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研究从 PREZISTA® 片剂中提取的高度纯化的达芦那韦乙醇酸盐的物理化学稳定性。

Investigating the Physicochemical Stability of Highly Purified Darunavir Ethanolate Extracted from PREZISTA® Tablets.

机构信息

Department of Industrial and Physical Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, Indiana, 47907, USA.

Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, 575 Stadium Mall Drive, West Lafayette, Indiana, 47907, USA.

出版信息

AAPS PharmSciTech. 2018 Jul;19(5):2407-2417. doi: 10.1208/s12249-018-1036-x. Epub 2018 Jun 4.

Abstract

Understanding physicochemical stability of darunavir ethanolate is expected to be of critical importance for the development and manufacturing of high-quality darunavir-related pharmaceutical products. However, there are no enabling monographs for darunavir to illustrate its solid-state chemistry, impurity profile, and assay methods. In addition, the US Pharmacopeia reference standard of darunavir is still not commercially available. It has been also challenging to find reliable vendors to obtain highly purified darunavir ethanolate crystals to conduct the physicochemical stability testing. In the present research, we developed a straightforward and cost-effective approach to extract and purify darunavir ethanolate from PREZISTA® tablets using reverse-engineering and crystallization. Using these highly purified crystals, we thoroughly evaluated the potential risks of degradation and form conversions of darunavir ethanolate at stressed conditions to define the manufacturing and packaging specifications for darunavir-related products. Amorphization was observed under thermal storage caused by desolvation of darunavir ethanolate. The ethanolate-to-hydrate conversion of darunavir was observed at high relative humidity conditions. Moreover, acid/base-induced degradations of darunavir have been investigated herein to determine the possible drug-excipient compatibility issues in formulations. Furthermore, it is of particular interests to allow the production of high-quality darunavir-ritonavir fixed dose combinations for marketing in Africa. Thus, a validated HPLC method was developed according to ICH guideline to simultaneously quantify assays of darunavir and ritonavir in a single injection. In summary, the findings of this study provide important information for pharmaceutical scientists to design and develop reliable formulations and processings for darunavir-related products with improved stability.

摘要

理解达芦那韦乙醇酸盐的物理化学稳定性对于开发和制造高质量的达芦那韦相关药物产品至关重要。然而,目前并没有关于达芦那韦的专论来阐明其固态化学、杂质概况和分析方法。此外,美国药典的达芦那韦参考标准仍然无法商业获得。此外,找到可靠的供应商来获得高纯度的达芦那韦乙醇酸盐晶体以进行物理化学稳定性测试也具有挑战性。在本研究中,我们开发了一种简单且经济有效的方法,使用反向工程和结晶从 PREZISTA®片剂中提取和纯化达芦那韦乙醇酸盐。使用这些高度纯化的晶体,我们彻底评估了达芦那韦乙醇酸盐在应激条件下降解和形态转化的潜在风险,以确定达芦那韦相关产品的制造和包装规格。在热储存过程中,由于达芦那韦乙醇酸盐的去溶剂化作用,观察到了无定形化。在高相对湿度条件下,观察到达芦那韦乙醇酸盐向水合物的转化。此外,本文还研究了酸/碱诱导的达芦那韦降解,以确定制剂中可能存在的药物-赋形剂相容性问题。此外,特别关注允许在非洲生产高质量的达芦那韦-利托那韦固定剂量组合用于上市。因此,根据 ICH 指南开发了一种经过验证的 HPLC 方法,可在单次注射中同时定量测定达芦那韦和利托那韦的含量。总之,本研究的结果为药物科学家提供了重要信息,有助于设计和开发具有改善稳定性的达芦那韦相关产品的可靠配方和工艺。

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