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Antibacterial activities of the methanol extract, fractions and compounds from Elaeophorbia drupifera (Thonn.) Stapf. (Euphorbiaceae).
Voukeng, Igor K; Nganou, Blaise K; Sandjo, Louis P; Celik, Ilhami; Beng, Veronique P; Tane, Pierre; Kuete, Victor.
  • Voukeng IK; Department of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
  • Nganou BK; Department of Chemistry, Faculty of Science, University of Dschang, Dschang, Cameroon.
  • Sandjo LP; Department of Pharmaceutical Sciences, CCS, Universidade Federal de Santa Catarina, Florianópolis, 88040-900, Santa Catarina, Brazil.
  • Celik I; Department of Chemistry, Faculty of Science, Anadolu University, Eskisehir, Turkey.
  • Beng VP; Department of Biochemistry, Faculty of Science, University of Yaounde I, Yaoundé, Cameroon.
  • Tane P; Department of Chemistry, Faculty of Science, University of Dschang, Dschang, Cameroon.
  • Kuete V; Department of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon. kuetevictor@yahoo.fr.
BMC Complement Altern Med ; 17(1): 28, 2017 Jan 07.
Article en En | MEDLINE | ID: mdl-28061888
ABSTRACT

BACKGROUND:

Elaeophorbia drupifera (Thonn.) Stapf. (Euphorbiaceae) is used in Cameroonian folk medicine to treat several ailments including bacterial-related diseases such as skin infections. In this study, the methanol extract from the leaves (EDL), fractions (EDLa-d), sub-fractions EDLc1-7 and EDLc31-35 as well as isolated compounds were tested for their antimicrobial activities against a panel of Gram-negative and Gram-positive bacteria including multidrug resistant (MDR) phenotypes.

METHODS:

The broth microdilution method was used to determine the minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) of the above samples; column chromatography was used for the fractionation and purification of the leaves extract whilst the chemical structures of compounds were determined using spectroscopic techniques.

RESULTS:

Phytochemical investigation lead to the isolation of a mixture (13) of stigmasterol and ß-sitosterol (1 + 2), euphol (3), sitosterol-O-ß- D -xylopyranoside (4), 3,3',4'-tri-O-methylellagic acid (5), a mixture (11) of afzelin and quercetin-3-O-ß-D-xylopyranoside (6 + 7), 3,3',4'-tri-O-methylellagic acid 4-O-ß-D-glucopyranoside (8), ellagic acid-4-O-ß-xylopyranoside-3,3',4'-trimethyl ether (9) from EDLc. Crude extract and fractions displayed selective activities with MIC values ranged from 32 to 1024 µg/mL for EDL against 84.9% of the 33 tested bacteria, 93.9% for EDLc, 69.7% for EDLb, 33.4% for EDLa and 0.03% for EDLd. MIC values ranged from 16 to 1024 µg/mL were obtained with EDLc3 and EDLc4 on all tested bacteria meanwhile other sub-fractions displayed selective activities. MIC value of 32 µg/mL was obtained with fractions EDLa against Escherichia coli AG100, EDLc against Enterobacer aerogenes ATCC13048 and EA298. For sub-fractions obtained from EDLc, the lowest MIC value of 16 µg/mL was recorded with EDLc3 against Staphylococcus aureus MRSA11. A corresponding value of 8 µg/mL against Providencia stuartii NAE16 was recorded with EDLc33 obtained from further fractionation of EDLc3. EDLc3 had MIC values below 100 µg/mL against all tested bacteria. Compound 5 as well as the mixture (11) of 6 and 7 inhibited the growth of all the tested bacteria with MICs ranged from 64 to 256 µg/mL.

CONCLUSION:

Elaeophorbia drupifera is a potential source of phytomedicine to tackle MDR bacteria. Sub-fraction EDLc3 was more active than all isolated compounds and deserves further investigations to develop natural drug to combat Gram-negative, Gram-positive bacteria and otherwise MDR phenotypes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Euphorbiaceae / Antibacterianos Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Euphorbiaceae / Antibacterianos Idioma: En Año: 2017 Tipo del documento: Article