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新型第一代溶出模型研究口服淋巴靶向药物制剂的释放和摄取。

Novel First-Generation Dissolution Models to Investigate the Release and Uptake of Oral Lymphotropic Drug Products.

机构信息

Faculty of Pharmacy and Pharmaceutical Sciences, Katz Group-Rexall Centre for Pharmacy & Health Research, University of Alberta, 11315 - 87 Avenue, Edmonton, AB, T6G 2T9, Canada.

College of Pharmacy, Jeju National University, Jeju, 63243, Republic of Korea.

出版信息

AAPS PharmSciTech. 2024 Aug 14;25(6):187. doi: 10.1208/s12249-024-02866-y.

Abstract

Conventional dissolution tests only assess the aqueous release of drugs to ensure quality and performance, without indicating whether absorption occurs through the portal or the lymphatic circulation. To address this issue, this study aimed to develop novel first-generation dissolution models that could investigate the release and uptake of oral lymphotropic drugs and examine relevant formulation issues. Dissolution of three commercial lymphotropic drug products (Terbinafina, Apo-terbinafine, and Lamisil) was done using modified versions of USP Apparatus II and IV. The developed models contained a lymphatic compartment filled with artificial chylomicrons to account for absorption through intestinal lymphatic pathway. The various products exhibited different release profiles into the aqueous media and the lymphatic media across the two tested models. The modified USP IV apparatus demonstrated greater distinction in aqueous release patterns. However, the release pattern into the lymphatic media remained similar in both models. This work represents a progress in meeting the challenges posed by the increasing complexity of pharmaceutical products containing lipophilic drugs or formulations, and has the potential to contribute towards the development of in-vitro bioequivalence standards for formulations targeting intestinal lymphatics.

摘要

传统的溶解试验仅评估药物在水性介质中的释放,以确保质量和性能,但并不能指示药物是否通过门静脉或淋巴循环吸收。为了解决这个问题,本研究旨在开发新的第一代溶解模型,以研究口服淋巴靶向药物的释放和摄取,并研究相关的制剂问题。使用 USP 仪器 II 和 IV 的改良版本对三种市售淋巴靶向药物产品(特比萘芬、阿朴特比萘芬和兰美抒)进行溶解。所开发的模型包含充满人工乳糜微粒的淋巴室,以解释通过肠淋巴途径的吸收。各种产品在两种测试模型中均表现出不同的水性介质和淋巴介质中的释放模式。改良的 USP IV 仪器在水性释放模式方面表现出更大的区别。然而,在两种模型中,进入淋巴介质的释放模式仍然相似。这项工作代表了在满足含有亲脂性药物或制剂的药物产品日益复杂的挑战方面取得的进展,并有可能为针对肠淋巴的制剂制定体外生物等效性标准做出贡献。

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