{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T15:21:39Z","timestamp":1787844099688,"version":"build-2784847793"},"reference-count":25,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","license":[{"start":{"date-parts":[[2018,5,1]],"date-time":"2018-05-01T00:00:00Z","timestamp":1525132800000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2018,5]]},"abstract":"<jats:sec>\n                    <jats:title>OBJECTIVE:<\/jats:title>\n                    <jats:p>\n                      <jats:italic toggle=\"yes\">Amaranthus viridis<\/jats:italic>\n                      (\n                      <jats:italic toggle=\"yes\">Amaranthaceae<\/jats:italic>\n                      ) widely distributed all over the world, growing under a wide range of climatic conditions and has been utilized as a medicinal herb in traditional Ayurvedic medicine as antipyretic agents, also for the treatment of inflammation, ulcer, diabetic, asthma and hyperlipidemia. The aim of the study was designed to evaluate the chemical composition and antioxidant and biological properties of different fractions obtained from\n                      <jats:italic toggle=\"yes\">A. viridis<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>MATERIALS AND METHODS:<\/jats:title>\n                    <jats:p>\n                      Four different extracts of\n                      <jats:italic toggle=\"yes\">A. viridis<\/jats:italic>\n                      were prepared using aqueous, methanol, chloroform, and hexane and investigated their antioxidant potential using free radical scavenging activities such as 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2'-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS), and nitric oxide (NO) radical scavenging activity, as well as metal chelating activity. In addition, antityrosinase and antigenotoxicity properties were also evaluated by the standard\n                      <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                      methods. Finally, the active methanolic extract (ME) was investigated for identifying the phenolic compounds using UPLC-MS\/MS.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>RESULTS:<\/jats:title>\n                    <jats:p>\n                      In the present study, chlorogenic acid, gulonic acid, and kaempferol were found to be the major components responsible for the antioxidant activity of\n                      <jats:italic toggle=\"yes\">A. viridis<\/jats:italic>\n                      extract as evidenced from UPLC-MS\/MS. Furthermore, the ME of\n                      <jats:italic toggle=\"yes\">A. viridis<\/jats:italic>\n                      revealed excellent antioxidant activities such as DPPH radical scavenging activity (IC\n                      <jats:sub>50<\/jats:sub>\n                      = 47.23 \u00b1 0.66 \u03bcg\/mL), NO radical scavenging activity (IC\n                      <jats:sub>50<\/jats:sub>\n                      = 64.33 \u00b1 2.01 \u03bcg\/mL), hydrogen peroxide (H\n                      <jats:sub>2<\/jats:sub>\n                      O\n                      <jats:sub>2<\/jats:sub>\n                      ) radical scavenging activity (IC\n                      <jats:sub>50<\/jats:sub>\n                      = 33.21 \u00b1 3.3 \u03bcg\/mL), ABTS radical scavenging activity (IC\n                      <jats:sub>50<\/jats:sub>\n                      = 47.61 \u00b1 1.31 \u03bcg\/mL), metal chelating activity (IC\n                      <jats:sub>50<\/jats:sub>\n                      = 32.1 \u00b1 1.11 \u03bcg\/mL), as well as lipid peroxidation inhibiting activity (IC\n                      <jats:sub>50<\/jats:sub>\n                      = 112 \u00b1 1.21 \u03bcg\/mL). Furthermore, ME revealed that the protective effects of extract were observed on H\n                      <jats:sub>2<\/jats:sub>\n                      O\n                      <jats:sub>2<\/jats:sub>\n                      -induced DNA damages with alkaline comet assay.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>CONCLUSIONS:<\/jats:title>\n                    <jats:p>\n                      Taken together, the study concluded that the promising antioxidant capacities of\n                      <jats:italic toggle=\"yes\">A. viridis<\/jats:italic>\n                      extract can further be utilized in various agricultural, pharmaceutical, and food applications.\n                    <\/jats:p>\n                  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