One-pot synthesis creates antimicrobial microcapsules with sustained-release properties, indicating potential for medical applications.
Natural, low-toxicity, and controlled-release antimicrobial microcapsules were synthesized via one-pot emulsion crosslinking of esterification and amidation condensation. The controlled-release microcapsules (MCs) exhibited adjustable surface charge, a satisfactory porous structure, and sustained-release capabilities. The core agent release performance adhered to the Ritger-Peppas model, characterized by Fickian diffusion.
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Xiang et al. (2025) studied this question.
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