Optical Spectroscopy of Hydrophobic Sunscreen Molecules Adsorbed to Dielectric Nanospheres
Fluorescence and absorption spectra of hydrophobic sunscreens, weakly fluorescent octyl methoxycinnamate, moderately fluorescent octyl salicylate and highly fluorescent 2-ethylhexyl-4-(dimethylamino)benzoate (padimate O) adsorbed to dielectric microspheres in aqueous suspension, have been compared w...
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Veröffentlicht in: | Photochemistry and photobiology 2004-06, Vol.79 (6), p.531-539 |
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description | Fluorescence and absorption spectra of hydrophobic sunscreens, weakly fluorescent octyl methoxycinnamate, moderately fluorescent octyl salicylate and highly fluorescent 2-ethylhexyl-4-(dimethylamino)benzoate (padimate O) adsorbed to dielectric microspheres in aqueous suspension, have been compared with spectra in organic solution. The fluorescence of adsorbed salicylate and padimate is enhanced compared with fluorescence in methanol: about a factor of 6 and 30 in terms of fluorescence yield per molecule of salicylate and padimate, respectively. Cinnamate, which has a low fluorescence yield, does not show a comparable fluorescence enhancement. The fluorescence amplification is independent of sphere diameter from 30 to 1500 nm, at least for salicylate. The enhancement, as well as the location of absorption spectral peaks, is consistent with a low–dielectric constant environment of the molecules, in spite of the presumed location near the interface between polystyrene (ϵ = 2.4–3.8) and water (ϵ = 78). The adsorbed state of these sunscreens represents a proposed improved in vitro model for the environment of sunscreens in vivo, as well as a general model for chromophores in heterogeneous environments. |
doi_str_mv | 10.1562/2004-01-05-RA.1 |
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The fluorescence of adsorbed salicylate and padimate is enhanced compared with fluorescence in methanol: about a factor of 6 and 30 in terms of fluorescence yield per molecule of salicylate and padimate, respectively. Cinnamate, which has a low fluorescence yield, does not show a comparable fluorescence enhancement. The fluorescence amplification is independent of sphere diameter from 30 to 1500 nm, at least for salicylate. The enhancement, as well as the location of absorption spectral peaks, is consistent with a low–dielectric constant environment of the molecules, in spite of the presumed location near the interface between polystyrene (ϵ = 2.4–3.8) and water (ϵ = 78). The adsorbed state of these sunscreens represents a proposed improved in vitro model for the environment of sunscreens in vivo, as well as a general model for chromophores in heterogeneous environments.</description><identifier>ISSN: 0031-8655</identifier><identifier>EISSN: 1751-1097</identifier><identifier>DOI: 10.1562/2004-01-05-RA.1</identifier><identifier>PMID: 15291305</identifier><identifier>CODEN: PHCBAP</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>4-Aminobenzoic Acid - chemistry ; Absorption ; Adsorption ; Cinnamates - chemistry ; Hydrophobic and Hydrophilic Interactions ; Microspheres ; Molecular Structure ; Nanotechnology ; para-Aminobenzoates ; Particle Size ; Research s ; Salicylates - chemistry ; Solutions - chemistry ; Spectrometry, Fluorescence ; Sunscreening Agents - chemistry ; Water - chemistry</subject><ispartof>Photochemistry and photobiology, 2004-06, Vol.79 (6), p.531-539</ispartof><rights>American Society for Photobiology</rights><rights>Copyright American Society of Photobiology Jun 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b358t-7219da753341256c17a8112c6061bc98ee8094ce97548a4f47628f021794202c3</citedby><cites>FETCH-LOGICAL-b358t-7219da753341256c17a8112c6061bc98ee8094ce97548a4f47628f021794202c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bioone.org/doi/pdf/10.1562/2004-01-05-RA.1$$EPDF$$P50$$Gbioone$$H</linktopdf><link.rule.ids>314,780,784,26978,27924,27925,52363</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15291305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krishnan, Rajagopal</creatorcontrib><creatorcontrib>Carr, Aaron</creatorcontrib><creatorcontrib>Blair, Elizabeth</creatorcontrib><creatorcontrib>Nordlund, Thomas M.</creatorcontrib><title>Optical Spectroscopy of Hydrophobic Sunscreen Molecules Adsorbed to Dielectric Nanospheres</title><title>Photochemistry and photobiology</title><addtitle>Photochem Photobiol</addtitle><description>Fluorescence and absorption spectra of hydrophobic sunscreens, weakly fluorescent octyl methoxycinnamate, moderately fluorescent octyl salicylate and highly fluorescent 2-ethylhexyl-4-(dimethylamino)benzoate (padimate O) adsorbed to dielectric microspheres in aqueous suspension, have been compared with spectra in organic solution. The fluorescence of adsorbed salicylate and padimate is enhanced compared with fluorescence in methanol: about a factor of 6 and 30 in terms of fluorescence yield per molecule of salicylate and padimate, respectively. Cinnamate, which has a low fluorescence yield, does not show a comparable fluorescence enhancement. The fluorescence amplification is independent of sphere diameter from 30 to 1500 nm, at least for salicylate. The enhancement, as well as the location of absorption spectral peaks, is consistent with a low–dielectric constant environment of the molecules, in spite of the presumed location near the interface between polystyrene (ϵ = 2.4–3.8) and water (ϵ = 78). The adsorbed state of these sunscreens represents a proposed improved in vitro model for the environment of sunscreens in vivo, as well as a general model for chromophores in heterogeneous environments.</description><subject>4-Aminobenzoic Acid - chemistry</subject><subject>Absorption</subject><subject>Adsorption</subject><subject>Cinnamates - chemistry</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Microspheres</subject><subject>Molecular Structure</subject><subject>Nanotechnology</subject><subject>para-Aminobenzoates</subject><subject>Particle Size</subject><subject>Research s</subject><subject>Salicylates - chemistry</subject><subject>Solutions - chemistry</subject><subject>Spectrometry, Fluorescence</subject><subject>Sunscreening Agents - chemistry</subject><subject>Water - chemistry</subject><issn>0031-8655</issn><issn>1751-1097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqF0L1P3EAQBfBVlCgcJHW6yEqRbmFmvR_e8gQEkCBIkDRpVvZ6LIx8XrNrF_ffZ093EhIN1TS_eXp6jH1DOEWlxZkAkByQg-IP61P8wFZoFHIEaz6yFUCJvNJKHbHjlJ4BUFqDn9kRKmGxBLVi_-6nuff1UDxO5OcYkg_Ttghdcb1tY5ieQtP74nEZk49EY3EXBvLLQKlYtynEhtpiDsVFT8PuO9Pf9RjS9ESR0hf2qauHRF8P94T9_XX55_ya395f3Zyvb3lTqmrmRqBta6PKUqJQ2qOpK0ThNWhsvK2IKrDSkzVKVrXspNGi6kCgsVKA8OUJ-7nPnWJ4WSjNbtMnT8NQjxSW5LQ2WprKZvjjDXwOSxxzNyfKXENlmdHZHvk8RorUuSn2mzpuHYLbbe52mztAB8o9rB3mj--H2KXZUPvqDyNnwPeg6UMY6d3A_-PMiO8</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>Krishnan, Rajagopal</creator><creator>Carr, Aaron</creator><creator>Blair, Elizabeth</creator><creator>Nordlund, Thomas M.</creator><general>Blackwell Publishing Ltd</general><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>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7TM</scope><scope>7U7</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20040601</creationdate><title>Optical Spectroscopy of Hydrophobic Sunscreen Molecules Adsorbed to Dielectric Nanospheres</title><author>Krishnan, Rajagopal ; Carr, Aaron ; Blair, Elizabeth ; Nordlund, Thomas M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b358t-7219da753341256c17a8112c6061bc98ee8094ce97548a4f47628f021794202c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>4-Aminobenzoic Acid - chemistry</topic><topic>Absorption</topic><topic>Adsorption</topic><topic>Cinnamates - chemistry</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Microspheres</topic><topic>Molecular Structure</topic><topic>Nanotechnology</topic><topic>para-Aminobenzoates</topic><topic>Particle Size</topic><topic>Research s</topic><topic>Salicylates - chemistry</topic><topic>Solutions - chemistry</topic><topic>Spectrometry, Fluorescence</topic><topic>Sunscreening Agents - chemistry</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krishnan, Rajagopal</creatorcontrib><creatorcontrib>Carr, Aaron</creatorcontrib><creatorcontrib>Blair, Elizabeth</creatorcontrib><creatorcontrib>Nordlund, Thomas M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Nursing & Allied Health Database</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Photochemistry and photobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krishnan, Rajagopal</au><au>Carr, Aaron</au><au>Blair, Elizabeth</au><au>Nordlund, Thomas M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optical Spectroscopy of Hydrophobic Sunscreen Molecules Adsorbed to Dielectric Nanospheres</atitle><jtitle>Photochemistry and photobiology</jtitle><addtitle>Photochem Photobiol</addtitle><date>2004-06-01</date><risdate>2004</risdate><volume>79</volume><issue>6</issue><spage>531</spage><epage>539</epage><pages>531-539</pages><issn>0031-8655</issn><eissn>1751-1097</eissn><coden>PHCBAP</coden><abstract>Fluorescence and absorption spectra of hydrophobic sunscreens, weakly fluorescent octyl methoxycinnamate, moderately fluorescent octyl salicylate and highly fluorescent 2-ethylhexyl-4-(dimethylamino)benzoate (padimate O) adsorbed to dielectric microspheres in aqueous suspension, have been compared with spectra in organic solution. The fluorescence of adsorbed salicylate and padimate is enhanced compared with fluorescence in methanol: about a factor of 6 and 30 in terms of fluorescence yield per molecule of salicylate and padimate, respectively. Cinnamate, which has a low fluorescence yield, does not show a comparable fluorescence enhancement. The fluorescence amplification is independent of sphere diameter from 30 to 1500 nm, at least for salicylate. The enhancement, as well as the location of absorption spectral peaks, is consistent with a low–dielectric constant environment of the molecules, in spite of the presumed location near the interface between polystyrene (ϵ = 2.4–3.8) and water (ϵ = 78). The adsorbed state of these sunscreens represents a proposed improved in vitro model for the environment of sunscreens in vivo, as well as a general model for chromophores in heterogeneous environments.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>15291305</pmid><doi>10.1562/2004-01-05-RA.1</doi><tpages>9</tpages></addata></record> |
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subjects | 4-Aminobenzoic Acid - chemistry Absorption Adsorption Cinnamates - chemistry Hydrophobic and Hydrophilic Interactions Microspheres Molecular Structure Nanotechnology para-Aminobenzoates Particle Size Research s Salicylates - chemistry Solutions - chemistry Spectrometry, Fluorescence Sunscreening Agents - chemistry Water - chemistry |
title | Optical Spectroscopy of Hydrophobic Sunscreen Molecules Adsorbed to Dielectric Nanospheres |
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