Selectively functionalized mesoporous silica particles with the PEGylated outer surface and the doxorubicin-grafted inner surface: Improvement of loading content and solubility

被引:17
作者
Kim, Min Soo [1 ]
Jeon, Jae Bum [1 ]
Chang, Ji Young [1 ]
机构
[1] Seoul Natl Univ, Coll Engn, Dept Mat Sci & Engn, Seoul 151744, South Korea
关键词
Mesoporous silica; Drug delivery; Doxorubicin; pH-sensitive; Surface modification; CANCER-CELL-LINE; DRUG-DELIVERY; CONTROLLED-RELEASE; GUEST MOLECULES; IN-VITRO; NANOPARTICLES; SYSTEM; RESISTANCE; CARRIERS; MCM-41;
D O I
10.1016/j.micromeso.2013.01.028
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We prepared selectively functionalized, spherical mesoporous silica particles (SMSPs) with a polyethylene glycol (PEG)-grafted outer surface and a doxorubicin-grafted inner surface for drug delivery. The SMSPs were fabricated by co-condensation of an amphiphilic organotriethoxysilane with a thermally cleavable urethane bond and tetraethoxysilane (TEOS) in the presence of cetyltrimethylammonium bromide (CTAB) under basic conditions. The outer surface of the as-precipitated silica particles was functionalized by grafting with 3-(triethoxysilyl)propyloxy-PEG. The PEG-grafted SMSPs were refluxed in methanol in the presence of HCl, resulting in the removal of surfactant molecules and the formation of a methoxy urethane group tethered to the pore wall. After the reaction of the methoxy urethane group with hydrazine, doxorubicin was chemically introduced into the pores through a pH-sensitive hydrazone linkage. A high loading content was achieved through chemical loading followed by physical loading. The doxorubicin-loaded SMSPs showed a pH-sensitive and sustained release behavior. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:118 / 124
页数:7
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