Department of Pharmacy, University of Navarra, 31008 Pamplona, Spain.
Eur J Pharm Sci. 2009 Nov 5;38(4):405-13. doi: 10.1016/j.ejps.2009.09.010. Epub 2009 Sep 16.
The aim of this work was to study the effect of the combination between 2-hydroxypropyl-beta-cyclodextrin (HPCD) and bioadhesive nanoparticles on the encapsulation and intestinal permeability of paclitaxel (PTX). In this context, a solid inclusion complex between PTX and HPCD was prepared by an evaporation method. Then, the complex was incorporated in poly(anhydride) nanoparticles by a solvent displacement method. The resulting nanoparticles, PTX-HPCD NP, displayed a size of about 300 nm and a drug loading of about 170 microg/mg (500-fold higher than in the absence of HPCD). The effect of these nanoparticles on the permeability of intestinal epithelium was investigated using the Ussing chamber technique. The apparent permeability (P(app)) of PTX was found to be 12-fold higher when formulated as PTX-HPCD NP than when formulated as Taxol (control). Furthermore, when interaction between nanoparticles and the mucosa was avoided, the permeability of PTX significantly decreased. In summary, the association between PTX-HPCD and poly(anhydride) nanoparticles would induce a positive effect over the intestinal permeability of paclitaxel, being the bioadhesion a mandatory condition in this phenomena.
本工作旨在研究 2-羟丙基-β-环糊精(HPCD)与生物黏附纳米粒子联合对紫杉醇(PTX)包封率和肠道通透性的影响。在此背景下,采用蒸发法制备了 PTX 与 HPCD 的固体包合物。然后,通过溶剂置换法将该复合物包封于聚(酸酐)纳米粒子中。所得的纳米粒子,即 PTX-HPCD NP,粒径约为 300nm,载药量约为 170μg/mg(载药量比不含 HPCD 时高 500 倍)。采用 Ussing 室技术研究了这些纳米粒子对肠上皮通透性的影响。结果发现,与 Taxol(对照)相比,将 PTX 制成 PTX-HPCD NP 时,PTX 的表观渗透系数(P(app))提高了 12 倍。此外,当避免纳米粒子与黏膜相互作用时,PTX 的通透性显著降低。总之,PTX-HPCD 与聚(酸酐)纳米粒子的结合会对紫杉醇的肠道通透性产生积极影响,而生物黏附是这一现象的必要条件。