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Punica granatum peel extracts: HPLC fractionation and LC MS analysis to quest compounds having activity against multidrug resistant bacteria.
Khan, Ilyas; Rahman, Hazir; Abd El-Salam, Nasser M; Tawab, Abdul; Hussain, Anwar; Khan, Taj Ali; Khan, Usman Ali; Qasim, Muhammad; Adnan, Muhammad; Azizullah, Azizullah; Murad, Waheed; Jalal, Abdullah; Muhammad, Noor; Ullah, Riaz.
Afiliación
  • Khan I; Departmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
  • Rahman H; Departmen of Microbiology, Abdul Wali Khan University, Mardan, Pakistan. hazirrahman@hotmail.com.
  • Abd El-Salam NM; Riyadh Community College, King Saud University, Riyadh, 11437, Saudi Arabia.
  • Tawab A; National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan.
  • Hussain A; Department of Botany, Abdul Wali Khan University, Mardan, Pakistan.
  • Khan TA; Departmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
  • Khan UA; Departmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
  • Qasim M; Departmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
  • Adnan M; Department of Botany, Kohat University of Science & Technology, Kohat, Pakistan.
  • Azizullah A; Department of Botany, Kohat University of Science & Technology, Kohat, Pakistan.
  • Murad W; Department of Botany, Kohat University of Science & Technology, Kohat, Pakistan.
  • Jalal A; Institute of Biotechnology & Genetic Engineering, The University of Agriculture, Peshawar, Pakistan.
  • Muhammad N; Department of Biotechnology & Genetic Engineering, Kohat University of Science & Technology, Kohat, Pakistan.
  • Ullah R; Department of Chemistry, Government College Ara Khel, Frontier Region Kohat, Pakistan.
BMC Complement Altern Med ; 17(1): 247, 2017 May 03.
Article en En | MEDLINE | ID: mdl-28468660
ABSTRACT

BACKGROUND:

Medicinal plants are rich source of traditional herbal medicine around the globe. Most of the plant's therapeutic properties are due to the presence of secondary bioactive compounds.

METHODS:

The present study analyzed the High Pressure Liquid Chromatography (HPLC) fractions of Puncia granatum (peel) extracts (aqueous, chloroform, ethanol and hexane) against multidrug resistant bacterial pathogens (Acinetobacter baumannii, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus). All the fractions having antibacterial activity was processed for bioactive compounds identification using LC MS/MS analysis.

RESULTS:

Among total HPLC fractions (n = 30), 4 HPLC fractions of P. granatum (peel) showed potential activity against MDR pathogens. Fraction 1 (F1) and fraction 4 (F4) collected from aqueous extract showed maximum activity against P. aeruginosa. Fraction 2 (F2) of hexane showed antibacterial activity against three pathogens, while ethanol F4 exhibited antibacterial activity against A. baumannii. The active fractions were processed for LC MS/MS analysis to identify bioactive compounds. Valoneic acid dilactone (aqueous F1 and F4), Hexoside (ethanol F4) and Coumaric acid (hexane F2) were identified as bioactive compounds in HPLC fractions.

CONCLUSION:

Puncia granatum peel extracts HPLC fractions exhibited potential inhibitory activity against MDR bacterial human pathogens. Several bioactive compounds were identified from the HPLC fractions. Further characterization of these compounds may be helpful to conclude it as therapeutic lead molecules against MDR pathogens.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Bacterias / Extractos Vegetales / Resistencia a Múltiples Medicamentos / Lythraceae / Antibacterianos Idioma: En Revista: BMC Complement Altern Med Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2017 Tipo del documento: Article País de afiliación: Pakistán

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Bacterias / Extractos Vegetales / Resistencia a Múltiples Medicamentos / Lythraceae / Antibacterianos Idioma: En Revista: BMC Complement Altern Med Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2017 Tipo del documento: Article País de afiliación: Pakistán