PRELIMINARY PHYTOCHEMICAL STUDY AND EVALUATION OF CYTOTOXIC ACTIVITY OF EUPHORBIA LAURIFOLIA JUSS. EX. LAM LATEX ON ARTEMIA SALINA
DOI:
https://doi.org/10.47187/perf.v2i20.27Keywords:
Euphorbia laurifolia, cytotoxic activity, artemia salina, latex, terpenes, EuphorbiaceaeAbstract
Euphorbia laurifolia is a plant species that belongs to the family Euphorbiaceae located in colombia, venezuela and Ecuador. traditionally, it is used for liver affections and to avoid the formation of skin abscesses and warts. due to its high availability and variety of uses, it has phytochemical and phar- macological importance. the aim of this investigation was to carry out preliminary phytochemical study and evaluation of the cytotoxic activity of E. laurifolia latex on artemia salina. several latex extracts, separation and identification of compounds was performed by Thin Layer Chromatography (tlc). the evaluation of the cytotoxic activity on artemia salina was carried out using the hexanic fraction at concentrations of 0, 31, 62, 125, 250, 500, 1000 ppm. it was established that E. laurifolia contains terpene compounds, identified by TLC molecules such as borneol (Rf 0.24) and cineole (Rf0.40). regarding the cytotoxicity of the hexane fraction, the lethal concentration (lc50) was 214.50 ppm, showing that the extract is toxic. the latex of E. laurifolia is rich in terpene compounds with high cytotoxic activity; therefore, it presents a remarkable potential for future pharmacological studies.
Downloads
References
Ávila L, Pérez M, Sánchez-Duffhues G, Hernández-Galán R, Muñoz E. Effects of diterpenes from latex of Euphorbia lactea and Euphorbia laurifolia on Human Immunodeficiency Virus Type 1 Reactivation. Phytochemistry. 2010; 7: 243–248
Ahmed, A, Couladis, M., Mahmoud, A., De Adams, A., Mabry, T. Ingol diterpene ester from the latex of Euphorbia lactea. fitoterapia.1999; 70: 140–143.
Lu Z, Yang M, Zhang J, Chen G, Huang, H., Guan S, Ingenane diterpenoids from Euphorbia esula. phytochemistry. 2008; 69: 812–819.
Blanco-Molina M., Tron G, Macho A, Lucena C, Calzado M, Muñoz E, Appendino, G., Ingenol Esters induce apoptosis in Jurkat cells through an ap 1 and NF-UB independent pathway. 2001; 8:767–778
Vigone A, Tron G, Surico D, Baj G, Appendino G, Surico N. Ingenol derivatives inhibit proliferation and induce apoptosis in breast cancer cell lines. Eur. J. gynaecol. oncol. 2005; 26, 526–530.
Jijón C. Euphorbia laurifolia. [internet]. 2014 [citado 12 noviembre 2014]; http://plantasnativas.visitavirtualjbq.com/index.php?option=com_content&view=article&id=13:euphorbia-laurifolia&cati- d=14:siglo-xviii-coleccion-de-joseph-de-jussieu&itemid=108
Ulloa C, Moller P. Árboles y arbustos de los Andes. [internet]. 2014 [citado 11 noviembre 2014]; http://www.efloras.org/florataxon.aspx?flora_id=201&taxon_id=112355
Singh SK, Yadav RP, Singh, D, Singh, A. Toxic Effect of two common Euphorbiales latices on the freshwater snail lymnaea acuminate. Enviro Toxicol Pharmacol. 2004; 15: 87–93.
Hassan AA, Mahmoud AE, Hassan RA, Huseein EAM. Evaluation of Euphorbia aphylla, Ziziphus spina-christi and Enterolobium contortisiliquum as molluscicidal agents. J am sci. 2011; 7: 511-20.
Al-Zanbagi NA, Banaja AEA, Barrett, J. Molluscicidal Activity of Some Saudi Arabian Euphorbiales against the snail biomphalaria pfeifferi. J Ethnopharmacol. 2010; 70: 119–25.
Prashant Y, et al. Ijppr.Human, 2015; 4: 56-67
Mogollón-Morales JA, Nieves E, Rondón M, Rondón-Rivas ME. Propiedad molusquicida de Euphorbia laurifolia a. Juss (Euphorbiaceae) contra biomphalaria glabrata say Hospedador intermediario de schistosoma mansoni. avan biomed 2016; 5: 83-9.
González J, Basabe P, Sexmero M, Sánchez Isidoro. Diterpenes from the latex of Euphorbia bro- teri.phytochemistry 1988; 7: 207-212.
Smith I. Chromatographic and Electrophoretic Techniques. Zone Electrophoresis. 1960; 2: 200-215
Ferreira-Dias S, Valente D, Abreu J. Pattern recognition of acorns from different quercus species Based on Oil Content and Fatty Acid Profile. 2003; 54.
Wagner H, Blant S. Análisis de medicamentos de plantas. 2.ª ed. atlas de cromatografía en capa fina. Springer. 1996: 315-350
Finney D, Probit analysis. 3.ª ed.,Cambridge University Press, UK. 1971; 1: 76-80.
Jaramillo B, Olivero J, Muñoz K. composición química volátil y toxicidad aguda (Cl50) frente a artemia salina del aceite esencial del Croton malambo colectado en la costa norte colombiana. scientia et technica. 2007; 1: 299-302
Ospina V, Mantilla J, Conde C, Escobar P. Permeación en piel humana de una nanoemulsión de ftalocianina de aluminio clorada para la optimización de tratamientos tópicos de leishmaniasis cutánea. revista ciencias de la salud, 12(2), 2014: 195-211.
Chudzik M, Korzonek-Szlacheta i, Król W. Triterpenos como compuestos potencialmente citotóxicos. Molecules. 2015; 20(1): 1610-1625
Zhao H-C, Wang, J-b. The accumulation of phytoalexin in cucumber plant after stress. Colloids and Surfaces B: Biointerfaces. 2005: 187-193.
Borroto J, Trujillo R, de la Torre y, Waksman N, Hernández M y Salazar R. Actividad antimicrobiana y toxicidad frente a artemia salina del extracto diclorometánico de raíces de Morinda royoc L. Revista Cubana de Plantas Medicinales. 2011:34-42.
Timoleon M, Pascal W, Ramsay S, Raduis M. Uzor P, Zulfiqar A. Terpenoids From the Stem Bark of neoboutonia macrocalyx (Euphorbiaceae). Phytochemistry Letters 2015; 12: 328–331
Downloads
Published
How to Cite
Issue
Section
License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.