Investigation of the Potential of Nebivolol Hydrochloride-Loaded Chitosomal Systems for Tissue Regeneration: In Vitro Characterization and In Vivo Assessment
In this study, we evaluated the synergistic effect of nebivolol hydrochloride (NVH), a third-generation beta-blocker and NO donor drug, and chitosan on the tissue regeneration. Ionic gelation method was selected for the preparation of NVH-loaded chitosomes using chitosan lactate and sodium tripolyph...
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Veröffentlicht in: | Pharmaceutics 2021-05, Vol.13 (5), p.700 |
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creator | Elsherif, Noha Ibrahim Al-Mahallawi, Abdulaziz Mohsen Abdelkhalek, Abdelfattah Ahmed Shamma, Rehab Nabil |
description | In this study, we evaluated the synergistic effect of nebivolol hydrochloride (NVH), a third-generation beta-blocker and NO donor drug, and chitosan on the tissue regeneration. Ionic gelation method was selected for the preparation of NVH-loaded chitosomes using chitosan lactate and sodium tripolyphosphate. The effect of different formulation variables was studied using a full factorial design, and NVH entrapment efficiency percentages and particle size were selected as the responses. The chosen system demonstrated high entrapment efficiency (73.68 ± 3.61%), small particle size (404.05 ± 11.2 nm), and good zeta potential value (35.6 ± 0.25 mV). The best-achieved formula demonstrated spherical morphology in transmission electron microscopy and amorphization of the crystalline drug in differential scanning calorimetry and X-ray diffraction. Cell culture studies revealed a significantly higher proliferation of the fibroblasts in comparison with the drug suspensions and the blank formula. An in vivo study was conducted to compare the efficacy of the proposed formula on wound healing. The histopathological examination showed the superiority of NVH-loaded chitosomes on the wound proliferation and the non-significant difference in the collagen deposition after 15 days of the injury to that of intact skin. In conclusion, NVH-loaded chitosomes exhibited promising results in enhancing skin healing and tissue regeneration. |
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Ionic gelation method was selected for the preparation of NVH-loaded chitosomes using chitosan lactate and sodium tripolyphosphate. The effect of different formulation variables was studied using a full factorial design, and NVH entrapment efficiency percentages and particle size were selected as the responses. The chosen system demonstrated high entrapment efficiency (73.68 ± 3.61%), small particle size (404.05 ± 11.2 nm), and good zeta potential value (35.6 ± 0.25 mV). The best-achieved formula demonstrated spherical morphology in transmission electron microscopy and amorphization of the crystalline drug in differential scanning calorimetry and X-ray diffraction. Cell culture studies revealed a significantly higher proliferation of the fibroblasts in comparison with the drug suspensions and the blank formula. An in vivo study was conducted to compare the efficacy of the proposed formula on wound healing. The histopathological examination showed the superiority of NVH-loaded chitosomes on the wound proliferation and the non-significant difference in the collagen deposition after 15 days of the injury to that of intact skin. In conclusion, NVH-loaded chitosomes exhibited promising results in enhancing skin healing and tissue regeneration.</description><identifier>ISSN: 1999-4923</identifier><identifier>EISSN: 1999-4923</identifier><identifier>DOI: 10.3390/pharmaceutics13050700</identifier><identifier>PMID: 34064916</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Biodegradation ; Cellulose ; chitosan lactate ; chitosomes ; Collagen ; Diabetes ; Diabetic neuropathy ; Efficiency ; Fibroblasts ; Hemodialysis ; Hyaluronic acid ; nebivolol hydrochloride ; Particle size ; Polymers ; Tissue engineering ; tissue regeneration ; Variance analysis ; Wound healing</subject><ispartof>Pharmaceutics, 2021-05, Vol.13 (5), p.700</ispartof><rights>2021 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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Ionic gelation method was selected for the preparation of NVH-loaded chitosomes using chitosan lactate and sodium tripolyphosphate. The effect of different formulation variables was studied using a full factorial design, and NVH entrapment efficiency percentages and particle size were selected as the responses. The chosen system demonstrated high entrapment efficiency (73.68 ± 3.61%), small particle size (404.05 ± 11.2 nm), and good zeta potential value (35.6 ± 0.25 mV). The best-achieved formula demonstrated spherical morphology in transmission electron microscopy and amorphization of the crystalline drug in differential scanning calorimetry and X-ray diffraction. Cell culture studies revealed a significantly higher proliferation of the fibroblasts in comparison with the drug suspensions and the blank formula. An in vivo study was conducted to compare the efficacy of the proposed formula on wound healing. The histopathological examination showed the superiority of NVH-loaded chitosomes on the wound proliferation and the non-significant difference in the collagen deposition after 15 days of the injury to that of intact skin. In conclusion, NVH-loaded chitosomes exhibited promising results in enhancing skin healing and tissue regeneration.</description><subject>Biodegradation</subject><subject>Cellulose</subject><subject>chitosan lactate</subject><subject>chitosomes</subject><subject>Collagen</subject><subject>Diabetes</subject><subject>Diabetic neuropathy</subject><subject>Efficiency</subject><subject>Fibroblasts</subject><subject>Hemodialysis</subject><subject>Hyaluronic acid</subject><subject>nebivolol hydrochloride</subject><subject>Particle size</subject><subject>Polymers</subject><subject>Tissue engineering</subject><subject>tissue regeneration</subject><subject>Variance analysis</subject><subject>Wound healing</subject><issn>1999-4923</issn><issn>1999-4923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><sourceid>DOA</sourceid><recordid>eNptkltrFDEUxwdRbGn7EYSAL76s5jKXxAehLGoXFitafQ2Z5Mxulpk5a5JZWL-L39VMt4gV85Jwzj-_cy2KF4y-FkLRN_utCYOxMCVvIxO0og2lT4pzppRalIqLp3-9z4qrGHc0HyGYFOp5cSZKWpeK1efFr9V4gJj8xiSPI8GOpC2Qz5hgTN70s-ETtP6APfbk5ugC2m2PwTtYrNE4cGS59QkjDln89RgTDJF0GMidj3EC8gU2MEK4p78lq5F89ylg_mSCsQmC_3kKbEZ38h6QXMcIMQ45g8viWWf6CFcP90Xx7cP7u-XNYn37cbW8Xi9sKXlayKbOLZC2rRteOqmAV4wKkKqtaFtJ4LYxtuaOqhZa5YxlHWWtkZTKpuRNLS6K1Ynr0Oz0PvjBhKNG4_W9AcNGm5B73YOWtTK2ahxjFS8lOMnKpmu6ruIW6kp2mfXuxNpP7QDO5jKC6R9BH3tGv9UbPGjJcg2qyYBXD4CAP6Y8HD34aKHvzQg4Rc0rMQ9PyDnvl_9IdziFMbdqVnFWl7KUWVWdVDZgjAG6P8kwqud90v_dJ_Ebs6rDfQ</recordid><startdate>20210511</startdate><enddate>20210511</enddate><creator>Elsherif, Noha Ibrahim</creator><creator>Al-Mahallawi, Abdulaziz Mohsen</creator><creator>Abdelkhalek, Abdelfattah Ahmed</creator><creator>Shamma, Rehab Nabil</creator><general>MDPI AG</general><general>MDPI</general><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/0000-0002-7635-6842</orcidid><orcidid>https://orcid.org/0000-0003-1694-1342</orcidid></search><sort><creationdate>20210511</creationdate><title>Investigation of the Potential of Nebivolol Hydrochloride-Loaded Chitosomal Systems for Tissue Regeneration: In Vitro Characterization and In Vivo Assessment</title><author>Elsherif, Noha Ibrahim ; Al-Mahallawi, Abdulaziz Mohsen ; Abdelkhalek, Abdelfattah Ahmed ; Shamma, Rehab Nabil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-8760508cb6724d89e25103e89b50b58e2c7ac62d09beb9dac1f01ba8008742763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biodegradation</topic><topic>Cellulose</topic><topic>chitosan lactate</topic><topic>chitosomes</topic><topic>Collagen</topic><topic>Diabetes</topic><topic>Diabetic neuropathy</topic><topic>Efficiency</topic><topic>Fibroblasts</topic><topic>Hemodialysis</topic><topic>Hyaluronic acid</topic><topic>nebivolol hydrochloride</topic><topic>Particle size</topic><topic>Polymers</topic><topic>Tissue engineering</topic><topic>tissue regeneration</topic><topic>Variance analysis</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elsherif, Noha Ibrahim</creatorcontrib><creatorcontrib>Al-Mahallawi, Abdulaziz Mohsen</creatorcontrib><creatorcontrib>Abdelkhalek, Abdelfattah Ahmed</creatorcontrib><creatorcontrib>Shamma, Rehab Nabil</creatorcontrib><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 UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest - 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>Directory of Open Access Journals</collection><jtitle>Pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elsherif, Noha Ibrahim</au><au>Al-Mahallawi, Abdulaziz Mohsen</au><au>Abdelkhalek, Abdelfattah Ahmed</au><au>Shamma, Rehab Nabil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of the Potential of Nebivolol Hydrochloride-Loaded Chitosomal Systems for Tissue Regeneration: In Vitro Characterization and In Vivo Assessment</atitle><jtitle>Pharmaceutics</jtitle><date>2021-05-11</date><risdate>2021</risdate><volume>13</volume><issue>5</issue><spage>700</spage><pages>700-</pages><issn>1999-4923</issn><eissn>1999-4923</eissn><abstract>In this study, we evaluated the synergistic effect of nebivolol hydrochloride (NVH), a third-generation beta-blocker and NO donor drug, and chitosan on the tissue regeneration. Ionic gelation method was selected for the preparation of NVH-loaded chitosomes using chitosan lactate and sodium tripolyphosphate. The effect of different formulation variables was studied using a full factorial design, and NVH entrapment efficiency percentages and particle size were selected as the responses. The chosen system demonstrated high entrapment efficiency (73.68 ± 3.61%), small particle size (404.05 ± 11.2 nm), and good zeta potential value (35.6 ± 0.25 mV). The best-achieved formula demonstrated spherical morphology in transmission electron microscopy and amorphization of the crystalline drug in differential scanning calorimetry and X-ray diffraction. Cell culture studies revealed a significantly higher proliferation of the fibroblasts in comparison with the drug suspensions and the blank formula. An in vivo study was conducted to compare the efficacy of the proposed formula on wound healing. The histopathological examination showed the superiority of NVH-loaded chitosomes on the wound proliferation and the non-significant difference in the collagen deposition after 15 days of the injury to that of intact skin. In conclusion, NVH-loaded chitosomes exhibited promising results in enhancing skin healing and tissue regeneration.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34064916</pmid><doi>10.3390/pharmaceutics13050700</doi><orcidid>https://orcid.org/0000-0002-7635-6842</orcidid><orcidid>https://orcid.org/0000-0003-1694-1342</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biodegradation Cellulose chitosan lactate chitosomes Collagen Diabetes Diabetic neuropathy Efficiency Fibroblasts Hemodialysis Hyaluronic acid nebivolol hydrochloride Particle size Polymers Tissue engineering tissue regeneration Variance analysis Wound healing |
title | Investigation of the Potential of Nebivolol Hydrochloride-Loaded Chitosomal Systems for Tissue Regeneration: In Vitro Characterization and In Vivo Assessment |
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