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Tuftsin-bearing liposomes as rifampin vehicles in treatment of tuberculosis in mice.

DIR@IMTECH: CSIR-Institute of Microbial Technology

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Title Tuftsin-bearing liposomes as rifampin vehicles in treatment of tuberculosis in mice.
 
Creator Agarwal, A
Kandpal, H
Gupta, H P
Singh, N B
Gupta, C M
 
Subject QR Microbiology
 
Description The antitubercular activity of rifampin was considerably increased when it was encapsulated in egg phosphatidylcholine liposomes. A further increase in the activity was observed when the macrophage activator tetrapeptide tuftsin was grafted on the surface of the drug-loaded liposomes. Intermittent treatments (twice weekly) with these preparations were significantly more effective than the continuous treatments. Rifampin delivered twice weekly for 2 weeks in tuftsin-bearing liposomes was at least 2,000 times more effective than the free drug in lowering the load of lung bacilli in infected animals. However, pretreatment with drug-free tuftsin-bearing liposomes did not render the pretreated animals resistant to the Mycobacterium tuberculosis infections, neither did it appreciably increase the chemotherapeutic efficacy of the liposomized rifampin. These results clearly demonstrate that liposome targeting to macrophages could considerably increase the antitubercular activity of liposomized drugs such as rifampin. Also, it shows that immunoprophylactic treatment with macrophage activators such as tuftsin does not afford any advantage in treatment of tuberculosis infections, presumably because of inactivation of the primed macrophages by the mycobacterial sulfatides.
 
Publisher ASM
 
Date 1994-03
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://crdd.osdd.net/open/411/1/gupta94.pdf
Agarwal, A and Kandpal, H and Gupta, H P and Singh, N B and Gupta, C M (1994) Tuftsin-bearing liposomes as rifampin vehicles in treatment of tuberculosis in mice. Antimicrobial agents and chemotherapy, 38 (3). pp. 588-93. ISSN 0066-4804
 
Relation http://aac.asm.org/content/38/3/588.long
http://crdd.osdd.net/open/411/