Gong Yaqi, Mohd Shabbir, Wu Simei, Liu Shilin, Pei Ying, Luo Xiaogang
School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, LiuFang Campus, No.206, Guanggu 1st road, Donghu New & High Technology Development Zone, Wuhan, 430205 Hubei Province, P.R. China.
College of Food Science and Technology, Huazhong Agricultural University, Wuhan, 430205 Hubei Province, China.
ACS Omega. 2021 Jan 25;6(4):2734-2741. doi: 10.1021/acsomega.0c04946. eCollection 2021 Feb 2.
Functional modified cellulose microsphere (CMs) materials exhibit great application potential in drug various fields. Here, we designed pH-responsive carboxylated cellulose microspheres (CCMs) by the citric/hydrochloric acid hydrolysis method to enhance oral bioavailability of insulin by a green route. The CMs were high purity cellulose that dissolved and regenerated from a green solvent by the green sol-gel method. The prepared microspheres were characterized by spectroscopic techniques, such as field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectrum (FT-IR), X-ray diffraction (XPS), etc. The spherical porous structure and carboxylation of cellulose were confirmed by FESEM and FT-IR, respectively. Insulin was loaded into the CCMs by electrostatic interactions, and the insulin release was controlled through ionization of carboxyl groups and proton balance. In vitro insulin release profiles demonstrated the suppression of insulin release in artificial gastric fluid (AGF), while a significant increase at artificial intestinal fluid (AIF) was observed. The insulin release profile was fitted in Korsmeyer-Peppas kinetic model, and insulin release was governed by the Fickian diffusion mechanism. The stability of the secondary structure of insulin was studied by dichroism circular. Excellent biocompatibility and no cytotoxicity of designed CCMs cast them as a potential oral insulin carrier.
功能性改性纤维素微球(CMs)材料在药物各个领域展现出巨大的应用潜力。在此,我们通过柠檬酸/盐酸水解法设计了pH响应性羧化纤维素微球(CCMs),以通过绿色途径提高胰岛素的口服生物利用度。CMs是通过绿色溶胶-凝胶法从绿色溶剂中溶解并再生得到的高纯度纤维素。制备的微球通过场发射扫描电子显微镜(FE-SEM)、傅里叶变换红外光谱(FT-IR)、X射线衍射(XPS)等光谱技术进行表征。FESEM和FT-IR分别证实了纤维素的球形多孔结构和羧化作用。胰岛素通过静电相互作用负载到CCMs中,并通过羧基的离子化和质子平衡来控制胰岛素的释放。体外胰岛素释放曲线表明在人工胃液(AGF)中胰岛素释放受到抑制,而在人工肠液(AIF)中观察到显著增加。胰岛素释放曲线符合Korsmeyer-Peppas动力学模型,胰岛素释放受菲克扩散机制控制。通过圆二色性研究了胰岛素二级结构的稳定性。所设计的CCMs具有优异的生物相容性且无细胞毒性,使其成为一种潜在的口服胰岛素载体。