Solvent-Free Direct PEGylation of Collagen Fibers

The addition of poly(ethylene glycol) (PEG) to biomolecules and biomaterials is a well-established approach to modify their properties for therapeutic applications. For biomaterials, the approach is typically to blend or electrospray the synthetic polymer with the biomaterial. Effective surface modification approaches such as surface-initiated polymer brushes are challenging since the harsh solvents required for brush synthesis may destroy the biomaterial. Herein, we describe the PEGylation of collagen fibers by surface-initiated PEG brushes using a living anionic grafting-from mechanism. This brush synthesis is done in the absence of solvents to minimize the degradation of the native collagen structure. We quantify the effect the brush synthesis has on the native structure of the collagen fiber using differential scanning calorimetry (DSC) and find that even at long reaction times a significant fraction of the native structure remains. Dynamic mechanical analysis indicates the collagen undergoes only modest structural degradation, while adhesion studies find a significant improvement of antifouling properties. Further, our approach opens the way for further chemistry, as the growing polymer chain is a potassium alkoxy group that can be functionalized by termination or by subsequent reaction by a wide variety of molecules.

Automated summary

The addition of PEG is a well-established method to modify the properties of biomolecules and biomaterials for therapeutic applications. However, surface modification approaches using harsh solvents may damage the biomaterials. In this study, we describe a solvent-free approach to PEGylate collagen fibers using surface initiated PEG brushes, which effectively maintains the native structure of collagen. The modified collagen fibers show improved antifouling properties and offer opportunities for further chemical reactions.