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依非韦伦与γ-环糊精包合物的固态研究及其对溶解度的影响。

Inclusion Compound of Efavirenz and γ-Cyclodextrin: Solid State Studies and Effect on Solubility.

机构信息

LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.

Ashland Specialty Ingredients, Paul-Thomas Strasse, 56, D-40599 Düsseldorf, Germany.

出版信息

Molecules. 2021 Jan 20;26(3):519. doi: 10.3390/molecules26030519.

Abstract

Efavirenz is an antiretroviral drug of widespread use in the management of infections with human immunodeficiency virus type 1 (HIV-1). Efavirenz is also used in paediatrics, but due to its very poor aqueous solubility the liquid formulations available resort to oil-based excipients. In this report we describe the interaction of γ-cyclodextrin with efavirenz in solution and in the solid state. In aqueous solution, the preferential host-guest stoichiometry was determined by the continuous variation method using H NMR, which indicated a 3:2 host-to-guest proportion. Following, the solid inclusion compound was prepared at different stoichiometries by co-dissolution and freeze-drying. Solid-state characterisation of the products using FT-IR, C{H} CP-MAS NMR, thermogravimetry, and X-ray powder diffraction has confirmed that the 3:2 stoichiometry is the adequate starting condition to isolate a solid inclusion compound in the pure form. The effect of γ-cyclodextrin on the solubility of efavirenz is studied by the isotherm method.

摘要

依非韦伦是一种广泛用于治疗人类免疫缺陷病毒 1 型(HIV-1)感染的抗逆转录病毒药物。依非韦伦也用于儿科,但由于其水溶性极差,现有的液体制剂采用油基赋形剂。在本报告中,我们描述了γ-环糊精在溶液中和固态下与依非韦伦的相互作用。在水溶液中,通过使用 H NMR 的连续变化法确定了优先的主客体化学计量比,表明主客体比例为 3:2。随后,通过共溶解和冷冻干燥制备了不同化学计量比的固体包合物。使用傅里叶变换红外光谱(FT-IR)、C{H} CP-MAS NMR、热重分析和 X 射线粉末衍射对产物进行固态表征,证实 3:2 的化学计量比是分离纯形式的固体包合物的合适起始条件。通过等温法研究了γ-环糊精对依非韦伦溶解度的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7c9/7863942/7a7f1cca4a7e/molecules-26-00519-g001.jpg

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