Nanoparticle Encapsulated Lipopeptide Conjugate of Antitubercular Drug Isoniazid: In Vitro Intracellular Activity and in Vivo Efficacy in a Guinea Pig Model of Tuberculosis-Reference-Cited by-同舟云学术

Nanoparticle Encapsulated Lipopeptide Conjugate of Antitubercular Drug Isoniazid: In Vitro Intracellular Activity and in Vivo Efficacy in a Guinea Pig Model of Tuberculosis

Published:2014-11-26 Issue:12 Volume:25 Page:2260-2268
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Horváti Kata,Bacsa Bernadett,Kiss Éva,Gyulai Gergő,Fodor Kinga,Balka Gyula,Rusvai Miklós,Szabó Eleonóra¹,Hudecz Ferenc,Bősze Szilvia

Affiliation:

1. Laboratory of Bacteriology, Korányi National Institute for Tuberculosis and Respiratory Medicine, Budapest, 1122 Hungary

Funder

Hungarian Research Fund

Social Renewal Operational Programme

National Research and Development Programme

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/bc500476x

Reference60 articles.

1. Antibiotics for Emerging Pathogens

2. The challenge of new drug discovery for tuberculosis

3. The catalase—peroxidase gene and isoniazid resistance of Mycobacterium tuberculosis

4. Isoniazid: the magic molecule

5. Action of 1-isonicotinyl-2-palmitoyl hydrazine against the Mycobacterium avium complex and enhancement of its activity by m-fluorophenylalanine

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