A method for preparing oxiracetam oral film by hot-melt extrusion

An oral film and hot-melt technology, applied in the field of oxiracetam, can solve the problems of difficult control of disintegration time and tensile strength, restrictions on the development and application of oral film, and complex liposome preparation process, etc., to achieve Increased bioavailability, avoid elimination effects, uniform and complete appearance

Active Publication Date: 2018-10-23
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 injection, and vascular inflammation caused by intravenous injection are all problems in clinical application.
[0006] CN101732251A discloses a liposome of oxiracetam, which is prepared from oxiracetam, phospholipids, cholesterol, Tween 80 and an appropriate amount of osmotic pressure regulator and buffer solution; the liposome has good stability and encapsulation efficiency High, low toxicity and side effects; but the liposome preparation process is complicated, not suitable for large-scale production; more importantly, the curative effect of liposomes in the human body remains to be further studied, and there are few liposome preparations for clinical use in China at present
Although the oral film has many advantages, the limitations of its film-forming materials and preparation technology lead to low drug loading, the disintegration time and tensile strength are not easy to control, and most of the time it needs to mask the taste, which restricts the oral film. development and application of

Method used

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  • A method for preparing oxiracetam oral film by hot-melt extrusion
  • A method for preparing oxiracetam oral film by hot-melt extrusion
  • A method for preparing oxiracetam oral film by hot-melt extrusion

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Experimental program
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Effect test

Embodiment 1

[0038] Mix 6g oxiracetam, 87g chitosan, 4g propylene alcohol, 2g malic acid, and 1g fructose, fully grind and mix evenly, then send it to the hot melt zone through the feed zone of the hot melt laminator, and place it at 80- Hot melt at 85°C, the molten mixture is continuously output through the metering area, poured into the mold, and forms a film after cooling.

Embodiment 2

[0040] Mix 7g oxiracetam, 85g chitosan, 5g propylene alcohol, 2g citric acid, and 1g glucose, fully grind and mix evenly, and then send it to the hot-melt zone through the feed zone of the hot-melt film laminating machine. Hot melt at 90°C, the molten mixture is continuously output through the metering area, poured into the mold, and forms a film after cooling.

[0041] The hot-melt lamination process can be carried out with reference to the following documents: Repka MA, Battu SK, Upadhye SB, etal.Pharmaceutical applications of hot-melt extrusion: part II[J].Drug Dev IndPharm, 2007,33(10):1043-1057 .

Embodiment 3

[0043] Mix 8g of oxiracetam, 86g of hyaluronic acid, 3g of triethyl citrate, 2g of saliva stimulant, and 1g of xylitol. After fully grinding and mixing evenly, send it to the The hot melting zone is hot-melted at 85-90°C, and the molten mixture is continuously output through the metering zone, poured into the mold, and forms a film after cooling.

[0044] With reference to embodiment 1-3, prepare following embodiment: (consumption is weight g in the following table)

[0045]

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Abstract

The invention discloses a method for preparing an oxiracetam oral membrane. The method comprises the following steps of fully grinding and uniformly mixing oxiracetam, a membrane forming material, a plasticizing agent, a saliva stimulating agent and a flavoring agent, and forming a membrane by hot melting and extruding. The method solves the technical problems of easiness in breaking of the membrane, poor strength and toughness, delaying of disintegration, longer dissolving time, difficulty in medicine absorbing and the like. The oxiracetam oral membrane preparation has the beneficial effects that the stripping property is good, the medicine membrane is flexible, the easiness in breaking is avoided, and the dissolving time is short.

Description

technical field [0001] The invention relates to oxiracetam, in particular to a method for preparing oxiracetam oral film by hot-melt extrusion. 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 oxir...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/06A61K31/4015A61K47/36A61P25/28
CPCA61K9/006A61K31/4015A61K47/36
Inventor 叶雷
Owner CHONGQING RUNZE PHARM CO LTD
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