Enhancing therapeutic loading and delaying transport via molecular imprinting and living/controlled polymerization

Asa D. Vaughan, Jeney B. Zhang, Mark Byrne

    Research output: Contribution to journalArticlepeer-review

    28 Scopus citations

    Abstract

    This work demonstrates for the first time molecular imprinting using a "living/controlled" polymerization (LCP) strategy to enhance template loading/affinity and delay release in weakly crosslinked gels. Two gel systems were studied: poly(DEAEM-co-HEMA-co-PEG200DMA) gels imprinted for diclofenac sodium and poly(MAA-co-EGDMA) gels imprinted for ethyl adenine-9-acetate. Experimental evidence confirms that template diffusion coefficients within imprinted gels can be heavily influenced by template binding affinity. Recognition studies revealed significant increases in template loading/affinity with large increases in loading for LCP, and dynamic template release studies showed that imprinting via LCP extends the template release profile by twofold over that of imprinting via conventional free-radical polymerization techniques and fourfold over the control network (less Fickian and toward zero-order release with a profile coefficient of 0.70). Analysis of reaction kinetics indicated that LCP with reversible termination events increases the chemically controlled chain propagation mechanism, and that binding sites are formed during this phase of the polymerization.

    Original languageEnglish (US)
    Pages (from-to)268-279
    Number of pages12
    JournalAIChE Journal
    Volume56
    Issue number1
    DOIs
    StatePublished - Jan 1 2010

    All Science Journal Classification (ASJC) codes

    • Biotechnology
    • Environmental Engineering
    • Chemical Engineering(all)

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