Citrate-Based Polyester Elastomer with Artificially Regulatable Degradation Rate on Demand

Citrate-based polymers are commonly used to create biodegradable implants. In an era of personalized medicine, it is highly desired that the degradation rates of citrate-based implants can be artificially regulated as required during clinical applications. Unfortunately, current citrate-based polyme...

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Veröffentlicht in:Biomacromolecules 2023-09, Vol.24 (9), p.4123-4137
Hauptverfasser: Wan, Lu, Lu, Liangliang, Liang, Xuejiao, Liu, Zhichang, Huang, Xinxin, Du, Ruichun, Luo, Qiong, Xu, Qiang, Zhang, Qiuhong, Jia, Xudong
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Sprache:eng
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Zusammenfassung:Citrate-based polymers are commonly used to create biodegradable implants. In an era of personalized medicine, it is highly desired that the degradation rates of citrate-based implants can be artificially regulated as required during clinical applications. Unfortunately, current citrate-based polymers only undergo passive degradation, which follows a specific degradation profile. This presents a considerable challenge for the use of citrate-based implants. To address this, a novel citrate-based polyester elastomer (POCSS) with artificially regulatable degradation rate is developed by incorporating disulfide bonds (S–S) into the backbone chains of the crosslinking network of poly­(octamethylene citrate) (POC). This POCSS exhibits excellent and tunable mechanical properties, notable antibacterial properties, good biocompatibility, and low biotoxicity of its degradation products. The degradation rate of the POCSS can be regulated by breaking the S–S in its crosslinking network using glutathione (GSH). After a period of subcutaneous implantation of POCSS scaffolds in mice, the degradation rate eventually increased by 2.46 times through the subcutaneous administration of GSH. Notably, we observed no significant adverse effects on its surrounding tissues, the balance of the physiological environment, major organs, and the health status of the mice during degradation.
ISSN:1525-7797
1526-4602
DOI:10.1021/acs.biomac.3c00479