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This study presents a microfluidic approach combined with a design of experiments (DoE) strategy to optimize the production of PEGylated liposomes with maleimide groups for targeted drug delivery to placental tissues. The research successfully identified optimal conditions for liposome formulation, achieving suitable size and polydispersity, and confirmed the absence of cytotoxicity while demonstrating high grafting efficiency for peptide conjugation. Overall, the findings indicate that this method enables

Author

yamalk48

Language

EN