Controlling release kinetics of gentamicin from silica nano-carriers

被引:17
|
作者
Perni, Stefano [1 ]
Martini-Gilching, Kerstin [1 ]
Prokopovich, Polina [1 ]
机构
[1] Cardiff Univ, Sch Pharm Pharmaceut Sci, Redwood Bldg,King Edward VII Ave, Cardiff CF10 3NB, S Glam, Wales
关键词
Silica nanoparticles; Gentamicin; LbL; Antibiotic release; BETA-LACTAM ANTIBIOTICS; CONTINUOUS-INFUSION; POLYELECTROLYTE MULTILAYERS; DRUG-DELIVERY; NANOPARTICLES; LAYER; FILMS; PH; ASSEMBLIES; INFECTION;
D O I
10.1016/j.colsurfa.2017.04.063
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Antibiotic release from a carrier can be employed to reduce the frequency of administration or prolong efficacy. In this work, we prepared silica nanoparticles loaded with gentamicin through different synthetis routes (entrapment, adsorption, covalent bonding and Layer-by-Layer (LbL)). The nanocarriers physical-chemical properties were characterised and antibiotic release from the nanocarriers was monitored. The nanoparticles prepared entrapping gentamicin gave the highest drug load but completed the release over a period of 4 h. No significant differences in antibiotic load were noticed between absorption or binding of gentamicin onto the silica nanoparticles surface; moreover the release of the drug occurred over 2 days in both cases. The nanoparticles coated with gentamicin through LbL technique released the antibiotic for 3 weeks. This work demonstrates that silica nanoparticles can be employed as antibiotic carriers providing a continuous release of antibiotic over a period that can be tuned through the choice of preparation method.
引用
收藏
页码:212 / 221
页数:10
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