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Liposomal-lupane system as alternative chemotherapy against cutaneous leishmaniasis: macrophage as target cell.
Author: BarrosNeuza B, CiancagliniPietro, FacundoValdir A, MigliaccioVanessa, NicoleteRoberto, Silva-JardimIzaltina, StábeliRodrigo G
Original Abstract of the Article :
Leishmania amazonensis causes human diseases that range from self-healing to diffusion cutaneous lesions. The chemotherapy of leishmaniasis requires long-term treatment and has been based on the use of pentavalent antimonials. Liposomes have been used as antileishmanial drug carries and have adjuvan...See full text at original site
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引用元:
https://doi.org/10.1016/j.exppara.2013.07.022
データ提供:米国国立医学図書館(NLM)
Liposomal-Lupane System for Cutaneous Leishmaniasis
The vast desert of tropical medicine presents unique challenges. This research focuses on cutaneous leishmaniasis, a parasitic disease that causes skin lesions. The study investigates a novel approach for treating the disease, utilizing a liposomal formulation containing lupane, a natural compound with anti-leishmanial properties.Liposomal-Lupane System: A New Therapeutic Strategy
The researchers developed a liposomal formulation containing lupane, a natural compound isolated from the fruits of Combretum leprosum. This is like encasing a potent medicinal ingredient in a protective capsule, ensuring its safe and effective delivery to the target area. The study evaluated the efficacy of liposomal-lupane in a mouse model of Leishmania amazonensis infection.Implications for Leishmaniasis Treatment
This research presents a promising new approach for treating cutaneous leishmaniasis. The liposomal-lupane system, like a skilled desert traveler carrying a precious remedy, could offer a more effective and potentially safer treatment option, reducing the need for long-term and often toxic treatments.Dr. Camel's Conclusion
This study explores a new frontier in the treatment of cutaneous leishmaniasis. The liposomal-lupane system offers a beacon of hope in the desert of parasitic diseases, potentially leading to improved therapeutic strategies and enhanced patient outcomes.Date :
- Date Completed 2013-12-05
- Date Revised 2013-10-14
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