A novel polymer planar biomimetic membrane with self-differentiating intestinal-like structural for drug permeability prediction.

IF 4.7 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Weishuo Ju, Ran Zhang, Jingxuan Guo, Shuo Li, Huimin Zhang, Huijia Song, Yanping Sun, Zibin Gao
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引用次数: 0

Abstract

Accurately and efficiently assessing drug permeability has emerged as a critical challenge in early drug discovery and development, prompting the development of various models. In this study, a polymer planar biomimetic membrane permeation assay (PPBMPA) model was established using a Transwell chamber, and its permeability assessment capability was evaluated using model drugs with high, medium, and low permeability. The underlying permeation mechanism was also investigated. The results demonstrated that the biomimetic membrane spontaneously differentiated into an intestinal-like structure comprising a hydrated layer, a polymersome layer, and a basal layer, thereby mimicking the sequential process of drug permeation across the mucus layer, intestinal epithelium, interstitial space, and into the bloodstream. This highly biomimetic permeation pattern enabled effective differentiation between high and low absorption drugs, exhibiting a strong correlation with Caco-2 permeability (R2 = 0.85). Collectively, these findings suggest that the novel PPBMPA model holds promise as a reliable tool for rapid and reproducible drug permeability prediction.

一种具有自分化肠样结构的新型聚合物平面仿生膜用于药物透性预测。
准确有效地评估药物渗透性已成为早期药物发现和开发的关键挑战,促使各种模型的发展。本研究采用Transwell实验室建立了聚合物平面仿生膜渗透试验(PPBMPA)模型,并采用高、中、低渗透率模型药物对其渗透性评价能力进行了评价。并对其渗透机理进行了研究。结果表明,仿生膜自发分化为由水合层、聚合体层和基底层组成的肠样结构,从而模拟药物通过黏液层、肠上皮、间质间隙和进入血液的顺序过程。这种高度仿生的渗透模式能够有效区分高吸收和低吸收药物,与Caco-2渗透率有很强的相关性(R2 = 0.85)。总的来说,这些发现表明,新的PPBMPA模型有望成为快速和可重复的药物渗透性预测的可靠工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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