Heteroatom modified MCM-41-silica carriers for Lomefloxacin delivery systems

被引:43
作者
Brezoiu, Ana-Maria [1 ]
Deaconu, Mihaela [1 ]
Nicu, Ioana [2 ]
Vasile, Eugeniu [3 ]
Mitran, Raul-Augustin [4 ]
Matei, Cristian [1 ]
Berger, Daniela [1 ]
机构
[1] Univ Politehn Bucuresti, Dept Inorgan Chem Phys Chem & Electrochem, Polizu St 1-7, Bucharest 011061, Romania
[2] Natl Inst Chem Pharmaceut Res & Dev, Vitan Ave 112, Bucharest 031299, Romania
[3] Univ Politehn Bucuresti, Dept Sci & Engn Oxide Mat & Nanomat, Polizu St 1-7, Bucharest 011061, Romania
[4] Romanian Acad, Ilie Murgulescu Inst Phys Chem, Splaiul Independentei 202, Bucharest 060021, Romania
关键词
Drug delivery systems; Heteroatom modified MCM-41; Mesoporous silica; Fluoroquinolone; Antibiotic; MESOPOROUS SILICA NANOPARTICLES; DRUG-DELIVERY; MESOSTRUCTURED SILICA; ALUMINOSILICATE CARRIERS; CATALYTIC OZONATION; RELEASE; CIPROFLOXACIN; ADSORPTION; EFFICIENT; FE-MCM-41;
D O I
10.1016/j.micromeso.2018.08.031
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The paper presents novel Lomefloxacin delivery systems based on heteroatom modified MCM-41-type silica materials. The modification of MCM-41 mesoporous silica with Mg, Fe, Ce or Zn was performed by ion-exchange approach and the resulted materials exhibited an ordered pore framework, high specific surface area (in the range of 510-813 m(2)/g), total pore volume (from 0.47 to 0.96 cm(3)/g), and uniform distribution of heteroatoms, which allow their use as carriers in drug delivery systems. The heteroatom modification of MCM-41 silica led either to the formation of amorphous metal oxide on the inner pore surface in the case of Mg and Zn, or materials with a crystalline oxide phase (CeO2 or Fe2O3) on the silica surface. The drug release profiles from heteroatom modified MCM-41 carriers were determined in simulated body fluid pH 7.4 and all Lomefloxacin-loaded samples exhibited a slower release kinetics than the antibiotic dissolution, the lowest delivery rate being obtained for Mg modified MCM-41 material. All the prepared antibiotic delivery systems presented good bactericide activity against E. coli strain.
引用
收藏
页码:214 / 222
页数:9
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