Red wine-inspired tannic acid-KH561 copolymer: its adhesive properties and its application in wound healing

Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid-KH561 (TA561) copolymer was fabricated by phenol-silanol reaction and polycondensation of...

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Published inRSC advances Vol. 11; no. 9; pp. 5182 - 5191
Main Authors Chen, Chen, Yang, Xiao, Li, Shu-jing, Ma, Feng-jun, Yan, Xiao, Ma, Yu-ning, Ma, Yu-xia, Ma, Qing-hai, Gao, Shu-zhong, Huang, Xiao-jun
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 27.01.2021
The Royal Society of Chemistry
Subjects
Ability tests
Aluminum
ambient temperature
Antiinfectives and antibacterials
Aqueous solutions
bioadhesives
Chemistry
color
composite polymers
condensation reactions
Copolymers
dyeing
fabrics
films (materials)
heat
In vivo methods and tests
liquids
methicillin-resistant Staphylococcus aureus
Nanoparticles
Oligomers
Polyphenols
Polytetrafluoroethylene
red wines
Room temperature
rubber
silane
silicon
siloxanes
Skin preparations
Sol-gel processes
Staphylococcus infections
Tannic acid
Thin films
Vinyl chloride
wood
Wound healing
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Abstract Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid-KH561 (TA561) copolymer was fabricated by phenol-silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol-gel transition via continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag + or Au 3+ ions to form the corresponding nanoparticles. An in vivo antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant Staphylococcus aureus (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations. Inspired by the coating properties of red wine on various surfaces, tannic acid hardened KH561 (TA561) copolymer was fabricated for wound dressings. The synthetic route was facile, robust and the related raw material was low-cost.
AbstractList Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid-KH561 (TA561) copolymer was fabricated by phenol-silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol-gel transition via continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag+ or Au3+ ions to form the corresponding nanoparticles. An in vivo antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant Staphylococcus aureus (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations.Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid-KH561 (TA561) copolymer was fabricated by phenol-silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol-gel transition via continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag+ or Au3+ ions to form the corresponding nanoparticles. An in vivo antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant Staphylococcus aureus (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations.
Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid–KH561 (TA561) copolymer was fabricated by phenol–silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol–gel transition via continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag + or Au 3+ ions to form the corresponding nanoparticles. An in vivo antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant Staphylococcus aureus (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations. Inspired by the coating properties of red wine on various surfaces, tannic acid hardened KH561 (TA561) copolymer was fabricated for wound dressings. The synthetic route was facile, robust and the related raw material was low-cost.
Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid–KH561 (TA561) copolymer was fabricated by phenol–silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol–gel transition via continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag⁺ or Au³⁺ ions to form the corresponding nanoparticles. An in vivo antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant Staphylococcus aureus (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations.
Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid–KH561 (TA561) copolymer was fabricated by phenol–silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol–gel transition via continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag + or Au 3+ ions to form the corresponding nanoparticles. An in vivo antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant Staphylococcus aureus (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations.
Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid-KH561 (TA561) copolymer was fabricated by phenol-silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol-gel transition continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag or Au ions to form the corresponding nanoparticles. An antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations.
Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin care effect of pyrogallol-rich red wine, tannic acid–KH561 (TA561) copolymer was fabricated by phenol–silanol reaction and polycondensation of silane in an aqueous medium under mild conditions. This copolymer could undergo sol–gel transition via continuous heating or when simply placed at room temperature, during which liquid TA561 oligomers connected with each other to form solid TA561 as a bulk resin or thin film. Combining the advantages of the polyphenols and polysiloxane, TA561 can be used as an adhesive for multiple surfaces, including wood, polytetrafluoroethylene, poly(vinyl chloride), aluminum chips and silicon rubber. Furthermore, TA561 also possessed reducing activity towards Ag+ or Au3+ ions to form the corresponding nanoparticles. An in vivo antimicrobial ability test indicated that TA561 could promote wound healing and showed resistance to methicillin-resistant Staphylococcus aureus (MRSA) infection in comparison with KH561. Indeed, TA561 has the potential to be utilized as a low-cost, green bioadhesive material for skin preparations.
Author Ma, Yu-xia
Chen, Chen
Li, Shu-jing
Yan, Xiao
Ma, Feng-jun
Gao, Shu-zhong
Ma, Yu-ning
Huang, Xiao-jun
Ma, Qing-hai
Yang, Xiao
AuthorAffiliation Department of Polymer Science and Engineering
Shandong University of Traditional Chinese Medicine
The First Affiliated Hospital of Shandong First Medical University (Shandong Provincial Qianfoshan Hospital)
Key Laboratory of New Material Research Institute
Department of Acupuncture-Moxibustion and Tuina
Zhejiang University
MOE Key Laboratory of Macromolecular Synthesis and Functionalization
AuthorAffiliation_xml – name: Shandong University of Traditional Chinese Medicine
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Cites_doi 10.1021/acsmacrolett.9b00091
10.1038/415389a
10.1016/j.jece.2018.08.009
10.1093/jac/dkv367
10.1039/c3ra46342g
10.1002/anie.201310509
10.1097/SLA.0b013e318176c4b3
10.1016/j.envint.2018.12.065
10.1002/smll.201902440
10.1016/j.reactfunctpolym.2019.02.001
10.1016/j.foodres.2018.07.019
10.1002/adfm.201809110
10.1007/s00114-004-0501-4
10.1007/s10965-018-1616-1
10.1007/s00289-016-1868-z
10.1038/nmat4635
10.1016/j.pmatsci.2017.06.003
10.1021/acsabm.9b00353
10.32725/jab.2008.015
10.1039/C6NJ00185H
10.1038/nrdp.2018.33
10.1039/C9CS00285E
10.1016/j.compscitech.2019.04.016
10.1021/acsami.9b14538
10.1021/acs.jafc.9b03947
10.1160/TH12-08-0543
10.1016/j.cis.2018.06.001
10.1016/j.carbpol.2011.09.059
10.1021/acsbiomaterials.9b00130
10.2147/IJN.S124442
10.1002/adma.201503565
10.1002/pola.29028
10.1016/j.dyepig.2008.05.008
10.1021/acsami.8b03569
10.2174/1568026615666150414142209
10.1128/mBio.00880-19
10.1016/j.jallcom.2009.07.094
10.1128/CMR.19.2.403-434.2006
10.1111/j.1601-183X.2006.00249.x
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References Zhao (D0RA07342C-(cit24)/*[position()=1]) 2018; 25
Ge (D0RA07342C-(cit33)/*[position()=1]) 2019; 67
Guo (D0RA07342C-(cit20)/*[position()=1]) 2014; 53
Gao (D0RA07342C-(cit35)/*[position()=1]) 2018; 10
Jeschke (D0RA07342C-(cit2)/*[position()=1]) 2008; 248
He (D0RA07342C-(cit25)/*[position()=1]) 2019; 137
Penders (D0RA07342C-(cit32)/*[position()=1]) 2017; 12
Moghaddam (D0RA07342C-(cit17)/*[position()=1]) 2014; 4
Reitzer (D0RA07342C-(cit15)/*[position()=1]) 2018; 257
Korey (D0RA07342C-(cit38)/*[position()=1]) 2018; 56
Du (D0RA07342C-(cit22)/*[position()=1]) 2019; 5
Barthelemy (D0RA07342C-(cit36)/*[position()=1]) 2004; 91
Deng (D0RA07342C-(cit13)/*[position()=1]) 2019; 29
Meziane (D0RA07342C-(cit37)/*[position()=1]) 2007; 6
Xu (D0RA07342C-(cit39)/*[position()=1]) 2012; 87
Wang (D0RA07342C-(cit21)/*[position()=1]) 2019; 11
Chang (D0RA07342C-(cit29)/*[position()=1]) 2016; 71
Xu (D0RA07342C-(cit10)/*[position()=1]) 2019; 2
Zhu (D0RA07342C-(cit18)/*[position()=1]) 2019; 15
Szymanska-Chargot (D0RA07342C-(cit34)/*[position()=1]) 2009; 486
Burkinshaw (D0RA07342C-(cit19)/*[position()=1]) 2009; 80
Kumar (D0RA07342C-(cit7)/*[position()=1]) 2019; 124
Khatoon (D0RA07342C-(cit30)/*[position()=1]) 2018; 6
Nash (D0RA07342C-(cit14)/*[position()=1]) 2018; 113
Lee (D0RA07342C-(cit6)/*[position()=1]) 2017; 89
Franks (D0RA07342C-(cit28)/*[position()=1]) 2013; 109
Panyala (D0RA07342C-(cit8)/*[position()=1]) 2008; 6
Marin (D0RA07342C-(cit11)/*[position()=1]) 2015; 15
Zheng (D0RA07342C-(cit9)/*[position()=1]) 2019; 8
Church (D0RA07342C-(cit3)/*[position()=1]) 2006; 19
Lee (D0RA07342C-(cit4)/*[position()=1]) 2018; 4
Zasloff (D0RA07342C-(cit12)/*[position()=1]) 2002; 415
Yang (D0RA07342C-(cit23)/*[position()=1]) 2019; 177
Shang (D0RA07342C-(cit27)/*[position()=1]) 2019; 10
Castleberry (D0RA07342C-(cit5)/*[position()=1]) 2015; 28
Liu (D0RA07342C-(cit31)/*[position()=1]) 2016; 40
Hong (D0RA07342C-(cit26)/*[position()=1]) 2017; 74
Yu (D0RA07342C-(cit1)/*[position()=1]) 2016; 15
Zhang (D0RA07342C-(cit16)/*[position()=1]) 2020; 49
References_xml – volume: 8
  start-page: 326
  year: 2019
  ident: D0RA07342C-(cit9)/*[position()=1]
  publication-title: ACS Macro Lett.
  doi: 10.1021/acsmacrolett.9b00091
– volume: 415
  start-page: 389
  year: 2002
  ident: D0RA07342C-(cit12)/*[position()=1]
  publication-title: Nature
  doi: 10.1038/415389a
– volume: 6
  start-page: 5837
  year: 2018
  ident: D0RA07342C-(cit30)/*[position()=1]
  publication-title: J. Environ. Chem. Eng.
  doi: 10.1016/j.jece.2018.08.009
– volume: 71
  start-page: 449
  year: 2016
  ident: D0RA07342C-(cit29)/*[position()=1]
  publication-title: J. Antimicrob. Chemother.
  doi: 10.1093/jac/dkv367
– volume: 4
  start-page: 8711
  year: 2014
  ident: D0RA07342C-(cit17)/*[position()=1]
  publication-title: RSC Adv.
  doi: 10.1039/c3ra46342g
– volume: 53
  start-page: 1
  year: 2014
  ident: D0RA07342C-(cit20)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201310509
– volume: 248
  start-page: 387
  year: 2008
  ident: D0RA07342C-(cit2)/*[position()=1]
  publication-title: Ann. Surg.
  doi: 10.1097/SLA.0b013e318176c4b3
– volume: 124
  start-page: 448
  year: 2019
  ident: D0RA07342C-(cit7)/*[position()=1]
  publication-title: Environ. Int.
  doi: 10.1016/j.envint.2018.12.065
– volume: 15
  start-page: 1902440
  year: 2019
  ident: D0RA07342C-(cit18)/*[position()=1]
  publication-title: Small
  doi: 10.1002/smll.201902440
– volume: 137
  start-page: 104
  year: 2019
  ident: D0RA07342C-(cit25)/*[position()=1]
  publication-title: React. Funct. Polym.
  doi: 10.1016/j.reactfunctpolym.2019.02.001
– volume: 113
  start-page: 277
  year: 2018
  ident: D0RA07342C-(cit14)/*[position()=1]
  publication-title: Food Res. Int.
  doi: 10.1016/j.foodres.2018.07.019
– volume: 29
  start-page: 1809110
  year: 2019
  ident: D0RA07342C-(cit13)/*[position()=1]
  publication-title: Adv. Funct. Mater.
  doi: 10.1002/adfm.201809110
– volume: 91
  start-page: 135
  year: 2004
  ident: D0RA07342C-(cit36)/*[position()=1]
  publication-title: Naturwissenschaften
  doi: 10.1007/s00114-004-0501-4
– volume: 25
  start-page: 225
  year: 2018
  ident: D0RA07342C-(cit24)/*[position()=1]
  publication-title: J. Polym. Res.
  doi: 10.1007/s10965-018-1616-1
– volume: 74
  start-page: 2861
  year: 2017
  ident: D0RA07342C-(cit26)/*[position()=1]
  publication-title: Polym. Bull.
  doi: 10.1007/s00289-016-1868-z
– volume: 15
  start-page: 911
  year: 2016
  ident: D0RA07342C-(cit1)/*[position()=1]
  publication-title: Nat. Mater.
  doi: 10.1038/nmat4635
– volume: 89
  start-page: 392
  year: 2017
  ident: D0RA07342C-(cit6)/*[position()=1]
  publication-title: Prog. Mater. Sci.
  doi: 10.1016/j.pmatsci.2017.06.003
– volume: 2
  start-page: 3329
  year: 2019
  ident: D0RA07342C-(cit10)/*[position()=1]
  publication-title: ACS Appl. Bio Mater.
  doi: 10.1021/acsabm.9b00353
– volume: 6
  start-page: 117
  year: 2008
  ident: D0RA07342C-(cit8)/*[position()=1]
  publication-title: J. Appl. Biomed.
  doi: 10.32725/jab.2008.015
– volume: 40
  start-page: 6332
  year: 2016
  ident: D0RA07342C-(cit31)/*[position()=1]
  publication-title: New J. Chem.
  doi: 10.1039/C6NJ00185H
– volume: 4
  start-page: 18033
  year: 2018
  ident: D0RA07342C-(cit4)/*[position()=1]
  publication-title: Nat. Rev. Dis. Primers
  doi: 10.1038/nrdp.2018.33
– volume: 49
  start-page: 433
  year: 2020
  ident: D0RA07342C-(cit16)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C9CS00285E
– volume: 177
  start-page: 18
  year: 2019
  ident: D0RA07342C-(cit23)/*[position()=1]
  publication-title: Compos. Sci. Technol.
  doi: 10.1016/j.compscitech.2019.04.016
– volume: 11
  start-page: 37502
  year: 2019
  ident: D0RA07342C-(cit21)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.9b14538
– volume: 67
  start-page: 11489
  year: 2019
  ident: D0RA07342C-(cit33)/*[position()=1]
  publication-title: J. Agric. Food Chem.
  doi: 10.1021/acs.jafc.9b03947
– volume: 109
  start-page: 684
  year: 2013
  ident: D0RA07342C-(cit28)/*[position()=1]
  publication-title: Thromb. Haemostasis
  doi: 10.1160/TH12-08-0543
– volume: 257
  start-page: 31
  year: 2018
  ident: D0RA07342C-(cit15)/*[position()=1]
  publication-title: Adv. Colloid Interface Sci.
  doi: 10.1016/j.cis.2018.06.001
– volume: 87
  start-page: 1589
  year: 2012
  ident: D0RA07342C-(cit39)/*[position()=1]
  publication-title: Carbohydr. Polym.
  doi: 10.1016/j.carbpol.2011.09.059
– volume: 5
  start-page: 2610
  year: 2019
  ident: D0RA07342C-(cit22)/*[position()=1]
  publication-title: ACS Biomater. Sci. Eng.
  doi: 10.1021/acsbiomaterials.9b00130
– volume: 12
  start-page: 2457
  year: 2017
  ident: D0RA07342C-(cit32)/*[position()=1]
  publication-title: Int. J. Nanomed.
  doi: 10.2147/IJN.S124442
– volume: 28
  start-page: 1809
  year: 2015
  ident: D0RA07342C-(cit5)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201503565
– volume: 56
  start-page: 1468
  year: 2018
  ident: D0RA07342C-(cit38)/*[position()=1]
  publication-title: J. Polym. Sci., Part A: Polym. Chem.
  doi: 10.1002/pola.29028
– volume: 80
  start-page: 53
  year: 2009
  ident: D0RA07342C-(cit19)/*[position()=1]
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2008.05.008
– volume: 10
  start-page: 17352
  year: 2018
  ident: D0RA07342C-(cit35)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.8b03569
– volume: 15
  start-page: 1596
  year: 2015
  ident: D0RA07342C-(cit11)/*[position()=1]
  publication-title: Curr. Top. Med. Chem.
  doi: 10.2174/1568026615666150414142209
– volume: 10
  start-page: e00880
  year: 2019
  ident: D0RA07342C-(cit27)/*[position()=1]
  publication-title: mBio
  doi: 10.1128/mBio.00880-19
– volume: 486
  start-page: 66
  year: 2009
  ident: D0RA07342C-(cit34)/*[position()=1]
  publication-title: J. Alloys Compd.
  doi: 10.1016/j.jallcom.2009.07.094
– volume: 19
  start-page: 403
  year: 2006
  ident: D0RA07342C-(cit3)/*[position()=1]
  publication-title: Clin. Microbiol. Rev.
  doi: 10.1128/CMR.19.2.403-434.2006
– volume: 6
  start-page: 192
  year: 2007
  ident: D0RA07342C-(cit37)/*[position()=1]
  publication-title: Genes, Brain Behav.
  doi: 10.1111/j.1601-183X.2006.00249.x
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Snippet Damaged tissue with an open wound is one of the daily injuries and can have different levels of severity. Inspired by the textile dyeing, coloration and skin...
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SubjectTerms Ability tests
Aluminum
ambient temperature
Antiinfectives and antibacterials
Aqueous solutions
bioadhesives
Chemistry
color
composite polymers
condensation reactions
Copolymers
dyeing
fabrics
films (materials)
heat
In vivo methods and tests
liquids
methicillin-resistant Staphylococcus aureus
Nanoparticles
Oligomers
Polyphenols
Polytetrafluoroethylene
red wines
Room temperature
rubber
silane
silicon
siloxanes
Skin preparations
Sol-gel processes
Staphylococcus infections
Tannic acid
Thin films
Vinyl chloride
wood
Wound healing
Title Red wine-inspired tannic acid-KH561 copolymer: its adhesive properties and its application in wound healing
URI https://www.ncbi.nlm.nih.gov/pubmed/35424430
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