Curcumin-Polyethylene Glycol Loaded on Chitosan-Gelatin Nanoparticles Enhances Burn Wound Healing in Rat
Abstract The aim of the present study was to evaluate effects of curcumin-polyethylene glycol loaded on chitosan-gelatin nanoparticles (C-PEG-CGNPs) on burn wound healing in rat as a model study. Sixty healthy male White Wistar rats were randomized into four experimental groups of 15 animals each: C...
Gespeichert in:
Veröffentlicht in: | Journal of burn care & research 2022-11, Vol.43 (6), p.1399-1409 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1409 |
---|---|
container_issue | 6 |
container_start_page | 1399 |
container_title | Journal of burn care & research |
container_volume | 43 |
creator | Ravanfar, Kimia Amniattalab, Amir Mohammadi, Rahim |
description | Abstract
The aim of the present study was to evaluate effects of curcumin-polyethylene glycol loaded on chitosan-gelatin nanoparticles (C-PEG-CGNPs) on burn wound healing in rat as a model study. Sixty healthy male White Wistar rats were randomized into four experimental groups of 15 animals each: Control group (Control) was treated with normal saline. Carrier group was treated with CGNPs-based ointment (0.05 mg/ml). Silver sulfadiazine group was treated with silver sulfadiazine 1% ointment. Treatment group was treated with C-PEG-CGNPs (0.05 mg/ml). Wound size was measured on 7, 14, and 21 days after surgery. The expression of p53, Bcl-2, caspase-3 were evaluated using reverse transcription-polymerase chain reaction and immunohistochemical staining. Reduction in wound area indicated that there was significant difference between Treatment group and other groups (P < .05). Quantitative histological and morphometric studies, and mean rank of the qualitative studies demonstrated that there was a significant difference between Treatment group and other groups (P < .05). Observations demonstrated C-PEG-CGNPs significantly shortened the inflammatory phase and accelerated the cellular proliferation. Accordingly, the animals in Treatment group revealed significantly (P < .05) higher fibroblast distribution/one mm2 of wound area and rapid reepithelialization. The mRNA levels of Bcl-2, p53, and caspase-3 were remarkably (P < .05) higher in Treatment group compared to control animals. The immunohistochemical analyses confirmed the reverse transcription-polymerase chain reaction findings. C-PEG-CGNPs offered potential advantages in burn wound healing acceleration and improvement. |
doi_str_mv | 10.1093/jbcr/irac048 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2650254300</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/jbcr/irac048</oup_id><sourcerecordid>2650254300</sourcerecordid><originalsourceid>FETCH-LOGICAL-c323t-d3cb82e9dbd786f6f3cae5c00f81ebcb3c527c2f2501c5db331191f6948447923</originalsourceid><addsrcrecordid>eNp9kLtOwzAARS0EoqWwMSNvMBDqR5zHCFFpkSpACARb5DgOSeXYwY6H_D2pWjoy3TscneEAcInRHUYpnW8KYeeN5QKFyRGYYsbSYLzJ8eHHXxNw5twGoTBEMTsFE8pCgqI4nYI681b4ttHBq1GD7OtBSS3hUg3CKLg2vJQlNBpmddMbx3WwlIr3jYbPXJuO274RSjq40DXXYjwP3mr4abwu4Upy1ehvOMJvvD8HJxVXTl7sdwY-Hhfv2SpYvyyfsvt1ICihfVBSUSREpmVRxklURRUVXDKBUJVgWYiCCkZiQSrCEBasLCjFOMVVlIZJGMYpoTNws_N21vx46fq8bZyQSnEtjXc5iRgiLKQIjejtDhXWOGdllXe2abkdcozybdt82zbftx3xq73ZF60sD_BfzBG43gHGd_-rfgE9foTB</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2650254300</pqid></control><display><type>article</type><title>Curcumin-Polyethylene Glycol Loaded on Chitosan-Gelatin Nanoparticles Enhances Burn Wound Healing in Rat</title><source>Oxford Journals</source><creator>Ravanfar, Kimia ; Amniattalab, Amir ; Mohammadi, Rahim</creator><creatorcontrib>Ravanfar, Kimia ; Amniattalab, Amir ; Mohammadi, Rahim</creatorcontrib><description>Abstract
The aim of the present study was to evaluate effects of curcumin-polyethylene glycol loaded on chitosan-gelatin nanoparticles (C-PEG-CGNPs) on burn wound healing in rat as a model study. Sixty healthy male White Wistar rats were randomized into four experimental groups of 15 animals each: Control group (Control) was treated with normal saline. Carrier group was treated with CGNPs-based ointment (0.05 mg/ml). Silver sulfadiazine group was treated with silver sulfadiazine 1% ointment. Treatment group was treated with C-PEG-CGNPs (0.05 mg/ml). Wound size was measured on 7, 14, and 21 days after surgery. The expression of p53, Bcl-2, caspase-3 were evaluated using reverse transcription-polymerase chain reaction and immunohistochemical staining. Reduction in wound area indicated that there was significant difference between Treatment group and other groups (P < .05). Quantitative histological and morphometric studies, and mean rank of the qualitative studies demonstrated that there was a significant difference between Treatment group and other groups (P < .05). Observations demonstrated C-PEG-CGNPs significantly shortened the inflammatory phase and accelerated the cellular proliferation. Accordingly, the animals in Treatment group revealed significantly (P < .05) higher fibroblast distribution/one mm2 of wound area and rapid reepithelialization. The mRNA levels of Bcl-2, p53, and caspase-3 were remarkably (P < .05) higher in Treatment group compared to control animals. The immunohistochemical analyses confirmed the reverse transcription-polymerase chain reaction findings. C-PEG-CGNPs offered potential advantages in burn wound healing acceleration and improvement.</description><identifier>ISSN: 1559-047X</identifier><identifier>EISSN: 1559-0488</identifier><identifier>DOI: 10.1093/jbcr/irac048</identifier><identifier>PMID: 35420679</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><ispartof>Journal of burn care & research, 2022-11, Vol.43 (6), p.1399-1409</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the American Burn Association. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the American Burn Association. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-d3cb82e9dbd786f6f3cae5c00f81ebcb3c527c2f2501c5db331191f6948447923</citedby><cites>FETCH-LOGICAL-c323t-d3cb82e9dbd786f6f3cae5c00f81ebcb3c527c2f2501c5db331191f6948447923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35420679$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ravanfar, Kimia</creatorcontrib><creatorcontrib>Amniattalab, Amir</creatorcontrib><creatorcontrib>Mohammadi, Rahim</creatorcontrib><title>Curcumin-Polyethylene Glycol Loaded on Chitosan-Gelatin Nanoparticles Enhances Burn Wound Healing in Rat</title><title>Journal of burn care & research</title><addtitle>J Burn Care Res</addtitle><description>Abstract
The aim of the present study was to evaluate effects of curcumin-polyethylene glycol loaded on chitosan-gelatin nanoparticles (C-PEG-CGNPs) on burn wound healing in rat as a model study. Sixty healthy male White Wistar rats were randomized into four experimental groups of 15 animals each: Control group (Control) was treated with normal saline. Carrier group was treated with CGNPs-based ointment (0.05 mg/ml). Silver sulfadiazine group was treated with silver sulfadiazine 1% ointment. Treatment group was treated with C-PEG-CGNPs (0.05 mg/ml). Wound size was measured on 7, 14, and 21 days after surgery. The expression of p53, Bcl-2, caspase-3 were evaluated using reverse transcription-polymerase chain reaction and immunohistochemical staining. Reduction in wound area indicated that there was significant difference between Treatment group and other groups (P < .05). Quantitative histological and morphometric studies, and mean rank of the qualitative studies demonstrated that there was a significant difference between Treatment group and other groups (P < .05). Observations demonstrated C-PEG-CGNPs significantly shortened the inflammatory phase and accelerated the cellular proliferation. Accordingly, the animals in Treatment group revealed significantly (P < .05) higher fibroblast distribution/one mm2 of wound area and rapid reepithelialization. The mRNA levels of Bcl-2, p53, and caspase-3 were remarkably (P < .05) higher in Treatment group compared to control animals. The immunohistochemical analyses confirmed the reverse transcription-polymerase chain reaction findings. C-PEG-CGNPs offered potential advantages in burn wound healing acceleration and improvement.</description><issn>1559-047X</issn><issn>1559-0488</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kLtOwzAARS0EoqWwMSNvMBDqR5zHCFFpkSpACARb5DgOSeXYwY6H_D2pWjoy3TscneEAcInRHUYpnW8KYeeN5QKFyRGYYsbSYLzJ8eHHXxNw5twGoTBEMTsFE8pCgqI4nYI681b4ttHBq1GD7OtBSS3hUg3CKLg2vJQlNBpmddMbx3WwlIr3jYbPXJuO274RSjq40DXXYjwP3mr4abwu4Upy1ehvOMJvvD8HJxVXTl7sdwY-Hhfv2SpYvyyfsvt1ICihfVBSUSREpmVRxklURRUVXDKBUJVgWYiCCkZiQSrCEBasLCjFOMVVlIZJGMYpoTNws_N21vx46fq8bZyQSnEtjXc5iRgiLKQIjejtDhXWOGdllXe2abkdcozybdt82zbftx3xq73ZF60sD_BfzBG43gHGd_-rfgE9foTB</recordid><startdate>20221102</startdate><enddate>20221102</enddate><creator>Ravanfar, Kimia</creator><creator>Amniattalab, Amir</creator><creator>Mohammadi, Rahim</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20221102</creationdate><title>Curcumin-Polyethylene Glycol Loaded on Chitosan-Gelatin Nanoparticles Enhances Burn Wound Healing in Rat</title><author>Ravanfar, Kimia ; Amniattalab, Amir ; Mohammadi, Rahim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-d3cb82e9dbd786f6f3cae5c00f81ebcb3c527c2f2501c5db331191f6948447923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ravanfar, Kimia</creatorcontrib><creatorcontrib>Amniattalab, Amir</creatorcontrib><creatorcontrib>Mohammadi, Rahim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of burn care & research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ravanfar, Kimia</au><au>Amniattalab, Amir</au><au>Mohammadi, Rahim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Curcumin-Polyethylene Glycol Loaded on Chitosan-Gelatin Nanoparticles Enhances Burn Wound Healing in Rat</atitle><jtitle>Journal of burn care & research</jtitle><addtitle>J Burn Care Res</addtitle><date>2022-11-02</date><risdate>2022</risdate><volume>43</volume><issue>6</issue><spage>1399</spage><epage>1409</epage><pages>1399-1409</pages><issn>1559-047X</issn><eissn>1559-0488</eissn><abstract>Abstract
The aim of the present study was to evaluate effects of curcumin-polyethylene glycol loaded on chitosan-gelatin nanoparticles (C-PEG-CGNPs) on burn wound healing in rat as a model study. Sixty healthy male White Wistar rats were randomized into four experimental groups of 15 animals each: Control group (Control) was treated with normal saline. Carrier group was treated with CGNPs-based ointment (0.05 mg/ml). Silver sulfadiazine group was treated with silver sulfadiazine 1% ointment. Treatment group was treated with C-PEG-CGNPs (0.05 mg/ml). Wound size was measured on 7, 14, and 21 days after surgery. The expression of p53, Bcl-2, caspase-3 were evaluated using reverse transcription-polymerase chain reaction and immunohistochemical staining. Reduction in wound area indicated that there was significant difference between Treatment group and other groups (P < .05). Quantitative histological and morphometric studies, and mean rank of the qualitative studies demonstrated that there was a significant difference between Treatment group and other groups (P < .05). Observations demonstrated C-PEG-CGNPs significantly shortened the inflammatory phase and accelerated the cellular proliferation. Accordingly, the animals in Treatment group revealed significantly (P < .05) higher fibroblast distribution/one mm2 of wound area and rapid reepithelialization. The mRNA levels of Bcl-2, p53, and caspase-3 were remarkably (P < .05) higher in Treatment group compared to control animals. The immunohistochemical analyses confirmed the reverse transcription-polymerase chain reaction findings. C-PEG-CGNPs offered potential advantages in burn wound healing acceleration and improvement.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>35420679</pmid><doi>10.1093/jbcr/irac048</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1559-047X |
ispartof | Journal of burn care & research, 2022-11, Vol.43 (6), p.1399-1409 |
issn | 1559-047X 1559-0488 |
language | eng |
recordid | cdi_proquest_miscellaneous_2650254300 |
source | Oxford Journals |
title | Curcumin-Polyethylene Glycol Loaded on Chitosan-Gelatin Nanoparticles Enhances Burn Wound Healing in Rat |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T09%3A18%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Curcumin-Polyethylene%20Glycol%20Loaded%20on%20Chitosan-Gelatin%20Nanoparticles%20Enhances%20Burn%20Wound%20Healing%20in%20Rat&rft.jtitle=Journal%20of%20burn%20care%20&%20research&rft.au=Ravanfar,%20Kimia&rft.date=2022-11-02&rft.volume=43&rft.issue=6&rft.spage=1399&rft.epage=1409&rft.pages=1399-1409&rft.issn=1559-047X&rft.eissn=1559-0488&rft_id=info:doi/10.1093/jbcr/irac048&rft_dat=%3Cproquest_cross%3E2650254300%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2650254300&rft_id=info:pmid/35420679&rft_oup_id=10.1093/jbcr/irac048&rfr_iscdi=true |