介孔二氧化硅
体内
纳米颗粒
聚乙烯醇
材料科学
普萘洛尔
细胞毒性
体外
纳米技术
医学
药理学
化学
介孔材料
内科学
生物化学
生物
催化作用
复合材料
生物技术
作者
Haiwei Wu,Xuan Wang,Jiawei Zheng,Ling Zhang,Xiaoming Li,Weien Yuan,Xuejian Liu
标识
DOI:10.1002/adhm.201801261
摘要
Abstract Infantile hemangioma (IH) is one of the most common neoplasm of infancy. Although with the potential to involute slowly after proliferation, IH has several subsets that could develop severe complications and lead to functional impairment or permanent disfigurement. In the present study, a novel propranolol (PRN) delivery system is developed that encapsulated in mesoporous silica nanoparticles (MSN). The primary nanoparticles are further treated with polyvinyl alcohol (PVA) to form PVA‐MSN‐PRN nanoparticles. The encapsulation efficiency is 58.8% ± 7.2%, and nanoparticles could release PRN in a controlled‐release way. It is discovered that PVA‐MSN‐PRN could significantly suppress hemangioma stem cell (Hemsc) proliferation, promote Hemsc apoptosis in vitro, and inhibit the growth of hemangiomain xenografts in vivo. A conclusion could be made that this novel nanodrug delivery system has high therapeutic efficacy, low cytotoxicity, low administration frequency, and provides an attractive strategy for efficient IH therapy.
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