This study demonstrates significant drug loading efficiency in amphiphilic diblock copolymers, indicating potential for drug delivery applications.
This study investigates the self-assembly behavior of a series of amphiphilic diblock co-polymers, each consisting of a hydrophilic poly(N-vinyl pyrrolidone) (PNVP) block and a hydrophobic block derived from n-alkyl vinyl esters, namely poly(vinyl butyrate) (PVBu), poly(vinyl decanoate), (PVDc) and poly(vinyl stearate) (PVSt), in aqueous solutions. Dynamic and static light scattering (DLS and SLS) techniques were employed to monitor the micellization behavior. The effect of the nature of the hydrophobic block, the copolymer composition and the copolymer molecular weight on the self-assembly properties were thoroughly examined. The encapsulation of curcumin and indomethacin within the dry cores of the micellar structures was conducted in aqueous solutions for all block copolymers at various curcumin/indomethacin-to-polymer mass ratios. UV-Vis spectroscopy was used to evaluate the drug loading capacity and efficiency (%DLC and %DLE). In several cases, the encapsulation of both hydrophobic drugs was found to be nearly quantitative. Combined with the observed stability of the micellar structures, these findings suggest that the block copolymers demonstrate significant potential as carriers for drug delivery applications.
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Plachouras et al. (2025) studied this question.
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