Synthesis and characterization of valproic acid ester pro-drug micelles via an amphiphilic polycaprolactone block copolymer design
Literature Information
Suchithra A. Senevirathne, Suthida Boonsith, David Oupicky, Michael C. Biewer, Mihaela C. Stefan
The attachment of Histone deacetylase (HDAC) inhibitors via covalent bonds to biocompatible and biodegradable block copolymers provides a new research direction for cancer treatment. Herein, we report the synthesis and characterization of valproic acid ester pro-drug micelles of amphiphilic polycaprolactone block copolymers and their potential applications in drug delivery.
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Polymer Chemistry

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![2-(5-Bromo-1H-pyrrolo[2,3-B]pyridin-3-YL)acetic acid structure 2-(5-Bromo-1H-pyrrolo[2,3-B]pyridin-3-YL)acetic acid structure](https://static.chemtradehub.com/structs/106/1060795-03-0-0589.webp)
