نمایش مختصر رکورد

dc.contributor.authorVikas, Bibaen_US
dc.contributor.authorB S, Akhilen_US
dc.contributor.authorP, Remanien_US
dc.contributor.authorSujathan, Ken_US
dc.date.accessioned1399-07-08T18:03:45Zfa_IR
dc.date.accessioned2020-09-29T18:03:45Z
dc.date.available1399-07-08T18:03:45Zfa_IR
dc.date.available2020-09-29T18:03:45Z
dc.date.issued2017-10-01en_US
dc.date.issued1396-07-09fa_IR
dc.date.submitted2017-06-01en_US
dc.date.submitted1396-03-11fa_IR
dc.identifier.citationVikas, Biba, B S, Akhil, P, Remani, Sujathan, K. (2017). Free Radical Scavenging Properties of Annona squamosa. Asian Pacific Journal of Cancer Prevention, 18(10), 2725-2731. doi: 10.22034/APJCP.2017.18.10.2725en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttps://dx.doi.org/10.22034/APJCP.2017.18.10.2725
dc.identifier.urihttp://journal.waocp.org/article_50785.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/35371
dc.description.abstract<br /> <em><span style="font-size: small;">Annona squamosa </span></em><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">has extensively been used in the traditional and folkloric medicine and found to possess many biological activities. Different solvents, petroleum ether, chloroform, ethyl acetate and methanol extracts of </span></span><em><span style="font-size: small;">Annona squamosa </span></em><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">seeds (ASPE, ASCH, ASEA, ASME) have been used to prepare plant extracts. The present investigations dealt with the free radical scavenging activity of four extracts using various techniques such as total reducing power estimation, total phenolic count, 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical scavenging effect, evaluation of ABTS cation decolorisation capacity, FRAP assay, hdroxyl radical scavenging assay, super oxide assay and Nitric oxide radical scavenging assay of the extracts. The results showed that the four extracts of </span></span><em><span style="font-size: small;">Annona squamosa </span></em><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">showed significant </span></span><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">reducing power in four extracts. The total phenolic contents in petroleum ether, chloroform, ethyl acetate, methanol </span></span><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">extracts and positive control were 0.64±0.17, 0.54±0.27, 0.49±0.24, 0.57±0.22 and 0.66±0.33. The antioxidant capacity by ABTS assay of ASPE, ASCH, ASEA, ASME and positive control, trolox showed 77.75±0.5,73.25±1.7,78.5± 1.2 , 80 ± 0.8 μg/ml and 94.2 ± 0.9 respectively. The (50 % scavenging activity) SA</span></span><span style="font-family: Times New Roman,Times New Roman; font-size: xx-small;"><span style="font-family: Times New Roman,Times New Roman; font-size: xx-small;">50 </span></span><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">of ASPE and ASCH, ASEA and ASME was </span></span><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">found to be 34.4 μg/ml, 43.8 μg/ml 34.7 μg/m and 28.8 μg/ml respectively by DPPH assay. The percentage of </span></span><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">hydroxyl radical scavenging increased with the increasing concentration of the extracts. ASPE, ASCH, ASEA and </span></span><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">ASME showed superoxide radical scavenging activity, as indicated by their values 66 ± 0.5, 68 ± 1 ,63 ± 1 and 70 ± 0.5 μg/ml respectively compared to gallic acid which was 97 ± 0.5 μg/ml. The values for scavenging of nitric oxide for ASPE, ASCH, ASEA and ASME were 91.0 ± 1.0, 66.75 ± 0.5, 71.75 ± 1.1 and 75.75 ± 1.15 μg/ml while value for standard ascorbic acid was 91.0 ± 1.0 μg/ml. The results revealed strong antioxidants in four extracts may lead to the </span></span><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">development of potent antioxidant agents from </span></span><em><span style="font-size: small;">Annona squamosa </span></em><span style="font-family: Times New Roman,Times New Roman; font-size: small;"><span style="font-family: Times New Roman,Times New Roman; font-size: small;">seeds. </span></span>en_US
dc.format.extent1031
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.relation.isversionofhttps://dx.doi.org/10.22034/APJCP.2017.18.10.2725
dc.subjectAnnona squamosaen_US
dc.subjectAntioxidant activityen_US
dc.subjectFree radical scavenging activityen_US
dc.subjectBiology generalen_US
dc.titleFree Radical Scavenging Properties of Annona squamosaen_US
dc.typeTexten_US
dc.typeResearch Articlesen_US
dc.contributor.departmentDivision of Cancer Research, Regional Cancer Centre, Trivandrum, India.en_US
dc.contributor.departmentDivision of Cancer Research, Regional Cancer Centre, Trivandrum, India.en_US
dc.contributor.departmentDivision of Cancer Research, Regional Cancer Centre, Trivandrum, India.en_US
dc.contributor.departmentDivision of Cancer Research, Regional Cancer Centre, Trivandrum, India.en_US
dc.citation.volume18
dc.citation.issue10
dc.citation.spage2725
dc.citation.epage2731


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