Evidence map›Paper›PMID 28468660›Full record

ArticleBMC complementary and alternative medicine2017

Punica granatum peel extracts: HPLC fractionation and LC MS analysis to quest compounds having activity against multidrug resistant bacteria.

Ilyas Khan, Hazir Rahman, Nasser M Abd El-Salam, Abdul Tawab, Anwar Hussain, Taj Ali Khan, Usman Ali Khan, Muhammad Qasim, Muhammad Adnan, Azizullah Azizullah and 4 more

Abstract read
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Article in BMC complementary and alternative medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

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  15. A phenolic small molecule inhibitor of RNase L prevents cell death from ADAR1 deficiency.Proceedings of the National Academy of Sciences of the United States of America · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Ilyas KhanDepartmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
Hazir RahmanDepartmen of Microbiology, Abdul Wali Khan University, Mardan, Pakistan. hazirrahman@hotmail.com.
Nasser M Abd El-SalamRiyadh Community College, King Saud University, Riyadh, 11437, Saudi Arabia.
Abdul TawabNational Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan.
Anwar HussainDepartment of Botany, Abdul Wali Khan University, Mardan, Pakistan.
Taj Ali KhanDepartmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
Usman Ali KhanDepartmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
Muhammad QasimDepartmen of Microbiology, Kohat University of Science & Technology, Kohat, Pakistan.
Muhammad AdnanDepartment of Botany, Kohat University of Science & Technology, Kohat, Pakistan.
Azizullah AzizullahDepartment of Botany, Kohat University of Science & Technology, Kohat, Pakistan.
Waheed MuradDepartment of Botany, Kohat University of Science & Technology, Kohat, Pakistan.
Abdullah JalalInstitute of Biotechnology & Genetic Engineering, The University of Agriculture, Peshawar, Pakistan.
Noor MuhammadDepartment of Biotechnology & Genetic Engineering, Kohat University of Science & Technology, Kohat, Pakistan.
Riaz UllahDepartment of Chemistry, Government College Ara Khel, Frontier Region Kohat, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMedicinal 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.

methodsThe 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.

resultsAmong 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.

conclusionPuncia 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.

Indexed as

LythraceaeAcinetobacter baumanniiAnti-Bacterial AgentsBacteriaChemical FractionationChromatography, High Pressure LiquidDrug Resistance, MultipleEscherichia coliFruitMicrobial Sensitivity TestsPlant ExtractsPseudomonas aeruginosaStaphylococcus aureusTandem Mass SpectrometryAnti-Bacterial AgentsPlant ExtractsAnti-MDR activityCoumaric acidHexosideHPLC fractionsPuncia granatum peel extractsValoneic acid dilactone

Identifiers

PMID28468660
PMCPMC5415797

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.