Treprostinil palmitil 吸入粉利用内源性肺部酶提供持续的曲普瑞司替尼。

Expert opinion on drug delivery Pub Date : 2024-08-01 Epub Date: 2024-09-12 DOI:10.1080/17425247.2024.2395444
Tam Nguyen, Christina Chang, David Cipolla, Vladimir Malinin, Walter Perkins, Veronica Viramontes, Junguo Zhou, Michel Corboz
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引用次数: 0

摘要

研究背景研究设计与方法:我们进行了体外活性测定,以确定肺部水解 TP 的酶,并进行了细胞测定和免疫染色,以确定肺部的可能位置:结果:脂蛋白脂肪酶(LPL)的活性高于其他测试的肺酶。在体外和体内目标 TP 剂量下都存在过高的 LPL 活性:结论:LPL 可能是实现 TP 转化的关键酶。限速步骤可能是 TP 的可及性,而不是酶的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treprostinil palmitil inhalation powder leverages endogenous lung enzymes to provide sustained treprostinil.

Background: To determine key enzymes enabling treprostinil palmitil (TP) conversion to treprostinil and the main converting sites in the respiratory system.

Research design and methods: We performed in vitro activity assays to identify lung enzymes hydrolyzing TP, and cell-based assays and immunostainings to establish the likely locations within the lung.

Results: Lipoprotein lipase (LPL) had greater activity than the other tested lung enzymes. Excess LPL activity was present both in vitro and at the target TP dose in vivo.

Conclusions: LPL is likely the key enzyme enabling TP conversion. The rate-limiting step is likely the accessibility of TP and not the enzyme activity.

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