Carlos Eliel Maya Ramírez

Dr. Carlos Eliel Maya Ramírez

orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 May 2024 in Phycology
Verified
Journal Article
Open access
PDF file
Haresh S. KalasariyaHaresh S. Kalasariya
Haresh S. Kalasariya
CRCarlos Eliel Maya Ramírez
Carlos Eliel Maya Ramírez
João CotasJoão Cotas
João Cotas
Leonel PereiraLeonel Pereira
Leonel Pereira
The term ‘cosmeceutical’ refers to cosmetic products that offer medicinal or drug-like benefits. Marine algae are rich sources of bioactive compounds, particularly carbohydrates and peptides, which have gained attention for their potential in cosmeceuticals. These compounds are abundant, safe, and have minimal cytotoxicity effects. They offer various benefits to the skin, including addressing rashes, pigmentation, aging, and cancer. Additionally, they exhibit properties such as antimicrobial, skin-whitening, anti-aging, antioxidant, and anti-melanogenic effects. This review surveys the literature on the cosmeceutical potentials of algae-derived compounds, focusing on their roles in skin whitening, anti-aging, anticancer, antioxidant, anti-inflammatory, and antimicrobial applications. The discussion also includes current challenges and future opportunities for using algae for cosmeceutical purposes.

28 January 2025 in Life
Verified
Journal Article
Open access
PDF file
CRCarlos Eliel Maya Ramírez
Carlos Eliel Maya Ramírez
ASAsmae SAIH
Asmae SAIH
AMAlfonso Mendez-Tenorio
Alfonso Mendez-Tenorio
CWCarlos Wong-Baeza
Carlos Wong-Baeza
BTBenjamin Nogueda Torres
Benjamin Nogueda Torres
JHJuan Carlos Santiago Hernández
Juan Carlos Santiago Hernández
Chagas disease, caused by the protozoan Trypanosoma cruzi, represents a significant public health challenge, particularly in Latin America’s endemic regions. The limited efficacy and frequent adverse effects of current treatments underscore the need for novel therapeutic options. This research explores marine natural compounds as potential candidates for Chagas disease treatment using virtual screening and in silico evaluation methods. Techniques such as molecular docking, drug-likeness evaluation, and pharmacokinetic analysis were employed to identify promising anti-parasitic compounds. Among the candidates, chandrananimycin A, venezueline A, and dispacamide demonstrated high binding affinities to key targets in T. cruzi alongside favorable docking scores and compliance with essential drug-likeness criteria. Pharmacokinetic profiling further supported their therapeutic potential, revealing desirable properties like effective absorption and minimal toxicity. These findings underscore the promise of marine-derived compounds as a valuable source of new drugs, emphasizing the need for further in vitro and in vivo investigations to elucidate their molecular mechanisms and optimize their development as viable treatments for Chagas disease.