Author/Authors :
Ha، نويسنده , , Seung Hee and Hwang، نويسنده , , Jong-Ho and Kim، نويسنده , , Do Hyung and Kim، نويسنده , , Min-Dae and Choi، نويسنده , , Cheol-Woong and Jeong، نويسنده , , Young-Il and Chung، نويسنده , , Chung Wook and Kim، نويسنده , , Cy Hyun and Kang، نويسنده , , Dae Hwan، نويسنده ,
Abstract :
The aim of this study was to prepare sunitinib-loaded biodegradable films using poly(l-lactide-co-ɛ-caprolactone) (PLCL) for anti-tumor drug delivery. Sunitinib-loaded PLCL film has a rough surface, while empty film has a smooth surface. PLCL film loaded with 5% (w/w) sunitinib showed an absence of a crystalline peak of sunitinib, while sharp peaks were observed at 10% (w/w) loading, indicating that sunitinib was molecularly distributed in the polymer matrix at 5% (w/w). A drug release study revealed an initial burst during the first 2 h, followed by continuous release until 24 h. Since weight loss of film was <10% for 1 week, drug release mechanism was dominantly dependent on the diffusion-mediated release of drugs to the medium. Sunitinib has a dose-dependent anti-proliferation effect against HuCC-T1 human cholangiocarcinoma cells in vitro. These results indicate that sunitinib-loaded PLCL film is a appropriate candidate as a vehicle for anti-tumor drug delivery.
Keywords :
D. Microstructure , A. Thin films , D. Diffusion , A. Polymers