化学
介孔二氧化硅
赫拉
Zeta电位
纳米颗粒
药物输送
赖氨酸
共聚物
介孔材料
聚合
生物物理学
体外
高分子化学
核化学
纳米技术
有机化学
聚合物
生物化学
氨基酸
材料科学
催化作用
生物
作者
Chunbo Yang,Zheng-Zheng Shi,Cong Feng,Rui Li,Sihao Luo,Xiangfeng Li,Liping Ruan
标识
DOI:10.1002/mabi.202000034
摘要
Abstract In this study, an adjustable pH‐responsive drug delivery system using mesoporous silica nanoparticles (MSNs) as the host materials and the modified polypeptides as the nanovalves is reported. Since the polypeptide can self‐assemble via electrostatic interaction at pH 7.4 and be disassembled by pH changes, the modified poly( l ‐lysine) and poly( l ‐glutamate) are utilized for pore blocking and opening in the study. Poly( l ‐lysine)‐MSN (PLL‐MSN) and poly( l ‐glutamate)‐MSN (PLG‐MSN) are synthesized via the ring opening polymerization of N‐carboxyanhydrides onto the surface of mesoporous silica nanoparticles. The successful modification of the polypeptide on MSN is proved by Zeta potential change, X‐ray photoelectron spectroscopy (XPS), solid state NMR, and MALDI‐TOF MS. In vitro simulated dye release studies show that PLL‐MSN and PLG‐MSN can successfully load the dye molecules. The release study shows that the controlled release can be constructed at different pH by adjusting the ratio of PLL‐MSN to PLG‐MSN. Cellular uptake study indicates that the drug is detected in both cytoplasm and nucleus, especially in the nucleus. In vitro cytotoxicity assay indicates that DOX loaded mixture nanoparticles (ratio of PLL‐MSN to PLG‐MSN is 1:1) can be triggered for drug release in HeLa cells, resulting in 88% of cell killing.
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