Hasinah Rafiq, Yu‐I Hsu, Mitsuharu Suzuki, Supritha Muppuri, Kenichi Nakayama, Hiroshi Uyama
Electrospinning of bio-based poly(lactic acid) (PLA) is a straightforward approach for encapsulating hydrophilic bioactive compounds within biodegradable polymers for sustained release. PLA offers good mechanical properties, biocompatibility, and non-toxic degradation under physiological conditions. However, its intrinsic hydrophobicity hinders the uniform dispersion of hydrophilic drugs, leading to recrystallization, phase separation, and incomplete drug dissolution. In this study, a fluorinated covalent organic framework (COF) was employed as a nanocarrier to encapsulate the hydrophilic anticancer drug, 5-fluorouracil (5-FU), within electrospun PLA fibers containing polyethylene glycol (PEG) as a compatibilizer. The fluorinated COF achieved a 5-FU loading of 65%, enabling efficient drug incorporation within electrospun PLA/PEG fibers, while suppressing drug recrystallization and achieving sustained, pH-responsive release. Compared to directly loaded fibers, the 5-FU@COF/fibers exhibited enhanced cumulative release at acidic pH (pH 5.4) compared to physiological pH (pH 7.4), due to the pH-induced degradation of both the COF and PLA/PEG fibers. Furthermore, embedding 5-FU@COF particles within the fibrous matrix reduced burst release and provided sustained release in aqueous environments. The presence of COF increased the maximum degradation temperature of the fibers, enhancing the thermal stability of the fiber composite. Additionally, the lowered initial degradation temperature of 5-FU/COF fibers at 200°C relative to drug-free COF/fibers served as a clear indicator of successful drug loading. Overall, these findings establish pH-responsive COF-polymer composites as a sustainable platform for selective anticancer drug delivery in acidic conditions.