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In Vitro Antioxidant and Antiaging Activities of Collagen and Its Hydrolysate from Mackerel Scad Skin (Decapterus macarellus)
The skin of mackerel scad fish (Decapterus macarellus) is a new source for pepsin-soluble collagen and its hydrolysate, both of which have never been explored. This study aims to characterize and determine the in vitro antioxidant, antiglycation, and antityrosinase activity of pepsin-soluble collage...
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Published in: | Marine drugs 2022-08, Vol.20 (8), p.516 |
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description | The skin of mackerel scad fish (Decapterus macarellus) is a new source for pepsin-soluble collagen and its hydrolysate, both of which have never been explored. This study aims to characterize and determine the in vitro antioxidant, antiglycation, and antityrosinase activity of pepsin-soluble collagen (PSC) and hydrolyzed collagen (HC) from mackerel scad skin. PSC was extracted using 0.5 M acetic acid containing 0.1% pepsin for 48 h at 4 °C. The obtained PSC was then hydrolyzed with collagenase type II (6250 U/g) to produce HC. The PSC yield obtained was 6.39 ± 0.97%, with a pH of 6.76 ± 0.18, while the HC yield was 96% from PSC. SDS-PAGE and Fourier Transform Infrared (FTIR) analysis showed the typical features of type I collagen. HC demonstrated high solubility (66.75–100%) throughout the entire pH range (1–10). The PSC and HC from mackerel scad skin showed antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH), with IC50 values of 148.55 ± 3.14 ppm and 34.966 ± 0.518 ppm, respectively. In the antiglycation test, PSC had an IC50 value of 239.29 ± 15.67 ppm, while HC had an IC50 of 68.43 ± 0.44 ppm. PSC also exhibited antityrosinase activity, with IC50 values of 234.66 ± 0.185 ppm (on the L-DOPA substrate), while HC had an IC50 value of 79.35 ± 0.5 ppm. Taken together, these results suggest that the skin of mackerel scad fish has potential antiaging properties and can be further developed for pharmaceutical and cosmetic purposes. |
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This study aims to characterize and determine the in vitro antioxidant, antiglycation, and antityrosinase activity of pepsin-soluble collagen (PSC) and hydrolyzed collagen (HC) from mackerel scad skin. PSC was extracted using 0.5 M acetic acid containing 0.1% pepsin for 48 h at 4 °C. The obtained PSC was then hydrolyzed with collagenase type II (6250 U/g) to produce HC. The PSC yield obtained was 6.39 ± 0.97%, with a pH of 6.76 ± 0.18, while the HC yield was 96% from PSC. SDS-PAGE and Fourier Transform Infrared (FTIR) analysis showed the typical features of type I collagen. HC demonstrated high solubility (66.75–100%) throughout the entire pH range (1–10). The PSC and HC from mackerel scad skin showed antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH), with IC50 values of 148.55 ± 3.14 ppm and 34.966 ± 0.518 ppm, respectively. In the antiglycation test, PSC had an IC50 value of 239.29 ± 15.67 ppm, while HC had an IC50 of 68.43 ± 0.44 ppm. PSC also exhibited antityrosinase activity, with IC50 values of 234.66 ± 0.185 ppm (on the L-DOPA substrate), while HC had an IC50 value of 79.35 ± 0.5 ppm. Taken together, these results suggest that the skin of mackerel scad fish has potential antiaging properties and can be further developed for pharmaceutical and cosmetic purposes.</description><identifier>ISSN: 1660-3397</identifier><identifier>EISSN: 1660-3397</identifier><identifier>DOI: 10.3390/md20080516</identifier><identifier>PMID: 36005519</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acetic acid ; Aging ; antiaging ; antioxidant ; Antioxidants ; Collagen ; Collagen (type I) ; Collagen (type II) ; Collagenase ; Decapterus macarellus ; Enzymes ; Fish ; Fish skin ; Fourier analysis ; Fourier transforms ; Gel electrophoresis ; Hydrolysates ; hydrolyzed collagen ; Infrared analysis ; Levodopa ; Low income groups ; Mackerel ; mackerel scad skin ; Marine fishes ; Molecular weight ; Morphology ; Pepsin ; Peptides ; pH effects ; Proteins ; Scanning electron microscopy ; Sodium lauryl sulfate ; Spectrum analysis ; Substrates ; Tuna</subject><ispartof>Marine drugs, 2022-08, Vol.20 (8), p.516</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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This study aims to characterize and determine the in vitro antioxidant, antiglycation, and antityrosinase activity of pepsin-soluble collagen (PSC) and hydrolyzed collagen (HC) from mackerel scad skin. PSC was extracted using 0.5 M acetic acid containing 0.1% pepsin for 48 h at 4 °C. The obtained PSC was then hydrolyzed with collagenase type II (6250 U/g) to produce HC. The PSC yield obtained was 6.39 ± 0.97%, with a pH of 6.76 ± 0.18, while the HC yield was 96% from PSC. SDS-PAGE and Fourier Transform Infrared (FTIR) analysis showed the typical features of type I collagen. HC demonstrated high solubility (66.75–100%) throughout the entire pH range (1–10). The PSC and HC from mackerel scad skin showed antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH), with IC50 values of 148.55 ± 3.14 ppm and 34.966 ± 0.518 ppm, respectively. In the antiglycation test, PSC had an IC50 value of 239.29 ± 15.67 ppm, while HC had an IC50 of 68.43 ± 0.44 ppm. PSC also exhibited antityrosinase activity, with IC50 values of 234.66 ± 0.185 ppm (on the L-DOPA substrate), while HC had an IC50 value of 79.35 ± 0.5 ppm. Taken together, these results suggest that the skin of mackerel scad fish has potential antiaging properties and can be further developed for pharmaceutical and cosmetic purposes.</description><subject>Acetic acid</subject><subject>Aging</subject><subject>antiaging</subject><subject>antioxidant</subject><subject>Antioxidants</subject><subject>Collagen</subject><subject>Collagen (type I)</subject><subject>Collagen (type II)</subject><subject>Collagenase</subject><subject>Decapterus macarellus</subject><subject>Enzymes</subject><subject>Fish</subject><subject>Fish skin</subject><subject>Fourier analysis</subject><subject>Fourier transforms</subject><subject>Gel electrophoresis</subject><subject>Hydrolysates</subject><subject>hydrolyzed collagen</subject><subject>Infrared analysis</subject><subject>Levodopa</subject><subject>Low income groups</subject><subject>Mackerel</subject><subject>mackerel scad skin</subject><subject>Marine fishes</subject><subject>Molecular weight</subject><subject>Morphology</subject><subject>Pepsin</subject><subject>Peptides</subject><subject>pH effects</subject><subject>Proteins</subject><subject>Scanning electron microscopy</subject><subject>Sodium lauryl sulfate</subject><subject>Spectrum 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Vitro Antioxidant and Antiaging Activities of Collagen and Its Hydrolysate from Mackerel Scad Skin (Decapterus macarellus)</title><author>Herawati, Elisa ; Akhsanitaqwim, Yochidamai ; Agnesia, Pipin ; Listyawati, Shanti ; Pangastuti, Artini ; Ratriyanto, Adi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-4e22be35bd65e962f6973c89fb9d83abb1db4918a70d8bf01ffbe526c8d34fe73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acetic acid</topic><topic>Aging</topic><topic>antiaging</topic><topic>antioxidant</topic><topic>Antioxidants</topic><topic>Collagen</topic><topic>Collagen (type I)</topic><topic>Collagen (type II)</topic><topic>Collagenase</topic><topic>Decapterus macarellus</topic><topic>Enzymes</topic><topic>Fish</topic><topic>Fish skin</topic><topic>Fourier analysis</topic><topic>Fourier transforms</topic><topic>Gel electrophoresis</topic><topic>Hydrolysates</topic><topic>hydrolyzed collagen</topic><topic>Infrared analysis</topic><topic>Levodopa</topic><topic>Low income groups</topic><topic>Mackerel</topic><topic>mackerel scad skin</topic><topic>Marine fishes</topic><topic>Molecular weight</topic><topic>Morphology</topic><topic>Pepsin</topic><topic>Peptides</topic><topic>pH effects</topic><topic>Proteins</topic><topic>Scanning electron microscopy</topic><topic>Sodium lauryl sulfate</topic><topic>Spectrum analysis</topic><topic>Substrates</topic><topic>Tuna</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Herawati, Elisa</creatorcontrib><creatorcontrib>Akhsanitaqwim, Yochidamai</creatorcontrib><creatorcontrib>Agnesia, Pipin</creatorcontrib><creatorcontrib>Listyawati, Shanti</creatorcontrib><creatorcontrib>Pangastuti, Artini</creatorcontrib><creatorcontrib>Ratriyanto, Adi</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central 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Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herawati, Elisa</au><au>Akhsanitaqwim, Yochidamai</au><au>Agnesia, Pipin</au><au>Listyawati, Shanti</au><au>Pangastuti, Artini</au><au>Ratriyanto, Adi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vitro Antioxidant and Antiaging Activities of Collagen and Its Hydrolysate from Mackerel Scad Skin (Decapterus macarellus)</atitle><jtitle>Marine drugs</jtitle><date>2022-08-13</date><risdate>2022</risdate><volume>20</volume><issue>8</issue><spage>516</spage><pages>516-</pages><issn>1660-3397</issn><eissn>1660-3397</eissn><abstract>The skin of mackerel scad fish (Decapterus macarellus) is a new source for pepsin-soluble collagen and its hydrolysate, both of which have never been explored. This study aims to characterize and determine the in vitro antioxidant, antiglycation, and antityrosinase activity of pepsin-soluble collagen (PSC) and hydrolyzed collagen (HC) from mackerel scad skin. PSC was extracted using 0.5 M acetic acid containing 0.1% pepsin for 48 h at 4 °C. The obtained PSC was then hydrolyzed with collagenase type II (6250 U/g) to produce HC. The PSC yield obtained was 6.39 ± 0.97%, with a pH of 6.76 ± 0.18, while the HC yield was 96% from PSC. SDS-PAGE and Fourier Transform Infrared (FTIR) analysis showed the typical features of type I collagen. HC demonstrated high solubility (66.75–100%) throughout the entire pH range (1–10). The PSC and HC from mackerel scad skin showed antioxidant activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH), with IC50 values of 148.55 ± 3.14 ppm and 34.966 ± 0.518 ppm, respectively. In the antiglycation test, PSC had an IC50 value of 239.29 ± 15.67 ppm, while HC had an IC50 of 68.43 ± 0.44 ppm. PSC also exhibited antityrosinase activity, with IC50 values of 234.66 ± 0.185 ppm (on the L-DOPA substrate), while HC had an IC50 value of 79.35 ± 0.5 ppm. Taken together, these results suggest that the skin of mackerel scad fish has potential antiaging properties and can be further developed for pharmaceutical and cosmetic purposes.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>36005519</pmid><doi>10.3390/md20080516</doi><orcidid>https://orcid.org/0000-0002-3162-9261</orcidid><orcidid>https://orcid.org/0000-0001-9656-9135</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetic acid Aging antiaging antioxidant Antioxidants Collagen Collagen (type I) Collagen (type II) Collagenase Decapterus macarellus Enzymes Fish Fish skin Fourier analysis Fourier transforms Gel electrophoresis Hydrolysates hydrolyzed collagen Infrared analysis Levodopa Low income groups Mackerel mackerel scad skin Marine fishes Molecular weight Morphology Pepsin Peptides pH effects Proteins Scanning electron microscopy Sodium lauryl sulfate Spectrum analysis Substrates Tuna |
title | In Vitro Antioxidant and Antiaging Activities of Collagen and Its Hydrolysate from Mackerel Scad Skin (Decapterus macarellus) |
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