Literature DB >> 23612869

Unexpectedly high levels of antimony (III) in the pentavalent antimonial drug Glucantime: insights from a new voltammetric approach.

Pascal Salaün1, Frédéric Frézard.   

Abstract

Glucantime, a pentavalent antimonial drug, is commonly used for the treatment of leishmaniasis but the presence of residual trivalent antimony, Sb(III), is thought to be responsible for toxic side-effects observed in patients. Numerous analytical studies have focused on determining Sb(III) concentrations in Glucantime but without reaching a consensus: results span over 3 orders of magnitude. In this study, we present a detailed new analytical approach showing that: (1) Sb(III) levels are much higher than previously reported and represent more than 30% of total Sb; (2) determination of Sb(III) concentrations in acidic conditions is hampered by fast oxidation rates. This latter point explains the large variations in previously reported results of Sb(III) concentrations in Glucantime. Measurements were made here at a vibrated gold microwire electrode by stripping voltammetry enabling measurement of Sb(III) in acidic, neutral or alkaline conditions. The developed methods are sensitive (e.g., detection limits of 19 pM for 120 s deposition at pH 4.5), stable (<6%, N = 100), precise (5%, N = 5) and robust (same electrode used for weeks) at all pH values. In diluted solutions of Glucantime, Sb(III) levels were strongly dependent both on pH and ionic strength. At pH < 3, Sb(III) is oxidized with oxidation rates that increase as pH is decreased. At high pH, Sb(III) forms electro-inactive complexes. Highest Sb(III) levels were detected at pH ~3 and at low ionic strength. The presence of several Sb(III) and Sb(V) species was demonstrated by different reduction waves obtained by stripping scanned voltammetry. As an implication of these unexpectedly high Sb(III) concentrations, an alternative model can be proposed for the mode of action of pentavalent antimonials against leishmaniasis, in which antimony complexes may act as molecular carrier of Sb(III) and release it specifically in the acidic intracellular compartment where the Leishmania parasites reside.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23612869     DOI: 10.1007/s00216-013-6947-5

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  7 in total

Review 1.  Antimony transport mechanisms in resistant leishmania parasites.

Authors:  Frédéric Frézard; Rubens Monte-Neto; Priscila G Reis
Journal:  Biophys Rev       Date:  2014-01-25

2.  Genistein and Ascorbic Acid Reduce Oxidative Stress-Derived DNA Damage Induced by the Antileishmanial Meglumine Antimoniate.

Authors:  Luís Cláudio Lima de Jesus; Rossy-Eric Pereira Soares; Vanessa Ribeiro Moreira; Raissa Lacerda Pontes; Patrícia Valéria Castelo-Branco; Silma Regina Ferreira Pereira
Journal:  Antimicrob Agents Chemother       Date:  2018-08-27       Impact factor: 5.191

3.  First report on ototoxicity of meglumine antimoniate.

Authors:  Cláudia Maria Valete-Rosalino; Maria Helena Araujo-Melo; Débora Cristina de Oliveira Bezerra; Renata Oliveira de Barcelos; Vanessa de Melo-Ferreira; Tânia Salgado de Sousa Torraca; Ana Cristina da Costa Martins; João Soares Moreira; Mirian Catherine Melgares Vargas; Frederico Pereira Bom Braga; Mariza de Matos Salgueiro; Maurício Naoto Saheki; Armando Oliveira Schubach
Journal:  Rev Inst Med Trop Sao Paulo       Date:  2014 Sep-Oct       Impact factor: 1.846

4.  Hepatotoxicity of pentavalent antimonial drug: possible role of residual Sb(III) and protective effect of ascorbic acid.

Authors:  Kelly C Kato; Eliane Morais-Teixeira; Priscila G Reis; Neila M Silva-Barcellos; Pascal Salaün; Paula P Campos; José Dias Corrêa-Junior; Ana Rabello; Cynthia Demicheli; Frédéric Frézard
Journal:  Antimicrob Agents Chemother       Date:  2013-11-04       Impact factor: 5.191

5.  Species-specific antimonial sensitivity in Leishmania is driven by post-transcriptional regulation of AQP1.

Authors:  Goutam Mandal; Srotoswati Mandal; Mansi Sharma; Karen Santos Charret; Barbara Papadopoulou; Hiranmoy Bhattacharjee; Rita Mukhopadhyay
Journal:  PLoS Negl Trop Dis       Date:  2015-02-25

6.  Treatment Outcome of the Drug-resistant Zoonotic Cutaneous Leishmaniasis by Glucantime.

Authors:  Simindokht Soleimanifard; Reza Arjmand; Sedighe Saberi; Mansoor Salehi; Seyed Hossain Hejazi
Journal:  Adv Biomed Res       Date:  2017-03-01

7.  Association of liposome-encapsulated trivalent antimonial with ascorbic acid: an effective and safe strategy in the treatment of experimental visceral leishmaniasis.

Authors:  Renata A O Castro; Neila M Silva-Barcellos; Carolina S A Licio; Janine B Souza; Míriam C Souza-Testasicca; Flávia M Ferreira; Mauricio A Batista; Denise Silveira-Lemos; Sandra L Moura; Frédéric Frézard; Simone A Rezende
Journal:  PLoS One       Date:  2014-08-08       Impact factor: 3.240

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.