Chitosan oligosaccharide coated mesoporous silica nanoparticles for pH-stimuli responsive drug delivery applications

被引:23
作者
Moorthy, Madhappan Santha [1 ,2 ]
Hoang, Giang [1 ,2 ]
Manivasagan, Panchanathan [1 ,2 ]
Mondal, Sudip [1 ,2 ]
Thi Tuong Vy Phan [3 ]
Kim, Hyehyun [3 ]
Oh, Junghwan [1 ,2 ,3 ]
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.
引用
收藏
页码:217 / 226
页数:10
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