纳米载体
生物利用度
壳聚糖
渗透
普罗布考
甲基丙烯酰胺
粘液
纳米颗粒
化学
聚合物
化学工程
材料科学
纳米技术
共聚物
有机化学
药理学
膜
生物化学
生态学
工程类
生物
医学
抗氧化剂
丙烯酰胺
作者
Hong‐Yan Lü,Guangzhao Yang,Ran Fu,Tianbin Gao,Changshan Sun,Qinfu Zhao,Siling Wang
标识
DOI:10.1016/j.carbpol.2019.115508
摘要
Oral administration of nanoparticles is extremely limited due to the two processes of mucus permeation and epithelial absorption, which requires completely opposite surface properties of the nanocarriers. To tackle the contradiction, we developed a rational strategy to modify the surface of mesoporous carbon nanoparticles with chitosan concealed by a hydrophilic N-(2-hydroxypropyl) methacrylamide copolymer (pHPMA) layer. Probucol (PB) with the low poor permeability and solubility was loaded in optimal nanocarriers to realize the high loading efficacy and controlled release. The pHPMA polymer is a hydrophilic "mucus-inert" material, which could be dissociable from the surface of nanoparticles in the mucus, thus promoting their mucus permeation and causing exposure of chitosan in transepithelial transport. The swelling effect of chitosan under acidic conditions allowed regulation of PB release behavior. In conclusion, the mucus-permeable nanocarrier could effectively overcome multiple gastrointestinal absorption barriers and the oral bioavailability of PB-loaded HCMCN was 2.76-fold that of commercial preparation.
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