Microencapsulation of coupled folate and chitosan nanoparticles for targeted delivery of combination drugs to colon
Version 2 2024-06-06, 02:59Version 2 2024-06-06, 02:59
Version 1 2015-08-20, 14:31Version 1 2015-08-20, 14:31
journal contribution
posted on 2024-06-06, 02:59authored byP Li, Z Yang, Y Wang, Z Peng, S Li, Lingxue KongLingxue Kong, Q Wang
Folate-chitosan nanoparticles, co-loaded with 5-fluourouacil (5-FU) and leucovorin (LV) and prepared by ionic gelation technology were physically microencapsulated by enteric polymer using a solvent evaporation method. Average particle size of the microencapsulated particles was in the range of 15 to 35 µm. High drug encapsulation efficiency was obtained for both 5-FU and LV in the microencapsulated particles. Both drugs were in amorphous state in the microencapsulated particles. By enteric coating, excellent pH-dependent release profile was achieved and no drug release was observed in simulated gastric and intestinal fluids. However, when the pH value reached the soluble threshold of Eudragit S-100, a constant and slow drug release was observed. The results indicated that these microencapsulated particles are a promising vehicle for selectively targeting drugs to colon in the chemotherapy of colon cancer.