Penfluridol polyanhydride pellets and penfluridol long-acting controlled-release tablets and preparation method thereof

A technology of pentafluridopolyanhydride pellets and penfluridol, which is applied to medical preparations with no active ingredients, medical preparations containing active ingredients, sugar-coated pills, etc., and can solve increased muscle tension, dull face, and slow movements , muscle tremor, salivation, fidgeting, repeated wandering; ④ tardive dyskinesia, great interference with the normal life of mentally ill patients, etc., to reduce clinical adverse reactions, reduce hospitalization costs and other treatment costs, and facilitate family treatment.

Active Publication Date: 2020-03-10
湖南中南制药有限责任公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] However, it is worth noting that since the drug has been used in clinical practice for decades, many patients with mental illness have experienced various adverse reactions of varying degrees. Parkinson's syndrome-like symptoms such as tremor and salivation; ②Acute dystonia: such as compulsive mouth opening, tongue protruding, torticollis, respiratory movement disorder, and dysphagia; ③Akathisia: such as restlessness and repeated wandering; ④Delayed onset Sexual dyskinesia: mouth-tongue-buccal triad, such as sucking, tongue licking, chewing, etc., the most common ones are tremor, akinesia, tachycardia, etc., the incidence rate is as high as 40%, and it may even cause a transient Once serious adverse reactions occur, the normal life of mentally ill patients will be greatly disturbed. In severe cases, there are many cases of suicide to get rid of pain.

Method used

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  • Penfluridol polyanhydride pellets and penfluridol long-acting controlled-release tablets and preparation method thereof
  • Penfluridol polyanhydride pellets and penfluridol long-acting controlled-release tablets and preparation method thereof
  • Penfluridol polyanhydride pellets and penfluridol long-acting controlled-release tablets and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] Preparation of poly(fumaric acid--sebacic acid) [P(FA--SA)] (FA:SA=20:80):

[0050] 1. Fumaric acid prepolymer (A) preparation:

[0051] In a 1000ml four-necked reaction flask equipped with a mechanical stirrer, a thermometer, a reflux tube, a heater, a vacuum tube and an addition funnel, add 29 g (0.25 mol) of fumaric acid, remove the air in the reaction flask under high vacuum, and then turn off the vacuum Finally, slowly feed nitrogen gas to make the pressure in the bottle consistent with the atmospheric pressure, and repeat the operation once more. Add 250 ml of acetic anhydride (313.2 g, 3.07 mol) from the separatory funnel, under the protection of nitrogen, stir and heat to an inner temperature of 135° C. for reflux reaction for 1.5 hours. After the reaction is completed, the reaction solvent is recovered by vacuum distillation (mainly acetic anhydride and acetic acid generated by the reaction, and the inner temperature of the distillation is controlled to be not...

Embodiment 2

[0058] Prescription: (weight)

[0059]

[0060] 105g of penfluridol polyanhydride pellets contain 26.25g of penfluridol.

[0061] A total of 1000 pieces were made, shallow arc punching die The tablet weighs 189mg, and each tablet contains 26.25mg of penfluridol.

[0062] making process:

[0063] Dissolve penfluridol raw material in ethanol, heat (fumaric acid--sebacic acid) polyanhydride to melt, then add penfluridol ethanol solution at 65°C, stir and mix at 70°C for 40 minutes, then vacuum distill at 70°C Remove ethanol, vacuum dry, cool and solidify, pulverize, vacuum dry, and pulverize again to obtain pentafluridomeric anhydride pellets;

[0064] 1. Granulation: According to the dosage in the above formula, mix starch, sucrose powder (the powdered sugar that has been crushed and passed through a 80-mesh sieve), dextrin and penfluridol pellets in sequence, and add 21 g of ethanol with a volume concentration of 50%. Add edge and mix to make wet material, and granulate...

Embodiment 3

[0071] prescription:

[0072]

[0073] A total of 200g of materials, a total of 1000 pieces were made, shallow arc punching die The tablet weighs 200mg, and each tablet contains 26.25mg of penfluridol.

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Abstract

The invention discloses a penfluridol polyanhydride pellet and a penfluridol long-acting controlled release tablet as well as a preparation method of the penfluridol long-acting controlled release tablet. The penfluridol long-acting controlled release tablet is prepared from the following components in percentage by weight: 50-60 % of penfluridol polyanhydride pellets, 15-20 % of starch, 10-16 % of sucrose powder, 5-10 % of polysaccharide, 0.2-1.0 % of magnesium stearate, and 1-3 % of hydroxypropylcellulose, wherein the penfluridol polyanhydride pellets are mixture particles composed of (fumaric acid--sebacic acid) polyanhydride [P(FA--SA)] (FA:SA=0.25:1) and penfluridol, and the weight percentage of penfluridol is 15-25 %. The penfluridol long-acting controlled release tablet has the long-acting controlled release effect, and is orally taken twice per month, 2 tablets each time, or the tablets are increased or decreased according to the diseases, or the administration is carried out following the doctor's advice, so that the untoward effects of penfluridol can be greatly reduced, the clinical efficacies can be improved, the home treatment for psychopaths is conveniently maintained, and the hospitalization expenses and other treatment cost of the psychopaths are reduced. Compared with the other clinical medicines for treating schizophrenia, the penfluridol long-acting controlled release tablet has better economic applicability and better clinical efficiency.

Description

technical field [0001] The present invention relates to penfluridol preparations. Background technique [0002] Penfluridol is a commonly used antipsychotic drug in clinical practice. At present, long-acting sugar-coated tablets are taken orally in clinical practice. The usual dosage is to take 1-3 tablets orally once a week, 20 mg per tablet. It has definite curative effect on the treatment of various types of acute and chronic schizophrenia [1] , becoming one of the first-line antipsychotic drugs in psychiatry. [0003] However, it is worth noting that since the drug has been used in clinical practice for decades, many patients with mental illness have experienced various adverse reactions of varying degrees. Parkinson's syndrome-like symptoms such as tremor and salivation; ②Acute dystonia: such as compulsive mouth opening, tongue protruding, torticollis, respiratory movement disorder, and dysphagia; ③Akathisia: such as restlessness and repeated wandering; ④Delayed onset...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/16A61K31/451A61K9/22A61K9/36A61K47/34A61P25/18
CPCA61K9/0002A61K9/1641A61K9/2031A61K9/2866A61K31/451
Inventor 申玉良曹春宇郑良彬舒志坚申玉军肖云生刘红
Owner 湖南中南制药有限责任公司
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