CHENG-MING PENG2026-10-162026-10-162022-12-01Pure ID: 15448824Pure UUID: 0a52d7fc-b5bb-47ac-b834-ec52e0cba9b910.1016/j.mtcomm.2022.104284https://www.scopus.com/pages/publications/85136508920https://scholars.csmu.edu.tw/handle/123456789/32037A direct drug delivery system of with the inhibition of multidrug resistance was developed in this study by the polymer mixing of Pluronic block copolymer F127, L121, polyethylene glycol (PEG), and polyvinyl alcohol (PVA). The polymer mixing was defined as Pluronic blending composites (PBCs) and optimized through adjusting the ratio of two different water-soluble homopolymers, PEG and PVA. The chemotherapeutic drugs of 5-fluorouracil (5-FU) were released from Pluronic blending composites nearly one month without continuous supplementary. Also, the effective ingredient of L121 inhibited multidrug resistance in human pancreatic cancer and caused the malfunction of the ATP binding cassette subfamily C (ABCC) transporter as evidenced by the flow cytometer studies. PBC-3 effectively suppresses the function of ABCC transporter up to 25 days. 5-FU are able to accumulate in the cancer cells of AsPC-1 and PANC-1 at a designated effective concentration. Then, a surgical dressing was prepared by 3D bio-printing technology with Pluronic blending composites cross-linked by sodium alginate. Results show that the surgical dressing of 24 layers with 10 mm × 10 mm would continuously release 5-FU in effective anticancer concentration for six days.enjournal article