Journal of Global Pharma Technology
Volume 08 Issue 07

Antileishmanial Activity of 2-Phenoxy Nicotinic Acid Hydrazide Sulfonamide against Leishmania (L) Major [MRHO/IR/75/ER] Promastigotes: An In-Vitro Study

Parisa Kianfar (Unknown)



Article Info

Publish Date
30 Jun 2017

Abstract

Introduction: cutaneous leishmaniasis is parasitic disease in Iran and a major health problem in the country. The aim of this study was to compare the efficacy-achieved derivatives of 2-phenoxy nicotinic acid hydrazide sulfonamide and glucantime is in the treatment of leishmaniasis. Material and method: In this experimental- laboratory study Leishmania major promastigotes, a standard strain MRHO / IR / 75 / ER were cultured in NNN medium. Then in tubes containing medium, 105 Leishmania (equivalently100 ml) and 0.5 ml of dilution of 2-phenoxy nicotinic acid hydrazide sulfonamide and glucantime at a concentration of 2/0, 1, 5, 25 and 125 µg/ml separately added. Cell proliferation assay done by using BrdU (XTT) kit. Result: The results of variance analysis showed that 2-phenoxy nicotinic acid hydrazide sulfonamide derivatives and Glucantime have inhibitory effect on the parasite Leishmania. all concentrations tested 2.0, 1, 5, 25 and 125 µg/ml decreased the number of Leishmania parasites that their effects compared to control group was statistically significant (P = 0.000). Conclusion: 2-phenoxy nicotinic acid hydrazide sulfonamide derivatives able to inhibit the in vitro proliferation of Leishmania major and compared to Glucantime had better inhibitory effect on major promastigotes growth of Iranian rural leishmaniasis. Keywords: 2-phenoxy nicotinic acid hydrazide sulfonamide, Leishmania major, Glucantime, promastigotes.

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Journal Info

Abbrev

jgpt

Publisher

Subject

Medicine & Pharmacology

Description

ournal of Global Pharma Technology is a monthly, open access, Peer review journal of Pharmacy published by JGPT Journal publishes peer-reviewed original research papers, case reports and systematic reviews. The journal allows free access to its contents, which is likely to attract more readers and ...