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Hybrid Lipid/Clay Carrier Systems Containing Annatto Oil for Topical Formulations
Nanocomposites formed by clay and lipid carriers (NLCs) show a high potential for providing controlled release and specific delivery of bioactive molecules and have recently gained attention in the pharmaceutical sector due to their ability to transport hydrophilic and hydrophobic drugs. Recent stud...
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Published in: | Pharmaceutics 2022-05, Vol.14 (5), p.1067 |
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creator | Barbosa, Raquel de Melo Leite, Aliana Monteiro García-Villén, Fátima Sánchez-Espejo, Rita Cerezo, Pilar Viseras, César Faccendini, Angela Sandri, Giuseppina Raffin, Fernanda Nervo Moura, Túlio Flávio Accioly de Lima E |
description | Nanocomposites formed by clay and lipid carriers (NLCs) show a high potential for providing controlled release and specific delivery of bioactive molecules and have recently gained attention in the pharmaceutical sector due to their ability to transport hydrophilic and hydrophobic drugs. Recent studies have recognized the biological activity of the oil of Bixa orellana L. (AO) with regards to its healing, antioxidant, antibacterial, and anti-leishmanial properties. Therefore, the purpose of this study is the preparation and characterization of hybrid systems based on lipid nanocarriers and laponite for the delivery of AO. NLCs were prepared by the fusion-emulsification method, using cetyl palmitate (CP) or myristyl myristate (MM), AO, and Poloxamer 188. The morphology, hydrodynamic diameters, zeta potential (ZP), polydispersity index (PDI), thermal analysis, X-ray diffraction analysis (XRD), viscosity behavior, and cytotoxicity testing of the hybrid systems were performed. The thermal study and X-ray diffraction analyses (XRD) revealed polymorphic structural changes compatible with the amorphization of the material. Rheological assays highlighted a typical pseudoplastic behavior in all systems (MM and CP with LAP). The hybrid systems’ morphology, size diameters, and PDIs were similar, preset spherical and monodisperse structures (≈200 nm; |
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Recent studies have recognized the biological activity of the oil of Bixa orellana L. (AO) with regards to its healing, antioxidant, antibacterial, and anti-leishmanial properties. Therefore, the purpose of this study is the preparation and characterization of hybrid systems based on lipid nanocarriers and laponite for the delivery of AO. NLCs were prepared by the fusion-emulsification method, using cetyl palmitate (CP) or myristyl myristate (MM), AO, and Poloxamer 188. The morphology, hydrodynamic diameters, zeta potential (ZP), polydispersity index (PDI), thermal analysis, X-ray diffraction analysis (XRD), viscosity behavior, and cytotoxicity testing of the hybrid systems were performed. The thermal study and X-ray diffraction analyses (XRD) revealed polymorphic structural changes compatible with the amorphization of the material. Rheological assays highlighted a typical pseudoplastic behavior in all systems (MM and CP with LAP). The hybrid systems’ morphology, size diameters, and PDIs were similar, preset spherical and monodisperse structures (≈200 nm; <0.3), without significant change up to sixty days. The ZP values differed from each other, becoming higher with increasing AO concentration. XEDS spectra and elemental X-ray maps show peaks of lipids (organic components, C and O) and inorganic components O, Mg, and Si. All samples showed cell viability above 60%. The results indicated a stable, biocompatible hybrid system that can be an alternative for topical application.</description><identifier>ISSN: 1999-4923</identifier><identifier>EISSN: 1999-4923</identifier><identifier>DOI: 10.3390/pharmaceutics14051067</identifier><identifier>PMID: 35631653</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Bixa orellana L ; Chemical properties ; Clay ; colloidal suspension ; Dosage and administration ; Drug resistance ; Essences and essential oils ; Fibroblasts ; Heat resistance ; hybrid system ; Hydrogels ; Lipids ; Medicinal plants ; Nanocomposites ; Nanomedicine ; Nanoparticles ; Particle size ; topical formulations ; Transdermal medication ; Ulcers ; Wound healing</subject><ispartof>Pharmaceutics, 2022-05, Vol.14 (5), p.1067</ispartof><rights>COPYRIGHT 2022 MDPI AG</rights><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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Recent studies have recognized the biological activity of the oil of Bixa orellana L. (AO) with regards to its healing, antioxidant, antibacterial, and anti-leishmanial properties. Therefore, the purpose of this study is the preparation and characterization of hybrid systems based on lipid nanocarriers and laponite for the delivery of AO. NLCs were prepared by the fusion-emulsification method, using cetyl palmitate (CP) or myristyl myristate (MM), AO, and Poloxamer 188. The morphology, hydrodynamic diameters, zeta potential (ZP), polydispersity index (PDI), thermal analysis, X-ray diffraction analysis (XRD), viscosity behavior, and cytotoxicity testing of the hybrid systems were performed. The thermal study and X-ray diffraction analyses (XRD) revealed polymorphic structural changes compatible with the amorphization of the material. Rheological assays highlighted a typical pseudoplastic behavior in all systems (MM and CP with LAP). The hybrid systems’ morphology, size diameters, and PDIs were similar, preset spherical and monodisperse structures (≈200 nm; <0.3), without significant change up to sixty days. The ZP values differed from each other, becoming higher with increasing AO concentration. XEDS spectra and elemental X-ray maps show peaks of lipids (organic components, C and O) and inorganic components O, Mg, and Si. All samples showed cell viability above 60%. The results indicated a stable, biocompatible hybrid system that can be an alternative for topical application.</description><subject>Bixa orellana L</subject><subject>Chemical properties</subject><subject>Clay</subject><subject>colloidal suspension</subject><subject>Dosage and administration</subject><subject>Drug resistance</subject><subject>Essences and essential oils</subject><subject>Fibroblasts</subject><subject>Heat resistance</subject><subject>hybrid system</subject><subject>Hydrogels</subject><subject>Lipids</subject><subject>Medicinal plants</subject><subject>Nanocomposites</subject><subject>Nanomedicine</subject><subject>Nanoparticles</subject><subject>Particle size</subject><subject>topical formulations</subject><subject>Transdermal medication</subject><subject>Ulcers</subject><subject>Wound healing</subject><issn>1999-4923</issn><issn>1999-4923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptksFq3DAQhk1paUKaR2gx9NLLJpIlW9alsCxNE1gIpelZjOTRRostuZJd2Levtpsm2RDNQWL0_5-Y0RTFR0ouGJPkcryHOIDBeXImUU5qShrxpjilUsoFlxV7--x8UpyntCV5MUZbJt8XJ6xuGG1qdlr8uN7p6Lpy7UbXXa562JUriNFhLH_u0oRDKlfBT-C885ty6T1MUyhvXV_aEMu7MDoDfXkV4jD3MLng04finYU-4fnDflb8uvp2t7perG-_36yW64WpRTUtrOTIoWkQRWu7NgdooUFzbK2p6xYpcqOJNaLh0rQaKku4AVJxrQEEZWfFzYHbBdiqMboB4k4FcOpfIsSNgpj706OithFAiSQMCedU6BYbynnFWk2I4JhZXw-scdYDdgb9FKE_gh7feHevNuGPkpQLSdoM-PIAiOH3jGlSg0sG-x48hjmpqhG0ErQWdZZ-fiHdhjn63Kq9Kv9RJVrxpNpALsB5G_K7Zg9VS1ExThvJ96qLV1Q5OhycCR6ty_kjQ30wmBhSimgfa6RE7UdLvTpa2ffpeYMeXf8Hif0FDXLNDA</recordid><startdate>20220517</startdate><enddate>20220517</enddate><creator>Barbosa, Raquel de Melo</creator><creator>Leite, Aliana Monteiro</creator><creator>García-Villén, Fátima</creator><creator>Sánchez-Espejo, Rita</creator><creator>Cerezo, Pilar</creator><creator>Viseras, César</creator><creator>Faccendini, Angela</creator><creator>Sandri, Giuseppina</creator><creator>Raffin, Fernanda Nervo</creator><creator>Moura, Túlio Flávio Accioly de Lima E</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2219-3566</orcidid><orcidid>https://orcid.org/0000-0001-6766-9321</orcidid><orcidid>https://orcid.org/0000-0002-8818-817X</orcidid><orcidid>https://orcid.org/0000-0001-7623-4485</orcidid></search><sort><creationdate>20220517</creationdate><title>Hybrid Lipid/Clay Carrier Systems Containing Annatto Oil for Topical Formulations</title><author>Barbosa, Raquel de Melo ; Leite, Aliana Monteiro ; García-Villén, Fátima ; Sánchez-Espejo, Rita ; Cerezo, Pilar ; Viseras, César ; Faccendini, Angela ; Sandri, Giuseppina ; Raffin, Fernanda Nervo ; Moura, Túlio Flávio Accioly de Lima E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-f94e4a66ee78fd8d8dab7bab4e8fc558e1e4cb0fc7649c8ba2f04ca024bbaa713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Bixa orellana L</topic><topic>Chemical properties</topic><topic>Clay</topic><topic>colloidal suspension</topic><topic>Dosage and administration</topic><topic>Drug resistance</topic><topic>Essences and essential oils</topic><topic>Fibroblasts</topic><topic>Heat resistance</topic><topic>hybrid system</topic><topic>Hydrogels</topic><topic>Lipids</topic><topic>Medicinal plants</topic><topic>Nanocomposites</topic><topic>Nanomedicine</topic><topic>Nanoparticles</topic><topic>Particle size</topic><topic>topical formulations</topic><topic>Transdermal medication</topic><topic>Ulcers</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbosa, Raquel de Melo</creatorcontrib><creatorcontrib>Leite, Aliana Monteiro</creatorcontrib><creatorcontrib>García-Villén, Fátima</creatorcontrib><creatorcontrib>Sánchez-Espejo, Rita</creatorcontrib><creatorcontrib>Cerezo, Pilar</creatorcontrib><creatorcontrib>Viseras, César</creatorcontrib><creatorcontrib>Faccendini, Angela</creatorcontrib><creatorcontrib>Sandri, Giuseppina</creatorcontrib><creatorcontrib>Raffin, Fernanda Nervo</creatorcontrib><creatorcontrib>Moura, Túlio Flávio Accioly de Lima E</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest_Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbosa, Raquel de Melo</au><au>Leite, Aliana Monteiro</au><au>García-Villén, Fátima</au><au>Sánchez-Espejo, Rita</au><au>Cerezo, Pilar</au><au>Viseras, César</au><au>Faccendini, Angela</au><au>Sandri, Giuseppina</au><au>Raffin, Fernanda Nervo</au><au>Moura, Túlio Flávio Accioly de Lima E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hybrid Lipid/Clay Carrier Systems Containing Annatto Oil for Topical Formulations</atitle><jtitle>Pharmaceutics</jtitle><addtitle>Pharmaceutics</addtitle><date>2022-05-17</date><risdate>2022</risdate><volume>14</volume><issue>5</issue><spage>1067</spage><pages>1067-</pages><issn>1999-4923</issn><eissn>1999-4923</eissn><abstract>Nanocomposites formed by clay and lipid carriers (NLCs) show a high potential for providing controlled release and specific delivery of bioactive molecules and have recently gained attention in the pharmaceutical sector due to their ability to transport hydrophilic and hydrophobic drugs. Recent studies have recognized the biological activity of the oil of Bixa orellana L. (AO) with regards to its healing, antioxidant, antibacterial, and anti-leishmanial properties. Therefore, the purpose of this study is the preparation and characterization of hybrid systems based on lipid nanocarriers and laponite for the delivery of AO. NLCs were prepared by the fusion-emulsification method, using cetyl palmitate (CP) or myristyl myristate (MM), AO, and Poloxamer 188. The morphology, hydrodynamic diameters, zeta potential (ZP), polydispersity index (PDI), thermal analysis, X-ray diffraction analysis (XRD), viscosity behavior, and cytotoxicity testing of the hybrid systems were performed. The thermal study and X-ray diffraction analyses (XRD) revealed polymorphic structural changes compatible with the amorphization of the material. Rheological assays highlighted a typical pseudoplastic behavior in all systems (MM and CP with LAP). The hybrid systems’ morphology, size diameters, and PDIs were similar, preset spherical and monodisperse structures (≈200 nm; <0.3), without significant change up to sixty days. The ZP values differed from each other, becoming higher with increasing AO concentration. XEDS spectra and elemental X-ray maps show peaks of lipids (organic components, C and O) and inorganic components O, Mg, and Si. All samples showed cell viability above 60%. The results indicated a stable, biocompatible hybrid system that can be an alternative for topical application.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35631653</pmid><doi>10.3390/pharmaceutics14051067</doi><orcidid>https://orcid.org/0000-0002-2219-3566</orcidid><orcidid>https://orcid.org/0000-0001-6766-9321</orcidid><orcidid>https://orcid.org/0000-0002-8818-817X</orcidid><orcidid>https://orcid.org/0000-0001-7623-4485</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bixa orellana L Chemical properties Clay colloidal suspension Dosage and administration Drug resistance Essences and essential oils Fibroblasts Heat resistance hybrid system Hydrogels Lipids Medicinal plants Nanocomposites Nanomedicine Nanoparticles Particle size topical formulations Transdermal medication Ulcers Wound healing |
title | Hybrid Lipid/Clay Carrier Systems Containing Annatto Oil for Topical Formulations |
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