Abstract |
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.
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Authors | S Maya, S Indulekha, V Sukhithasri, K T Smitha, Shantikumar V Nair, R Jayakumar, Raja Biswas |
Journal | International journal of biological macromolecules
(Int J Biol Macromol)
Vol. 51
Issue 4
Pg. 392-9
(Nov 2012)
ISSN: 1879-0003 [Electronic] Netherlands |
PMID | 22705573
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 Elsevier B.V. All rights reserved. |
Chemical References |
- Anti-Bacterial Agents
- Biocompatible Materials
- Capsules
- Drug Carriers
- Gels
- O-carboxymethylchitosan
- Chitosan
- Tetracycline
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Topics |
- Anti-Bacterial Agents
(chemistry, pharmacology)
- Biocompatible Materials
(chemistry, metabolism, toxicity)
- Capsules
- Chitosan
(analogs & derivatives, chemistry, metabolism, toxicity)
- Drug Carriers
(chemistry, metabolism, toxicity)
- Endocytosis
- Gels
- HEK293 Cells
- Hemolysis
(drug effects)
- Humans
- Intracellular Space
(drug effects, microbiology)
- Nanoparticles
- Particle Size
- Platelet Activation
(drug effects)
- Staphylococcus aureus
(drug effects, metabolism, physiology)
- Tetracycline
(chemistry, pharmacology)
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