Université Paris-Sud, UMR CNRS 8612, Faculté de Pharmacie, 5, Rue J.B. Clément, 92296, Châtenay-Malabry, France.
Pharm Res. 2012 Apr;29(4):943-52. doi: 10.1007/s11095-011-0634-z. Epub 2011 Dec 7.
To evaluate of the effect of size and surface characteristics of poly(isobutylcyanoacrylate) nanoparticles coated with pluronic F68 and thiolated chitosan on mucoadhesion.
Nanoparticles were obtained by radical emulsion polymerization in presence of different amounts of F68 (0-4%w/v). Mucoadhesion was ex vivo evaluated by applying nanoparticle suspension on rat intestinal mucosa and quantifying the amount of attached nanoparticles after incubation.
F68 unimers added in the polymerization medium allowed decreasing nanoparticle size from 251 to 83 nm, but resulted in nanoparticle surface modification. The amount of thiolated chitosan onto nanoparticle surface was decreased resulting in lower thiol groups and zeta potential. Consequently, the decrease of nanoparticle hydrodynamic diameter resulted in eight-fold-increase of the number of nanoparticles attached to the mucosa but a significant decrease of the weight of attached nanoparticles was observed. This unexpected result was due to a decrease of the amount of chitosan and thiolated chitosan available to interact with mucus upon addition of F68 in the polymerization medium.
Addition of F68 should not be recommended to improve the amount of mucoadherent nanoparticles. Further studies could allow understanding if the low amount of small size nanoparticles could be able to improve oral bioavailability.
评估聚异丁基氰基丙烯酸酯纳米粒子的大小和表面特性,以及包覆聚乙二醇-聚丙二醇-聚乙二醇(Pluronic F68)和巯基化壳聚糖对黏附性的影响。
通过在不同量的 F68(0-4%w/v)存在下的自由基乳液聚合获得纳米粒子。通过将纳米粒子悬浮液施加到大鼠肠黏膜上,并在孵育后定量附着的纳米粒子的量,来评估体外黏附性。
在聚合介质中添加的 F68 单体允许将纳米粒子的粒径从 251nm 减小到 83nm,但导致纳米粒子表面发生修饰。纳米粒子表面的巯基化壳聚糖的量减少,导致硫醇基团和zeta 电位降低。因此,纳米粒子水动力直径的减小导致附着在黏膜上的纳米粒子数量增加了 8 倍,但附着的纳米粒子的重量显著降低。这一意外的结果是由于在聚合介质中添加 F68 导致与黏液相互作用的壳聚糖和巯基化壳聚糖的量减少。
不应建议添加 F68 来增加黏附性纳米粒子的数量。进一步的研究可以了解小粒径纳米粒子的低含量是否能够提高口服生物利用度。