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Non-steroidal anti-inflammatory drug ultra-fine powder and preparation method thereof

A non-steroidal anti-inflammatory drug and ultrafine powder technology, which is applied in the field of medicine, can solve the problem that the temperature and pressure of the supercritical fluid state are greatly affected, the types and quantities of non-steroidal anti-inflammatory drugs are small, and the production equipment is not easy to configure and other problems, to achieve the effect of good parallelism of production process, stable powder shape and high bioavailability

Inactive Publication Date: 2015-12-30
WUXI XINRENTANG PHARMA TECH +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the high requirements of supercritical technology on equipment and the state of supercritical fluid is greatly affected by temperature and pressure, it is difficult to maintain the state, and the research on related application equipment still needs to be further strengthened
[0028] Anti-solvent recrystallization, solvent diffusion, solvent evaporation, reaction precipitation and other methods, due to uncontrollable crystal growth, resulting in large product size differences, and generally accompanied by high-speed stirring or high-speed centrifugation or high-pressure homogenization, while spray drying and freezing Drying is used as a drying method to collect dry particles and usually needs to be combined with other methods; the above methods are not easy to configure industrial production equipment, the operation risk factor is high, and the cost is high
[0029] The various defects of the above-mentioned ultrafine powder preparation method are the main factors that lead to the extremely small number and types of drugs that are currently listed as non-steroidal anti-inflammatory drugs in the form of ultrafine powder.

Method used

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  • Non-steroidal anti-inflammatory drug ultra-fine powder and preparation method thereof
  • Non-steroidal anti-inflammatory drug ultra-fine powder and preparation method thereof
  • Non-steroidal anti-inflammatory drug ultra-fine powder and preparation method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0053] Aspirin raw material 10g, add 40ml methanol, heat to dissolve, room temperature, 20kHz, 150W ultrasonic, obtain white crystal; Obtain superfine powder after collecting, washing, drying (electron microscope XSP-BM-2C, attached Figure 4 ).

Embodiment 2

[0055] Add 100g of aspirin raw material, add 397ml of methanol, heat to dissolve, add 81ml of water, cool down in an ice bath, 40kHz, 250W ultrasonic to obtain white crystals; collect, wash and dry to obtain ultrafine powder.

Embodiment 3

[0057] Diclofenac sodium raw material 10g, add 50ml of methanol, heat to dissolve, add 10ml of water, cool down in ice bath, 20kHz, 200W ultrasonic, to obtain white crystals; collect, wash and dry to obtain ultrafine powder.

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Abstract

The invention relates to non-steroidal anti-inflammatory drug ultra-fine powder and a preparation method thereof. A non-steroidal anti-inflammatory drug has the functions of resisting inflammations and rheumatism, relieving pain, bringing down a fever and resisting blood coagulation and is widely used for alleviating osteoarthritis, rheumatoid arthritis, various fevers and various painful symptoms in clinic. The method for preparing the non-steroidal anti-inflammatory drug ultra-fine powder comprises the steps that non-steroidal anti-inflammatory drug crystals are rapidly obtained by exerting ultrasonic waves with the frequency ranging from 10 kHz to 500 kHz, the power ranging from 1 mW to 5000 W and the sound intensity ranging from 0.1 mW / cm<2> to 500 w / cm<2> into a homogeneous solution containing the non-steroidal anti-inflammatory drug, and then the non-steroidal anti-inflammatory drug ultra-fine powder is directly obtained after normal operations such as solid collection, washing and drying are conducted. The non-steroidal anti-inflammatory drug ultra-fine powder is free of substrate materials and has the advantages that the drug-loading rate is high, the dissolution velocity is high, higher bioavailability is easy to achieve, and the stability and the safety are achieved, so that the requirements for improving the bioavailability of the drug, decreasing the drug dosage and reducing adverse reactions are met, and a wide application prospect in clinic is achieved.

Description

technical field [0001] The invention relates to the technical field of medicine, in particular to an ultrafine powder of non-steroidal anti-inflammatory drugs and a preparation method thereof. Background technique [0002] Non-steroidal anti-inflammatory drugs (NSAIDs) are called non-steroidal anti-inflammatory drugs (NSAIDs) because of their chemical structure and anti-inflammatory mechanism are different from glucocorticoid steroidal anti-inflammatory drugs (SAIDS); pain effect. In addition to the commonly used oral and injection dosage forms, it is also widely used in topical medicine such as eyes. At present, NSAIDs are one of the most used drugs in the world, and about 30 million people in the world use them every day. [0003] Aspirin is slightly soluble in water and easily soluble in ethanol. It is one of the three classic drugs in the history of medicine, and is the most widely used antipyretic and analgesic anti-inflammatory drug in clinical practice. If the dos...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C69/157C07C67/52C07C229/42C07C227/42C07D209/28C07C57/30C07C51/43C07D417/12C07C65/10A61K9/14A61P29/00
Inventor 毛宇锋张兆勇周成林岳力群
Owner WUXI XINRENTANG PHARMA TECH
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