Literature DB >> 26653559

In vitro and in vivo antileishmanial properties of a 2-n-propylquinoline hydroxypropyl β-cyclodextrin formulation and pharmacokinetics via intravenous route.

Kaluvu Balaraman1, Nashira Campos Vieira2, Fathi Moussa3, Joël Vacus4, Sandrine Cojean1, Sébastien Pomel1, Christian Bories1, Bruno Figadère5, Ventikasamy Kesavan6, Philippe M Loiseau7.   

Abstract

2-n-propylquinoline (2-n-PQ) had shown interesting in vivo antileishmanial activities after administration by oral route on leishmaniasis animal models. However, the lipophilic properties of this compound avoid its use by intravenous route, this route being indicated in cases of severe visceral leishmaniasis with vomiting. Thus, a 2-n-propylquinoline hydroxypropyl beta-cyclodextrin (2-n-PQ-HPC) formulation was set up in this aim. The formulation was active in vitro both on Leishmania donovani axenic and intramacrophage amastigotes with IC50 values at 6.22±0.82μM and 20.01±0.52μM, respectively, without any toxicity on macrophages. 2-n-PQ-HPC exhibited similar activity on WT and drug-resistant parasites. Its in vitro interactions with antimonials, amphotericin B and miltefosine were found as additive both in axenic amastigotes and intramacrophage amastigotes. 2-n-PQ-HPC was not able to generate drug resistance after in vitro drug pressure since the resistance index was less than 4. 2-n-PQ-HPC was also active on the L. donovani/Balb/c mice model with an intravenous treatment regimen at 10mgkg(-1)day(-1) on 10 consecutive days without hepatic, renal and blood toxicity. The pharmacokinetics of 2-n-PQ in rats showed that after an intravenous treatment of the formulation at 10mgkg(-1), the plasma drug concentrations rapidly declined bi-exponentially with a half-life of 58.7min and a total clearance of 18.63lh(-1)kg(-1). The apparent volume of distribution was higher than the blood volume in rats, indicating that 2-n-PQ was well distributed in tissues, allowing parasite elimination. Such a formulation is worth of further antiparasitic and toxicological evaluations.
Copyright © 2015 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  2-n-propylquinoline; In vitro and in vivo antileishmanial activity; Pharmacokinetics; Toxicity

Mesh:

Substances:

Year:  2015        PMID: 26653559     DOI: 10.1016/j.biopha.2015.10.028

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  4 in total

1.  Exploring In Vitro Biological Cellular Responses of Pegylated β-Cyclodextrins.

Authors:  Juliana Rincón-López; Miguelina Martínez-Aguilera; Patricia Guadarrama; Karla Juarez-Moreno; Yareli Rojas-Aguirre
Journal:  Molecules       Date:  2022-05-08       Impact factor: 4.927

2.  Synthesis and biological evaluation against Leishmania donovani of novel hybrid molecules containing indazole-based 2-pyrone scaffolds.

Authors:  M El Ghozlani; L Bouissane; M Berkani; S Mojahidi; A Allam; C Menendez; S Cojean; P M Loiseau; M Baltas; E M Rakib
Journal:  Medchemcomm       Date:  2018-11-19       Impact factor: 3.597

Review 3.  Recent synthetic efforts in the preparation of 2-(3,4)-alkenyl (aryl) quinoline molecules towards anti-kinetoplastid agents.

Authors:  Dayana Orozco; Vladimir V Kouznetsov; Armando Bermúdez; Leonor Y Vargas Méndez; Arturo René Mendoza Salgado; Carlos Mario Meléndez Gómez
Journal:  RSC Adv       Date:  2020-01-29       Impact factor: 4.036

Review 4.  The Potential of 2-Substituted Quinolines as Antileishmanial Drug Candidates.

Authors:  Philippe M Loiseau; Kaluvu Balaraman; Gillian Barratt; Sébastien Pomel; Rémy Durand; Frédéric Frézard; Bruno Figadère
Journal:  Molecules       Date:  2022-04-02       Impact factor: 4.411

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.