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報告人：陳榮軍教授(Prof. Rongjun Chen)

報告人單位：英國帝國理工學院(Imperial College London)

報告時間：2023年6月29日（星期四）15:30

會議地點：江浦校區潤德樓B511報告廳

舉辦單位：材料科學與工程學院

報告人簡介：Rongjun Chen obtained his PhD degree and did his postdoctoral work in the Department of Chemical Engineering and Biotechnology at the University of Cambridge. He is Currently Professor of Biomaterials Engineering and Head of the Biomaterials and Nanomedicine Laboratory in the Department of Chemical Engineering at Imperial College London. His research focuses on design, synthesis and manufacturing of polymers, lipids and bio-inspired nanoparticles for targeted delivery of active pharmaceutical agents through fundamental understanding of their transport processes across extracellular and intracellular barriers. He has developed a translational research programme on targeted nanomedicine, thermostable RNA vaccine formulation, cell and gene therapy. His research work has been recognised by various awards including the IChemE Global Team Award in 2021, Imperial College President’s Award for Outstanding Research Team in 2021, and highly commended for IChemE Global Biotechnology Award in 2018. He is an Editor for Chemical Engineering Journal.

報告摘要：Biomacromolecules represent a powerful new class of vaccines and therapies with potential for treatment of a wide variety of previously intractable human diseases. However, it remains a major challenge to effectively deliver them to a target site. There is a need to better understand the mechanisms of delivery across extracellular and intracellular barriers in order to design optimal delivery systems for biological molecules. On the one hand, this would open up significant opportunities to protect and deliver potent macromolecules of therapeutic interest to positively impact human health. In addition, this would enable us to develop a more general understanding of the rules governing the extracellular and intracellular delivery of biological molecules.

This talk will cover our efforts on design, synthesis and biological evaluation in-vitro and in-vivo of novel bio-inspired nanostructures. Strict control over their structure, size, charge and hydrophobicity-hydrophilicity balance can effectively manipulate their physicochemical properties and interactions with lipid membrane, cell, tissue and animal models at different length scales. It has been demonstrated that the non-toxic and biocompatible nano-formulations display favourable in-vivo biodistribution, enhanced three-dimensional tissue penetration, and efficient intracellular delivery of payloads with a range of different sizes and charges, including peptides, proteins and nucleic acids such as RNA. Our work presents promising platforms suitable for development of targeted nanomedicines and vaccines.

審核：沈岳松