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Carvedilol tablet and preparation method thereof

A technology of carvedilol tablet and filler, which is applied in the field of carvedilol tablet and its preparation, and can solve the problems that carvedilol tablet is not easy, cannot achieve the effect of rapid drug release, slow onset and the like , to achieve the effect of rapid release, easy operation and quick effect

Inactive Publication Date: 2015-06-17
ZIBO DEV ZONE YADA PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Carvedilol tablets currently used are not easily soluble in water, have a slow onset of action, cannot achieve the effect of rapid drug release, and cannot be quickly absorbed by patients.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0011] Carvedilol tablet consists of the following raw materials in parts by weight: 30 parts of carvedilol, 15 parts of microcrystalline cellulose, 805 parts of Tween, 5 parts of starch, 10 parts of magnesium stearate, micronized silica gel 15 servings.

[0012] The preparation method of carvedilol tablets is to weigh the powder of each raw material according to the above ratio, first mix 30 parts of vedilol powder, 15 parts of microcrystalline cellulose, and 5 parts of Tween-805, and then add 5 parts of starch , 10 parts of magnesium stearate and 15 parts of micropowder silica gel, mixed evenly, and finally placed in a tablet machine to be compressed into tablets, and packed.

Embodiment 2

[0014] Carvedilol tablet is made up of the following raw materials in parts by weight: 50 parts of carvedilol, 25 parts of cellulose, 10 parts of sodium lauryl sulfate, 10 parts of polyvinylpyrrolidone, 15 parts of calcium stearate, Micropowder silica gel 20 parts.

[0015] The preparation method of carvedilol tablets is to weigh the powder of each raw material according to the above ratio, first mix 50 parts of vedilol powder, 25 parts of cellulose and 10 parts of sodium lauryl sulfate, and then add polyvinylpyrrolidone 10 parts, 15 parts of calcium stearate and 20 parts of micropowdered silica gel, mixed evenly, and finally placed in a tablet machine to be compressed into tablets and packaged.

Embodiment 3

[0017] The carvedilol tablet consists of the following raw materials in parts by weight: 25 parts of carvedilol, 10 parts of lactose, 10 parts of poloxamer, 2 parts of starch, 5 parts of talcum powder, and 5 parts of micronized silica gel.

[0018] The preparation method of carvedilol tablet, take the powder of each raw material according to the above ratio, mix 25 parts of carvedilol, 10 parts of lactose and 10 parts of poloxamer, then add 2 parts of starch, 5 parts of talcum powder and 5 parts of micro-powder silica gel, mixed evenly, and finally placed in a tablet machine to be compressed into tablets, packaged.

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PUM

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Abstract

The invention discloses a carvedilol tablet and a preparation method thereof and belongs to the field of pharmacy. The carvedilol tablet comprises, by weight, 5-50 parts of carvedilol, 10-30 parts of a filler, 2-10 parts of a surfactant, 2-10 parts of a binder, 5-15 parts of a lubricant and 5-20 parts of a flow aid. The preparation method comprises the following steps of weighing raw material powder according to the above ratio, mixing the carvedilol, filler and surfactant powder to obtain uniform powder, adding the lubricant, binder and flow aid into the mixture, carrying out mixing to obtain a uniform mixture, putting the mixture into a tablet machine, preparing tablets and carrying out packaging. The carvedilol tablet can be dissolved in water easily, is suitable for oral administration, has a fast release rate and produces effects fast. The preparation method has simple processes, can be operated easily and is suitable for batch production.

Description

technical field [0001] The invention belongs to the field of pharmacy, and in particular relates to a carvedilol tablet and a preparation method thereof. Background technique [0002] Carvedilol is an α and β receptor blocker, which can relax blood vessels while blocking receptors. It is used to treat mild and moderate hypertension or hypertensive patients with renal insufficiency and diabetes. Carvedilol is easily absorbed after oral administration, with an absolute bioavailability (F) of about 25% to 35%, a significant first-pass effect, and an elimination phase half-life (t1 / 2b) of about 7 to 10 hours. When taken with food, its absorption is slowed, but has no significant effect on bioavailability, and can reduce the risk of orthostatic hypotension. Carvedilol is a basic lipophilic compound with a binding rate of more than 98% to plasma proteins. Its steady-state volume of distribution is about 1.5L, and its plasma clearance rate is 500-700ml / min. Carvedilol is complet...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/20A61K31/403A61P9/08A61P9/12A61P13/12A61P3/10
Inventor 隋英祝
Owner ZIBO DEV ZONE YADA PHARMA
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