J Biomed Nanotechnol. 2020 Jul 1;16(7):1160-1168. doi: 10.1166/jbn.2020.2956.
The oral administration of paclitaxel suffering obstacles like poorly solubility and low permeability, causing extremely low oral bioavailability. In this study, we aim to study the role of transmembrane pathway on the absorption mechanisms of PTX-Micelles. In addition, we will further study the permeability of PTX-Micelles by employing perfusion model. The results showed the PTX-Micelles could be up taken by caco-2 intact. In addition, we found that the endocytosis pathway and M cells pathway attended, while paracellular pathway absented in the transport process of PTX-Micelles. The study on perfusion showed the absorption rate constant (Ka) of PTX was enhanced from 6.3, 6.1, 10.6 and 13.6 × 10/min to 15.1, 18.4, 45.6 and 42.9 × 10/min by micelles in duodenum, jejunum, ileum and colon, respectively, indicating the PTX-Micelles could enhance the permeability of PTX in intestinal membrane. This study indicating that transmembrane pathway-mediated transport is an important part in the transport process of polymeric micelles, and designing formulation based on transmembrane pathways may be a promising route for oral bioavailability enhancement of poor-soluble drugs.
紫杉醇口服给药存在溶解度差和渗透性低等障碍,导致口服生物利用度极低。本研究旨在探讨跨膜途径在 PTX-胶束吸收机制中的作用。此外,我们将通过灌流模型进一步研究 PTX-胶束的渗透性。结果表明,PTX-胶束可以被完整的 Caco-2 细胞摄取。此外,我们发现内吞途径和 M 细胞途径参与了 PTX-胶束的转运过程,而细胞旁途径不存在。灌流研究表明,PTX 的吸收速率常数(Ka)分别从十二指肠、空肠、回肠和结肠中的 6.3、6.1、10.6 和 13.6×10/min 增加到 15.1、18.4、45.6 和 42.9×10/min,表明 PTX-胶束可以增强 PTX 在肠膜中的渗透性。本研究表明,跨膜途径介导的转运是聚合物胶束转运过程中的重要组成部分,基于跨膜途径设计制剂可能是提高难溶性药物口服生物利用度的有前途的途径。