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Jun-Sheng Wang

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Open access Aug 2026

Viscoelasticity-tuned hyaluronic acid-gelatin microcarriers with thermoresponsive polymer grafts for scalable cell expansion and gentle harvesting.

Three-dimensional (3D) cell culture using microcarriers is an effective strategy for scalable cell expansion; however, conventional enzymatic detachment can compromise cell viability, surface proteins, and native signalling. We report viscoelasticity-tuneable hyaluronic acid (HA)-gelatin microspheres as microcarriers, engineered with a thermoresponsive polymer coating to enhance cell attachment and enable gentle harvesting. Gelatin-only (GLA), gelatin-HA (G-HA), and gelatin-HA-L-lysine (G-HA-L) microspheres were fabricated. HA incorporation and lysine functionalization were used to tune microsphere mechanics and interfacial stability. Frequencysweep rheology revealed that HA-containing formulations exhibited higher elastic dominance (G' > G″) and a broader, more stable viscoelastic response than gelatin-only and a commercial gelatin microcarrier benchmark, with G-HA-L showing the most favorable balance of stiffness and damping (highest G'/G″ across the tested window). The microspheres were subsequently coated with poly (N-isopropylacrylamide-co-acrylic acid) (P(NIPAM-AAc)), producing a temperature-responsive interface. Importantly, the thermoresponsive coating enhanced early cell attachment, particularly on G-HA-L (reaching ~70% within 4 h and approaching ~90% by 24 h), outperforming both coated G-HA and commercial microcarriers. For harvesting, lowtemperature conditioning markedly improved cell release and recovery compared to trypsinonly controls, consistent with temperature-triggered polymer swelling facilitating detachment. Collectively, these results demonstrate that coupling viscoelastic microcarrier design with thermoresponsive surface engineering provides a promising platform for efficient cell growth and gentle, process-friendly harvesting, with potential applications in tissue engineering and regenerative medicine.

Rizka Musdalifah Amsar, Xiangqiang Lin, Jun-Sheng Wang et al. · 0 citations