Dynamic structure model of polyelectrolyte complex based controlled-release matrix tablets visualized by synchrotron radiation micro-computed tomography | |
Yin, XZ; Li, L; Gu, XQ; Wang, HM; Wu, L; Qin, W; Xiao, TQ; York, P; Zhang, JW; Mao, SR | |
刊名 | MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS |
2020 | |
卷号 | 116页码:- |
关键词 | MAGNETIC-RESONANCE MICROSCOPY DRUG-RELEASE MORPHOLOGICAL-CHANGES EXCIPIENTS KINETICS DELIVERY |
ISSN号 | 0928-4931 |
DOI | 10.1016/j.msec.2020.111137 |
文献子类 | 期刊论文 |
英文摘要 | Hydrophilic matrix tablets are the most commonly used dosage forms to fabricate oral controlled-release systems. It is highly desirable to design delivery system with novel mechanism to achieve sustained drug release through a simplified preparation process. The chitosan-anionic polymers based matrix tablets is assumed to produce self-assembly in the gastrointestinal tract, then transferring into film-coated tablets from original matrix type. But its dynamic behavior during dissolution process and the on-going internal microstructural changes during drug release were still in the dark. In this study, by using synchrotron radiation X-ray micro-tomography (SR-mu CT) with phase contrast imaging, the micro-structure characteristics of chitosan-lambda-carrageenan (CS-lambda-CG) matrix based tablets during the dissolution were successfully elucidated for the first time. The qualitative and quantitative analyses of intensity distribution distinguished a hydrated CS-lambda-CG layer from a solid core. Visualization based on 3D models provided quantitative details on the micro-structural characteristics of hydration dynamics. After CS-lambda-CG matrix tablets were immersed in simulated gastric fluid (SGF) pH 1.2 medium for 0.5-2.0 h, the hydrated layer transformed into a gel layer and a solid swollen layer. The erosion front, swelling front, and solvent penetration front were also defined from the distinguishable micro-structures. More importantly, once the matrix tablet was transferred from SGF to the simulated intestinal fluid (SIF) pH 6.8 medium, a new layer with the enhanced strength and compactness in comparison to common gels was formed on the surface of tablets. The temporal and spatial variation of 3D models further provided direct evidence for this cross-linking behavior, the new layer was composed of CS-lambda-CG polyelectrolyte complexes (PEC) which subsequently dominated release mechanisms. In summary, the phase contrast SR-mu CT technique was utilized to investigate the hydration dynamics of CS-lambda-CG matrix tablets which was supposed to provide a novel drug release mechanism. Based on the structure feature obtained from the high contrast image, different hydration region was distinguished and the cross-linked film was identified and visualized directly for the first time. |
语种 | 英语 |
内容类型 | 期刊论文 |
源URL | [http://ir.sinap.ac.cn/handle/331007/32817] |
专题 | 上海应用物理研究所_中科院上海应用物理研究所2011-2017年 |
作者单位 | 1.Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China 2.Univ Bradford, Bradford BD7 1DP, W Yorkshire, England 3.Chinese Acad Sci, Ctr Drug Delivery Syst, Shanghai 201203, Peoples R China 4.Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China |
推荐引用方式 GB/T 7714 | Yin, XZ,Li, L,Gu, XQ,et al. Dynamic structure model of polyelectrolyte complex based controlled-release matrix tablets visualized by synchrotron radiation micro-computed tomography[J]. MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS,2020,116:-. |
APA | Yin, XZ.,Li, L.,Gu, XQ.,Wang, HM.,Wu, L.,...&Mao, SR.(2020).Dynamic structure model of polyelectrolyte complex based controlled-release matrix tablets visualized by synchrotron radiation micro-computed tomography.MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS,116,-. |
MLA | Yin, XZ,et al."Dynamic structure model of polyelectrolyte complex based controlled-release matrix tablets visualized by synchrotron radiation micro-computed tomography".MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS 116(2020):-. |
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