1993
DOI: 10.1128/aac.37.12.2584
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In vitro activities of free and liposomal drugs against Mycobacterium avium-M. intracellulare complex and M. tuberculosis

Abstract: We compared MICs and MBCs of various free-and liposome-incorporated antimicrobial agents against several patient isolates of Mycobacterium avium-M. intracellulare complex and certain American Type Culture Collection strains of M. avium, M. intracellulare, and Mycobacterium tuberculosis. Seven of 19 agents were selected for incorporation into liposomes. The MICs of these agents for 50 and 90% of isolates tested (MIC50s and MIC90s, respectively) ranged from 0.5 to 62 ,ug/ml. Members of the M. avium-M. intracelul… Show more

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Cited by 55 publications
(39 citation statements)
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“…The therapeutic activity of free and encapsulated INH and RIF was evaluated at both therapeutic and sub-therapeutic dose [47]. Parenteral clofazimine liposomes were [48] evaluated in acute and chronic murine infections [49]. Liposomes significantly reduced the toxicity of the drug both in vitro and in vivo and showed enhanced anti-TB activity in acute and chronic models.…”
Section: Drug Delivery Explored In Tb Chemotherapy Liposomesmentioning
confidence: 99%
“…The therapeutic activity of free and encapsulated INH and RIF was evaluated at both therapeutic and sub-therapeutic dose [47]. Parenteral clofazimine liposomes were [48] evaluated in acute and chronic murine infections [49]. Liposomes significantly reduced the toxicity of the drug both in vitro and in vivo and showed enhanced anti-TB activity in acute and chronic models.…”
Section: Drug Delivery Explored In Tb Chemotherapy Liposomesmentioning
confidence: 99%
“…Overall, a significant increase in the anti-TB activity was found. With the aim of improving the anti-TB activity, reducing the toxicity and enabling the parenteral administration of highly lipophilic clofazimine, drug-loaded liposomes were produced [65] and preclinically evaluated in acute and chronic murine infections [66]. Encapsulation reduced the in vitro and in vivo toxicity of the drug and enhanced the anti-TB activity in both acute and chronic models.…”
Section: (B)nonpolymeric Nanocarrier Liposomementioning
confidence: 99%
“…Elimination of mycobacterium from liver and spleen was found higher with liposomal drugs when compared with free drugs which offer more promising therapeutic approach for the chemotherapy of tuberculosis [31]. Clofazimine, Resorcinomycin A, and PD 117558 loaded liposome incorporated against several patients with microbial infection showed complete killing of bacteria at concentrations ranging from 8 to 31 µg/ml and thus liposomes, would help to reduce the toxicities of the drugs and could be used to target macrophages [32]. AMK encapsulated liposomes were found to be in high and sustained drug levels in infected tissues, exceeding the MIC for M. avium for at least 28 days while comparing with ciprofloxacin (CPF) encapsulated liposome in M. avium infected murine model.…”
Section: Liposomesmentioning
confidence: 99%