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作 者:Mochamad Chalid Gifrandy Gustiraharjo Azizah Intan Pangesty Alyssa Adyandra Yudan Whulanza Sugeng Supriadi
机构地区:[1]Department of Metallurgical and Material Engineering,Faculty of Engineering,University of Indonesia,Depok City,16424,Indonesia [2]Department of Mechanical Engineering,Faculty of Engineering,University of Indonesia,Depok City,16424,Indonesia
出 处:《Journal of Renewable Materials》2023年第7期3043-3056,共14页可再生材料杂志(英文)
基 金:Funding Statement:This work was supported by Universitas Indonesia under Grant PUTI 2020(No.NKB-4325/UN2.RST/HKP.05.00/2020).
摘 要:Polyethylene glycol(PEG)was added at different concentrations to the blend of poly(L-lactic acid)(PLLA)and poly(D,L-lactic acid)(PDLLA)to tailor the properties.The differential scanning calorimetry(DSC)measurement showed that all blends were miscible due to shifting a single glass transition temperature into a lower temperature for increasing PEG content.The DSC,FTIR,and XRD results implied the crystallinity enhancement for PEG content until 8 wt%,then decreased at 12 wt%PEG.The XRD result indicated the homo crystalline phase formation in all blends and no stereocomplex crystal.The in vitro degradation study indicated that PEG content is proportional to the degradation rate.The highest weight loss after 28 days was achieved at 12 wt%PEG.The FTIR analysis showed a structural evolution overview during hydrolytic degradation,viz.increasing and decreasing crystallinity during 14 days for the blend without and with PEG,respectively.In conclusion,the PEG addition increased crystallinity and degradation rate of the PLLA/PDLLA mixture,but PEG higher amounts led to a decrease in crystallinity,and the weight loss was intensified.This can be useful for tuning PLA-based biomaterials with the desired physicochemical properties and appropriate degradation rates for applications in drug delivery/tissue engineering.
关 键 词:PLLA PDLLA PEG CRYSTALLINITY degradation
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