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pH-responsive drug release and real-time fluorescence detection of porous silica nanoparticles

Published on Aug 1, 2017in Materials Science and Engineering: C4.959
· DOI :10.1016/j.msec.2017.03.224
Xu Zhang4
Estimated H-index: 4
(Henan University),
Yamin Wang1
Estimated H-index: 1
+ 1 AuthorsLei Sun11
Estimated H-index: 11
(Henan University)
Abstract
Abstract In this work, pH-sensitive “dual-switch” porous silica (pSiO2) nanoparticles (NPs) were constructed for drug delivery. Poly(acrylic acid) (PAA) was grafting onto the internal and external surfaces of amino groups functionalized porous silica (pSiO2-NH2) NPs by the amidation between the amino groups and the carboxyl groups of PAA for pH triggered drug release. The resultant pSiO2/PAA NPs have an average diameter of 50–60 nm and high specific surface area (914 m2·g− 1). To improve the loading capacity, ZnO quantum dots (QDs) were used to block the partial pores of pSiO2/PAA and the loading capacity reached to 28% for methotrexate (MTX) model drug. The in vitro cellular cytotoxicity test and a hemolysis assay demonstrated that the pSiO2/PAA/ZnO NPs were highly biocompatible and suitable to utilize as drug carriers. The MTX-loaded pSiO2/PAA/ZnO NPs displayed more efficient cytotoxic to HepG2 cells than free MTX. The pSiO2/PAA/ZnO NPs displayed low premature, pH-responsive release and pH-dependent fluorescence. Moreover, pH-dependent fluorescence enables to trace MTX release behavior.
  • References (13)
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