm in diameter and weighing 200 mg (tamusulosin HCl content: 0.2
mg).
EXAMPLE 19
[0211]
42 Indeloxazine Hydrochloride 60 (mg) Sucrose 37 HPMC (90SH30000)
180 Lubricant 3
[0212] Indeloxazine hydrochloride, sucrose, HPMC and lubricant were
mixed and dry-granulated. The granules were then compression-molded
to provide tablets each measuring 9 mm in diameter and 280 mg
(indeloxazine HCl content: 60 mg).
EXAMPLE 20
[0213]
43 Formoterol Fumarate 0.16 (mg) Anhydrous Maltose 47.84 Carbopol
940 100 Lubricant 2
[0214] Formoterol fumarate, anhydrous maltose, Carbopol 940 and
lubricant were mixed and the resulting composition was
compression-molded to provide tablets each measuring 7 mm in
diameter and weighing 150 mg (formoterol fumarate content: 0.2
mg).
EXAMPLE 21
[0215]
44 AAP 100 (mg) PEG6000 200 PEO (Polyox WSR N-60K) 300
[0216] Acetaminophen (AAP), PEG6000 and PEO (Polyox WSR N-60K, mean
molecular weight: 200 million) were mixed in a mortar and using an
oil press the mixture was compression-molded at a pressure of 1
ton/punch to provide tablets each measuring 11 mm in diameter and
weighing 600 mg (AAP content: 100 mg).
Comparative Example 5
[0217]
45 AAP 100 (mg) PEO (Polyox WSR N-60K) 300
[0218] AAP and PEO (POLYOX WSR N-60K) were mixed in a mortar and
using an oil press the mixture was compression-molded at a pressure
of 1 ton/punch to provide tables each measuring 9 mm in diameter
and weighing 400 mg (AAP content: 100 mg).
[0219] (1) Dissolution Test
[0220] Using JP Disintegration Test Fluid 2, a dissolution test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 200 rpm. Sampling was carried out at predetermined
intervals and AAP in each sample solution was assayed by the UV
method.
[0221] (2) Gelation Test
[0222] Using JP Disintegration Test Fluid 2, a gelation test was
carried out by JP Dissolution Test Method 2 (paddle method) at a
paddle speed of 25 rpm. After 2 hours, the tablets were taken out
and the diameter (D obs) of the portion not forming a gel was
measured. From the D obs value thus found, the gelation index (G)
was calculated.
[0223] (3) Dosage Test in Dogs
[0224] Male beagle dogs (n=6) fasted for about 20 hours were orally
dosed with the preparation of Comparative Example 5 (AAP: 100 mg)
or the preparation of Example 20 (AAP: 100 mg), together with 30 ml
of water. Blood sampling was carried out at predetermined intervals
and the plasma concentration of the drug was determined by the
HPLC/UV method.
[0225] Results
[0226] In the in vitro dissolution test, the preparation of
Comparative Example 5 and that of Example 20 were substantially
identical in the pattern of dissolution but the preparation of
Example 20, which contained a hydrophilic base, showed a gelation
index greater than that of the preparation of Comparative Example
5. When these preparations were respectively administered orally to
dogs, the plasma concentration of the drug was definitely better
sustained in the case of Example 21 as compared with Comparative
Example 5. The maximum plasma concentration (C max) of the drug
after administration of the preparation of Example 21 was
substantially equal to that after administration of the preparation
of Comparative Example 5 but the former preparation was superior in
AUC and MRT. Moreover, after administration of the preparation of
Example 21, the blood concentration of the drug was sustained at a
high level up to 12 hours.
INDUSTRIAL APPLICABILITY
[0227] The preparation of the present invention absorbs water to
undergo substantially complete gelation during its stay in the
upper digestive tract and moves down into the lower digestive tract
undergoing constant erosion and continues to release the drug on
further erosion. Therefore, this preparation provides for a
favorable sustained release of the drug even in the colon which is
low in water content to insure drug release lasting for about 6 to
18 hours (about 12 to 24 hours if the release in the upper
digestive tract is taken into account) and, hence, insures a steady
drug concentration in the blood.
[0228] Since the conventional sustained-release preparations
release drugs only in the upper digestive tract, the duration of
release is about 6 hours at most and subsequent maintenance of
blood concentration is relied on the biological half-life inherent
to the drug. In contrast, with respect to the preparation of the
present invention, the duration of drug release per se is
increased. Accordingly, even when the drug is that having a short
biological half-life and the sustained release thereof has
heretofore been considered difficult, a sufficient blood
concentration can be maintained over a time period of more than 12
hours.
[0229] Thus, the preparation of the present invention is capable of
sustaining the efficacy of the drug and the number of
administration can be reduced. Further, the side effect of the drug
can be reduced by suppressing rapid increase of blood concentration
of the drug and the constant blood concentration of the drug can be
maintained.
[0230] As demonstrated in the examples described above, the present
invention is capable of prolonging the absorption of various types
of drugs such as acetaminophen, which is a neutral drug,
nicardipine hydrochloride, which is a basic drug, and diclofenac
Na, which is an acidic drug. Therefore, the present invention
provides a pharmaceutical technology having a great versatility
without depending on physical properties of drugs.
* * * * *