citric acid coated magnetite nanoparticles to overcome intrinsic rifampicin resistance in...

1
EPOSTER PRESENTATION Open Access Citric acid coated magnetite nanoparticles to overcome intrinsic rifampicin resistance in Mycobacterium smegmatis Priyanka Padwal, Rajdip Bandyopadhyaya, Sarika Mehra * From 2nd International Science Symposium on HIV and Infectious Diseases (HIV SCIENCE 2014) Chennai, India. 30 January - 1 February 2014 Background The major problem faced in current tuberculosis (TB) therapy is intrinsic drug resistance of mycobacterium. Hence, there is a need to develop ways to overcome these resistance mechanisms. In the current work, we have investigated the effect of citric acid coated magne- tite nanoparticles in combination with rifampicin against a wild type strain of Mycobacterium smegmatis. Methods We have studied the effect of rifampicin on growth of cells, with and without the nanoparticles. Further, cellu- lar uptake of nanoparticles was studied by transmission electron microscopy. Since, permeability barrier and drug efflux are responsible for intrinsic drug resistance, we have performed accumulation and efflux studies on common efflux pump substrate ethidium bromide (EtBr) by semi automated fluorometric method in the presence and absence of nanoparticles. Results Citric acid coated magnetite nanoparticles exhibited a significant growth inhibition when used in combination with rifampicin. However, nanoparticles alone did not have any effect on mycobacterial growth. Enhanced growth inhibition was seen in the presence of a combina- tion of rifampicin and nanoparticles, which was even more than rifampicin alone at the same concentration. Uptake studies revealed that nanoparticles were interna- lized by M. smegmatis. Transport studies on EtBr demon- strate that, in presence of nanoparticles, the net EtBr accumulation inside the cells was increased. Conclusion Citric acid coated magnetite nanoparticles enhanced the antibacterial effect of rifampicin when used in combina- tion with the drug. Increased accumulation of EtBr in presence of nanoparticles indicates that, one of the pos- sible reasons for this enhanced effect is enhanced intra- cellular drug accumulation. Published: 27 May 2014 doi:10.1186/1471-2334-14-S3-E42 Cite this article as: Padwal et al.: Citric acid coated magnetite nanoparticles to overcome intrinsic rifampicin resistance in Mycobacterium smegmatis. BMC Infectious Diseases 2014 14(Suppl 3):E42. Submit your next manuscript to BioMed Central and take full advantage of: Convenient online submission Thorough peer review No space constraints or color figure charges Immediate publication on acceptance Inclusion in PubMed, CAS, Scopus and Google Scholar Research which is freely available for redistribution Submit your manuscript at www.biomedcentral.com/submit * Correspondence: [email protected] Department of Chemical Engineering, Indian Institute of Technology Bombay, Mumbai, India Padwal et al. BMC Infectious Diseases 2014, 14(Suppl 3):E42 http://www.biomedcentral.com/1471-2334/14/S3/E42 © 2014 Padwal et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http:// creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Upload: sarika

Post on 20-Jan-2017

213 views

Category:

Documents


1 download

TRANSCRIPT

EPOSTER PRESENTATION Open Access

Citric acid coated magnetite nanoparticles toovercome intrinsic rifampicin resistance inMycobacterium smegmatisPriyanka Padwal, Rajdip Bandyopadhyaya, Sarika Mehra*

From 2nd International Science Symposium on HIV and Infectious Diseases (HIV SCIENCE 2014)Chennai, India. 30 January - 1 February 2014

BackgroundThe major problem faced in current tuberculosis (TB)therapy is intrinsic drug resistance of mycobacterium.Hence, there is a need to develop ways to overcomethese resistance mechanisms. In the current work, wehave investigated the effect of citric acid coated magne-tite nanoparticles in combination with rifampicin againsta wild type strain of Mycobacterium smegmatis.

MethodsWe have studied the effect of rifampicin on growth ofcells, with and without the nanoparticles. Further, cellu-lar uptake of nanoparticles was studied by transmissionelectron microscopy. Since, permeability barrier anddrug efflux are responsible for intrinsic drug resistance,we have performed accumulation and efflux studies oncommon efflux pump substrate ethidium bromide (EtBr)by semi automated fluorometric method in the presenceand absence of nanoparticles.

ResultsCitric acid coated magnetite nanoparticles exhibited asignificant growth inhibition when used in combinationwith rifampicin. However, nanoparticles alone did nothave any effect on mycobacterial growth. Enhancedgrowth inhibition was seen in the presence of a combina-tion of rifampicin and nanoparticles, which was evenmore than rifampicin alone at the same concentration.Uptake studies revealed that nanoparticles were interna-lized by M. smegmatis. Transport studies on EtBr demon-strate that, in presence of nanoparticles, the net EtBraccumulation inside the cells was increased.

ConclusionCitric acid coated magnetite nanoparticles enhanced theantibacterial effect of rifampicin when used in combina-tion with the drug. Increased accumulation of EtBr inpresence of nanoparticles indicates that, one of the pos-sible reasons for this enhanced effect is enhanced intra-cellular drug accumulation.

Published: 27 May 2014

doi:10.1186/1471-2334-14-S3-E42Cite this article as: Padwal et al.: Citric acid coated magnetitenanoparticles to overcome intrinsic rifampicin resistance inMycobacterium smegmatis. BMC Infectious Diseases 2014 14(Suppl 3):E42.

Submit your next manuscript to BioMed Centraland take full advantage of:

• Convenient online submission

• Thorough peer review

• No space constraints or color figure charges

• Immediate publication on acceptance

• Inclusion in PubMed, CAS, Scopus and Google Scholar

• Research which is freely available for redistribution

Submit your manuscript at www.biomedcentral.com/submit

* Correspondence: [email protected] of Chemical Engineering, Indian Institute of TechnologyBombay, Mumbai, India

Padwal et al. BMC Infectious Diseases 2014, 14(Suppl 3):E42http://www.biomedcentral.com/1471-2334/14/S3/E42

© 2014 Padwal et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative CommonsAttribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction inany medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.