Complex and Intelligent Systems Research Center, East China University of Science and Technology, Shanghai, PR China; Division of Biomedical Engineering, University of Saskatchewan, Saskatoon, Canada.
Changzhou Institute of Advanced Materials, Beijing University of Chemical Technology, Changzhou, Jiangsu, PR China.
Int J Biol Macromol. 2019 Mar 1;124:724-732. doi: 10.1016/j.ijbiomac.2018.11.261. Epub 2018 Nov 28.
The glucose-responsive behavior of the Con A-sugar affinity based hydrogels, microgels, films and nanoparticles has been widely investigated in the application of drug delivery and biosensors. However, the principle or mechanism of such systems is not well known in literature. In this study, for the first time, the glucose-responsive principle (or principle) of the Con A-sugar based system was detailedly explained through the binding interactions test by isothermal titration calorimetry and ligand binding theory. The study also successfully resolved the controversy regarding the principle of such systems in literature. The other contribution of the study is the experimental validation that the insulin-loaded microgels with different hydrogel-network compositions (based on Con A-sugar affinity) respond to different glucose concentrations. Particularly, the result of the in vitro insulin release suggests that the microgels be able to maintain bolus and basal insulin release in response to different glucose concentrations and the network composition be able to affect the burst release, release rate and overall release amount of insulin. Further, the released insulin has been shown to remain active and the microgels possess no in vitro cytotoxicity to HDF cells. The second contribution is a first step towards the realization of personalized diabetes care.
基于 ConA 糖亲和性的水凝胶、微凝胶、薄膜和纳米粒子的葡萄糖响应行为已在药物输送和生物传感器的应用中得到了广泛研究。然而,文献中对于此类系统的原理或机制尚不清楚。在这项研究中,首次通过等温滴定微量热法和配体结合理论的结合相互作用测试,详细解释了基于 ConA 糖的系统的葡萄糖响应原理(或原则)。该研究还成功解决了文献中此类系统原理的争议。该研究的另一个贡献是实验验证了具有不同水凝胶网络组成(基于 ConA 糖亲和性)的载胰岛素微凝胶对不同葡萄糖浓度的响应。特别是,体外胰岛素释放的结果表明,微凝胶能够根据不同的葡萄糖浓度保持胰岛素的突释和基础释放,并且网络组成能够影响胰岛素的爆发释放、释放率和整体释放量。此外,释放的胰岛素保持活性,并且微凝胶对 HDF 细胞没有体外细胞毒性。第二个贡献是实现个性化糖尿病护理的第一步。