Conjugation of PDLA onto MgO microspheres: comparison between solution grafting and melt grafting methods.

J Mater Chem B

Engineering Research Centre for Biomedical Materials of Ministry of Education, Key Laboratory for Ultrafine Materials of Ministry of Education, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.

Published: January 2025

Magnesium oxide (MgO) is known for its bioactivity and osteoconductivity when incorporated into biodegradable poly(lactic acid) (PLA), whereas the weak interfacial bonding between MgO microspheres (mMPs) and PLA often leads to suboptimal composite properties with uncontrollable functionality. Conjugation of mMPs with PLA may offer a good way to enhance their compatibility. In this study, we systematically investigated two grafting techniques, solution grafting (Sol) and melt grafting (Mel), to decorate poly (D-lactic acid) (PDLA) on mMPs pre-treated by prioritized hydration to obtain Sol MPs and Mel MPs, in order to optimize the grafting efficiency and improve their controllability in the properties including the crystal structure and surface morphology. Meanwhile, the Sol method showed an improved grafting ratio (2.9 times higher) compared to the Mel method. The conjugation of mMPs with PDLA effectively neutralized the rapid pH increase during the degradation of pure mMPs, which could be used for sustainable delivery of the Mg ions. Moreover, the Sol MPs exhibited the lowest degradation rate constant, which could be well fitted by the first-order dynamic model, suggesting a transformation of the mMP degradation mode from bulk degradation to surface degradation. This change in the biodegradation mode was beneficial for decreasing the over-basic effect caused by the quick degradation of pure mMPs, thus extending their application in the development of PDLA/MgO composites towards tissue engineering or regenerative medicine.

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Source
http://dx.doi.org/10.1039/d4tb02692fDOI Listing

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