介孔二氧化硅
药物输送
介孔有机硅
解吸
材料科学
阿霉素
药品
吸附
介孔材料
控制释放
纳米颗粒
纳米技术
化学工程
生物物理学
核化学
化学
有机化学
药理学
化疗
医学
催化作用
外科
工程类
生物
作者
Nian Wu,Xian Zeng,Bing Liu,Fang Xiang Song,Meng Lan Chen,Xiao Qin Cai,Hong Huan Luo,Yan Li
标识
DOI:10.1016/j.jddst.2022.104102
摘要
Hollow (hollow periodic mesoporous organosilica, HPMO), core-shell (mSiO2@PMO), and bowl (nanobowl periodic mesoporous organosilica, BPMO) organic mesoporous silica nanoparticles were produced in this work. According to adsorption and desorption studies, all three have large pore diameters (2–10 nm), high specific surfaces (567–726 m2g-1), and large pore volumes (0.4–1.4 cm3g-1). After transporting the antitumor pharmaceutical doxorubicin (DOX) and ZnO-controlled pH stimulation response modification, the obtained [email protected]@ZnO has a high drug loading rate (17–37%, with the largest drug loading capacity up to 378 μg/mg). Cell uptake and apoptosis tests revealed that the three morphologies of [email protected]@ZnO had high cellular uptake and inhibitory effects. These results showed that the [email protected]@ZnO preparation may be beneficial for tumor-targeted therapy. More importantly, when three unique morphologies of [email protected]@ZnO were analyzed in terms of drug loading, cell uptake, and apoptosis, the findings showed that the hollow structure of [email protected]@ZnO and the bowl-like structure of [email protected]@ZnO had more substantial impacts in all areas.
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