Healthy articular cartilage has excellent lubricating properties, with friction coefficients reaching extremely low values at physiological pressures. Such high-performing lubricating layer in joints is attributed to the surface hydration arising from the interplay between multiple hydrophilic biopolymers (such as hyaluronic acid, proteoglycans, and lubricin) and phospholipids in the cartilage matrix. Mimicking such molecular structure, hydrogels, composed of a hydrophilic polymer network, have the potential to replicate the lubricating feature and possibly replace natural cartilages. In this study, we have synthesized a poly(2-methacryloyloxyethyl phosphorylcholine-co-N-isopropylacrylamide) (PMPC-co-PNIPAM, PMN)random copolymer with highly-hydrated lubricious 2-methacryloyloxyethyl phosphorylcholine moieties and less hydrated N-isopropylacrylamide moieties. Incorporation of PMN copolymers within various hydrogels significantly reduces the gels sliding surface friction, resulting in low friction coefficients against different counter surfaces, including stainless steel (hard metal surface), polyethylene (hydrophobic surface), and polyHEMA (soft hydrogel surface). Additionally, hydrogels containing PMN are shown to be biocompatible and have excellent antifouling properties, making them an ideal coating for commercially available stents. With these qualities, hydrogels containing PMN stand out as a promising new material with numerous possible applications.