Versatile dopamine-functionalized hyaluronic acid-recombinant human collagen hydrogel promoting diabetic wound healing via inflammation control and vascularization tissue regeneration

The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctio...

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Published inBioactive materials Vol. 35; pp. 330 - 345
Main Authors Wang, Yong, Zhang, Yuan, Yang, Yun-Peng, Jin, Ming-Yuan, Huang, Sha, Zhuang, Ze-Ming, Zhang, Tao, Cao, Li-Li, Lin, Xiao-Ying, Chen, Jun, Du, Yong-Zhong, Chen, Jian, Tan, Wei-Qiang
Format Journal Article
LanguageEnglish
Published China Elsevier B.V 01.05.2024
KeAi Publishing Communications Ltd
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Abstract The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctional hydrogels. Here, we have produced HA-DA@rhCol hydrogels consisting of dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol) by oxidative coupling of the catechol group using the H2O2/HRP catalytic system. The post-reactive hydrogel has a good porous structure, swelling rate, reasonable degradation, rheological and mechanical properties, and the catechol group and dopamine impart to the hydrogel tissue adhesiveness, antioxidant capacity, and excellent photothermal effects leading to superior in vitro antimicrobial activity. In addition, the ability of rhCol to confer hydrogels to promote angiogenesis and wound repair has also been investigated. Cytotoxicity and hemolysis tests demonstrated the good biocompatibility of the hydrogel. Wound closure, collagen deposition and immunohistochemical examination confirmed the ability of the hydrogel to promote diabetic wound healing. In summary, the adhesive hemostatic antioxidative hydrogel with rhCol to promote wound healing in diabetic rat is an excellent chronic wound dressing. [Display omitted] •This hydrogel is formulated by combining dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol).•The hydrogel demonstrates tissue adhesiveness, antioxidant capacity, and photothermal effect coupled with antibacterial activity.•The introduction of dopamine enhances the anti-inflammatory effect of hyaluronic acid in diabetic wound.•RhCol promotes angiogenesis in diabetic wound, rendering it a kind of promising bioactive material for chronic wound dressing.
AbstractList The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctional hydrogels. Here, we have produced HA-DA@rhCol hydrogels consisting of dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol) by oxidative coupling of the catechol group using the H2O2/HRP catalytic system. The post-reactive hydrogel has a good porous structure, swelling rate, reasonable degradation, rheological and mechanical properties, and the catechol group and dopamine impart to the hydrogel tissue adhesiveness, antioxidant capacity, and excellent photothermal effects leading to superior in vitro antimicrobial activity. In addition, the ability of rhCol to confer hydrogels to promote angiogenesis and wound repair has also been investigated. Cytotoxicity and hemolysis tests demonstrated the good biocompatibility of the hydrogel. Wound closure, collagen deposition and immunohistochemical examination confirmed the ability of the hydrogel to promote diabetic wound healing. In summary, the adhesive hemostatic antioxidative hydrogel with rhCol to promote wound healing in diabetic rat is an excellent chronic wound dressing. [Display omitted] •This hydrogel is formulated by combining dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol).•The hydrogel demonstrates tissue adhesiveness, antioxidant capacity, and photothermal effect coupled with antibacterial activity.•The introduction of dopamine enhances the anti-inflammatory effect of hyaluronic acid in diabetic wound.•RhCol promotes angiogenesis in diabetic wound, rendering it a kind of promising bioactive material for chronic wound dressing.
The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctional hydrogels. Here, we have produced HA-DA@rhCol hydrogels consisting of dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol) by oxidative coupling of the catechol group using the H2O2/HRP catalytic system. The post-reactive hydrogel has a good porous structure, swelling rate, reasonable degradation, rheological and mechanical properties, and the catechol group and dopamine impart to the hydrogel tissue adhesiveness, antioxidant capacity, and excellent photothermal effects leading to superior in vitro antimicrobial activity. In addition, the ability of rhCol to confer hydrogels to promote angiogenesis and wound repair has also been investigated. Cytotoxicity and hemolysis tests demonstrated the good biocompatibility of the hydrogel. Wound closure, collagen deposition and immunohistochemical examination confirmed the ability of the hydrogel to promote diabetic wound healing. In summary, the adhesive hemostatic antioxidative hydrogel with rhCol to promote wound healing in diabetic rat is an excellent chronic wound dressing.
The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctional hydrogels. Here, we have produced HA-DA@rhCol hydrogels consisting of dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol) by oxidative coupling of the catechol group using the H O /HRP catalytic system. The post-reactive hydrogel has a good porous structure, swelling rate, reasonable degradation, rheological and mechanical properties, and the catechol group and dopamine impart to the hydrogel tissue adhesiveness, antioxidant capacity, and excellent photothermal effects leading to superior in vitro antimicrobial activity. In addition, the ability of rhCol to confer hydrogels to promote angiogenesis and wound repair has also been investigated. Cytotoxicity and hemolysis tests demonstrated the good biocompatibility of the hydrogel. Wound closure, collagen deposition and immunohistochemical examination confirmed the ability of the hydrogel to promote diabetic wound healing. In summary, the adhesive hemostatic antioxidative hydrogel with rhCol to promote wound healing in diabetic rat is an excellent chronic wound dressing.
The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctional hydrogels. Here, we have produced HA-DA@rhCol hydrogels consisting of dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol) by oxidative coupling of the catechol group using the H 2 O 2 /HRP catalytic system. The post-reactive hydrogel has a good porous structure, swelling rate, reasonable degradation, rheological and mechanical properties, and the catechol group and dopamine impart to the hydrogel tissue adhesiveness, antioxidant capacity, and excellent photothermal effects leading to superior in vitro antimicrobial activity. In addition, the ability of rhCol to confer hydrogels to promote angiogenesis and wound repair has also been investigated. Cytotoxicity and hemolysis tests demonstrated the good biocompatibility of the hydrogel. Wound closure, collagen deposition and immunohistochemical examination confirmed the ability of the hydrogel to promote diabetic wound healing. In summary, the adhesive hemostatic antioxidative hydrogel with rhCol to promote wound healing in diabetic rat is an excellent chronic wound dressing. Image 1 • This hydrogel is formulated by combining dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol). • The hydrogel demonstrates tissue adhesiveness, antioxidant capacity, and photothermal effect coupled with antibacterial activity. • The introduction of dopamine enhances the anti-inflammatory effect of hyaluronic acid in diabetic wound. • RhCol promotes angiogenesis in diabetic wound, rendering it a kind of promising bioactive material for chronic wound dressing.
The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctional hydrogels. Here, we have produced HA-DA@rhCol hydrogels consisting of dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol) by oxidative coupling of the catechol group using the H2O2/HRP catalytic system. The post-reactive hydrogel has a good porous structure, swelling rate, reasonable degradation, rheological and mechanical properties, and the catechol group and dopamine impart to the hydrogel tissue adhesiveness, antioxidant capacity, and excellent photothermal effects leading to superior in vitro antimicrobial activity. In addition, the ability of rhCol to confer hydrogels to promote angiogenesis and wound repair has also been investigated. Cytotoxicity and hemolysis tests demonstrated the good biocompatibility of the hydrogel. Wound closure, collagen deposition and immunohistochemical examination confirmed the ability of the hydrogel to promote diabetic wound healing. In summary, the adhesive hemostatic antioxidative hydrogel with rhCol to promote wound healing in diabetic rat is an excellent chronic wound dressing.The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection, and elevated risk of reopening, highlighting the need for effective chronic wound management with innovative approaches such as multifunctional hydrogels. Here, we have produced HA-DA@rhCol hydrogels consisting of dopamine-modified hyaluronic acid and recombinant human collagen type-III (rhCol) by oxidative coupling of the catechol group using the H2O2/HRP catalytic system. The post-reactive hydrogel has a good porous structure, swelling rate, reasonable degradation, rheological and mechanical properties, and the catechol group and dopamine impart to the hydrogel tissue adhesiveness, antioxidant capacity, and excellent photothermal effects leading to superior in vitro antimicrobial activity. In addition, the ability of rhCol to confer hydrogels to promote angiogenesis and wound repair has also been investigated. Cytotoxicity and hemolysis tests demonstrated the good biocompatibility of the hydrogel. Wound closure, collagen deposition and immunohistochemical examination confirmed the ability of the hydrogel to promote diabetic wound healing. In summary, the adhesive hemostatic antioxidative hydrogel with rhCol to promote wound healing in diabetic rat is an excellent chronic wound dressing.
Author Zhuang, Ze-Ming
Lin, Xiao-Ying
Yang, Yun-Peng
Huang, Sha
Chen, Jun
Chen, Jian
Wang, Yong
Jin, Ming-Yuan
Tan, Wei-Qiang
Du, Yong-Zhong
Zhang, Yuan
Cao, Li-Li
Zhang, Tao
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  surname: Wang
  fullname: Wang, Yong
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 2
  givenname: Yuan
  orcidid: 0009-0004-8911-7471
  surname: Zhang
  fullname: Zhang, Yuan
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 3
  givenname: Yun-Peng
  surname: Yang
  fullname: Yang, Yun-Peng
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 4
  givenname: Ming-Yuan
  surname: Jin
  fullname: Jin, Ming-Yuan
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
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  givenname: Sha
  surname: Huang
  fullname: Huang, Sha
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 6
  givenname: Ze-Ming
  surname: Zhuang
  fullname: Zhuang, Ze-Ming
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 7
  givenname: Tao
  surname: Zhang
  fullname: Zhang, Tao
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 8
  givenname: Li-Li
  surname: Cao
  fullname: Cao, Li-Li
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 9
  givenname: Xiao-Ying
  surname: Lin
  fullname: Lin, Xiao-Ying
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 10
  givenname: Jun
  orcidid: 0000-0002-4459-8804
  surname: Chen
  fullname: Chen, Jun
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 11
  givenname: Yong-Zhong
  surname: Du
  fullname: Du, Yong-Zhong
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
– sequence: 12
  givenname: Jian
  surname: Chen
  fullname: Chen, Jian
  email: chenjianzuj4h@zju.edu.cn
  organization: Department of Ultrasound in Medicine, The Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, 322000, China
– sequence: 13
  givenname: Wei-Qiang
  orcidid: 0000-0003-4951-0960
  surname: Tan
  fullname: Tan, Wei-Qiang
  email: tanweixxxx@zju.edu.cn
  organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, 3 East Qingchun Road, Hangzhou, 310016, China
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Keywords Hyaluronic acid hydrogel
Antibacterial
Antioxidant and anti-inflammation
Recombinant human collagen
Diabetic wound
Language English
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Snippet The management of chronic wounds in diabetes remains challenging due to the complexity of impaired wound healing, delayed healing, susceptibility to infection,...
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StartPage 330
SubjectTerms Adhesives
Angiogenesis
Antibacterial
Antimicrobial activity
Antioxidant and anti-inflammation
Antioxidants
Biocompatibility
Catechol
Chronic infection
Collagen
Cytotoxicity
Diabetes
Diabetes mellitus
Diabetic wound
Disease management
Dopamine
Effectiveness
Extracellular matrix
Hyaluronic acid
Hyaluronic acid hydrogel
Hydrocarbons
Hydrogels
Hydrogen peroxide
Infections
Inflammation
Mechanical properties
Pore size
Recombinant human collagen
Regeneration (physiology)
Rheological properties
Rheology
Skin
Spectrum analysis
Tissue engineering
Vascularization
Wound healing
Wound infection
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Title Versatile dopamine-functionalized hyaluronic acid-recombinant human collagen hydrogel promoting diabetic wound healing via inflammation control and vascularization tissue regeneration
URI https://dx.doi.org/10.1016/j.bioactmat.2024.02.010
https://www.ncbi.nlm.nih.gov/pubmed/38379700
https://www.proquest.com/docview/3076295919
https://www.proquest.com/docview/2929539835
https://pubmed.ncbi.nlm.nih.gov/PMC10876488
https://doaj.org/article/4ab1fc865c214577b4145d346db968a7
Volume 35
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