Self-Catalyzed Transesterification Transforms Ionizable Amphiphilic Janus Dendrimers into Multicomponent Vectors and Generates Complex Design Strategies for mRNA Delivery
In the authors' words
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Main result
Here we report that, unexpectedly, the least stable benzyl-ester-based IAJDs, which contain the 1-(2-hydroxyethyl)piperazine ionizable amine (IA), undergo an extraordinarily slow, self-catalyzed transesterification at room temperature that transforms the one-component system into a multicomponent one.
Appeared: Monday, September 21. Journal of the American Chemical Society. Peer-reviewed journal.
DOI: 10.1021/jacs.6c17127