Title of Invention

"SUSTAINED RELEASE COMPOSITION FOR ORAL ADMINISTRATION OF DRUGS"

Abstract A sustained-release composition for oral administration of a drug, comprising the drug, a mixture of sodium alginate and xanthan gum as a carrier for sustained release along with other optional ingredients and a mixture of hydroxypropyl methylcellulose and propylene glycol alginate as a gel hydration accelerator, which is capable of maintaining a constant drug level in blood for 24 hours or more owing to the fact that the drug release rate follows zero order kinetics and does not significantly vary with the degree of gastrointestinal motility due to rapid gel hydration without forming a non-gelated core.
Full Text Field of the Invention
The present invention relates to a sustained-release composition for oral administration of a drug, comprising the drug, a carrier for sustained release of the drug and a gel hydration accelerator, which is capable of maintaining a constant drug level in blood for 24 hours or more.
Background of the Invention
Once injected, the in vivo activity of a drug lasts only a short period of time and, for this reason, repeated administration of the drug is required for a long-term treatment. For example, in order to treat hypertension, drugs such as nifedipine should be administered more than 3 times a day.
Accordingly, there have been numerous efforts to develop a sustained-release formulation which can maintain an effective in vivo drug level for more than 24 hours. For instance, Japanese Patent Publication No. 6001716A (1994. 1. 11) discloses a solid dispersion formulation based on a hydroxypropyl methylcellulose matrix, and European Patent Publication No. 521310A(1993. 1. ' 7), a formulation based on a mixture of hydroxypropyl cellulose and hydroxypropyl methylcellulose which is a water-soluble polymer gelation agent. Further, Japanese Patent Publication No. 62077335A (1987. 4. 9) teaches a gel forming formulation based on carboxyvinyl polymer; Japanese Patent Publication No. 03169814A (1991. 7. 23), a formulation based on a mixture of a water-soluble polymer such as hydroxypropyl cellulose, hydroxypropyl methylcellulose, polyvinyl pyrrolidone and methylcellulose, and a water insoluble polymer such as microcystal cellulose; and European Patent No. 274176B (1992. 5. 27), a sustained release formulation based on polyvinyl pyrrolidone. However, these formulations have the drawback that a constant rate of drug release cannot be maintained for more than 24 hours due to the formation of a gel membrane on the outer shell of the formulation, leaving a non-gelated core.
Further, U.S. Patent Nos. 4,765,989A, 5,208,037A and 5,019,397A report osmotic release control formulations that exhibit a constant rate of drug release rate following zero order kinetics. However, the
manufacturing process of such formulations is very complicated and costly, besides the problem that the drug contained therein is not fully bioavailable (John S Grundy and Robert T. Foster, Clin. Pharmacokinet, 30(1): 28-51(1996)).
The present inventors have previously reported that a formulation of a drug prepared by using a monoglyceride gel carrier releases the drug at a constant rate that follows zero order kinetics for 24 hours, when brought into contact with a hydrophilic matrix or a water soluble matrix (Korean Patent No. 10-0216624 (1999. 5. 31)). However, this formulation is of an erosion type and has the problem of easy degradation by contractive movements of the gastrointestinals.
Summary of the Invention
Accordingly, it is an object of the present invention to provide a sustained release composition for oral administration of a drug, which, upon in vivo administration, is capable of releasing the drug at a constant rate following zero order kinetics for 24 hours or more, the rate being affected little by the degree of gastrointestinal motility.
In accordance with one aspect of the present invention, there is provided a sustained-release composition for oral administration of a drug, comprising the drug, a carrier for sustained release of the drug and a gel hydration accelerator.
Brief Description of Drawings
The above and other objects and features of the present invention will become apparent from the following description of the invention taken in conjunction with the following accompanying drawings, which respectively show:
Figs. 1A and IB : the time-dependent changes in the amount of the drug released in vitro (A: the formulation of the present invention; and B: the formulation of Korean Patent No. 10-0216624);
Fig. 2 : the time-dependent changes in the amount of the drug released in vitro by the formulation of the present invention;
Figs. 3A and 3B : dependencies of the drug release rate and the drag
release lag time on the amount of sodium alginate;
Figs. 4A and 4B : dependencies of the drug release rate and the drug release lag time on the amount of xanthan gum;
Figs. 5 A and 5B : dependencies of the drug release rate and the drug release lag time on the amount of propylene glycol ester;
Figs. 6A and 6B : the drug release rate changes with the amount of the carrier for sustained release (A: the formulation prepared in Example 18; and B: the formulation prepared in Example 19);
Figs. 7A and 7B : the drug release rate changes observed when locust bean gum is added to the carrier (A: the formulation prepared in Example 20; and B: the formulation prepared in Example 21); and
Figs. 8A to 8D : the time-dependent changes in the amount of the drug released in vitro by the inventive sustained-release formulation as compared with those of comparative formulations (A: Comparative Example 1; B: Comparative Example 2; C: Comparative Example 3; and D: Comparative Example 4).
Detailed Description of the Invention
The sustained-release composition for oral administration of the
present invention comprises a drug, comprising the drug, a carrier, for
sustained release of the drug and a gel hydratior accelerator.
The carrier is preferably a mixture of sodium alginate and xanthan gum, and the gel hydration accelerator, a mixture of hydroxypropyl methylcellulose and propylene glycol alginate.
The sustained-release composition of the present invention can maintain a constant drug level in the blood for 24 hours or more owing to the fact that the drug release rate follows zero order kinetics and does not significantly vary with the degree of gastrointestinal motility due to rapid gel hydration without forming a non-gelated core.
The components of the inventive composition are described in detail as follows:
(1) Pharmacologically active ingredient (drug)
The pharmacologically active ingredient of the inventive composition is any one of those dmgs which are suitable for use in
sustained-release drug formulations. Exemplary drugs include
antihypertensive drugs such as nifedipine, doxazocin, amosulralol, felodipine, lercanidipine, lacidipine, nicardipine, fosinopril, imidapril, clizapril, perindopril, lisinopril, losartan, irvesartan and candesartan; drugs for cardiovascular diseases such as isradipine; drugs for hyperlipemia such as lovastatin and simvastatin; non-steroidal anti-inflammatory drugs; drugs for asthma; anti-diabete drugs such as gliclazide, glimepiride and glipizide; calmative; antibiotic; antispasmodic; antispasmodic; and steroids, preferably nifedipine.
(2) Carrier for sustained release
The carrier for sustained release of the inventive composition is preferably a mixture of sodium alginate and xanthan gum with a mix ratio (weight by weight) in the range of 1 : 0.1-10, preferably, 1 : 0.2-0.6 to reduce initial burst release and change in the released amount of the drug.
Further, in order to enhance the structural integrity of the formulation, the inventive carrier may further comprise locust bean gum, the weight ratio of sodium alginate : xanthan gum : locust bean gum being the range of 1 : 0.2-10 : 0.1-5, preferably, 1:1-5: 0.5-3.
(3) Gel hydration accelerator
The gel hydration accelerator used in the present invention plays a critical role in forming a homogenous gelated core without leaving a non-gelated portion when the formulation is brought into contact with an aqueous medium. The gel hydration accelerator of the inventive composition is preferably a mixture of hydroxypropyl methylcellulose and propylene glycol alginate with a mix ratio (weight by weight) in the range of 1 : 0.05-20, preferably, 1 : 0.1-10. The hydroxypropyl methylcellulose used therein preferably has a viscosity ranging from 4,000 to 100,000 cps.
In accordance with the composition of the present invention, the weight ratio of the drug : the carrier for sustained release : the gel hydration accelerator is in the range of 1 : 3-30 : 0.1-15, preferably, 1 : 5-25 : 0.5-10.
The pharmaceutical composition of the present invention may be formulated for oral administration. The composition for oral administration may take various forms such as tablet, pill, powder, sachet, elixir, suspension, emulsion, solution, syrup, aerosol, granule, soft and hard gelatin capsule and
the like, which may contain conventional additives such as a diluent (e.g., lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and/or glycine), a lubricant (e.g., silica, talc, stearic acid or its zinc, magnesium or calcium salt and/or polyethylene glycol). In the tablet form, the composition may further comprise a binder (e.g., magnesium aluminum silicate, starch paste, gelatin, tragacanth, methyl cellulose, sodium carboxymethyl cellulose and/or polyvinylpyrrolidine, hydroxyprophyl cellulose and/or kofobidon (Kollidon VA64 , BASF, Germany) and optionally a disintegrant (e.g., starch, agar and alginic acid or its sodium salt), fizzy water and/or absorbent, colorant, flavor and sweetener.
The compositions may additionally include fillers, preservatives, antioxidants, stabilizers, pigments, anti-agglutinating agents, lubricating agents, wetting agents, flavoring agents, emulsifiers and the like.
The inventive pharmaceutical composition may be administered daily. A typical daily dose of the active ingredient ranges from about 0.15 to 2 mg/kg, preferably 0.5 to 1.5 mg/kg, and can be administered in a single dose or in divided doses. However, it should be understood that the amount of the active ingredient actually administered should be determined in light of various relevant factors including the condition to be treated, the chosen route of administration, the age and weight of the individual patient, and the severity of the patient's symptoms; and, therefore, the dosage suggested above should not be construed to limit the scope of the invention in any way.
The following Examples and Test Examples are intended to further illustrate the present invention without limiting its scope.
Further, percentages given below for solid in solid mixture, liquid in liquid, and solid in liquid are on a wt/wt, vol/vol and wt/vol basis, respectively, unless specifically indicated otherwise.
Examples 1 to 21: Preparation of Tablet
Nifedipine(Unique Chemicals, India), isradipine(Sun Pharm. India), lovastatin(CKD Pharm. KOREA), glipizide(Sun Pharm. India), sodium alginate(Keltone® HVCR, Keltoen® LVF, Kelcosol®, Kelset®, ISP USA), xanthan gum(Keltrol® F, Kelco, USA), Locust bean Gum(Cesagum® LN1,LR 200, Cesalpinia, Italy), propylene glycol alginate (Kelcoloid HVF,LVF, ISP, USA), hydroxypropyl methylcellusose (Meltose 90SH, 4,000SR, 100,000SR,
Shin-Et.su, Japan) and kopovidone (Kollidon VA64, BASF, Germany) were mixed as shown in Table 1 for 30 minutes, magnesium stearate and light anhydrous silicic acid (finer than mesh 30) were added thereto, and mixed for 5 minutes. Then, the resulting mixture was tableted under the common presser in accordance with the tablet preparation method to obtain a tablet preparation.
(Table Removed)
Comparative Examples I to 4: Preparation of Tablet
Comparative tablets were prepared by the procedure of Example 1 except that the ingredients listed in Table 2 were employed:
(Table Removed)
Test Example 1: In vitro Release-Test
The tablet prepared in Example 1 and the formulation described according to Korean Patent No. 10-0216624 were subjected to in vitro release-test in accordance with the release-test method described in Korea pharmacopoeia (the paddle method). The amount of released nifedipine from each of the tablets during the in vitro release-test conducted under the following conditions was measured by liquid chromatography. In order to avoid the drug degradation, the above tests were carried out at a long wavelength ( 420 nm)
- release-test system: Erweka DT 80
- release solution: the first release-test using 500 ml of artificial gastric juice (pH 1.2) for 2 hours and the secondary release-test using 400 ml of 0.235 M Na2HP04 containing 2.25% sodium lauryl sulfate(SLS) for 22 hours (a total release solution : pH 6.8, 1% SLS)
- temperature of release solution: 37 ± 0.5 °C
- rotation rate: 50, 100 and 150 rpm
- column: µ-Bondapak CI8® (Waters)
- mobile phase: acetonitrile : water (55:45 v/v)
- flow rate: 1.2 ml/min.
- detector: ultraviolet spectrophotometer (350 nm)
- injection volume: 20 µl
- calculation of released amount: cumulative release amount
The time-dependent changes in the amount of nifedipine released are shown in Fig. 1(A: the formulation of the present invention and B: the formulation of Korea Patent No. 10-0216624). As shown in Fig. 1, the time-dependent changes in the in vitro release pattern of the inventive formulation differ from that of the formulation of Korea Patent No. 10-0216624, exhibiting a steady release pattern which does not vary significantly with the degree of gastrointestinal motility.
Test Example 2: In vitro Release-Test
An in vitro release-test was conducted by employing the formulation prepared in Example 1 in accordance with the method of Test Example 1. The result in Fig. 2 shows that the lovastatin formulation releases the drug at
a constant release rate following zero order kinetics for 24 hours.
Test Example 3: In vitro Release-Test
In order to examine whether the release rate of the drug depends on the amount of sodium alginate of the carrier, an in vitro release-test was conducted by employing the formulations prepared in Examples 6 to 11 in accordance with the method of Test Example 1. The result in Fig. 3(A: the release rate of the drug and B: the release lag time of the drug) shows that the release rate of the drug becomes proportionally slower and the release lag time of the drug, longer, with the amount of sodium alginate.
Test Example 4: In vitro Release-Test
Also, in order to examine whether the release rate of the drug depends on the amount of xanthan gum of the carrier, an in vitro release-test was conducted by employing the formulations prepared in Examples 12 to 14 in accordance with the method of Test Example 1. The result in Fig. 4 (A: the release rate of the drug and B: the release lag time of the drug) shows that the release rate of the drug becomes proportionally slower, and the release lag time of the drug, longer, with the amount of xanthan gum.
Test Example 5: In vitro Release-Test
In order to examine whether the release rate of the drug depends on the amount of propyleneglycol alginate of the gel hydration accelerator, an in vitro release-test was conducted by employing the formulations prepared in Examples 15 to 17 in accordance with the method of Test Example 1. The result in Fig. 5 (A: the release rate of the drug and B: the release lag time of the drug) shows that the release rate of the drug becomes proportionally higher, and the release lag time of the drug, shorter, with the amount of propyleneglycol alginate.
Test Example 6: In vitro Release-Test
In order to examine whether the release rate of the drug depends on the amount of the carrier, an in vitro release-test was conducted by
employing the formulations prepared in Examples 18 and 19 in accordance with the method of Test Example 1. The result in Figs. 6A and 6B (A: the formulation of Example 18 and B: the formulation of Example 19) shows that the release rate of the drug follows zero order kinetics which does not depend on the amount of the carrier. That is, the formulations release the drug more or less at a constant rate when the mix ratio of the compounds of the carrier is unchanged.
Test Example 7: In vitro Release-Test
In order to examine whether the release rate of the drug changes when locust bean gum is added to the earner, an in vitro release-test was conducted by employing the formulations prepared in Examples 20 and 21 in accordance with the method of Test Example 1. The result in Figs. 7A and 7B (A: the formulation of Example 20 and B: the formulation of Example 21) shows that the formulation using a mixture of sodium alginate, xanthan gum and locust bean gum as the carrier has an excellent sustained release.
Test Example 8: In vitro Release-Test and Measurement of the Formation Rate of Non-Gelated Core and Gelated Core
In order to compare the release rates of the inventive and other formulations, an in vitro release-test was conducted by employing the formulations prepared in Example 20 and Comparative Examples 1 to 4 in accordance with the method of Test Example 1. The result in Figs. 8A to 8D (A: Comparative Example 1; B: Comparative Example 2; C: Comparative Example 3; and D: Comparative Example 4) shows that the time-dependent changes in the in vitro release pattern of the formulations prepared in Comparative Examples 1 to 4 differ from that of the inventive formulation. That is, the comparative formulations failed to exhibit zero order kinetics.
Further, at day 4 of the test, sections of the tablets were examined to detemiine the extents of gelated core and non-gelated core in accordance with the method of K. N. Park et al. (Controlled Drug Delivery, 18-23(2000)). The results are shown in Table 3.
Table 3

(Table Removed)
As shown in Table 3, the extent of core gelation is much more extensive for the inventive formulation than the formulations prepared in Comparative Examples 1 to 4.
While the invention has been described with respect to the above specific embodiments, it should be recognized that various modifications and changes may be made and also fall within the scope of the invention as defined by the claims that follow.







We claim :-
1. A sustained-release composition for oral administration of a
drug, comprising the drug, a carrier for sustained release of
the drug and a gel hydration accelerator, characterized in that
the weight ratio of the drug: : the carrier for sustained release
of the drug: : the gel hydration accelerator is in the range of 1
: 3 - 30 : 0.1 - 15; the carrier is a mixture of sodium alginate and xanthan gum having a weight ratio of 1 : 0.1 - 10 and the gel hydration accelerator is a mixture of hydroxypropyl methylcellulose and propylene glycol alginate having a weight ratio of 1 : 0.05-20.
2. A composition as claimed in claim 1, wherein said carrier optionally comprises locust bean gum.
3. A composition as claimed in claim 2, wherein the weight ratio of sodium alginate : xanthan gum : locust bean gum is in the range of 1 : 0.2 - 10 : 0.1 - 5.
4. A composition as claimed in claim 1, wherein the drug is selected from the group consisting of nifedipine, isradipine, lovastatin and glipizide.
5. A composition as claimed in claim 1, wherein the drug is selected from the group consisting of antihypertensive drugs, drugs for cardiovascular disease, drugs for hyperlipemia, non-steroidal anti-inflammatory drugs, drugs for asthma, anti-diabetes drugs, calmative, antibiotic, antispasmodic, steroids and a mixture thereof.

Documents:

1623-delnp-2005-abstract.pdf

1623-delnp-2005-assignment.pdf

1623-delnp-2005-cancelled claims.pdf

1623-delnp-2005-claims.pdf

1623-delnp-2005-complete specification (granted).pdf

1623-delnp-2005-correspondence-others.pdf

1623-delnp-2005-correspondence-po.pdf

1623-delnp-2005-description (complete).pdf

1623-delnp-2005-drawings.pdf

1623-delnp-2005-form-1.pdf

1623-delnp-2005-form-13.pdf

1623-delnp-2005-form-18.pdf

1623-delnp-2005-form-2.pdf

1623-delnp-2005-form-3.pdf

1623-delnp-2005-form-5.pdf

1623-delnp-2005-form-6.pdf

1623-delnp-2005-gpa.pdf

1623-delnp-2005-pct-210.pdf

1623-delnp-2005-pct-304.pdf

1623-delnp-2005-pct-409.pdf

1623-delnp-2005-pct-416.pdf

1623-delnp-2005-petition-137.pdf

1623-delnp-2005-petition-138.pdf


Patent Number 244379
Indian Patent Application Number 1623/DELNP/2005
PG Journal Number 50/2010
Publication Date 10-Dec-2010
Grant Date 06-Dec-2010
Date of Filing 21-Apr-2005
Name of Patentee HANMI PHARM. CO., LTD.
Applicant Address #893-5, HAJEO-RI, PALTAN-MYEON, HWASEONG-GUN, KYNGKI-DO, 445-910, REPUBLIC OF KOREA
Inventors:
# Inventor's Name Inventor's Address
1 WOO, JONG-SOO CHEONCHEONJUGONG APT., 118-203, #333, CHEONCHEON-DONG, JANGAN-GU, SUWON-SI, KYUNGKI-DO, 440-330, REPUBLIC OF KOREA
2 CHI, MOON-HYUK 201, #290-60, KOSAIK-DONG, KWONSUN-GU, SUWON-SI, KYUNGKI-DO, 441-360, REPUBLIC OF KOREA
PCT International Classification Number A61K 47/00
PCT International Application Number PCT/KR2003/002241
PCT International Filing date 2003-10-23
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 10-2002-0064940 2002-10-23 Republic of Korea