Preclinical and clinical studies to evaluate cutaneous biodistribution, safety and efficacy of UV filters encapsulated in mesoporous silica SBA-15
[Display omitted] Innovative technologies have been designed to improve efficacy and safety of chemical UV filters. Encapsulation can enhance efficacy and reduce transdermal permeation and systemic exposure. The aims of this work were (i) to determine the cutaneous biodistribution of avobenzone (AVO...
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Veröffentlicht in: | European journal of pharmaceutics and biopharmaceutics 2021-12, Vol.169, p.113-124 |
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container_title | European journal of pharmaceutics and biopharmaceutics |
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creator | Daneluti, André Luis Máximo Guerra, Lucas Offenbecker Velasco, Maria Valéria Robles do Rosário Matos, Jivaldo Baby, André Rolim Kalia, Yogeshvar N. |
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Innovative technologies have been designed to improve efficacy and safety of chemical UV filters. Encapsulation can enhance efficacy and reduce transdermal permeation and systemic exposure. The aims of this work were (i) to determine the cutaneous biodistribution of avobenzone (AVO), oxybenzone (OXY), and octyl methoxycinnamate (OMC) incorporated in mesoporous silica SBA-15 and (ii) to perform preclinical (in vitro) and (iii) clinical safety studies to demonstrate their innocuity and to evaluate sun protection factor (SPF) in humans. Skin penetration studies showed that deposition of OXY and AVO in porcine and human skin after application of stick formulation with incorporated filters (stick incorporated filters) was significantly lower than from a marketed (non-encapsulated) stick. Cutaneous deposition and transdermal permeation of OXY in and across human skin were 3.8-and 13.4- fold lower, respectively, after application of stick entrapped filters. Biodistribution results showed that encapsulation in SBA-15 decreased AVO and OXY penetration reaching porcine and human dermis. Greater deposition (and permeation) of OXY in porcine skin than in human skin, pointed to the role of follicular transport. Stick incorporated filters had good biocompatibility in vivo and safety profiles, even under sun-exposed conditions. Entrapment of UV filters improved the SPF by 26% and produced the same SPF profile as a marketed stick. Overall, the results showed that SBA-15 enabled safety and efficacy of UV filters to be increased. |
doi_str_mv | 10.1016/j.ejpb.2021.10.002 |
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Innovative technologies have been designed to improve efficacy and safety of chemical UV filters. Encapsulation can enhance efficacy and reduce transdermal permeation and systemic exposure. The aims of this work were (i) to determine the cutaneous biodistribution of avobenzone (AVO), oxybenzone (OXY), and octyl methoxycinnamate (OMC) incorporated in mesoporous silica SBA-15 and (ii) to perform preclinical (in vitro) and (iii) clinical safety studies to demonstrate their innocuity and to evaluate sun protection factor (SPF) in humans. Skin penetration studies showed that deposition of OXY and AVO in porcine and human skin after application of stick formulation with incorporated filters (stick incorporated filters) was significantly lower than from a marketed (non-encapsulated) stick. Cutaneous deposition and transdermal permeation of OXY in and across human skin were 3.8-and 13.4- fold lower, respectively, after application of stick entrapped filters. Biodistribution results showed that encapsulation in SBA-15 decreased AVO and OXY penetration reaching porcine and human dermis. Greater deposition (and permeation) of OXY in porcine skin than in human skin, pointed to the role of follicular transport. Stick incorporated filters had good biocompatibility in vivo and safety profiles, even under sun-exposed conditions. Entrapment of UV filters improved the SPF by 26% and produced the same SPF profile as a marketed stick. Overall, the results showed that SBA-15 enabled safety and efficacy of UV filters to be increased.</description><identifier>ISSN: 0939-6411</identifier><identifier>EISSN: 1873-3441</identifier><identifier>DOI: 10.1016/j.ejpb.2021.10.002</identifier><identifier>PMID: 34637918</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Administration, Cutaneous ; Animals ; Avobenzone ; Benzophenones - pharmacokinetics ; Biodistribution ; Cinnamates - pharmacokinetics ; Clinical safety ; Drug Compounding - methods ; Drug Evaluation, Preclinical ; Human skin ; Humans ; In vivo SPF ; Mesoporous silica ; Micropore Filters ; Octyl methoxycinnamate ; Oxybenzone ; Propiophenones - pharmacokinetics ; SBA-15 ; Silicon Dioxide - pharmacology ; Skin Absorption ; Stick incorporated UV filters ; Sun Protection Factor ; Sunscreening Agents - pharmacokinetics ; Swine ; Tissue Distribution</subject><ispartof>European journal of pharmaceutics and biopharmaceutics, 2021-12, Vol.169, p.113-124</ispartof><rights>2021 The Author(s)</rights><rights>Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-b15e55949eb457b7d74624771da91e02f972a256eeb8896cfa5893d16f26a4fd3</citedby><cites>FETCH-LOGICAL-c400t-b15e55949eb457b7d74624771da91e02f972a256eeb8896cfa5893d16f26a4fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejpb.2021.10.002$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34637918$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Daneluti, André Luis Máximo</creatorcontrib><creatorcontrib>Guerra, Lucas Offenbecker</creatorcontrib><creatorcontrib>Velasco, Maria Valéria Robles</creatorcontrib><creatorcontrib>do Rosário Matos, Jivaldo</creatorcontrib><creatorcontrib>Baby, André Rolim</creatorcontrib><creatorcontrib>Kalia, Yogeshvar N.</creatorcontrib><title>Preclinical and clinical studies to evaluate cutaneous biodistribution, safety and efficacy of UV filters encapsulated in mesoporous silica SBA-15</title><title>European journal of pharmaceutics and biopharmaceutics</title><addtitle>Eur J Pharm Biopharm</addtitle><description>[Display omitted]
Innovative technologies have been designed to improve efficacy and safety of chemical UV filters. Encapsulation can enhance efficacy and reduce transdermal permeation and systemic exposure. The aims of this work were (i) to determine the cutaneous biodistribution of avobenzone (AVO), oxybenzone (OXY), and octyl methoxycinnamate (OMC) incorporated in mesoporous silica SBA-15 and (ii) to perform preclinical (in vitro) and (iii) clinical safety studies to demonstrate their innocuity and to evaluate sun protection factor (SPF) in humans. Skin penetration studies showed that deposition of OXY and AVO in porcine and human skin after application of stick formulation with incorporated filters (stick incorporated filters) was significantly lower than from a marketed (non-encapsulated) stick. Cutaneous deposition and transdermal permeation of OXY in and across human skin were 3.8-and 13.4- fold lower, respectively, after application of stick entrapped filters. Biodistribution results showed that encapsulation in SBA-15 decreased AVO and OXY penetration reaching porcine and human dermis. Greater deposition (and permeation) of OXY in porcine skin than in human skin, pointed to the role of follicular transport. Stick incorporated filters had good biocompatibility in vivo and safety profiles, even under sun-exposed conditions. Entrapment of UV filters improved the SPF by 26% and produced the same SPF profile as a marketed stick. Overall, the results showed that SBA-15 enabled safety and efficacy of UV filters to be increased.</description><subject>Administration, Cutaneous</subject><subject>Animals</subject><subject>Avobenzone</subject><subject>Benzophenones - pharmacokinetics</subject><subject>Biodistribution</subject><subject>Cinnamates - pharmacokinetics</subject><subject>Clinical safety</subject><subject>Drug Compounding - methods</subject><subject>Drug Evaluation, Preclinical</subject><subject>Human skin</subject><subject>Humans</subject><subject>In vivo SPF</subject><subject>Mesoporous silica</subject><subject>Micropore Filters</subject><subject>Octyl methoxycinnamate</subject><subject>Oxybenzone</subject><subject>Propiophenones - pharmacokinetics</subject><subject>SBA-15</subject><subject>Silicon Dioxide - pharmacology</subject><subject>Skin Absorption</subject><subject>Stick incorporated UV filters</subject><subject>Sun Protection Factor</subject><subject>Sunscreening Agents - pharmacokinetics</subject><subject>Swine</subject><subject>Tissue Distribution</subject><issn>0939-6411</issn><issn>1873-3441</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2OFCEURonROO3oC7gwLF1YLVBQFImbceJfMokmOm4JBZeEDl2UQE3Sr-ETS9njLF0Rbr7vJPcehF5SsqeEDm8Pezgs054RRttgTwh7hHZ0lH3Xc04fox1RveoGTukFelbKgRDCpRifooueD71UdNyh398y2BjmYE3EZnb44VPq6gIUXBOGOxNXUwHbtZoZ0lrwFJILpeYwrTWk-Q0uxkM9_UWA941gTzh5fPsT-xAr5IJhtmYpa2wgh8OMj1DSkvJGKyG2Bv7-_qqj4jl64k0s8OL-vUS3Hz_8uP7c3Xz99OX66qaznJDaTVSAEIormLiQk3SSD4xLSZ1RFAjzSjLDxAAwjaMarDdiVL2jg2eD4d71l-j1mbvk9GuFUvUxFAsxnlfUTIx0JHzkrEXZOWpzKiWD10sOR5NPmhK9udAHvbnQm4tt1ly00qt7_jodwT1U_h2_Bd6dA9C2vAuQdbGhXQlcaFKqdin8j_8HdWqctA</recordid><startdate>202112</startdate><enddate>202112</enddate><creator>Daneluti, André Luis Máximo</creator><creator>Guerra, Lucas Offenbecker</creator><creator>Velasco, Maria Valéria Robles</creator><creator>do Rosário Matos, Jivaldo</creator><creator>Baby, André Rolim</creator><creator>Kalia, Yogeshvar N.</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope></search><sort><creationdate>202112</creationdate><title>Preclinical and clinical studies to evaluate cutaneous biodistribution, safety and efficacy of UV filters encapsulated in mesoporous silica SBA-15</title><author>Daneluti, André Luis Máximo ; Guerra, Lucas Offenbecker ; Velasco, Maria Valéria Robles ; do Rosário Matos, Jivaldo ; Baby, André Rolim ; Kalia, Yogeshvar N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-b15e55949eb457b7d74624771da91e02f972a256eeb8896cfa5893d16f26a4fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Administration, Cutaneous</topic><topic>Animals</topic><topic>Avobenzone</topic><topic>Benzophenones - pharmacokinetics</topic><topic>Biodistribution</topic><topic>Cinnamates - pharmacokinetics</topic><topic>Clinical safety</topic><topic>Drug Compounding - methods</topic><topic>Drug Evaluation, Preclinical</topic><topic>Human skin</topic><topic>Humans</topic><topic>In vivo SPF</topic><topic>Mesoporous silica</topic><topic>Micropore Filters</topic><topic>Octyl methoxycinnamate</topic><topic>Oxybenzone</topic><topic>Propiophenones - pharmacokinetics</topic><topic>SBA-15</topic><topic>Silicon Dioxide - pharmacology</topic><topic>Skin Absorption</topic><topic>Stick incorporated UV filters</topic><topic>Sun Protection Factor</topic><topic>Sunscreening Agents - pharmacokinetics</topic><topic>Swine</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Daneluti, André Luis Máximo</creatorcontrib><creatorcontrib>Guerra, Lucas Offenbecker</creatorcontrib><creatorcontrib>Velasco, Maria Valéria Robles</creatorcontrib><creatorcontrib>do Rosário Matos, Jivaldo</creatorcontrib><creatorcontrib>Baby, André Rolim</creatorcontrib><creatorcontrib>Kalia, Yogeshvar N.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of pharmaceutics and biopharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Daneluti, André Luis Máximo</au><au>Guerra, Lucas Offenbecker</au><au>Velasco, Maria Valéria Robles</au><au>do Rosário Matos, Jivaldo</au><au>Baby, André Rolim</au><au>Kalia, Yogeshvar N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preclinical and clinical studies to evaluate cutaneous biodistribution, safety and efficacy of UV filters encapsulated in mesoporous silica SBA-15</atitle><jtitle>European journal of pharmaceutics and biopharmaceutics</jtitle><addtitle>Eur J Pharm Biopharm</addtitle><date>2021-12</date><risdate>2021</risdate><volume>169</volume><spage>113</spage><epage>124</epage><pages>113-124</pages><issn>0939-6411</issn><eissn>1873-3441</eissn><abstract>[Display omitted]
Innovative technologies have been designed to improve efficacy and safety of chemical UV filters. Encapsulation can enhance efficacy and reduce transdermal permeation and systemic exposure. The aims of this work were (i) to determine the cutaneous biodistribution of avobenzone (AVO), oxybenzone (OXY), and octyl methoxycinnamate (OMC) incorporated in mesoporous silica SBA-15 and (ii) to perform preclinical (in vitro) and (iii) clinical safety studies to demonstrate their innocuity and to evaluate sun protection factor (SPF) in humans. Skin penetration studies showed that deposition of OXY and AVO in porcine and human skin after application of stick formulation with incorporated filters (stick incorporated filters) was significantly lower than from a marketed (non-encapsulated) stick. Cutaneous deposition and transdermal permeation of OXY in and across human skin were 3.8-and 13.4- fold lower, respectively, after application of stick entrapped filters. Biodistribution results showed that encapsulation in SBA-15 decreased AVO and OXY penetration reaching porcine and human dermis. Greater deposition (and permeation) of OXY in porcine skin than in human skin, pointed to the role of follicular transport. Stick incorporated filters had good biocompatibility in vivo and safety profiles, even under sun-exposed conditions. Entrapment of UV filters improved the SPF by 26% and produced the same SPF profile as a marketed stick. Overall, the results showed that SBA-15 enabled safety and efficacy of UV filters to be increased.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34637918</pmid><doi>10.1016/j.ejpb.2021.10.002</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Cutaneous Animals Avobenzone Benzophenones - pharmacokinetics Biodistribution Cinnamates - pharmacokinetics Clinical safety Drug Compounding - methods Drug Evaluation, Preclinical Human skin Humans In vivo SPF Mesoporous silica Micropore Filters Octyl methoxycinnamate Oxybenzone Propiophenones - pharmacokinetics SBA-15 Silicon Dioxide - pharmacology Skin Absorption Stick incorporated UV filters Sun Protection Factor Sunscreening Agents - pharmacokinetics Swine Tissue Distribution |
title | Preclinical and clinical studies to evaluate cutaneous biodistribution, safety and efficacy of UV filters encapsulated in mesoporous silica SBA-15 |
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