Efficacy of tetracycline encapsulated O-carboxymethyl chitosan nanoparticles against intracellular infections of Staphylococcus aureus

被引:132
作者
Maya, S.
Indulekha, S.
Sukhithasri, V.
Smitha, K. T.
Nair, Shantikumar V.
Jayakumar, R. [1 ]
Biswas, Raja
机构
[1] Amrita Vishwa Vidyapeetham, Amrita Inst Med Sci, Amrita Ctr Nanosci & Mol Med, Kochi 682041, India
关键词
Tetracycline; Intracellular bacterial infections; Carboxymethyl chitosan nanoparticles; Ionic gelation; Drug delivery; Staphylococcus aureus; DRUG-DELIVERY; ANTIBIOTICS; ADHERENCE;
D O I
10.1016/j.ijbiomac.2012.06.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intracellular bacterial infections are recurrent, persistent and are difficult to treat because of poor penetration and limited availability of antibiotics within macrophages and epithelial cells. We developed biocompatible, 200 nm sized tetracycline encapsulated O-carboxymethyl chitosan nanoparticles (Tet-O-CMC Nps) via ionic gelation for its sustained delivery of Tet into cells. S. aureus binds and aggregates with Tet-O-CMC Nps increasing drug concentrations at the infection site. Tet-O-CMC Nps were sixfold more effective in killing intracellular S. aureus compared to Tet alone in HEK-293 and differentiated THP1 macrophage cells proving it to be an efficient nanomedicine to treat intracellular S. aureus infections. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:392 / 399
页数:8
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