Antioxidant and anti-dermatophytic properties leaf and stem bark of Xylosma longifolium clos
The present study was carried out to assess the phytochemical and anti-dermatophytic effect of the leaf and bark extracts of Xylosma longifolium Clos. The leaf and stem bark are used by the indigenous people of Manipur, India for treatment of skin diseases. The leaves and stem barks of Xylosma longi...
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description | The present study was carried out to assess the phytochemical and anti-dermatophytic effect of the leaf and bark extracts of Xylosma longifolium Clos. The leaf and stem bark are used by the indigenous people of Manipur, India for treatment of skin diseases.
The leaves and stem barks of Xylosma longifolium were extracted using petroleum ether, chloroform and methanol respectively. The different extracts of each plant parts were tested for antioxidant activity using DPPH assay. The phenolic content was assayed using Folin-Ciocalteu colorimetric method. Each extracts was further analysed by RP-HPLC to quantify some individual flavonoid components. The anti-dermatophytic activity was evaluated both by agar diffusion method and micro wells dilution method against the Microsporum boullardii MTCC 6059, M. canis (MTCC 2820 and MTCC 32700), M. gypseum MTCC 2819, Trichophyton ajelloi MTCC 4878, T. rubrum (MTCC 296 and MTCC 3272).
The free radical scavenging activity values were ranged from 0.7 to 1.41 mg/ml and 0.6 to 1.23 mg/ml, respectively for leaf and stem bark extracts. The amount of total phenolic contents of the extracts occurred in both leaf and bark in the range of 12 to 56.6 mg GAE/100 g and 16 to 58 mg GAE/100 g respectively. RP-HPLC analysis for flavonoids revealed the presence of two major flavonoid compounds, rutin and catechin. Kaempferol was in trace or absent. Methanol leaf extract showed significant low inhibitory effect against tested fungus Trichophyton ajelloi MTCC 4878 (0.140625 mg/ml) as the most sensitive. These finding suggest that the methanol leaf extract tested contain compounds with antimicrobial properties.
The results of our study may partially justify the folkloric uses on the plant studied and further provide an evidence that the leaf extract of Xylosma longifolium might be indeed a potential sources of antimicrobial agents. |
doi_str_mv | 10.1186/1472-6882-13-155 |
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The leaves and stem barks of Xylosma longifolium were extracted using petroleum ether, chloroform and methanol respectively. The different extracts of each plant parts were tested for antioxidant activity using DPPH assay. The phenolic content was assayed using Folin-Ciocalteu colorimetric method. Each extracts was further analysed by RP-HPLC to quantify some individual flavonoid components. The anti-dermatophytic activity was evaluated both by agar diffusion method and micro wells dilution method against the Microsporum boullardii MTCC 6059, M. canis (MTCC 2820 and MTCC 32700), M. gypseum MTCC 2819, Trichophyton ajelloi MTCC 4878, T. rubrum (MTCC 296 and MTCC 3272).
The free radical scavenging activity values were ranged from 0.7 to 1.41 mg/ml and 0.6 to 1.23 mg/ml, respectively for leaf and stem bark extracts. The amount of total phenolic contents of the extracts occurred in both leaf and bark in the range of 12 to 56.6 mg GAE/100 g and 16 to 58 mg GAE/100 g respectively. RP-HPLC analysis for flavonoids revealed the presence of two major flavonoid compounds, rutin and catechin. Kaempferol was in trace or absent. Methanol leaf extract showed significant low inhibitory effect against tested fungus Trichophyton ajelloi MTCC 4878 (0.140625 mg/ml) as the most sensitive. These finding suggest that the methanol leaf extract tested contain compounds with antimicrobial properties.
The results of our study may partially justify the folkloric uses on the plant studied and further provide an evidence that the leaf extract of Xylosma longifolium might be indeed a potential sources of antimicrobial agents.</description><identifier>ISSN: 1472-6882</identifier><identifier>EISSN: 1472-6882</identifier><identifier>DOI: 10.1186/1472-6882-13-155</identifier><identifier>PMID: 23819459</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acids ; Agar ; Analysis ; Antifungal Agents - chemistry ; Antifungal Agents - pharmacology ; Antimicrobial agents ; Antioxidants ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Arthrodermataceae - drug effects ; Canis ; Care and treatment ; Chemical properties ; Dermatologic agents ; Dermatology ; Dermatomycoses - microbiology ; Ethanol ; Flavonoids ; Formulae, receipts, prescriptions ; Free radicals ; Fungal infections ; Health aspects ; Herbal medicine ; High performance liquid chromatography ; Humans ; Indigenous peoples ; Medicinal plants ; Methanol ; Microbial Sensitivity Tests ; Microorganisms ; Phenols ; Plant Bark - chemistry ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Plant Leaves - chemistry ; Polyphenols ; Salicaceae - chemistry ; Skin ; Skin diseases ; Solvents</subject><ispartof>BMC complementary and alternative medicine, 2013-07, Vol.13 (1), p.155-155, Article 155</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013 Devi et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2013 Devi et al.; licensee BioMed Central Ltd. 2013 Devi et al.; licensee BioMed Central Ltd.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b615t-e481dd0b42cb2ae39b8a78116a56d0aff4c37c12c6013d010dc88c3d72bcfce3</citedby><cites>FETCH-LOGICAL-b615t-e481dd0b42cb2ae39b8a78116a56d0aff4c37c12c6013d010dc88c3d72bcfce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718714/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718714/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23819459$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Devi, Wangkheirakpam Radhapiyari</creatorcontrib><creatorcontrib>Singh, S Brojendro</creatorcontrib><creatorcontrib>Singh, Chingakham B</creatorcontrib><title>Antioxidant and anti-dermatophytic properties leaf and stem bark of Xylosma longifolium clos</title><title>BMC complementary and alternative medicine</title><addtitle>BMC Complement Altern Med</addtitle><description>The present study was carried out to assess the phytochemical and anti-dermatophytic effect of the leaf and bark extracts of Xylosma longifolium Clos. The leaf and stem bark are used by the indigenous people of Manipur, India for treatment of skin diseases.
The leaves and stem barks of Xylosma longifolium were extracted using petroleum ether, chloroform and methanol respectively. The different extracts of each plant parts were tested for antioxidant activity using DPPH assay. The phenolic content was assayed using Folin-Ciocalteu colorimetric method. Each extracts was further analysed by RP-HPLC to quantify some individual flavonoid components. The anti-dermatophytic activity was evaluated both by agar diffusion method and micro wells dilution method against the Microsporum boullardii MTCC 6059, M. canis (MTCC 2820 and MTCC 32700), M. gypseum MTCC 2819, Trichophyton ajelloi MTCC 4878, T. rubrum (MTCC 296 and MTCC 3272).
The free radical scavenging activity values were ranged from 0.7 to 1.41 mg/ml and 0.6 to 1.23 mg/ml, respectively for leaf and stem bark extracts. The amount of total phenolic contents of the extracts occurred in both leaf and bark in the range of 12 to 56.6 mg GAE/100 g and 16 to 58 mg GAE/100 g respectively. RP-HPLC analysis for flavonoids revealed the presence of two major flavonoid compounds, rutin and catechin. Kaempferol was in trace or absent. Methanol leaf extract showed significant low inhibitory effect against tested fungus Trichophyton ajelloi MTCC 4878 (0.140625 mg/ml) as the most sensitive. These finding suggest that the methanol leaf extract tested contain compounds with antimicrobial properties.
The results of our study may partially justify the folkloric uses on the plant studied and further provide an evidence that the leaf extract of Xylosma longifolium might be indeed a potential sources of antimicrobial agents.</description><subject>Acids</subject><subject>Agar</subject><subject>Analysis</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antimicrobial agents</subject><subject>Antioxidants</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Arthrodermataceae - drug effects</subject><subject>Canis</subject><subject>Care and treatment</subject><subject>Chemical properties</subject><subject>Dermatologic agents</subject><subject>Dermatology</subject><subject>Dermatomycoses - microbiology</subject><subject>Ethanol</subject><subject>Flavonoids</subject><subject>Formulae, receipts, prescriptions</subject><subject>Free radicals</subject><subject>Fungal infections</subject><subject>Health aspects</subject><subject>Herbal medicine</subject><subject>High performance liquid chromatography</subject><subject>Humans</subject><subject>Indigenous peoples</subject><subject>Medicinal plants</subject><subject>Methanol</subject><subject>Microbial Sensitivity Tests</subject><subject>Microorganisms</subject><subject>Phenols</subject><subject>Plant Bark - chemistry</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Leaves - chemistry</subject><subject>Polyphenols</subject><subject>Salicaceae - chemistry</subject><subject>Skin</subject><subject>Skin diseases</subject><subject>Solvents</subject><issn>1472-6882</issn><issn>1472-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqNks-L1DAUx4so7rp69yQFQbx0zUvaNL0Iw-AvWPCyBw9CSJN0Jmua1CRdnP_e1FnHGVlBQkh47_O-vHzziuI5oEsARt9A3eKKMoYrIBU0zYPi_BB6eHQ_K57EeIMQtAzqx8UZJgy6uunOi68rl4z_YZRwqRRO5Z1MpXQYRfLTdpeMLKfgJx2S0bG0Wgy_sJj0WPYifCv9UH7ZWR9HUVrvNmbw1sxjKXPoafFoEDbqZ3fnRXH9_t31-mN19fnDp_XqquopNKnSNQOlUF9j2WOhSdczkRsFKhqqkBiGWpJWApYUAVEIkJKMSaJa3MtBanJRvN3LTnM_aiW1S0FYPgUzirDjXhh-mnFmyzf-lpMWWAt1FljvBXrj_yFwmpF-5Iu5fDGXA-HZ-6zy-q6N4L_POiY-mii1tcJpP8dcQOsGdYDof6D59Zh2ABl9-Rd64-fgsp0LhVnbEor-UBthNTdu8LlPuYjyVUNqShqMF-ryHiovpUcjvdODyfGTgldHBVstbNpGb-c8Mi6egmgPyuBjDHo4mAeIL6N6n10vjn_tUPB7NslPFP3jdQ</recordid><startdate>20130702</startdate><enddate>20130702</enddate><creator>Devi, Wangkheirakpam Radhapiyari</creator><creator>Singh, S Brojendro</creator><creator>Singh, Chingakham B</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>M7N</scope><scope>5PM</scope></search><sort><creationdate>20130702</creationdate><title>Antioxidant and anti-dermatophytic properties leaf and stem bark of Xylosma longifolium clos</title><author>Devi, Wangkheirakpam Radhapiyari ; Singh, S Brojendro ; Singh, Chingakham B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b615t-e481dd0b42cb2ae39b8a78116a56d0aff4c37c12c6013d010dc88c3d72bcfce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Acids</topic><topic>Agar</topic><topic>Analysis</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - pharmacology</topic><topic>Antimicrobial agents</topic><topic>Antioxidants</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - pharmacology</topic><topic>Arthrodermataceae - drug effects</topic><topic>Canis</topic><topic>Care and treatment</topic><topic>Chemical properties</topic><topic>Dermatologic agents</topic><topic>Dermatology</topic><topic>Dermatomycoses - microbiology</topic><topic>Ethanol</topic><topic>Flavonoids</topic><topic>Formulae, receipts, prescriptions</topic><topic>Free radicals</topic><topic>Fungal infections</topic><topic>Health aspects</topic><topic>Herbal medicine</topic><topic>High performance liquid chromatography</topic><topic>Humans</topic><topic>Indigenous peoples</topic><topic>Medicinal plants</topic><topic>Methanol</topic><topic>Microbial Sensitivity Tests</topic><topic>Microorganisms</topic><topic>Phenols</topic><topic>Plant Bark - chemistry</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Leaves - chemistry</topic><topic>Polyphenols</topic><topic>Salicaceae - chemistry</topic><topic>Skin</topic><topic>Skin diseases</topic><topic>Solvents</topic><toplevel>online_resources</toplevel><creatorcontrib>Devi, Wangkheirakpam Radhapiyari</creatorcontrib><creatorcontrib>Singh, S Brojendro</creatorcontrib><creatorcontrib>Singh, Chingakham B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Devi, Wangkheirakpam Radhapiyari</au><au>Singh, S Brojendro</au><au>Singh, Chingakham B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant and anti-dermatophytic properties leaf and stem bark of Xylosma longifolium clos</atitle><jtitle>BMC complementary and alternative medicine</jtitle><addtitle>BMC Complement Altern Med</addtitle><date>2013-07-02</date><risdate>2013</risdate><volume>13</volume><issue>1</issue><spage>155</spage><epage>155</epage><pages>155-155</pages><artnum>155</artnum><issn>1472-6882</issn><eissn>1472-6882</eissn><abstract>The present study was carried out to assess the phytochemical and anti-dermatophytic effect of the leaf and bark extracts of Xylosma longifolium Clos. The leaf and stem bark are used by the indigenous people of Manipur, India for treatment of skin diseases.
The leaves and stem barks of Xylosma longifolium were extracted using petroleum ether, chloroform and methanol respectively. The different extracts of each plant parts were tested for antioxidant activity using DPPH assay. The phenolic content was assayed using Folin-Ciocalteu colorimetric method. Each extracts was further analysed by RP-HPLC to quantify some individual flavonoid components. The anti-dermatophytic activity was evaluated both by agar diffusion method and micro wells dilution method against the Microsporum boullardii MTCC 6059, M. canis (MTCC 2820 and MTCC 32700), M. gypseum MTCC 2819, Trichophyton ajelloi MTCC 4878, T. rubrum (MTCC 296 and MTCC 3272).
The free radical scavenging activity values were ranged from 0.7 to 1.41 mg/ml and 0.6 to 1.23 mg/ml, respectively for leaf and stem bark extracts. The amount of total phenolic contents of the extracts occurred in both leaf and bark in the range of 12 to 56.6 mg GAE/100 g and 16 to 58 mg GAE/100 g respectively. RP-HPLC analysis for flavonoids revealed the presence of two major flavonoid compounds, rutin and catechin. Kaempferol was in trace or absent. Methanol leaf extract showed significant low inhibitory effect against tested fungus Trichophyton ajelloi MTCC 4878 (0.140625 mg/ml) as the most sensitive. These finding suggest that the methanol leaf extract tested contain compounds with antimicrobial properties.
The results of our study may partially justify the folkloric uses on the plant studied and further provide an evidence that the leaf extract of Xylosma longifolium might be indeed a potential sources of antimicrobial agents.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>23819459</pmid><doi>10.1186/1472-6882-13-155</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acids Agar Analysis Antifungal Agents - chemistry Antifungal Agents - pharmacology Antimicrobial agents Antioxidants Antioxidants - chemistry Antioxidants - pharmacology Arthrodermataceae - drug effects Canis Care and treatment Chemical properties Dermatologic agents Dermatology Dermatomycoses - microbiology Ethanol Flavonoids Formulae, receipts, prescriptions Free radicals Fungal infections Health aspects Herbal medicine High performance liquid chromatography Humans Indigenous peoples Medicinal plants Methanol Microbial Sensitivity Tests Microorganisms Phenols Plant Bark - chemistry Plant Extracts - chemistry Plant Extracts - pharmacology Plant Leaves - chemistry Polyphenols Salicaceae - chemistry Skin Skin diseases Solvents |
title | Antioxidant and anti-dermatophytic properties leaf and stem bark of Xylosma longifolium clos |
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