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In IPF treatment, Nintedanib can reduce the decline of forced vital capacity (FVC) and inhibit progression of pulmonary fibrosis ( Combination Therapies As mentioned above, pulmonary fibrosis is a complex pathological progression in which pathogenic factors activate complex fibrotic pathways in various cells (Schafer et al., 2020)

Furthermore, this technology allows for precise regulation of hydrogel porosity, which plays a crucial role in cell proliferation and differentiation

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