海藻酸钙
溶解
有孔小珠
材料科学
挤压
钙
化学工程
药物输送
动力学
复合材料
纳米技术
冶金
量子力学
物理
工程类
作者
Wan-Ping Voo,Chien Wei Ooi,M. Saïful Islam,Beng Ti Tey,Eng‐Seng Chan
标识
DOI:10.1016/j.eurpolymj.2015.12.029
摘要
Alginate hydrogel bead has been widely explored as a vehicle for controlled delivery application due to its non-toxicity, renewability, and ease of formation. However, alginate hydrogel beads are known to have a low stiffness, i.e., Young modulus <1 MPa, and a short dissolution time of between 1 h and 2 h in gastrointestinal fluid. This study aimed to fabricate calcium alginate hydrogel beads with desired properties like high stiffness and extended dissolution behaviour. A temperature-controlled extrusion–dripping method incorporating an immiscible interphase column was used to produce the ultra-high concentration (UHC) calcium hydrogel beads directly from unmodified alginate solution. The UHC beads have an extraordinary internal structure with thick calcium-alginate matrices and large pores in between the matrices. The Young’s modulus value of UHC calcium alginate beads was 3.6 MPa, which was approximately 8 times higher than the normal calcium alginate beads. The release profile for the model drug (i.e., methylene blue) encapsulated in UHC beads was found to be extended to 4 h at 80% of drug release (t80). The kinetics of drug release fitted well with the Korsmeyer–Peppas model (r2 ⩾ 0.99) and followed the non-Fickian mechanism. These findings show that the preparation of calcium alginate beads featuring high stiffness and extended dissolution profile can be achieved without any chemical modification or additives. The UHC calcium alginate bead holds excellent promise as an encapsulation carrier of drugs or food used in controlled delivery applications.
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