Polymer-coated mesoporous silica nanoparticles for controlled release of the prodrug sulfasalazine

被引:25
|
作者
Popova, M. [1 ,2 ]
Trendafilova, I. [1 ,2 ]
Zgureva, D. [3 ]
Kalvachev, Y. [4 ]
Boycheva, S. [5 ]
Tusar, N. Novak [6 ]
Szegedi, A. [7 ]
机构
[1] Bulgarian Acad Sci, Inst Organ Chem, BU-1113 Sofia, Bulgaria
[2] Bulgarian Acad Sci, Ctr Phytochem, BU-1113 Sofia, Bulgaria
[3] Tech Univ Sofia, Coll Energy & Elect, Sofia 1000, Bulgaria
[4] Bulgarian Acad Sci, Inst Catalysis, BU-1113 Sofia, Bulgaria
[5] Tech Univ Sofia, Dept Thermal & Nucl Power Engn, Sofia 1000, Bulgaria
[6] Natl Inst Chem Slovenia, Hajdrihova 19, Ljubljana 1001, Slovenia
[7] Hungarian Acad Sci, Inst Mat & Environm Chem, Res Ctr Nat Sci, H-1117 Budapest, Hungary
关键词
Prodrug sulfasalazine; Mesoporous silica; Polymer coating; Target delivery; DRUG-DELIVERY; AMINE FUNCTIONALIZATION; IN-VITRO; BIOCOMPATIBILITY; BIODISTRIBUTION; MCM-41; BIOADSORPTION; NANOSPHERES; MORPHOLOGY; VIVO;
D O I
10.1016/j.jddst.2018.01.020
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MCM-41 and SBA-15 silicas with particle sizes around 100 nm and 400 nm, respectively, were synthesized. The initial silica materials were modified with amino groups by post-synthesis method. Incipient wetness impregnation was applied for loading of prodrug sulfasalazine. The non-loaded and drug loaded mesoporous silica samples were characterized by XRD, TEM, SEM, N-2 physisorption, thermal analysis, and ATR FT-IR spectroscopy. The nanoparticles were post-coated twice by two different layers of polymers (Eudragit RL and Eudragit S), one of them being a pH sensitive one (Eudragit S). The functionalized and polymer coated mesoporous systems are suitable oral drug delivery carriers providing an opportunity to modify the release properties of the loaded drug.
引用
收藏
页码:415 / 420
页数:6
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