Literature DB >> 20201740

Drug delivery strategies for therapy of visceral leishmaniasis.

Swati Gupta1, Ajay Pal, Suresh P Vyas.   

Abstract

IMPORTANCE OF THE FIELD: Visceral leishmaniasis (VL) is the most overwhelming type of leishmaniasis associated with the poverty of developing countries and usually mortal if untreated. Most of the conventionally used dosage forms offer us the shortcomings of toxic side effects and emergence of drug resistance. Several efforts have been made to overcome the barriers involved in the treatment of VL. Colloidal carriers extensively represent the drug delivery systems (DDSs) for intracellular localization of antileishmanial compounds in macrophage-rich organs such as liver, spleen and bone marrow. These DDSs offer superior therapeutic efficacy over the conventional treatment in terms of site-specific drug delivery with reduced side effects. However, after 35 years of research in the field, AmBisome (Amphotericin B liposome for injection, Astellas Pharma US, Inc.) is the only DDS used against the VL. AREAS COVERED IN THIS REVIEW: A literature search was performed (for drugs and DDSs against VL) on PubMed and through Google. WHAT THE READER WILL GAIN: This review aims to describe the pathophysiology of VL and its current conventional treatment with special reference to DDSs designed against VL. TAKE HOME MESSAGE: On reviewing the conventional drugs and DDSs developed against VL, it is concluded that advances in the field of targeted drug delivery can result in more efficient strategies for the therapy of VL.

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Year:  2010        PMID: 20201740     DOI: 10.1517/17425240903548232

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  9 in total

1.  Cationic liposomal sodium stibogluconate (SSG), a potent therapeutic tool for treatment of infection by SSG-sensitive and -resistant Leishmania donovani.

Authors:  Roma Sinha; Jayeeta Roychoudhury; Partha Palit; Nahid Ali
Journal:  Antimicrob Agents Chemother       Date:  2014-11-03       Impact factor: 5.191

Review 2.  Bone marrow-targeted liposomal carriers.

Authors:  Keitaro Sou; Beth Goins; Babatunde O Oyajobi; Bruno L Travi; William T Phillips
Journal:  Expert Opin Drug Deliv       Date:  2011-01-31       Impact factor: 6.648

3.  Nanospheres encapsulating anti-leishmanial drugs for their specific macrophage targeting, reduced toxicity, and deliberate intracellular release.

Authors:  Anil Kumar Shukla; Sanjukta Patra; Vikash Kumar Dubey
Journal:  Vector Borne Zoonotic Dis       Date:  2012-08-27       Impact factor: 2.133

4.  Antileishmanial activity, uptake, and biodistribution of an amphotericin B and poly(α-Glutamic Acid) complex.

Authors:  Abeer H A Mohamed-Ahmed; Karin Seifert; Vanessa Yardley; Hollie Burrell-Saward; Stephen Brocchini; Simon L Croft
Journal:  Antimicrob Agents Chemother       Date:  2013-06-24       Impact factor: 5.191

5.  Preparation, optimization, and in vitro-in vivo evaluation of sorafenib-loaded polycaprolactone and cellulose acetate nanofibers for the treatment of cutaneous leishmaniasis.

Authors:  Mahsa Alemomen; Somayeh Taymouri; Sedigheh Saberi; Jaleh Varshosaz
Journal:  Drug Deliv Transl Res       Date:  2022-10-12       Impact factor: 5.671

Review 6.  Drug Trafficking into Macrophages via the Endocytotic Receptor CD163.

Authors:  Jonas Heilskov Graversen; Søren Kragh Moestrup
Journal:  Membranes (Basel)       Date:  2015-06-23

7.  Self-assembled amphotericin B-loaded polyglutamic acid nanoparticles: preparation, characterization and in vitro potential against Candida albicans.

Authors:  Qamar Zia; Aijaz Ahmed Khan; Zubair Swaleha; Mohammad Owais
Journal:  Int J Nanomedicine       Date:  2015-03-05

Review 8.  New Approaches to Overcome Transport Related Drug Resistance in Trypanosomatid Parasites.

Authors:  Jose A Garcia-Salcedo; Juan D Unciti-Broceta; Javier Valverde-Pozo; Miguel Soriano
Journal:  Front Pharmacol       Date:  2016-09-28       Impact factor: 5.810

9.  Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N'-Squaramide 17 towards Trypanosoma cruzi.

Authors:  Christian Rafael Quijia; Cínthia Caetano Bonatto; Luciano Paulino Silva; Milene Aparecida Andrade; Clenia Santos Azevedo; Camila Lasse Silva; Manel Vega; Jaime Martins de Santana; Izabela Marques Dourado Bastos; Marcella Lemos Brettas Carneiro
Journal:  Materials (Basel)       Date:  2020-12-02       Impact factor: 3.623

  9 in total

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