Neupane Rabin, Boddu Sai H S, Renukuntla Jwala, Babu R Jayachandra, Tiwari Amit K
Department of Pharmacology and Experimental Therapeutics, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH 43614, USA.
Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, Ajman University, Ajman 346, UAE.
Pharmaceutics. 2020 Feb 13;12(2):152. doi: 10.3390/pharmaceutics12020152.
The transdermal route of drugs has received increased attention in recent years due to numerous advantages over the oral and injectable routes, such as avoidance of the hepatic metabolism, protection of drugs from the gastrointestinal tract, sustained drug delivery, and good patient compliance. The assessment of ex vivo permeation during the pharmaceutical development process helps in understanding the product quality and performance of a transdermal delivery system. Generally, excised human skin relevant to the application site or animal skin is recommended for ex vivo permeation studies. However, the limited availability of the human skin and ethical issues surrounding the use of animal skin rendered these models less attractive in the permeation study. In the last three decades, enormous efforts have been put into developing artificial membranes and 3D cultured human skin models as surrogates to the human skin. This manuscript provides an insight on the European Medicines Agency (EMA) guidelines for permeation studies and the parameters affected when using Franz diffusion cells in the permeation study. The need and possibilities for skin alternatives, such as artificially cultured human skin models, parallel artificial membrane permeability assays (PAMPA), and artificial membranes for penetration and permeation studies, are comprehensively discussed.
近年来,药物的透皮给药途径因其相对于口服和注射途径具有诸多优势而受到越来越多的关注,这些优势包括避免肝脏代谢、保护药物免受胃肠道影响、持续给药以及良好的患者顺应性。在药物研发过程中进行体外渗透评估有助于了解透皮给药系统的产品质量和性能。一般来说,建议使用与应用部位相关的切除人体皮肤或动物皮肤进行体外渗透研究。然而,人体皮肤的有限可用性以及围绕动物皮肤使用的伦理问题使得这些模型在渗透研究中吸引力降低。在过去三十年中,人们付出了巨大努力来开发人工膜和3D培养的人体皮肤模型作为人体皮肤的替代物。本手稿深入探讨了欧洲药品管理局(EMA)关于渗透研究的指南以及在渗透研究中使用Franz扩散池时受到影响的参数。全面讨论了皮肤替代物的需求和可能性,如人工培养的人体皮肤模型、平行人工膜通透性测定(PAMPA)以及用于渗透和透皮研究的人工膜。