Topical Formulations Containing Pimenta pseudocaryophyllus Extract: In Vitro Antioxidant Activity and In Vivo Efficacy Against UV-B-Induced Oxidative Stress
Pimenta pseudocaryophyllus is a Brazilian native plant that presents high concentrations of flavonoids and other polyphenolic compounds. Herein, we evaluated: (1) the chemical properties of P. pseudocaryophyllus ethanolic extract (PPE), (2) the in vitro antioxidant activity (AA) of PPE and of two di...
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creator | Campanini, Marcela Z. Custódio, Dayana L. Ivan, Ana L. M. Martins, Sarah M. Paranzini, Maria J. R. Martinez, Renata M. Verri, Waldiceu A. Vicentini, Fabiana T. M. C. Arakawa, Nilton S. de J. Faria, Terezinha Baracat, Marcela M. Casagrande, Rúbia Georgetti, Sandra R. |
description | Pimenta pseudocaryophyllus
is a Brazilian native plant that presents high concentrations of flavonoids and other polyphenolic compounds. Herein, we evaluated: (1) the chemical properties of
P. pseudocaryophyllus
ethanolic extract (PPE), (2) the
in vitro
antioxidant activity (AA) of PPE and of two different topical formulations (F1 and F2) containing PPE, (3) physico-chemical and functional stability, (4)
in vitro
release of PPE, and (5)
in vivo
capacity of formulations to prevent UV-B irradiation-induced skin damage. Results show that the polyphenol and flavonoid contents in PPE were 199.33 and 28.32 mg/g, respectively, and HPLC results show the presence of eugenol, tannic acid, and rutin. Evaluation of the
in vitro
AA of PPE demonstrated a dose-dependent effect and an IC
50
of 4.75 μg/mL in 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 3.0 μg/mL in 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays. The ferric-reducing antioxidant power (FRAP assay) was 0.046 μmol/L trolox equivalent/μg/mL of extract. Among the AA, only the capacity to scavenge DPPH radical of PPE was maintained in F1 and F2. In addition, both formulations satisfactorily released the extract. The evaluation of the functional stability of F1 and F2 did not demonstrate loss of activity by storage at room temperature and at 4°C/6 months. In irradiated mice, treatment with F1 and F2 added with PPE significantly increased the capacity to scavenge ABTS radical and the FRAP of skin compared to vehicle-treated mice. In conclusion, the present results suggest that formulations containing PPE may be a topical source of antioxidant compounds to decrease oxidative damages of the skin. |
doi_str_mv | 10.1208/s12249-013-0049-8 |
format | Article |
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is a Brazilian native plant that presents high concentrations of flavonoids and other polyphenolic compounds. Herein, we evaluated: (1) the chemical properties of
P. pseudocaryophyllus
ethanolic extract (PPE), (2) the
in vitro
antioxidant activity (AA) of PPE and of two different topical formulations (F1 and F2) containing PPE, (3) physico-chemical and functional stability, (4)
in vitro
release of PPE, and (5)
in vivo
capacity of formulations to prevent UV-B irradiation-induced skin damage. Results show that the polyphenol and flavonoid contents in PPE were 199.33 and 28.32 mg/g, respectively, and HPLC results show the presence of eugenol, tannic acid, and rutin. Evaluation of the
in vitro
AA of PPE demonstrated a dose-dependent effect and an IC
50
of 4.75 μg/mL in 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 3.0 μg/mL in 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays. The ferric-reducing antioxidant power (FRAP assay) was 0.046 μmol/L trolox equivalent/μg/mL of extract. Among the AA, only the capacity to scavenge DPPH radical of PPE was maintained in F1 and F2. In addition, both formulations satisfactorily released the extract. The evaluation of the functional stability of F1 and F2 did not demonstrate loss of activity by storage at room temperature and at 4°C/6 months. In irradiated mice, treatment with F1 and F2 added with PPE significantly increased the capacity to scavenge ABTS radical and the FRAP of skin compared to vehicle-treated mice. In conclusion, the present results suggest that formulations containing PPE may be a topical source of antioxidant compounds to decrease oxidative damages of the skin.</description><identifier>ISSN: 1530-9932</identifier><identifier>EISSN: 1530-9932</identifier><identifier>DOI: 10.1208/s12249-013-0049-8</identifier><identifier>PMID: 24249253</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Animals ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Benzothiazoles - chemistry ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Biotechnology ; Biphenyl Compounds - chemistry ; Chemistry, Pharmaceutical - methods ; Ethanol - chemistry ; Mice ; Mice, Hairless ; Oxidative Stress - drug effects ; Pharmacology/Toxicology ; Pharmacy ; Phenols - chemistry ; Phenols - pharmacology ; Picrates - chemistry ; Pimenta ; Pimenta - chemistry ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Research Article ; Skin - drug effects ; Sulfonic Acids - chemistry ; Ultraviolet Rays - adverse effects</subject><ispartof>AAPS PharmSciTech, 2014-02, Vol.15 (1), p.86-95</ispartof><rights>American Association of Pharmaceutical Scientists 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-c54da09814cfa2002a1b98de87396ea82edbc47088f1ccb00025f14a711727d33</citedby><cites>FETCH-LOGICAL-c475t-c54da09814cfa2002a1b98de87396ea82edbc47088f1ccb00025f14a711727d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909169/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909169/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24249253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Campanini, Marcela Z.</creatorcontrib><creatorcontrib>Custódio, Dayana L.</creatorcontrib><creatorcontrib>Ivan, Ana L. M.</creatorcontrib><creatorcontrib>Martins, Sarah M.</creatorcontrib><creatorcontrib>Paranzini, Maria J. R.</creatorcontrib><creatorcontrib>Martinez, Renata M.</creatorcontrib><creatorcontrib>Verri, Waldiceu A.</creatorcontrib><creatorcontrib>Vicentini, Fabiana T. M. C.</creatorcontrib><creatorcontrib>Arakawa, Nilton S.</creatorcontrib><creatorcontrib>de J. Faria, Terezinha</creatorcontrib><creatorcontrib>Baracat, Marcela M.</creatorcontrib><creatorcontrib>Casagrande, Rúbia</creatorcontrib><creatorcontrib>Georgetti, Sandra R.</creatorcontrib><title>Topical Formulations Containing Pimenta pseudocaryophyllus Extract: In Vitro Antioxidant Activity and In Vivo Efficacy Against UV-B-Induced Oxidative Stress</title><title>AAPS PharmSciTech</title><addtitle>AAPS PharmSciTech</addtitle><addtitle>AAPS PharmSciTech</addtitle><description>Pimenta pseudocaryophyllus
is a Brazilian native plant that presents high concentrations of flavonoids and other polyphenolic compounds. Herein, we evaluated: (1) the chemical properties of
P. pseudocaryophyllus
ethanolic extract (PPE), (2) the
in vitro
antioxidant activity (AA) of PPE and of two different topical formulations (F1 and F2) containing PPE, (3) physico-chemical and functional stability, (4)
in vitro
release of PPE, and (5)
in vivo
capacity of formulations to prevent UV-B irradiation-induced skin damage. Results show that the polyphenol and flavonoid contents in PPE were 199.33 and 28.32 mg/g, respectively, and HPLC results show the presence of eugenol, tannic acid, and rutin. Evaluation of the
in vitro
AA of PPE demonstrated a dose-dependent effect and an IC
50
of 4.75 μg/mL in 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 3.0 μg/mL in 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays. The ferric-reducing antioxidant power (FRAP assay) was 0.046 μmol/L trolox equivalent/μg/mL of extract. Among the AA, only the capacity to scavenge DPPH radical of PPE was maintained in F1 and F2. In addition, both formulations satisfactorily released the extract. The evaluation of the functional stability of F1 and F2 did not demonstrate loss of activity by storage at room temperature and at 4°C/6 months. In irradiated mice, treatment with F1 and F2 added with PPE significantly increased the capacity to scavenge ABTS radical and the FRAP of skin compared to vehicle-treated mice. In conclusion, the present results suggest that formulations containing PPE may be a topical source of antioxidant compounds to decrease oxidative damages of the skin.</description><subject>Animals</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Benzothiazoles - chemistry</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Biphenyl Compounds - chemistry</subject><subject>Chemistry, Pharmaceutical - methods</subject><subject>Ethanol - chemistry</subject><subject>Mice</subject><subject>Mice, Hairless</subject><subject>Oxidative Stress - drug effects</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Phenols - chemistry</subject><subject>Phenols - pharmacology</subject><subject>Picrates - chemistry</subject><subject>Pimenta</subject><subject>Pimenta - chemistry</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Research Article</subject><subject>Skin - drug effects</subject><subject>Sulfonic Acids - chemistry</subject><subject>Ultraviolet Rays - adverse effects</subject><issn>1530-9932</issn><issn>1530-9932</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1DAUhS0EoqXwAGyQl2xC_ZM0Nguk6WgKI1UqEm23lsd2pq4SO9jOqPMuPCx3lLYqG1a-1v3Oub4-CH2k5AtlRJxmylgtK0J5RQgU4hU6pg0nlZScvX5RH6F3Od8TwjiV_C06YjXoWMOP0Z_rOHqje3wR0zD1uvgYMl7GULQPPmzxTz84uOAxu8lGo9M-jnf7vp8yXj2UpE35itcB3_qSIl4E0D94q0PBC1P8zpc91sHOxC7iVdfBNLPHiy3454Jvbqvzah3sZJzFVwcpqBz-VZLL-T160-k-uw-P5wm6uVhdL39Ul1ff18vFZWXqtimVaWqriRS0Np1msKWmGymsEy2XZ04L5uwGSCJER43ZECCajta6pbRlreX8BH2bfcdpMzhrYOGkezUmP8C-Kmqv_u0Ef6e2cae4JJKeSTD4_GiQ4u_J5aIGn43rex1cnLKiDWWcSSJqQOmMmhRzTq57HkOJOqSq5lQVpKoOqSoBmk8v3_eseIoRADYDGVph65K6j1MK8Gf_cf0LMGuxGg</recordid><startdate>20140201</startdate><enddate>20140201</enddate><creator>Campanini, Marcela Z.</creator><creator>Custódio, Dayana L.</creator><creator>Ivan, Ana L. M.</creator><creator>Martins, Sarah M.</creator><creator>Paranzini, Maria J. R.</creator><creator>Martinez, Renata M.</creator><creator>Verri, Waldiceu A.</creator><creator>Vicentini, Fabiana T. M. C.</creator><creator>Arakawa, Nilton S.</creator><creator>de J. Faria, Terezinha</creator><creator>Baracat, Marcela M.</creator><creator>Casagrande, Rúbia</creator><creator>Georgetti, Sandra R.</creator><general>Springer US</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>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20140201</creationdate><title>Topical Formulations Containing Pimenta pseudocaryophyllus Extract: In Vitro Antioxidant Activity and In Vivo Efficacy Against UV-B-Induced Oxidative Stress</title><author>Campanini, Marcela Z. ; Custódio, Dayana L. ; Ivan, Ana L. M. ; Martins, Sarah M. ; Paranzini, Maria J. R. ; Martinez, Renata M. ; Verri, Waldiceu A. ; Vicentini, Fabiana T. M. C. ; Arakawa, Nilton S. ; de J. 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M.</creatorcontrib><creatorcontrib>Martins, Sarah M.</creatorcontrib><creatorcontrib>Paranzini, Maria J. R.</creatorcontrib><creatorcontrib>Martinez, Renata M.</creatorcontrib><creatorcontrib>Verri, Waldiceu A.</creatorcontrib><creatorcontrib>Vicentini, Fabiana T. M. C.</creatorcontrib><creatorcontrib>Arakawa, Nilton S.</creatorcontrib><creatorcontrib>de J. Faria, Terezinha</creatorcontrib><creatorcontrib>Baracat, Marcela M.</creatorcontrib><creatorcontrib>Casagrande, Rúbia</creatorcontrib><creatorcontrib>Georgetti, Sandra R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>AAPS PharmSciTech</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Campanini, Marcela Z.</au><au>Custódio, Dayana L.</au><au>Ivan, Ana L. M.</au><au>Martins, Sarah M.</au><au>Paranzini, Maria J. R.</au><au>Martinez, Renata M.</au><au>Verri, Waldiceu A.</au><au>Vicentini, Fabiana T. M. C.</au><au>Arakawa, Nilton S.</au><au>de J. Faria, Terezinha</au><au>Baracat, Marcela M.</au><au>Casagrande, Rúbia</au><au>Georgetti, Sandra R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Topical Formulations Containing Pimenta pseudocaryophyllus Extract: In Vitro Antioxidant Activity and In Vivo Efficacy Against UV-B-Induced Oxidative Stress</atitle><jtitle>AAPS PharmSciTech</jtitle><stitle>AAPS PharmSciTech</stitle><addtitle>AAPS PharmSciTech</addtitle><date>2014-02-01</date><risdate>2014</risdate><volume>15</volume><issue>1</issue><spage>86</spage><epage>95</epage><pages>86-95</pages><issn>1530-9932</issn><eissn>1530-9932</eissn><abstract>Pimenta pseudocaryophyllus
is a Brazilian native plant that presents high concentrations of flavonoids and other polyphenolic compounds. Herein, we evaluated: (1) the chemical properties of
P. pseudocaryophyllus
ethanolic extract (PPE), (2) the
in vitro
antioxidant activity (AA) of PPE and of two different topical formulations (F1 and F2) containing PPE, (3) physico-chemical and functional stability, (4)
in vitro
release of PPE, and (5)
in vivo
capacity of formulations to prevent UV-B irradiation-induced skin damage. Results show that the polyphenol and flavonoid contents in PPE were 199.33 and 28.32 mg/g, respectively, and HPLC results show the presence of eugenol, tannic acid, and rutin. Evaluation of the
in vitro
AA of PPE demonstrated a dose-dependent effect and an IC
50
of 4.75 μg/mL in 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 3.0 μg/mL in 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays. The ferric-reducing antioxidant power (FRAP assay) was 0.046 μmol/L trolox equivalent/μg/mL of extract. Among the AA, only the capacity to scavenge DPPH radical of PPE was maintained in F1 and F2. In addition, both formulations satisfactorily released the extract. The evaluation of the functional stability of F1 and F2 did not demonstrate loss of activity by storage at room temperature and at 4°C/6 months. In irradiated mice, treatment with F1 and F2 added with PPE significantly increased the capacity to scavenge ABTS radical and the FRAP of skin compared to vehicle-treated mice. In conclusion, the present results suggest that formulations containing PPE may be a topical source of antioxidant compounds to decrease oxidative damages of the skin.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>24249253</pmid><doi>10.1208/s12249-013-0049-8</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antioxidants - chemistry Antioxidants - pharmacology Benzothiazoles - chemistry Biochemistry Biomedical and Life Sciences Biomedicine Biotechnology Biphenyl Compounds - chemistry Chemistry, Pharmaceutical - methods Ethanol - chemistry Mice Mice, Hairless Oxidative Stress - drug effects Pharmacology/Toxicology Pharmacy Phenols - chemistry Phenols - pharmacology Picrates - chemistry Pimenta Pimenta - chemistry Plant Extracts - chemistry Plant Extracts - pharmacology Research Article Skin - drug effects Sulfonic Acids - chemistry Ultraviolet Rays - adverse effects |
title | Topical Formulations Containing Pimenta pseudocaryophyllus Extract: In Vitro Antioxidant Activity and In Vivo Efficacy Against UV-B-Induced Oxidative Stress |
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