-
Something wrong with this record ?
Vancomycin-releasing cross-linked collagen sponges as wound dressings
JM. Hartinger, P. Lukáč, P. Mitáš, M. Mlček, M. Popková, T. Suchý, M. Šupová, J. Závora, V. Adámková, H. Benáková, O. Slanař, M. Šíma, M. Bartoš, H. Chlup, T. Grus
Language English Country Bosnia and Herzegovina
Document type Journal Article
NLK
Free Medical Journals
from 1998
PubMed Central
from 2004 to 2022
Europe PubMed Central
from 2006
Open Access Digital Library
from 2006-01-01
Medline Complete (EBSCOhost)
from 2008-08-01 to 2022-10-23
ROAD: Directory of Open Access Scholarly Resources
from 2008 to 2022
- MeSH
- Anti-Bacterial Agents pharmacokinetics MeSH
- Wound Healing drug effects MeSH
- Carps MeSH
- Carbodiimides pharmacokinetics MeSH
- Collagen pharmacokinetics MeSH
- Rats MeSH
- Methicillin-Resistant Staphylococcus aureus drug effects MeSH
- Bandages MeSH
- Vancomycin pharmacokinetics MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
The study presents a novel vancomycin-releasing collagen wound dressing derived from Cyprinus carpio collagen type I cross-linked with carbodiimide which retarded the degradation rate and increased the stability of the sponge. Following lyophilization, the dressings were subjected to gamma sterilization. The structure was evaluated via scanning electron microscopy images, micro-computed tomography, and infrared spectrometry. The structural stability and vancomycin release properties were evaluated in phosphate buffered saline. Microbiological testing and a rat model of a wound infected with methicillin-resistant Staphylococcus aureus (MRSA) were then employed to test the efficacy of the treatment of the infected wound. Following an initial mass loss due to the release of vancomycin, the sponges remained stable. After 7 days of exposure in phosphate buffered saline (37°C), 60% of the material remained with a preserved collagen secondary structure together with a high degree of open porosity (over 80%). The analysis of the release of vancomycin revealed homogeneous distribution of the antibiotic both across and between the sponges. The release of vancomycin was retarded as proved by in vitro testing and further confirmed by the animal model from which measurable concentrations were observed in blood samples 24 hours after the subcutaneous implantation of the sponge, which was more than observed following intraperitoneal administration. The sponge was also highly effective in terms of reducing the number of colony-forming units in biopsies extracted from the infected wounds 4 days following the inoculation of the wounds with the MRSA solution. The presented sponges have ideal properties to serve as wound dressing for prevention of surgical site infection or treatment of already infected wounds.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22004637
- 003
- CZ-PrNML
- 005
- 20240522102033.0
- 007
- ta
- 008
- 220113s2021 bn f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.17305/bjbms.2019.4496 $2 doi
- 035 __
- $a (PubMed)31782696
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a bn
- 100 1_
- $a Hartinger, Jan $u Department of Clinical Pharmacology and Pharmacy, Institute of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic $7 xx0224709
- 245 10
- $a Vancomycin-releasing cross-linked collagen sponges as wound dressings / $c JM. Hartinger, P. Lukáč, P. Mitáš, M. Mlček, M. Popková, T. Suchý, M. Šupová, J. Závora, V. Adámková, H. Benáková, O. Slanař, M. Šíma, M. Bartoš, H. Chlup, T. Grus
- 520 9_
- $a The study presents a novel vancomycin-releasing collagen wound dressing derived from Cyprinus carpio collagen type I cross-linked with carbodiimide which retarded the degradation rate and increased the stability of the sponge. Following lyophilization, the dressings were subjected to gamma sterilization. The structure was evaluated via scanning electron microscopy images, micro-computed tomography, and infrared spectrometry. The structural stability and vancomycin release properties were evaluated in phosphate buffered saline. Microbiological testing and a rat model of a wound infected with methicillin-resistant Staphylococcus aureus (MRSA) were then employed to test the efficacy of the treatment of the infected wound. Following an initial mass loss due to the release of vancomycin, the sponges remained stable. After 7 days of exposure in phosphate buffered saline (37°C), 60% of the material remained with a preserved collagen secondary structure together with a high degree of open porosity (over 80%). The analysis of the release of vancomycin revealed homogeneous distribution of the antibiotic both across and between the sponges. The release of vancomycin was retarded as proved by in vitro testing and further confirmed by the animal model from which measurable concentrations were observed in blood samples 24 hours after the subcutaneous implantation of the sponge, which was more than observed following intraperitoneal administration. The sponge was also highly effective in terms of reducing the number of colony-forming units in biopsies extracted from the infected wounds 4 days following the inoculation of the wounds with the MRSA solution. The presented sponges have ideal properties to serve as wound dressing for prevention of surgical site infection or treatment of already infected wounds.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a antibakteriální látky $x farmakokinetika $7 D000900
- 650 _2
- $a obvazy $7 D001458
- 650 _2
- $a karbodiimidy $x farmakokinetika $7 D002234
- 650 _2
- $a kapři $7 D002347
- 650 _2
- $a kolagen $x farmakokinetika $7 D003094
- 650 _2
- $a methicilin rezistentní Staphylococcus aureus $x účinky léků $7 D055624
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a vankomycin $x farmakokinetika $7 D014640
- 650 _2
- $a hojení ran $x účinky léků $7 D014945
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Lukáč, Peter $u 2nd Department of Cardiovascular Surgery, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Mitáš, Petr $u 2nd Department of Cardiovascular Surgery, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Mlček, Mikuláš $u Institute of Physiology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Popková, Michaela $u Institute of Physiology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Suchý, Tomáš $u Department of Composites and Carbon Materials, Institute of Rock Structure and Mechanics, Academy of Sciences of the Czech Republic, Prague, Czech Republic; Department of Mechanics, Biomechanics and Mechatronics, Faculty of Mechanical Engineering, Czech Technical University in Prague, Prague, Czech Republic
- 700 1_
- $a Šupová, Monika $u Department of Composites and Carbon Materials, Institute of Rock Structure and Mechanics, Academy of Sciences of the Czech Republic, Prague, Czech Republic
- 700 1_
- $a Závora, Jan $u Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Adámková, Václava $u Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Benáková, Hana $u Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Slanař, Ondřej $u Department of Clinical Pharmacology and Pharmacy, Institute of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Šíma, Martin $u Department of Clinical Pharmacology and Pharmacy, Institute of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Bartoš, Martin $u Department of Stomatology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 700 1_
- $a Chlup, Hynek $u Department of Mechanics, Biomechanics and Mechatronics, Faculty of Mechanical Engineering, Czech Technical University in Prague, Prague, Czech Republic
- 700 1_
- $a Grus, Tomáš $u 2nd Department of Cardiovascular Surgery, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic
- 773 0_
- $w MED00172976 $t Bosnian journal of basic medical sciences $x 1840-4812 $g Roč. 21, č. 1 (2021), s. 61-70
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31782696 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220113 $b ABA008
- 991 __
- $a 20240522102029 $b ABA008
- 999 __
- $a ok $b bmc $g 1751945 $s 1155786
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 21 $c 1 $d 61-70 $e 20210201 $i 1840-4812 $m Bosnian journal of basic medical sciences $n Bosn J Basic Med Sci $x MED00172976
- LZP __
- $a Pubmed-20220113