In vitro and in vivo assessment of curcumin-quercetin loaded multi-layered 3D-nanofibroporous matrix prepared by solution blow-spinning for full-thickness burn wound healing
Burn wounds (BWs) cause impairment of native skin tissue and may cause significant microbial infections that demand immediate care. Curcumin (Cur) and quercetin (Que) exhibit antimicrobial, hemocompatibility, ROS-scavenging, and anti-inflammatory properties. However, its instability, water insolubil...
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Veröffentlicht in: | International journal of biological macromolecules 2024-06, Vol.270 (Pt 1), p.132269 |
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creator | Katiyar, Soumya Singh, Divakar Tripathi, Abhay Dev Chaurasia, Avinash Kumar Singh, Ritika K Srivastava, Pradeep K Mishra, Abha |
description | Burn wounds (BWs) cause impairment of native skin tissue and may cause significant microbial infections that demand immediate care. Curcumin (Cur) and quercetin (Que) exhibit antimicrobial, hemocompatibility, ROS-scavenging, and anti-inflammatory properties. However, its instability, water insolubility, and low biological fluid absorption render it challenging to sustain local Cur and Que doses at the wound site. Therefore, to combat these limitations, we employed blow-spinning and freeze-drying to develop a multi-layered, Cur/Que-loaded gelatin/chitosan/PCL (GCP-Q/C) nanofibroporous (NFP) matrix. Morphological analysis of the NFP-matrix using SEM revealed a well-formed multi-layered structure. The FTIR and XRD plots demonstrated dual-bioactive incorporation and scaffold polymer interaction. Additionally, the GCP-Q/C matrix displayed high porosity (82.7 ± 2.07 %), adequate pore size (∼121 μm), enhanced water-uptake ability (∼675 % within 24 h), and satisfactory biodegradation. The scaffolds with bioactives had a long-term release, increased antioxidant activity, and were more effective against gram-positive (S. aureus) and gram-negative (E. coli) bacteria than the unloaded scaffolds. The in vitro findings of GCP-Q/C scaffolds showed promoted L929 cell growth and hemocompatibility. Additionally, an in vivo full-thickness BW investigation found that an implanted GCP-Q/C matrix stimulates rapid recuperation and tissue regeneration. In accordance with the findings, the Gel/Ch/PCL-Que/Cur NFP-matrix could represent an effective wound-healing dressing for BWs. |
doi_str_mv | 10.1016/j.ijbiomac.2024.132269 |
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Curcumin (Cur) and quercetin (Que) exhibit antimicrobial, hemocompatibility, ROS-scavenging, and anti-inflammatory properties. However, its instability, water insolubility, and low biological fluid absorption render it challenging to sustain local Cur and Que doses at the wound site. Therefore, to combat these limitations, we employed blow-spinning and freeze-drying to develop a multi-layered, Cur/Que-loaded gelatin/chitosan/PCL (GCP-Q/C) nanofibroporous (NFP) matrix. Morphological analysis of the NFP-matrix using SEM revealed a well-formed multi-layered structure. The FTIR and XRD plots demonstrated dual-bioactive incorporation and scaffold polymer interaction. Additionally, the GCP-Q/C matrix displayed high porosity (82.7 ± 2.07 %), adequate pore size (∼121 μm), enhanced water-uptake ability (∼675 % within 24 h), and satisfactory biodegradation. The scaffolds with bioactives had a long-term release, increased antioxidant activity, and were more effective against gram-positive (S. aureus) and gram-negative (E. coli) bacteria than the unloaded scaffolds. The in vitro findings of GCP-Q/C scaffolds showed promoted L929 cell growth and hemocompatibility. Additionally, an in vivo full-thickness BW investigation found that an implanted GCP-Q/C matrix stimulates rapid recuperation and tissue regeneration. In accordance with the findings, the Gel/Ch/PCL-Que/Cur NFP-matrix could represent an effective wound-healing dressing for BWs.</description><identifier>ISSN: 1879-0003</identifier><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2024.132269</identifier><identifier>PMID: 38744363</identifier><language>eng</language><publisher>Netherlands</publisher><subject>absorption ; Animals ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; antioxidant activity ; Antioxidants - chemistry ; Antioxidants - pharmacology ; bioactive compounds ; biocompatibility ; biodegradation ; Burns - drug therapy ; cell growth ; chitosan ; Chitosan - chemistry ; curcumin ; Curcumin - chemistry ; Curcumin - pharmacology ; Drug Liberation ; Escherichia coli ; Escherichia coli - drug effects ; freeze drying ; gelatin ; Gelatin - chemistry ; Mice ; Nanofibers - chemistry ; polymers ; Porosity ; quercetin ; Quercetin - chemistry ; Quercetin - pharmacology ; Rats ; Staphylococcus aureus - drug effects ; tissue repair ; Tissue Scaffolds - chemistry ; water solubility ; water uptake ; Wound Healing - drug effects</subject><ispartof>International journal of biological macromolecules, 2024-06, Vol.270 (Pt 1), p.132269</ispartof><rights>Copyright © 2024 Elsevier B.V. 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Curcumin (Cur) and quercetin (Que) exhibit antimicrobial, hemocompatibility, ROS-scavenging, and anti-inflammatory properties. However, its instability, water insolubility, and low biological fluid absorption render it challenging to sustain local Cur and Que doses at the wound site. Therefore, to combat these limitations, we employed blow-spinning and freeze-drying to develop a multi-layered, Cur/Que-loaded gelatin/chitosan/PCL (GCP-Q/C) nanofibroporous (NFP) matrix. Morphological analysis of the NFP-matrix using SEM revealed a well-formed multi-layered structure. The FTIR and XRD plots demonstrated dual-bioactive incorporation and scaffold polymer interaction. Additionally, the GCP-Q/C matrix displayed high porosity (82.7 ± 2.07 %), adequate pore size (∼121 μm), enhanced water-uptake ability (∼675 % within 24 h), and satisfactory biodegradation. The scaffolds with bioactives had a long-term release, increased antioxidant activity, and were more effective against gram-positive (S. aureus) and gram-negative (E. coli) bacteria than the unloaded scaffolds. The in vitro findings of GCP-Q/C scaffolds showed promoted L929 cell growth and hemocompatibility. Additionally, an in vivo full-thickness BW investigation found that an implanted GCP-Q/C matrix stimulates rapid recuperation and tissue regeneration. In accordance with the findings, the Gel/Ch/PCL-Que/Cur NFP-matrix could represent an effective wound-healing dressing for BWs.</description><subject>absorption</subject><subject>Animals</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>antioxidant activity</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>bioactive compounds</subject><subject>biocompatibility</subject><subject>biodegradation</subject><subject>Burns - drug therapy</subject><subject>cell growth</subject><subject>chitosan</subject><subject>Chitosan - chemistry</subject><subject>curcumin</subject><subject>Curcumin - chemistry</subject><subject>Curcumin - pharmacology</subject><subject>Drug Liberation</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>freeze drying</subject><subject>gelatin</subject><subject>Gelatin - chemistry</subject><subject>Mice</subject><subject>Nanofibers - chemistry</subject><subject>polymers</subject><subject>Porosity</subject><subject>quercetin</subject><subject>Quercetin - chemistry</subject><subject>Quercetin - pharmacology</subject><subject>Rats</subject><subject>Staphylococcus aureus - drug effects</subject><subject>tissue repair</subject><subject>Tissue Scaffolds - chemistry</subject><subject>water solubility</subject><subject>water uptake</subject><subject>Wound Healing - drug effects</subject><issn>1879-0003</issn><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1uFDEQhC0EIsnCK0Q-cvFiuz0zniMKf5EicYHzyvbYxIvHHvyTZB-Kd8QRQeLGqaulT1VdaoQuGd0zysa3x70_ap9WZfaccrFnwPk4P0PnTE4zoZTC83_0Gboo5djVODD5Ep2BnISAEc7Rr-uI73zNCau4YP-43HVdii1ltbHi5LBp2bTVR_Kz2Wxs7VRIarELXluongR1srlv8J5EFZPzOqct5dQKXlXN_gFv2W7qEdEnXFJo1aeIdUj3pGw-Rh-_Y5cydi0EUm-9-RF7PNYtR3yfWj_s1qrQqVfohVOh2NdPc4e-ffzw9eozufny6frq3Q3ZuBCVOCYHxaWlBoxzcpzUAnJYHIDTs3CTdlLMneQTgJEDiIEK57gzUhugboYdevPHd8uply71sPpibAgq2l7rAGyAkUsxsv-jdBi6P-1ZO3T5hDa92uWwZb-qfDr8_Qb8BnX-k2g</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Katiyar, Soumya</creator><creator>Singh, Divakar</creator><creator>Tripathi, Abhay Dev</creator><creator>Chaurasia, Avinash Kumar</creator><creator>Singh, Ritika K</creator><creator>Srivastava, Pradeep K</creator><creator>Mishra, Abha</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20240601</creationdate><title>In vitro and in vivo assessment of curcumin-quercetin loaded multi-layered 3D-nanofibroporous matrix prepared by solution blow-spinning for full-thickness burn wound healing</title><author>Katiyar, Soumya ; Singh, Divakar ; Tripathi, Abhay Dev ; Chaurasia, Avinash Kumar ; Singh, Ritika K ; Srivastava, Pradeep K ; Mishra, Abha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p244t-f185a28e0c3cff867ad385df33fb94f7bf8492442733c8534504ff2fc8bc30f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>absorption</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>antioxidant activity</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - pharmacology</topic><topic>bioactive compounds</topic><topic>biocompatibility</topic><topic>biodegradation</topic><topic>Burns - drug therapy</topic><topic>cell growth</topic><topic>chitosan</topic><topic>Chitosan - chemistry</topic><topic>curcumin</topic><topic>Curcumin - chemistry</topic><topic>Curcumin - pharmacology</topic><topic>Drug Liberation</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>freeze drying</topic><topic>gelatin</topic><topic>Gelatin - chemistry</topic><topic>Mice</topic><topic>Nanofibers - chemistry</topic><topic>polymers</topic><topic>Porosity</topic><topic>quercetin</topic><topic>Quercetin - chemistry</topic><topic>Quercetin - pharmacology</topic><topic>Rats</topic><topic>Staphylococcus aureus - drug effects</topic><topic>tissue repair</topic><topic>Tissue Scaffolds - chemistry</topic><topic>water solubility</topic><topic>water uptake</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Katiyar, Soumya</creatorcontrib><creatorcontrib>Singh, Divakar</creatorcontrib><creatorcontrib>Tripathi, Abhay Dev</creatorcontrib><creatorcontrib>Chaurasia, Avinash Kumar</creatorcontrib><creatorcontrib>Singh, Ritika K</creatorcontrib><creatorcontrib>Srivastava, Pradeep K</creatorcontrib><creatorcontrib>Mishra, Abha</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Katiyar, Soumya</au><au>Singh, Divakar</au><au>Tripathi, Abhay Dev</au><au>Chaurasia, Avinash Kumar</au><au>Singh, Ritika K</au><au>Srivastava, Pradeep K</au><au>Mishra, Abha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro and in vivo assessment of curcumin-quercetin loaded multi-layered 3D-nanofibroporous matrix prepared by solution blow-spinning for full-thickness burn wound healing</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-06-01</date><risdate>2024</risdate><volume>270</volume><issue>Pt 1</issue><spage>132269</spage><pages>132269-</pages><issn>1879-0003</issn><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>Burn wounds (BWs) cause impairment of native skin tissue and may cause significant microbial infections that demand immediate care. Curcumin (Cur) and quercetin (Que) exhibit antimicrobial, hemocompatibility, ROS-scavenging, and anti-inflammatory properties. However, its instability, water insolubility, and low biological fluid absorption render it challenging to sustain local Cur and Que doses at the wound site. Therefore, to combat these limitations, we employed blow-spinning and freeze-drying to develop a multi-layered, Cur/Que-loaded gelatin/chitosan/PCL (GCP-Q/C) nanofibroporous (NFP) matrix. Morphological analysis of the NFP-matrix using SEM revealed a well-formed multi-layered structure. The FTIR and XRD plots demonstrated dual-bioactive incorporation and scaffold polymer interaction. Additionally, the GCP-Q/C matrix displayed high porosity (82.7 ± 2.07 %), adequate pore size (∼121 μm), enhanced water-uptake ability (∼675 % within 24 h), and satisfactory biodegradation. The scaffolds with bioactives had a long-term release, increased antioxidant activity, and were more effective against gram-positive (S. aureus) and gram-negative (E. coli) bacteria than the unloaded scaffolds. The in vitro findings of GCP-Q/C scaffolds showed promoted L929 cell growth and hemocompatibility. Additionally, an in vivo full-thickness BW investigation found that an implanted GCP-Q/C matrix stimulates rapid recuperation and tissue regeneration. In accordance with the findings, the Gel/Ch/PCL-Que/Cur NFP-matrix could represent an effective wound-healing dressing for BWs.</abstract><cop>Netherlands</cop><pmid>38744363</pmid><doi>10.1016/j.ijbiomac.2024.132269</doi></addata></record> |
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subjects | absorption Animals Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology antioxidant activity Antioxidants - chemistry Antioxidants - pharmacology bioactive compounds biocompatibility biodegradation Burns - drug therapy cell growth chitosan Chitosan - chemistry curcumin Curcumin - chemistry Curcumin - pharmacology Drug Liberation Escherichia coli Escherichia coli - drug effects freeze drying gelatin Gelatin - chemistry Mice Nanofibers - chemistry polymers Porosity quercetin Quercetin - chemistry Quercetin - pharmacology Rats Staphylococcus aureus - drug effects tissue repair Tissue Scaffolds - chemistry water solubility water uptake Wound Healing - drug effects |
title | In vitro and in vivo assessment of curcumin-quercetin loaded multi-layered 3D-nanofibroporous matrix prepared by solution blow-spinning for full-thickness burn wound healing |
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