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Amorphous pharmaceutical fine particles and a method of manufacturing the same are produced by pulsed laser ablation in liquid

机译:通过在液体中进行脉冲激光烧蚀来生产非晶态药物细颗粒及其制造方法

摘要

The present disclosure relates to a method of using a laser in a liquid to produce a solution of an amorphous solid pharmaceutical compound microparticle, a solution of an amorphous pharmaceutical agent microparticle produced using the method, and the method Related to the fine particles produced. By using a target solidified via a phase transition method that converts the initial crystal structure to an amorphous solid, technical difficulties in handling a target compressed by hydraulic pressure are overcome. Amorphous solid pharmaceutical compound microparticles that improve the bioavailability and solubility of the pharmaceutical compound are produced by an ablation method using a laser. This improvement occurs as a result of the combination of an irregular crystal structure and an enlarged relative surface area due to particle size reduction. The method using a laser can be performed using an ultrashort pulse laser system or a UV-ns (ultraviolet nanosecond) laser. The results obtained with ultrashort near IR (infrared) lasers and UV-ns lasers demonstrate the formation of amorphous solid curcumin microparticles.
机译:本公开涉及一种在液体中使用激光来生产非晶态固体药物化合物微粒溶液的方法,使用该方法生产的非晶态药物制剂微粒溶液以及与所生产的微粒相关的方法。通过使用通过将初始晶体结构转化为非晶态固体的相变方法固化的靶材,克服了在处理被液压压缩的靶材方面的技术难题。通过使用激光的消融方法来生产提高药物化合物的生物利用度和溶解度的非晶态固体药物化合物微粒。由于不规则的晶体结构和由于减小的粒径而增大的相对表面积的结合而产生了这种改善。可以使用超短脉冲激光系统或UV-ns(紫外线纳秒)激光来执行使用激光的方法。用超短近红外(红外)激光器和UV-ns激光器获得的结果证明了非晶形固体姜黄素微粒的形成。

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