4.4 Article

Functionalized lactic acid macromonomers via polycondensation as an alternative to ring opening polymerization

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WILEY
DOI: 10.1002/cjce.24800

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kinetic model; lactic acid; lactide; polycondensation; ring-opening polymerization

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Engineered polylactic acid (PLA) nanoparticles synthesized from oligo(lactic acid) macromonomers have been studied for controlled drug delivery. This study compares the synthesis of PLA-based macromonomers via ring-opening polymerization (ROP) and direct polycondensation of lactic acid in the presence of 2-hydroxyethyl methacrylate (HEMA). It is found that polycondensation is a valuable alternative to ROP for macromonomers with an average chain length of up to 4, while ROP remains the main route for longer chains requiring strict control over the chain length distribution.
Engineered polylactic acid (PLA) nanoparticles synthesized from oligo(lactic acid) macromonomers have been studied over the last decades for controlled drug delivery. These macromonomers are typically produced via ring-opening polymerization (ROP) of the cyclic dimer lactide, initiated by 2-hydroxyethyl methacrylate (HEMA). This reaction route, despite leading to well-defined macromonomers, relies on the production of lactide from lactic acid, which burdens the ROP overall cost for more than 30%. In this work, we report the synthesis of PLA-based macromonomers by direct polycondensation of lactic acid in the presence of HEMA as a valuable alternative to ROP. In particular, we compare the two processes side by side, focusing on the production of three HEMA-LA(n) macromonomers, with n = 2, 4, and 6. Detailed kinetic models are developed for both reaction systems, and the corresponding parameters are estimated by fitting the experimental data. Through these models, the reaction kinetics as well as the time evolution of the entire chain length distributions of the products from polycondensation and ROP could be reliably predicted. This way, we demonstrated that polycondensation is a valuable alternative to ROP only for macromonomers with an average chain length of up to 4 and that ROP remains the main route to longer chains, when a strict control over the chain length distribution is required.

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