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Amlodipine and olmesartan medoxomil pharmaceutical composition and preparation method thereof

A technology of olmesartan medoxomil and amlodipine, which is applied in the field of medicine, can solve problems such as synergy, accumulation, limited complementary effects, low overall blood drug concentration, and slow onset of amlodipine, so as to improve bioavailability, Excellent in vitro dissolution, good disintegration performance and dissolution rate

Active Publication Date: 2013-01-23
HAINAN JINRUI PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] In the prior art, amlodipine and amlodipine salts (such as amlodipine maleate, amlodipine besylate, amlodipine mesylate, etc.) are almost insoluble in water and are slowly absorbed in the human body. The peak blood concentration is reached in 6-12 hours, and the overall level of blood drug concentration is low, especially the initial blood concentration after administration is very low, the drug has a very slow onset and slow action; while olmesartan medoxomil is administered 1-2 hours after administration Reach the peak concentration of the blood concentration, the drug has a rapid onset of action, and the time difference between the two drugs when they reach the peak blood concentration after simultaneous administration is far away, and the synergistic, cumulative and complementary effects are very limited
Disclosed as Chinese patent CN101766609A is a kind of compound preparation that is made up of amlodipine besylate, olmesartan medoxomil and auxiliary material, because the blood drug concentration-time curve of amlodipine and olmesartan medoxomil does not change respectively, ammonia Clodipine still works slowly, and the synergistic, additive and complementary effects of the two are very limited
[0011] In addition, in order to improve the bioavailability of amlodipine salt, the prior art uses the amlodipine salt of the racemate to be split into levamlodipine salt. After the administration of levamlodipine salt, although the bioavailability is somewhat However, the time to reach the peak blood concentration is still 6-12 hours, and the onset of effect is slow. The initial blood concentration after administration according to the dose required by the normal human body is very low, and its synergy, accumulation and complementarity with olmesartan medoxomil very limited
Chinese patent CN101416966A discloses a novel pharmaceutical composition for the treatment of hypertension, specifically related to levamlodipine and olmesartan medoxomil, and levamlodipine includes pharmaceutically acceptable salts, including besylate, malay However, after administration of the pharmaceutical composition, the plasma concentration-time curve of levamlodipine salt does not change, amlodipine takes effect slowly, and the synergistic effect of the two is very limited
And, amlodipine salt is split into levamlodipine salt, which increases the production process, and in the process of splitting, there is loss of dexamlodipine salt and the introduction of impurities, which greatly increases the cost of medicine

Method used

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  • Amlodipine and olmesartan medoxomil pharmaceutical composition and preparation method thereof
  • Amlodipine and olmesartan medoxomil pharmaceutical composition and preparation method thereof
  • Amlodipine and olmesartan medoxomil pharmaceutical composition and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0054] Add 9g of amlodipine maleate, 21ml of ethanol, 42ml of dimethyl sulfoxide, and 7ml of deionized water into a 100ml reaction kettle, adjust the pH to 6 with triethylamine or acetic acid, stir for 30min, seal it, and place it in an oven at 125°C After 3 days, take out the reaction kettle, place the reaction kettle in a 40KHz ultrasonic field to cool down naturally, wait for the reaction kettle to cool down slowly to 70°C, open the reaction kettle, add 70°C deionized water dropwise, white crystalline powder precipitates, and cool to room temperature And turn off the ultrasonic wave, filter, wash with dichloromethane and ethanol, and dry in vacuum for 2 hours to obtain amlodipine maleate hydrate crystals. The particle size range of the crystal is 75-150 μm, mp: 178-180°C.

[0055] Adopt U.S. Perkin-Elmer company PE 2400II elemental analyzer, elemental analysis (%) calculated value is: C (52.22), H (5.84), Cl (6.42), N (5.08), O (30.44); Elemental analysis (%) ) found: C (5...

Embodiment 2

[0059] Add 9g of amlodipine maleate, 21ml of ethanol, 42ml of dimethyl sulfoxide, and 7ml of deionized water into a 100ml reaction kettle, adjust the pH to 6.5 with triethylamine or acetic acid, stir for 30min, seal it, and place it in an oven at 130°C After 3 days, the reactor was taken out, and the reactor was placed in a 40KHz ultrasonic field to cool down naturally. After the reactor was slowly cooled to 75°C, the reactor was opened, and deionized water at 75°C was added dropwise. White crystalline powder precipitated, and cooled to room temperature. And turn off the ultrasonic wave, filter, wash with dichloromethane and ethanol, and dry in vacuum for 3 hours to obtain amlodipine maleate hydrate crystals. The particle size range of the crystal is 75-150 μm, mp: 178-180°C.

[0060] Adopt U.S. Perkin-Elmer company PE 2400II elemental analyzer, elemental analysis (%) calculated value is: C (52.22), H (5.84), Cl (6.42), N (5.08), O (30.44); Elemental analysis (%) ) found: C (...

Embodiment 3

[0064] Ingredients as follows:

[0065] Material name

First group

Second Group

The third group

Fourth group

fifth group

The sixth group

seventh group

Amlodipine

2.5

5

10g

10g

10g

10g

10g

Olmesartan medoxomil

20

30

40g

40g

40g

40g

40g

compressible starch

5

20

30g

36g

18g

50g

30g

Microcrystalline Cellulose PH102

10

15

46g

40g

60g

20g

38g

Low-substituted hydroxypropyl cellulose

15

20

32g

35g

15

28

40

Cross-linked polyvinylpyrrolidone

10

15

38g

30g

45g

30g

33g

essence

1

1.5

2g

2g

5g

2g

2g

Magnesium stearate

1

1

1g

1g

3g

1g

1g

[0066] 1000 pieces a...

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Abstract

The invention relates to an amlodipine and olmesartan medoxomil pharmaceutical composition and a preparation method thereof. The amlodipine and olmesartan medoxomil pharmaceutical composition comprises the following components in parts by weight: 2.5-10 parts of amlodipine, 20-40 parts of olmesartan medoxomil, 5-50 parts of compressible starch, 10-60 parts of microcrystalline cellulose, 15-40 parts of low-substituted hydroxypropyl cellulose, 10-45 parts of cross-linked polyvinylpyrrolidone, 1-5 parts of essence and 1-3 parts of magnesium stearate, wherein the amlodipine is an amlodipine maleate hydrate crystal. The pharmaceutical composition has the advantages of rapider and stable acting, strong synergism, accumulation and complementation effects, and high bioavailability.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to an amlodipine olmesartan medoxomil medicinal composition and a preparation method thereof. Background technique [0002] Olmesartan, Chinese alias: 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-(tetrazol-5-yl)phenyl]phenyl]methylimidazole -5-Carboxylic acid, English name: Olmesartan Medoxomil, molecular formula: C 24 h 26 N 6 o 3 , molecular weight: 446.5, the structural formula is as follows: [0003] [0004] Olmesartan medoxomil is a new angiotensin II receptor antagonist (ARB) drug launched in China in August 2006. Olmesartan medoxomil is the latest member of the angiotensin II receptor antagonist (ARB) class of drugs. It is a prodrug that can be rapidly and completely hydrolyzed into the active metabolite olmesartan after entering the gastrointestinal tract And its absorption is not affected by food. Because olmesartan medoxomil is not metabolized by the ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/4422A61K31/4178A61K9/28A61P9/12A61P9/10
Inventor 钟正明罗韬马鹰军王小树
Owner HAINAN JINRUI PHARMA CO LTD
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