α-Tocopherol liposome loaded chitosan hydrogel to suppress oxidative stress injury in cardiomyocytes.
Animals
Antioxidants
/ administration & dosage
Cell Adhesion
Cell Line
Cell Survival
Chitosan
/ chemistry
Humans
Hydrogels
/ chemistry
Hydrogen Bonding
Liposomes
Myocytes, Cardiac
/ metabolism
Oxidative Stress
/ drug effects
Rats
Reactive Oxygen Species
/ metabolism
Rheology
Spectrum Analysis
Temperature
alpha-Tocopherol
/ administration & dosage
Antioxidant
Cardiac tissue engineering
Chitosan hydrogel
Scaffold
α-Tocopherol liposome
Journal
International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578
Informations de publication
Date de publication:
15 Mar 2019
15 Mar 2019
Historique:
received:
11
06
2018
revised:
30
08
2018
accepted:
15
09
2018
pubmed:
19
9
2018
medline:
21
5
2019
entrez:
19
9
2018
Statut:
ppublish
Résumé
Myocardial infarction (MI) continues to be a major contributor to the morbidity and mortality across the globe. Injectable hydrogel, a tissue-engineered scaffold, recently demonstrated very promising in myocardial repair. However, the undesirable retention and survival of transplanted cells has limited their applications due to the oxidative stress microenvironment of MI lesions. In this work, a thermosensitive α-tocopherol (AT) liposome loaded chitosan hydrogel was developed to suppress the oxidative stress injury in cardiomyocytes. AT was embedded in the liposomes to improve its solubility and stability. The innovative AT liposome loaded chitosan hydrogel (AT-LCH) system had an appropriate sol-to-gel transition temperature. Hydrogels possessed a highly porous structure with irregular pores interconnected throughout the construct as shown by SEM, and liposomes distributed uniformly in the porous structure. A sustained AT release was observed in AT-LCH. In addition, AT-LCH has shown an excellent biocompatibility to support the adhesion and survival of cardiomyocytes. Moreover, it can resist the oxidative stress environment and improve the survival of cardiomyocytes. In general, this work suggests that AT-LCH may present an ideal scaffold material for injectable cardiac tissue engineering.
Identifiants
pubmed: 30227207
pii: S0141-8130(18)32715-6
doi: 10.1016/j.ijbiomac.2018.09.092
pii:
doi:
Substances chimiques
Antioxidants
0
Hydrogels
0
Liposomes
0
Reactive Oxygen Species
0
Chitosan
9012-76-4
alpha-Tocopherol
H4N855PNZ1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1192-1202Informations de copyright
Copyright © 2018. Published by Elsevier B.V.