Enzymatically modified isoquercitrin and its protective effects against photoaging: In-vitro and clinical studies
This research examines the anti-aging potential of the flavonoid derivative of isoquercitrin known as enzymatically modified isoquercitrin (EMIQ). Initial HPLC analyses showed that EMIQ used in the study contained 1-12 glucosides and 10.7% pentahydroxyflavonoids, promising potent antioxidant propert...
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Veröffentlicht in: | Photochemistry and photobiology 2024-09, Vol.100 (5), p.1475-1488 |
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description | This research examines the anti-aging potential of the flavonoid derivative of isoquercitrin known as enzymatically modified isoquercitrin (EMIQ). Initial HPLC analyses showed that EMIQ used in the study contained 1-12 glucosides and 10.7% pentahydroxyflavonoids, promising potent antioxidant properties. In subsequent in-vitro studies with UVA-exposed human dermal fibroblasts (HDFa), EMIQ demonstrated protective properties by reducing collagen damage. It modulated both the TGFβ/Smad pathway and the MMP1 pathway, contributing to collagen preservation. This protective effect was further confirmed using the T-Skin™ model, a reconstructed full-thickness human skin model, which illustrated that EMIQ could defend the physiological structures of both the epidermis and dermis against UV radiation. A 28-day clinical trial with 30 volunteers aged 31-55 years highlighted EMIQ's effectiveness. Participants using EMIQ-containing Essence displayed reduced facial trans-epidermal water loss and skin roughness, alongside improved skin elasticity. This study emphasizes EMIQ's potential as an anti-photoaging ingredient in cosmetics, warranting further research. The findings pave the way for developing innovative skincare products addressing photoaging effects. |
doi_str_mv | 10.1111/php.13891 |
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Initial HPLC analyses showed that EMIQ used in the study contained 1-12 glucosides and 10.7% pentahydroxyflavonoids, promising potent antioxidant properties. In subsequent in-vitro studies with UVA-exposed human dermal fibroblasts (HDFa), EMIQ demonstrated protective properties by reducing collagen damage. It modulated both the TGFβ/Smad pathway and the MMP1 pathway, contributing to collagen preservation. This protective effect was further confirmed using the T-Skin™ model, a reconstructed full-thickness human skin model, which illustrated that EMIQ could defend the physiological structures of both the epidermis and dermis against UV radiation. A 28-day clinical trial with 30 volunteers aged 31-55 years highlighted EMIQ's effectiveness. Participants using EMIQ-containing Essence displayed reduced facial trans-epidermal water loss and skin roughness, alongside improved skin elasticity. This study emphasizes EMIQ's potential as an anti-photoaging ingredient in cosmetics, warranting further research. The findings pave the way for developing innovative skincare products addressing photoaging effects.</description><identifier>ISSN: 0031-8655</identifier><identifier>ISSN: 1751-1097</identifier><identifier>EISSN: 1751-1097</identifier><identifier>DOI: 10.1111/php.13891</identifier><identifier>PMID: 38185856</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Collagen ; Cosmetics ; Dermis ; Epidermis ; Flavonoids ; Glucosides ; Physiological effects ; Radiation damage ; Skin ; Smad protein ; Thickness ; Ultraviolet radiation ; Water loss</subject><ispartof>Photochemistry and photobiology, 2024-09, Vol.100 (5), p.1475-1488</ispartof><rights>2024 American Society for Photobiology.</rights><rights>Copyright © 2024 American Society for Photobiology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c273t-47ffa12b4f8a3f58daae3b6e8b810787a8187868419d063d7a547cfc7562749f3</cites><orcidid>0000-0001-9748-087X ; 0009-0009-2208-7462</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38185856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bai, Xue-Dong</creatorcontrib><creatorcontrib>Fei, Wei-Cheng</creatorcontrib><creatorcontrib>Liu, Yu-Chen</creatorcontrib><creatorcontrib>Yang, Sheng-Ping</creatorcontrib><title>Enzymatically modified isoquercitrin and its protective effects against photoaging: In-vitro and clinical studies</title><title>Photochemistry and photobiology</title><addtitle>Photochem Photobiol</addtitle><description>This research examines the anti-aging potential of the flavonoid derivative of isoquercitrin known as enzymatically modified isoquercitrin (EMIQ). Initial HPLC analyses showed that EMIQ used in the study contained 1-12 glucosides and 10.7% pentahydroxyflavonoids, promising potent antioxidant properties. In subsequent in-vitro studies with UVA-exposed human dermal fibroblasts (HDFa), EMIQ demonstrated protective properties by reducing collagen damage. It modulated both the TGFβ/Smad pathway and the MMP1 pathway, contributing to collagen preservation. This protective effect was further confirmed using the T-Skin™ model, a reconstructed full-thickness human skin model, which illustrated that EMIQ could defend the physiological structures of both the epidermis and dermis against UV radiation. A 28-day clinical trial with 30 volunteers aged 31-55 years highlighted EMIQ's effectiveness. Participants using EMIQ-containing Essence displayed reduced facial trans-epidermal water loss and skin roughness, alongside improved skin elasticity. This study emphasizes EMIQ's potential as an anti-photoaging ingredient in cosmetics, warranting further research. The findings pave the way for developing innovative skincare products addressing photoaging effects.</description><subject>Collagen</subject><subject>Cosmetics</subject><subject>Dermis</subject><subject>Epidermis</subject><subject>Flavonoids</subject><subject>Glucosides</subject><subject>Physiological effects</subject><subject>Radiation damage</subject><subject>Skin</subject><subject>Smad protein</subject><subject>Thickness</subject><subject>Ultraviolet radiation</subject><subject>Water loss</subject><issn>0031-8655</issn><issn>1751-1097</issn><issn>1751-1097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkU1PwzAMhiMEYuPjwB9AkbjAoSNe0iblhhBf0iQucK7SNBmZ2qQ0KdL49WRscMAXW9bjV7ZfhM6AzCDFdf_ez4CKEvbQFHgOGZCS76MpIRQyUeT5BB2FsCIEWMnhEE2oAJGLvJiij3v3te5ktEq27Rp3vrHG6gbb4D9GPSgbB-uwdKkTA-4HH7WK9lNjbUyqApZLaV2IuH_30culdcsb_OyyzzTof-ZUa91GHYc4NlaHE3RgZBv06S4fo7eH-9e7p2zx8vh8d7vI1JzTmDFujIR5zYyQ1OSikVLTutCiFkC44DKdwEUhGJQNKWjDZc64MornxZyz0tBjdLnVTUunU0KsOhuUblvptB9DNS8BBGNlKRJ68Q9d-XFwabuKAtl8ilGeqKstpQYfwqBN1Q-2k8O6AlJtfKiSD9WPD4k93ymOdaebP_L38fQbaNWEfA</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Bai, Xue-Dong</creator><creator>Fei, Wei-Cheng</creator><creator>Liu, Yu-Chen</creator><creator>Yang, Sheng-Ping</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9748-087X</orcidid><orcidid>https://orcid.org/0009-0009-2208-7462</orcidid></search><sort><creationdate>20240901</creationdate><title>Enzymatically modified isoquercitrin and its protective effects against photoaging: In-vitro and clinical studies</title><author>Bai, Xue-Dong ; Fei, Wei-Cheng ; Liu, Yu-Chen ; Yang, Sheng-Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c273t-47ffa12b4f8a3f58daae3b6e8b810787a8187868419d063d7a547cfc7562749f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Collagen</topic><topic>Cosmetics</topic><topic>Dermis</topic><topic>Epidermis</topic><topic>Flavonoids</topic><topic>Glucosides</topic><topic>Physiological effects</topic><topic>Radiation damage</topic><topic>Skin</topic><topic>Smad protein</topic><topic>Thickness</topic><topic>Ultraviolet radiation</topic><topic>Water loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bai, Xue-Dong</creatorcontrib><creatorcontrib>Fei, Wei-Cheng</creatorcontrib><creatorcontrib>Liu, Yu-Chen</creatorcontrib><creatorcontrib>Yang, Sheng-Ping</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Photochemistry and photobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bai, Xue-Dong</au><au>Fei, Wei-Cheng</au><au>Liu, Yu-Chen</au><au>Yang, Sheng-Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzymatically modified isoquercitrin and its protective effects against photoaging: In-vitro and clinical studies</atitle><jtitle>Photochemistry and photobiology</jtitle><addtitle>Photochem Photobiol</addtitle><date>2024-09-01</date><risdate>2024</risdate><volume>100</volume><issue>5</issue><spage>1475</spage><epage>1488</epage><pages>1475-1488</pages><issn>0031-8655</issn><issn>1751-1097</issn><eissn>1751-1097</eissn><abstract>This research examines the anti-aging potential of the flavonoid derivative of isoquercitrin known as enzymatically modified isoquercitrin (EMIQ). Initial HPLC analyses showed that EMIQ used in the study contained 1-12 glucosides and 10.7% pentahydroxyflavonoids, promising potent antioxidant properties. In subsequent in-vitro studies with UVA-exposed human dermal fibroblasts (HDFa), EMIQ demonstrated protective properties by reducing collagen damage. It modulated both the TGFβ/Smad pathway and the MMP1 pathway, contributing to collagen preservation. This protective effect was further confirmed using the T-Skin™ model, a reconstructed full-thickness human skin model, which illustrated that EMIQ could defend the physiological structures of both the epidermis and dermis against UV radiation. A 28-day clinical trial with 30 volunteers aged 31-55 years highlighted EMIQ's effectiveness. Participants using EMIQ-containing Essence displayed reduced facial trans-epidermal water loss and skin roughness, alongside improved skin elasticity. This study emphasizes EMIQ's potential as an anti-photoaging ingredient in cosmetics, warranting further research. The findings pave the way for developing innovative skincare products addressing photoaging effects.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>38185856</pmid><doi>10.1111/php.13891</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-9748-087X</orcidid><orcidid>https://orcid.org/0009-0009-2208-7462</orcidid></addata></record> |
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subjects | Collagen Cosmetics Dermis Epidermis Flavonoids Glucosides Physiological effects Radiation damage Skin Smad protein Thickness Ultraviolet radiation Water loss |
title | Enzymatically modified isoquercitrin and its protective effects against photoaging: In-vitro and clinical studies |
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