Meloni Valentina, Halstenberg Laura, Mareczek Lena, Lu Jankin, Liang Bonnie, Gottschalk Nadine, Mueller Lena K
Merck Life Science KGaA, 64293 Darmstadt, Germany.
Merck Chemicals (Shanghai) Co., Ltd., Shanghai 201203, China.
Pharmaceutics. 2024 Nov 22;16(12):1499. doi: 10.3390/pharmaceutics16121499.
BACKGROUND/OBJECTIVES: This project aims to provide valuable insights into the formulation of orodispersible films (ODFs) for the delivery of PROTAC ARV-110. The primary objective of this drug delivery formulation is to enhance the solubility of PROTAC ARV-110, which faces significant challenges due to the low solubility of this active pharmaceutical ingredient, as it belongs to a molecular class that is considered to exceed the "Rule of Five".
We employed the concept of developing a rapidly disintegrating ODF to enhance the solubility of PROTAC ARV-110, utilizing polyvinyl alcohol as the polymer of choice. Given the high thermal stability of ARV-110, the PROTAC was subjected to two primary ODF manufacturing techniques: Hot melt extrusion (HME) and solvent casting. To establish the HME method, pre-screening through vacuum compression molding was performed. The films were characterized based on their disintegration in artificial saliva, drug release in a physiological environment, and mechanical strength.
All formulations demonstrated enhanced solubility of ARV-110, achieving exceptional results in terms of disintegration times and resistance to applied stress.
The findings from the experiments outlined herein establish a solid foundation for the successful production of orodispersible films for the delivery of PROTACs.
背景/目的:本项目旨在为用于递送PROTAC ARV - 110的口腔崩解膜(ODF)的配方提供有价值的见解。这种药物递送配方的主要目标是提高PROTAC ARV - 110的溶解度,由于这种活性药物成分的低溶解度,它面临着重大挑战,因为它属于被认为超过“五规则”的分子类别。
我们采用开发快速崩解的ODF的概念来提高PROTAC ARV - 110的溶解度,选用聚乙烯醇作为聚合物。鉴于ARV - 110的高热稳定性,该PROTAC采用了两种主要的ODF制造技术:热熔挤出(HME)和溶剂浇铸。为建立HME方法,通过真空压缩成型进行了预筛选。基于薄膜在人工唾液中的崩解、在生理环境中的药物释放以及机械强度对薄膜进行了表征。
所有配方均显示出ARV - 110溶解度的提高,在崩解时间和抗施加应力方面取得了优异的结果。
本文所述实验的结果为成功生产用于递送PROTAC的口腔崩解膜奠定了坚实的基础。