Advanced amphotericin-B gel formulation: An efficient approach to combat cutaneous leishmaniasis
Carla Veronica Rodarte de Moura1, Diego Botelho Campelo Leite2, Edvani Curti Muniz1
1Department of Chemistry, Federal University of Piauí, Teresina, PI, Brazil.
New amphotericin-B (AmB) gels using safe copolymers effectively treat cutaneous leishmaniasis by reducing parasites by 70%. These AmB-loaded gels minimize drug toxicity and improve delivery for leishmaniasis treatment.
Area of Science:
- Polymer chemistry
- Drug delivery systems
- Infectious disease research
Background:
- Conventional amphotericin-B (AmB) faces limitations like poor water solubility and gastrointestinal irritation.
- Cutaneous leishmaniasis requires effective drug delivery systems to overcome treatment challenges.
Purpose of the Study:
- To develop and characterize novel AmB-loaded copolymer gels (TMP-HPG-PCL and GLY-HPG-PCL) for cutaneous leishmaniasis treatment.
- To evaluate the safety, drug release profile, and therapeutic efficacy of these AmB-loaded gels.
Main Methods:
- Gels were synthesized using polyglycerol and ε-caprolactone copolymers incorporated with AmB.
- Characterization involved FTIR, NMR, TG, and DSC techniques.
- In vitro drug release, hemolytic, and cytotoxic studies were performed, followed by in vivo efficacy testing in Leishmania major-infected mice.
Main Results:
- AmB remained in its less toxic monomeric form within the copolymers.
- High AmB loading (31%) and encapsulation efficiency (93%) were achieved.
- The gels demonstrated controlled AmB release, significantly reduced parasite load (70%) in mice, and showed no toxicity to HaCat and MCF-7 cell lines.
Conclusions:
- The developed TMP-HPG-PCL and GLY-HPG-PCL copolymers are safe and effective drug carriers for AmB.
- These AmB-loaded gels show significant potential for combating cutaneous leishmaniasis with improved safety and efficacy.
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