Chen Li*, Liufang Gao, Yi Zhang and Benjamin K. Simpson Pages 945 - 954 ( 10 )
Background: Novel quercetin-loaded microparticles (QM) were fabricated using coaxial electrospraying, characterized for surface morphology and release profile, and evaluated for antitumor activity in vitro.
Methods: QM exhibited an average diameter of 1.69 ±1.13 mm, which was an appropriate size suitable for respiratory delivery. X-ray diffraction patterns showed that the components in QM existed in an amorphous physical form, leading to favorable interactions between the drug (quercetin), the polymer matrix (polyvinylpyrrolidone, PVP) and other excipients (sodium dodecyl sulfate and sucralose).
Results: QM performed much faster release rate compared with free quercetin powder (Q) in vitro. Furthermore, QM also showed more potent inhibitory effects on A549 cell growth with reduced cell viability, decreased cell migration and induced more G0/G1 phase cell cycle arrest than Q.
Conclusion: Thus, the quercetin loaded microparticles exhibited more potent inhibitory effects than free quercetin on A549 cell. The increased antitumor activity could be attributed to the enhanced accumulation of quercetin in the A549 cells with the QM. However, further studies are necessary to elucidate the exact mechanisms.
Quercetin, microparticle, fast-release, anti-tumor activity, lung cancer cells, microparticles.
School of Life Science, Shanxi University; No. 92, Wucheng Road, Taiyuan 030006, School of Life Science, Shanxi University; No. 92, Wucheng Road, Taiyuan 030006, Department of Food Science and Agricultural Chemistry, McGill University (Macdonald Campus); Ste-Anne-de-Bellevue, Québec H9X 3V9, Department of Food Science and Agricultural Chemistry, McGill University (Macdonald Campus); Ste-Anne-de-Bellevue, Québec H9X 3V9