Self-Assembly of Amphiphilic Block Copolypeptoids with C2-C5 Side Chains in Aqueous Solution

Nowadays, amphiphilic molecules play an important role in our life. In medical applications, amphiphilic block copolymers have attracted much attention as excipients in drug delivery systems. Here, the polymers are used as emulsifiers, micelles, or polymersomes with a hydrophilic corona block and a hydrophobic core or membrane. The aggregation behavior in aqueous solutions of a series of different amphiphilic block copolypeptoids comprising polysarcosine as a hydrophilic part is here reported. The formation of aggregates is investigated with 1H NMR spectroscopy and dynamic light scattering, and the determination of the critical micelle concentration (cmc) is performed using pyrene fluorescence spectroscopy. For the different block copolypeptoids cmc values ranging from 0.6 × 10−6m to 0.1 × 10−3m are found. The tendency to form micelles increases with increasing hydrophobicity at the nitrogen side chain in the hydrophobic moiety. Furthermore, in the case of the same hydrophobic side chain, a decreasing hydrophilic/lipophilic balance leads to the formation of larger aggregates. The aggregates formed in the buffer are able to solubilize the hydrophobic model compounds Reichardt's dye and pyrene, and exhibit versatile microenvironments. Final investigations about the cytotoxicity reveal that the block copolypeptoids are well tolerated by mammalian cells up to high concentrations. The aggregation behavior in aqueous solutions is reported for a series of different amphiphilic block copolypeptoids comprising polysarcosine as a hydrophilic part. The formation of aggregates is investigated with 1H NMR spectro­scopy and dynamic light scattering, and the critical micelle concentration is determined using pyrene fluorescence spectroscopy. Final investigations regarding cytotoxicity reveal that the block copolypeptoids are well tolerated by mammalian cells up to high concentrations.