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冷冻干燥法制备共非晶体系

Preparation of Co-Amorphous Systems by Freeze-Drying.

作者信息

Wostry Melvin, Plappert Hanna, Grohganz Holger

机构信息

Department of Pharmacy, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark.

出版信息

Pharmaceutics. 2020 Sep 30;12(10):941. doi: 10.3390/pharmaceutics12100941.

Abstract

Freeze-drying was evaluated as a production technique for co-amorphous systems of a poorly water-soluble drug. Naproxen was freeze-dried together with arginine and lysine as co-former. To increase the solubility of naproxen in the starting solution, the applicability of five surfactants was investigated, namely sodium dodecyl sulfate, pluronic F-127, polyoxyethylene (40) stearate, tween 20 and TPGS 1000. The influence of the surfactant type, surfactant concentration and total solid content to be freeze-dried on the solid state of the sample was investigated. X-ray powder diffraction and differential scanning calorimetry showed that the majority of systems formed co-amorphous one-phase systems. However, at higher surfactant concentrations, and depending on the surfactant type, surfactant reflections were observed in the XRPD analysis upon production. Crystallization of both naproxen and amino acid occurred from some combinations under storage. In conclusion, freeze-drying was shown to be a feasible technique for the production of a selection of co-amorphous drug-amino acid formulations.

摘要

冷冻干燥作为一种生产难溶性药物共无定形体系的技术进行了评估。萘普生与精氨酸和赖氨酸作为共形成剂一起进行冷冻干燥。为了提高萘普生在起始溶液中的溶解度,研究了五种表面活性剂的适用性,即十二烷基硫酸钠、普朗尼克F-127、聚氧乙烯(40)硬脂酸酯、吐温20和TPGS 1000。研究了表面活性剂类型、表面活性剂浓度和待冷冻干燥的总固体含量对样品固态的影响。X射线粉末衍射和差示扫描量热法表明,大多数体系形成了共无定形单相体系。然而,在较高的表面活性剂浓度下,根据表面活性剂类型的不同,在生产后的XRPD分析中观察到了表面活性剂的反射峰。在储存过程中,萘普生和氨基酸的某些组合会发生结晶。总之,冷冻干燥被证明是一种可行的技术,可用于生产一系列共无定形药物-氨基酸制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5266/7599809/1846a67fa76f/pharmaceutics-12-00941-g001.jpg

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