Results 91 to 100 of about 8,155 (173)

Thermoterapy effective and safer than miltefosine in the treatment of cutaneous leishmaniasis in Colombia

open access: yesRevista do Instituto de Medicina Tropical de São Paulo, 2013
In Colombia, pentavalent antimonials and miltefosine are the drugs of choice for the treatment of cutaneous leishmaniasis; however, their toxicity, treatment duration, (treatment adherence problems), cost, and decreased parasite sensitivity make the ...
Liliana López   +4 more
doaj   +1 more source

From lipid biophysics to first-in human test: topical liposomal treatment for cutaneous leishmaniasis

open access: yesPrecision Nanomedicine
Cutaneous leishmaniasis (CL) remains a major neglected disease with limited therapeutic op-tions and expanding geographic distribution. To develop a safe, accessible local treatment, we formulated topical Miltefosine gels incorporating different types of
Dolores Catalina Carrer
doaj   +1 more source

Miltefosine release profiles.

open access: yes, 2015
Miltefosine release from selected lipid nanocapsule formulations in PBS pH 7.4 at 37°C over a 24 h-study period. Data represent mean ± SD (n = 3). The inset is an enlargement of the release profiles for the first 8h of the release study.
Labiba K. El-Khordagui (827790)   +5 more
core   +1 more source

Miltefosine: een nieuw geneesmiddel voor leishmaniasis

open access: yes, 2006
There is a need for a safe and effective oral treatment for cutaneous and visceral leishmaniasis. Miltefosine is the first oral drug that is efficacious against different forms ofleishmaniasis, however it is not equally effective against all Leishmania ...
Dorlo, T. P. C.   +3 more
core  

Physicochemical properties of miltefosine-loaded chitosan nanoparticles.

open access: yes
Physicochemical properties of miltefosine-loaded chitosan nanoparticles.
Alireza Latifi (14593561)   +7 more
core   +1 more source

A policy for leishmaniasis with respect to the prevention and control of drug resistance. [PDF]

open access: yes, 2001
At the moment no country has a policy designed to control or prevent drug resistance in leishmaniasis. The risk of resistance is high in areas of anthroponotic visceral leishmaniasis, for example North Bihar, India, where the rate in some areas is 60 ...
Bryceson, A
core   +1 more source

Clinical, histopathological and parasitological follow-up of dogs naturally infected by Leishmania infantum before and after miltefosine treatment and associated therapies.

open access: yesPLoS ONE
In Brazil, Visceral Leishmaniases is caused by Leishmania infantum, and domestic dogs are the main reservoirs in its urban transmission cycle. As an alternative to euthanizing dogs, miltefosine has been used to treat canine visceral leishmaniasis since ...
Amábilli de Souza Rosar   +8 more
doaj   +1 more source

Leishmania miltefosine sensitivity.a

open access: yes, 2013
aCultured mid-log-phase promastigotes were seeded at 5×105 cells mL−1 with different miltefosine concentrations (5–200 µM), and the cell density was determined after 48 h.
Ricardo Andrade Zampieri (148278)   +4 more
core   +1 more source

Miltefosine (Impavido): the first oral treatment against leishmaniasis.

open access: yes, 2003
Miltefosine is a novel antileishmanial drug that has significant selectivity in both in vitro and in vivo models. Clinical efficacy was demonstrated for the treatment of visceral leishmaniasis with the advantage of oral administration over the currently ...
Engel, Kirsten-Rita   +17 more
core   +1 more source

Miltefosine Administration in Cats with Refractory Sporotrichosis [PDF]

open access: yes, 2018
Background: Sporotrichosis is a zoonosis caused by fungi of the Sporothrix schenckii complex. Cats have important zoonotic potential due to the high parasite load found in the cutaneous lesions.
Baptista, Vivian dos Santos   +6 more
core   +1 more source

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