以牛奶蛋白为载体提高水溶性差的药物的水溶性

Jaydeep S Chauhan, Jigar Vyas, U.M. Upadhyay
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引用次数: 0

摘要

导言:制剂科学家在开发治疗给药过程中面临的两大挑战是低水溶性药物的溶解性和可溶性。许多强效药物分子由于溶解性问题而无法产生治疗效果,但如果大剂量给药又会造成危险。固体分散技术是提高溶解度、溶出度和生物利用度的好方法。材料与方法:使用酪蛋白、婴儿配方奶粉和聚乙二醇 6000,通过传统的熔融法研制出了罗伐他汀的固体分散体,并对多个表征参数进行了表征。结论罗伐他汀的固体分散体得到了有效的开发。与罗伐他汀原料药相比,罗伐他汀固体分散液的溶解度明显提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancement of water solubility of Poorly Water-soluble drug using milk protein as carrier
Introduction: The two key challenges for formulation scientists in developing therapeutic delivery are the dissolution and solubility of a low aqueous-soluble drug. Many powerful drug molecules do not have therapeutic effects owing to solubility concerns, yet they can be dangerous when administered in large dosages. Solid dispersion technology is a good method for increasing solubility and dissolution, along with bioavailability. Material and Methods: solid dispersion of rosuvastatin was developed using casein, infant formula, and poly-ethylene glycol 6000 by conventional fusion method and characterized for several characterization parameters. Conclusion: Solid dispersion of rosuvastatin was efficiently developed. The dissolution of rosuvastatin solid dispersion was discovered to be noticeably increased as compared to rosuvastatin API, according to the current investigation, SD of rosuvastatin was a superior alternative for increasing the dissolution of weakly soluble therapeutic agent.
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