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A glimepiride tablet and a preparing method thereof

A glimepiride tablet and tablet technology, applied in the field of medicine, can solve the problems of difficult industrialization, complex process, and difficult filling, and achieve the effects of rapid dissolution, simple preparation process, and finer particle size

Inactive Publication Date: 2014-09-10
QINGDAO UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

From the test results, although surfactants are added to the dissolution test, only about 30% is dissolved in 10 minutes; the process is complicated, it is crushed after freeze-drying, it is easy to absorb moisture, it is difficult to fill, and it is difficult to industrialize

Method used

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  • A glimepiride tablet and a preparing method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Glimepiride 1g

[0037] Polyoxyethylene castor oil 5g

[0038] Chloroform 100ml

[0039] Micronized silica gel 100g

[0040] Lactose 50g

[0041] Crospovidone 5g

[0042] Magnesium Stearate 1g

[0043] Preparation Process

[0044] (1) Dissolve glimepiride in chloroform, add polyoxyethylene castor oil, and stir to obtain a homogeneous solution;

[0045] (2) Dry under reduced pressure to remove chloroform to obtain a viscous solution;

[0046] (3) Add micro-powder silica gel, stir well, then mix evenly with lactose, crospovidone, and magnesium stearate, and press into tablets.

Embodiment 2

[0048] Glimepiride 1g

[0049] Poloxamer 20g

[0050] Chloroform 100ml

[0051] Micronized silica gel 60g

[0052] Microcrystalline Cellulose 50g

[0053] Sodium carboxymethyl starch 10g

[0054] Micronized silica gel 2g

[0055] Preparation Process

[0056] (1) Dissolve glimepiride in chloroform, add poloxamer, stir to obtain a homogeneous solution;

[0057] (2) Dry under reduced pressure to remove chloroform to obtain a viscous solution;

[0058] (3) Add micropowder silica gel, stir well, then mix evenly with microcrystalline cellulose, sodium carboxymethyl starch, and micropowder silica gel, and press into tablets.

Embodiment 3

[0060] Glimepiride 1g

[0061] Polyoxyethylene castor oil 10g

[0062] Chloroform 100ml

[0063] Micronized silica gel 100g

[0064] Microcrystalline Cellulose 50g

[0065] Sodium carboxymethyl starch 5g

[0066] Magnesium Stearate 1g

[0067] Preparation Process

[0068] (1) Dissolve glimepiride in chloroform, add polyoxyethylene castor oil, and stir to obtain a homogeneous solution;

[0069] (2) Dry under reduced pressure to remove chloroform to obtain a viscous solution;

[0070] (3) Add micropowder silica gel, stir well, then mix evenly with microcrystalline cellulose, sodium carboxymethyl starch, and magnesium stearate, and press into tablets.

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PUM

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Abstract

A glimepiride tablet and a preparing method thereof are disclosed. The preparing method includes: dissolving glimepiride in chloroform, adding a surfactant, stirring to obtain a uniform solution, drying under reduced pressure, removing the chloroform to obtain a sticky solution, adding aerosol, fully stirring, adding pharmaceutically acceptable accessory materials, uniformly mixing, and tabletting.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to a glimepiride tablet and a preparation method thereof. Background technique [0002] Glimepiride is a new generation of sulfonylurea drugs developed by Hoechest Marion Roussel in Germany, and it is the first drug of this generation to be marketed. Glimepiride is a new oral hypoglycemic drug, suitable for non-insulin-dependent diabetes that is difficult to control with diet and physical exercise. The structural formula is as follows: [0003] [0004] Glimepiride is a poorly soluble drug, which is dissolved in chloroform and very slightly dissolved in methanol and ethanol. According to the "Japanese Medical Drug Quality Information Collection", it is dissolved in water, pH 1.2 hydrochloric acid, pH 4.0 acetate buffer, Solubility (37°C) in pH 6.8 phosphate buffer and pH 7.8 phosphate buffer is 2.7×l0-4, 7.0×10-6, 9.4×10-6, 1.0×10-3 and 7.1×10- 3mg / ml, is a hydrop...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/20A61K31/64A61P3/10
Inventor 沈若武张蓓孙勇徐晟伟夏玉军赵成晁凡管文敏
Owner QINGDAO UNIV
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