“…As described in Section , surface properties are crucial since they affect the interactions of the implant with proteins and cells, and intermediate hydrophilicities are generally preferred to achieve such interactions . Some easy and efficient methods to improve the biocompatibility and tailor the hydrolytic degradation rates of PCL, PLA, and PLGA, are to increase their hydrophilicity by coating or blending with natural polymers, such as decellularized ECM, − collagen, − gelatin, ,,, elastin, , other proteins, ,, and polysaccharides. ,− Grafting and coating with hydrophilic synthetic polymers, such as poly(glycerol sebacate) (PGS), , polyacrylamide, poly(vinyl alcohol) (PVA), , poly(ethylene oxide), polydopamine, polyurethane (PU) have also been performed, as well as plasma treatment. ,, Copolymerization and blending also help modulate the mechanical properties of these polymers. ,− Overall, PCL and PLA have been used in the TE of a wide variety of tissues, including cornea, skin, cartilage, and bone . The commercial availability and processability of such thermoplastic polyesters, combined with their established applications in products that have received FDA approval, are major factors that will, in our opinion, keep these polymers in the spotlight of the optimization of TE scaffolds.…”