Miltefosine: a review of its pharmacology and therapeutic efficacy in the treatment of leishmaniasis

TPC Dorlo, M Balasegaram, JH Beijnen… - Journal of …, 2012 - academic.oup.com
Miltefosine is an alkylphosphocholine drug with demonstrated activity against various
parasite species and cancer cells as well as some pathogenic bacteria and fungi. For 10 …

[HTML][HTML] Visceral leishmaniasis treatment: what do we have, what do we need and how to deliver it?

LH Freitas-Junior, E Chatelain, HA Kim… - International Journal for …, 2012 - Elsevier
Leishmaniasis is one of the most neglected tropical disease in terms of drug discovery and
development. Most antileishmanial drugs are highly toxic, present resistance issues or …

Increasing failure of miltefosine in the treatment of Kala-azar in Nepal and the potential role of parasite drug resistance, reinfection, or noncompliance

S Rijal, B Ostyn, S Uranw, K Rai… - Clinical Infectious …, 2013 - academic.oup.com
Abstract Background. Miltefosine (MIL), the only oral drug for visceral leishmaniasis (VL), is
currently the first-line therapy in the VL elimination program of the Indian subcontinent …

Leishmania–macrophage interactions: Insights into the redox biology

T Van Assche, M Deschacht, RAI da Luz, L Maes… - Free Radical Biology …, 2011 - Elsevier
Leishmaniasis is a neglected tropical disease that affects about 350 million individuals
worldwide. The protozoan parasite has a relatively simple life cycle with two principal …

Current screening methodologies in drug discovery for selected human diseases

OM Lage, MC Ramos, R Calisto, E Almeida… - Marine drugs, 2018 - mdpi.com
The increase of many deadly diseases like infections by multidrug-resistant bacteria implies
re-inventing the wheel on drug discovery. A better comprehension of the metabolisms and …

A Screen against Leishmania Intracellular Amastigotes: Comparison to a Promastigote Screen and Identification of a Host Cell-Specific Hit

G De Muylder, KKH Ang, S Chen… - PLoS neglected …, 2011 - journals.plos.org
The ability to screen compounds in a high-throughput manner is essential in the process of
small molecule drug discovery. Critical to the success of screening strategies is the proper …

PLGA nanoparticles and nanosuspensions with amphotericin B: potent in vitro and in vivo alternatives to Fungizone and AmBisome

H Van de Ven, C Paulussen, PB Feijens… - Journal of controlled …, 2012 - Elsevier
This paper describes the development of poly (D, L-lactide-co-glycolide)(PLGA)
nanoparticles (NPs) and nanosuspensions with the polyene antibiotic amphotericin B …

Tackling drug resistance and other causes of treatment failure in leishmaniasis

GJ Wijnant, F Dumetz, L Dirkx, D Bulté… - Frontiers in Tropical …, 2022 - frontiersin.org
Leishmaniasis is a tropical infectious disease caused by the protozoan Leishmania parasite.
The disease is transmitted by female sand flies and, depending on the infecting parasite …

Comparison of a high-throughput high-content intracellular Leishmania donovani assay with an axenic amastigote assay

M De Rycker, I Hallyburton, J Thomas… - Antimicrobial agents …, 2013 - Am Soc Microbiol
Visceral leishmaniasis is a neglected tropical disease with significant health impact. The
current treatments are poor, and there is an urgent need to develop new drugs. Primary …

An Image-Based High-Content Screening Assay for Compounds Targeting Intracellular Leishmania donovani Amastigotes in Human Macrophages

JL Siqueira-Neto, S Moon, J Jang, G Yang… - PLoS neglected …, 2012 - journals.plos.org
Leishmaniasis is a tropical disease threatening 350 million people from endemic regions.
The available drugs for treatment are inadequate, with limitations such as serious side …