Method for preparing oxiracetam oral dispersible film preparation

A technology for dispersing film and oral cavity is applied in the field of preparing oxiracetam orally dispersible film, which can solve the problem that disintegration time and tensile strength are not easy to control, restrict the development and application of orally dispersible film, and the preparation process of liposome is complicated. and other problems, to achieve the effect of improving bioavailability, avoiding elimination effect, and uniform and complete appearance

Inactive Publication Date: 2017-06-13
CHONGQING RUNZE PHARM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This type of preparation is directly injected into tissues or blood vessels, and there is no absorption process or the absorption process is very short, so the blood concentration can quickly reach the peak to play a role; Most require higher equipment conditions, and the drugs in the injection are generally dispersed in water as micron-sized solid particles in the molecular state, with a large degree of dispersion, and high-temperature sterilization often results in drug hydrolysis, oxidation, and solid particle coalescence Stability issues such as large size
At the same time, because the injection directly and quickly enters the human body without the protection of the normal physiological barrier of the human body, if the dosage is improper or the injection is too fast, or there is a problem with the quality of the drug, it may bring harm to the patient, or even cause irreparable consequences.
In addition, injection pain, inability to administer drugs by the patient, local induration of i...

Method used

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  • Method for preparing oxiracetam oral dispersible film preparation
  • Method for preparing oxiracetam oral dispersible film preparation
  • Method for preparing oxiracetam oral dispersible film preparation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Mix 8 parts of oxiracetam, 93 parts of polyoxyethylene, 8 parts of propylene glycol, 5 parts of citric acid, and 2 parts of fructose. After fully grinding and mixing evenly, send it to the hot-melt zone through the feed zone of the hot-melt laminator , heat-melted at 80-85°C, the molten mixture is continuously output through the metering area, poured into the mold, and forms a film after cooling.

Embodiment 2

[0037]Mix 10 parts of oxiracetam, 94 parts of polyoxyethylene, 8 parts of propylene glycol, 5 parts of malic acid, and 3 parts of glucose. After fully grinding and mixing evenly, send it to the hot melting area through the feeding area of ​​the hot melt laminating machine , heat-melted at 85-90°C, the molten mixture is continuously output through the metering area, poured into the mold, and forms a film after cooling.

[0038] The hot-melt lamination process can be carried out with reference to the following literature: Repka MA, Battu SK, Upadhye SB, et al. Pharmaceutical applications of hot-melt extrusion: part II [J]. Drug Dev IndPharm, 2007, 33 (10): 1043-1057.

Embodiment 3

[0040] Mix 12 parts of oxiracetam, 95 parts of hydroxypropyl methylcellulose, 8 parts of triethyl citrate, 4 parts of saliva stimulant, and 3 parts of xylitol. The feeding area of ​​the film machine is sent to the hot melting area, where it is melted at 85-90 ° C, and the molten mixture is continuously output through the metering area, poured into the mold, and forms a film after cooling.

[0041] With reference to Examples 1-3, the following examples are prepared: (amounts in the following table are parts by weight)

[0042]

[0043]

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Abstract

The invention discloses a method for preparing an oxiracetam oral dispersible film preparation. The method comprises the following steps of sufficiently grinding and uniformly mixing 1 to 15 parts of oxiracetam, 80 to 95 parts of film forming material, 5 to 10 parts of plasticizer, 2 to 5 parts of saliva irritant and 1 to 3 parts of sweetener, sending a mixture to a hot melting zone through a feeding zone of a hot-melt film laminator, hot melting the mixture at 70 to 95 DEG C, continuously outputting the molten mixture through a proportioning zone, pouring the molten mixture into a mold, and cooling the mixture to form the film preparation. According to the method, the film forming material of specific type and use level is selected to be combined with the plasticizer; thus, technical problems that the film preparation is easy to break, is poor in strength and toughness, is slow to disintegrate, is longer in dissolution time and is not beneficial to the absorption of a medicine, and the like, are solved; the made oxiracetam oral dispersible film preparation is enabled to be good in demolding performance; a medicinal film is flexible, is uneasy to break, and is short in the dissolution time.

Description

technical field [0001] The invention relates to oxiracetam, in particular to a method for preparing oxiracetam orodispersible film. Background technique [0002] Oxiracetam, chemically named 4-hydroxy-2-oxo-1-pyrrolidineacetamide, is a nootropic drug synthesized for the first time in 1974 by the Italian Shi Kebichem company. Aminobutyric acid (GABOB) derivatives are central nervous system drugs that can promote learning, enhance memory, and protect damaged nerve cells. Its structure is as follows: [0003] [0004] Since it was put on the market, due to its good effect, high safety, wide range of indications, few drug interactions and low toxicity, it has been the leading product in the treatment of dementia drugs, with injections, capsules, tablets and other dosage forms successively Development and listing. [0005] CN104069074A discloses a freeze-dried preparation of oxiracetam for injection, which is obtained by first forming an aqueous solution of oxiracetam with ...

Claims

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Application Information

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IPC IPC(8): A61K9/70A61K31/4015A61K47/10A61K47/14A61K47/38A61P25/28A61J3/00
CPCA61J3/00A61K9/0056A61K9/006A61K31/4015A61K47/10A61K47/14A61K47/38
Inventor 叶雷
Owner CHONGQING RUNZE PHARM CO LTD
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