Chemical Standardization of Extracts of CalophyllumBrasiliense with Antiplasmodial and Cytotoxic Activity

Malaria is considered one of the health problems in many parts of the world. The objective of this work is to implement standardized extraction strategies using analytical methodologies of the Calophyllum brasiliense Cambess. for the validation of antiplasmodial potential in vitro. Using HPLC chroma...

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Autores:
Mesa Vanegas, Ana María
Blair Trujillo, Silvia
Peláez Jaramillo, Carlos Alberto
Tipo de recurso:
Article of investigation
Fecha de publicación:
2019
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/45847
Acceso en línea:
https://hdl.handle.net/10495/45847
Palabra clave:
Antimaláricos
Antimalarials
Medicina de Hierbas
Herbal Medicine
Plasmodium falciparum
Extractos Vegetales
Plant Extracts
Citotoxicidad
Cytotoxicity
http://aims.fao.org/aos/agrovoc/c_34251
https://id.nlm.nih.gov/mesh/D000962
https://id.nlm.nih.gov/mesh/D029001
https://id.nlm.nih.gov/mesh/D010963
https://id.nlm.nih.gov/mesh/D010936
ODS 3: Salud y bienestar. Garantizar una vida sana y promover el bienestar de todos a todas las edades
Rights
openAccess
License
http://creativecommons.org/licenses/by/4.0/
Description
Summary:Malaria is considered one of the health problems in many parts of the world. The objective of this work is to implement standardized extraction strategies using analytical methodologies of the Calophyllum brasiliense Cambess. for the validation of antiplasmodial potential in vitro. Using HPLC chromatographic and chemical characterization techniques (13C-NMR, 1H-NMR), the marker substance was identified and quantified on continuous cultures of Plasmodium falciparum chloroquine-sensitive strain NF-54 and cytotoxicity in cell lines U-937 and HepG2used the antimalarial potential of the C. brasiliense. The best extracts were stems with ethyl acetate and extraction after 4 hours, presented a yield of 4.154±0.301%, a promising antiplasmodial activity of IC50 = 9.013 } 1.288 μg/mL, a cytotoxicity of CC50HepG2 =43.340±3.159 μg/mL, an IS = 4.808 and a content of marker substancesnamedsoulatrolide (1)of C1 =0.257±0.021%. A new analytical method for the quantification of marker substances was established and the best extracts were obtained. The extracts presented promising pharmacological activities for studies that guarantee reproducibility and effectiveness in biological tests in vivo and framed in the transformation of a phytotherapeutic product.