介孔二氧化硅
材料科学
纳米技术
纳米颗粒
药物输送
胶束
模板
纳米尺度
介孔材料
化学
有机化学
水溶液
催化作用
作者
Zhinan Fu,Li Li,Yiming Wang,Qiao-Lin Chen,Fang Zhao,Liheng Dai,Zhuo Chen,Dianhua Liu,Xuhong Guo
标识
DOI:10.1016/j.cej.2019.122905
摘要
The present work demonstrates how drug-loaded mesoporous silica nanoparticles (MSNPs) can be prepared by a sequential flash nanoprecipitation (FNP) technique. A sequential FNP technique is developed relying on a combination of two multi-inlet vortex mixers (MIVM), by which a continuous process that involves the formation of micelle-based templates followed by an in situ formation of MSNPs is achieved. Moreover, a widely used biological nematicide, abamectin (Abm), is added during the formation of micelles, ultimately leading to Abm-loaded MSNPs with high encapsulation efficiency. The obtained Abm-loaded MSNPs show excellent stability and inhibition activity against the livability of Meloidogyne incognita. Importantly, the parameters of the resulting MSNPs, such as silica shell thickness and inner cavity size of MSNPs, can be easily controlled by tuning the compositions of the reactant streams. We believe that such a simple approach towards direct preparation of drug-loaded MSNPs would find promising up-scale applications in various fields, such as drug delivery, bioimaging, and formulation technology.
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