共 41 条
Chitosan oligosaccharide coated mesoporous silica nanoparticles for pH-stimuli responsive drug delivery applications
被引:23
作者:

Moorthy, Madhappan Santha
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机构:
Pukyong Natl Univ, Dept Biomed Engn, Busan 48513, South Korea
Pukyong Natl Univ, Ctr Marine Integrated Biotechnol BK21 Plus, Busan 48513, South Korea Pukyong Natl Univ, Dept Biomed Engn, Busan 48513, South Korea

Hoang, Giang
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机构:
Pukyong Natl Univ, Dept Biomed Engn, Busan 48513, South Korea
Pukyong Natl Univ, Ctr Marine Integrated Biotechnol BK21 Plus, Busan 48513, South Korea Pukyong Natl Univ, Dept Biomed Engn, Busan 48513, South Korea

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Kim, Hyehyun
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机构:
Pukyong Natl Univ, Marine Integrated Bion Res Ctr, Busan 48513, South Korea Pukyong Natl Univ, Dept Biomed Engn, Busan 48513, South Korea

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机构:
[1] Pukyong Natl Univ, Dept Biomed Engn, Busan 48513, South Korea
[2] Pukyong Natl Univ, Ctr Marine Integrated Biotechnol BK21 Plus, Busan 48513, South Korea
[3] Pukyong Natl Univ, Marine Integrated Bion Res Ctr, Busan 48513, South Korea
关键词:
Silica nanoparticles;
pH-Stimuli;
Chitosan oligosaccharide;
Drug delivery;
Biopolymer;
CONTROLLED-RELEASE;
TRIGGERED RELEASE;
IN-VITRO;
NANOCARRIERS;
SYSTEMS;
HYBRIDS;
DESIGN;
D O I:
10.1007/s10934-018-0646-8
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Biopolymer-coated drug delivery system with high drug-loading efficiency and pH-stimuli responsive drug release to the target site receives much research interest in cancer therapy. In this study, we have synthesized a marine biopolymer, namely chitosan oligosaccharide (COS) coated mesoporous silica nanoparticle (MSNs@COS NPs) system for pH-responsive drug delivery applications. The COS coating onto the silica nanoparticles was performed through metal-ligand complex coordination approaches. The prepared MSNs@COS NPs system were characterized by low-angle X-ray diffraction (XRD), Fourier-transform infrared (FTIR), N-2 adsorption-desorption and transmission electron microscopic (TEM), and thermogravimetric analyses. The COS-coated MSNs@COS NPs system shows high drug-loading capacity, good drug retention efficiency under physiological pH (pH 7.4) conditions, and an intracellular pH-responsive drug release behavior under acidic pH (pH 6.5, 5.0, and 4.0) environments. Furthermore, the biocompatibility and the intracellular uptake behavior of the MSNs@COS NPs system were evaluated by using MDA-MB-231 cells. The in vitro cytotoxicity and fluorescence microscopic analysis results evidenced that the synthesized MSNs@COS NPs system is biocompatible and could be readily taken up by MDA-MB-231 cells. Therefore, we believe that the proposed system could be applicable for pH-stimuli responsive controlled drug delivery applications in cancer therapy.
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页码:217 / 226
页数:10
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