» Articles » PMID: 33966377

Nano- and Microformulations to Advance Therapies for Visceral Leishmaniasis

Overview
Date 2021 May 10
PMID 33966377
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Visceral leishmaniasis (VL) is a deadly, vector-borne, neglected tropical disease endemic to arid parts of the world and is caused by a protozoan parasite of the genus . Chemotherapy is the primary treatment for this systemic disease, and multiple potent therapies exist against this intracellular parasite. However, several factors, such as systemic toxicity, high costs, arduous treatment regimen, and rising drug resistance, are barriers for effective therapy against VL. Material-based platforms have the potential to revolutionize chemotherapy for leishmaniasis by imparting a better pharmacokinetic profile and creating patient-friendly routes of administration, while also lowering the risk for drug resistance. This review highlights promising drug delivery strategies and novel therapies that have been evaluated in preclinical models, demonstrating the potential to advance chemotherapy for VL.

Citing Articles

Antiparasitic activity of the iron-containing milk protein lactoferrin and its potential derivatives against human intestinal and blood parasites.

Anand N Front Parasitol. 2025; 2():1330398.

PMID: 39816822 PMC: 11731944. DOI: 10.3389/fpara.2023.1330398.


Innovating Leishmaniasis Treatment: A Critical Chemist's Review of Inorganic Nanomaterials.

Bessa I, DAmato D, Souza A, Levita D, Mello C, da Silva A ACS Infect Dis. 2024; 10(8):2485-2506.

PMID: 39001837 PMC: 11320585. DOI: 10.1021/acsinfecdis.4c00231.


Curcumin-loaded nanostructured systems for treatment of leishmaniasis: a review.

Dourado D, Medeiros T, Alencar E, Matos Sales E, Formiga F Beilstein J Nanotechnol. 2024; 15:37-50.

PMID: 38213574 PMC: 10777206. DOI: 10.3762/bjnano.15.4.


Micro and nanotechnologies: The little formulations that could.

Stiepel R, Duggan E, Batty C, Ainslie K Bioeng Transl Med. 2023; 8(2):e10421.

PMID: 36925714 PMC: 10013823. DOI: 10.1002/btm2.10421.


Mechanistic insight into the role of mevalonate kinase by a natural fatty acid-mediated killing of Leishmania donovani.

Prasad S, Kumar P, Mandal S, Mohan A, Chaurasia R, Shrivastava A Sci Rep. 2022; 12(1):16453.

PMID: 36180490 PMC: 9525708. DOI: 10.1038/s41598-022-20509-9.


References
1.
Peine K, Gupta G, Brackman D, Papenfuss T, Ainslie K, Satoskar A . Liposomal resiquimod for the treatment of Leishmania donovani infection. J Antimicrob Chemother. 2013; 69(1):168-75. PMC: 3861330. DOI: 10.1093/jac/dkt320. View

2.
Duarte M, Lage L, Pagliara Lage D, Martins V, Carvalho A, Roatt B . Treatment of murine visceral leishmaniasis using an 8-hydroxyquinoline-containing polymeric micelle system. Parasitol Int. 2016; 65(6 Pt A):728-736. DOI: 10.1016/j.parint.2016.07.005. View

3.
Croft S, Sundar S, Fairlamb A . Drug resistance in leishmaniasis. Clin Microbiol Rev. 2006; 19(1):111-26. PMC: 1360270. DOI: 10.1128/CMR.19.1.111-126.2006. View

4.
Rosler A, Vandermeulen G, Klok H . Advanced drug delivery devices via self-assembly of amphiphilic block copolymers. Adv Drug Deliv Rev. 2001; 53(1):95-108. DOI: 10.1016/s0169-409x(01)00222-8. View

5.
Soga O, van Nostrum C, Fens M, Rijcken C, Schiffelers R, Storm G . Thermosensitive and biodegradable polymeric micelles for paclitaxel delivery. J Control Release. 2005; 103(2):341-53. DOI: 10.1016/j.jconrel.2004.12.009. View