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

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 liposomes. Preclinical tests using low-dose Miltefosine (0.015% w/v) and ultrafluid liposomes were ineffective, leading us to increase the drug concentration and revise the liposomal design. At 0.5% w/v, Miltefosine—whether used alone or with fluid liposomes—produced complete lesion healing in a murine L. amazonensis model, with no relapse and sterile lesions at 30 days. Liposomes further accelerated the healing process. A first-in-human compassionate-use case with a patient refractory to standard therapies confirmed good local tolerance and eventual clinical cure using 0.5–1% Miltefosine gels + short Amphotericin B treatment. The experience also showed that ultrafluid liposomes are unsuitable for open ulcers, informing future optimization. Overall, topical Miltefosine at adequate concentration is a promising local treatment for CL, and liposomes can enhance therapeutic performance.

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Publication Details

Journal
Precision Nanomedicine
Published
2025-11-20
DOI
https://doi.org/10.33218/001c.147690
Primary Topic
Research on Leishmaniasis Studies
Type
article
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article

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

Dolores C. Carrer
Precision Nanomedicine
Research on Leishmaniasis Studies
article

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

Dolores C. Carrer
article en

Abstract

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 liposomes. Preclinical tests using low-dose Miltefosine (0.015% w/v) and ultrafluid liposomes were ineffective, leading us to increase the drug concentration and revise the liposomal design. At 0.5% w/v, Miltefosine—whether used alone or with fluid liposomes—produced complete lesion healing in a murine L. amazonensis model, with no relapse and sterile lesions at 30 days. Liposomes further accelerated the healing process. A first-in-human compassionate-use case with a patient refractory to standard therapies confirmed good local tolerance and eventual clinical cure using 0.5–1% Miltefosine gels + short Amphotericin B treatment. The experience also showed that ultrafluid liposomes are unsuitable for open ulcers, informing future optimization. Overall, topical Miltefosine at adequate concentration is a promising local treatment for CL, and liposomes can enhance therapeutic performance.

Precision NanomedicineVol. 8(ICRAN)
Universidad Nacional de Córdoba (AR), Instituto de Investigación Médica Mercedes y Martín Ferreyra (AR)
Openalex Percentile: Top 54%
Research on Leishmaniasis Studies
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From lipid biophysics to first-in human test: topical liposomal treatment for cutaneous leishmaniasis — Dolores C. Carrer · Precision Nanomedicine (2025) | TGRS Research Map | TGRS