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Optimization of an α‐(Amino acid)‐N‐carboxyanhydride polymerization using the high vacuum technique: Examining the effects of monomer concentration,polymerization kinetics,polymer molecular weight,and monomer purity
Authors:Robert A. Kowtoniuk  Tao Pei  Caitlin M. DeAngelo  Jacob H. Waldman  Erin N. Guidry  J. Michael Williams  Robert M. Garbaccio  Stephanie E. Barrett
Affiliation:1. Department of RNA Medicinal Chemistry, Merck Research Laboratories, Merck & Co., Inc., , West Point, Pennsylvania, 19486;2. Department of Process Chemistry, Merck Research Laboratories, Merck & Co., Inc., Rahway, , New Jersey, 07065
Abstract:l ‐Ornithine‐based poly(peptides) have been widely utilized in the field of drug delivery, however few studies have been conducted examining the details of polymerization. In this article, the effects of monomer concentration, polymerization kinetics, polymer molecular weight and monomer purity were investigated using l ‐carboxybenzyl (Cbz)‐ornithine as a model monomer. The mechanism of polymerization herein follows the normal amine mechanism to produce poly(peptides) having controlled molecular weights, known chain ends and a narrow polydispersity index (PDI). A preferred monomer concentration range was determined, which required minimal polymerization times and allowed for predictable and reproducible molecular weights with narrow PDIs. The impact of monomer purity on the polymerization was established and monomer purification conditions are reported, which produce high‐purity monomer after a single recrystallization. Additionally, the optimized polymerization conditions and monomer purification protocol were combined with a sequential monomer addition technique to produce high molecular weight poly(ornithine) with a narrow PDI and known chain ends. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1385–1391
Keywords:biodegradable  biopolymers  peptides  ring‐opening polymerization  α  ‐amino acid N‐carboxyanhydride
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