PLGA公司
核化学
生物结合
药物输送
介孔材料
化学
控制释放
表面改性
抗菌活性
傅里叶变换红外光谱
介孔二氧化硅
药品
组合化学
纳米技术
材料科学
体外
化学工程
有机化学
细菌
药理学
生物化学
催化作用
物理化学
医学
生物
工程类
遗传学
作者
Merina Paul Das,Gaurav Pandey,Bernaurdshaw Neppolian,Jayabrata Das
标识
DOI:10.1016/j.colsurfb.2021.111700
摘要
In this research, a core-shell type pH-responsive poly-l-glutamic acid embedded mesoporous bioactive glass nanospheres (MBAG/PLGA) was designed via aminosilane functionalization of MBAG using 3-aminopropyltriethoxysilane (APTES). The formation of MBAG/PLGA was well dispersed in an aqueous medium and demonstrated high drug loading efficacy and enhanced drug delivery rate. Daunomycin (DAN) was considered as a model chemotherapeutic drug for loading and release study. The cumulative in vitro release of DAN from DAN loaded MBAG/PLGA (MBAG/[email protected]) was observed to be pH-dependent and, the DAN release rate was much higher at pH ∼ 5.5 compared to pH at 7.4. The modified Kirby-Bauer microbial assay results showed that the MBAG is a potential antimicrobial agent and susceptibility for Gram-negative bacteria is observed to be much higher than Gram-positive ones. Advanced characterization studies such as SEM coupled with EDX, HRTEM, FTIR, XPS, TGA, XRD, and BET analysis were performed to support the findings of this research. Overall, these results demonstrated that MBAG/PLGA is a promising candidate for a pH-responsive localized drug delivery system in bioconjugate science.
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