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Sugar-Based Self-Assembly of Hydrogel Nanotubes Manifesting ESIPT: Theoretical Insight and Application in Live Cell Imaging

机译:基于糖的水凝胶纳米管的自组装表现出ESIPT:实时细胞成像中的理论洞察力和应用

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A biopolymeric hydrogel nanotubes (BTHBC) using 3-(benzo[d] thiazol-2-yl)-2-hydroxybenzaldehyde and chitosan have been synthesized which exhibits excited state intramolecular proton transfer (ESIPT) in both gel and solution phase. The optimized spatial structure of the monomer of BTHBC having lower energy (Energy: -1085688.464 kcal/mol) is found to be planar. FE-SEM analysis reveals that the spherical assemblies (20-100 nm) preceded gelation. Upon aging, gelation can be observed owing to the fusion of these spherical aggregates into nanotubes (200-500 nm). DFT study of BTHBC establishes that the migration of H atom from phenolic -OH group to the nitrogen of 2-(2' Hydroxyphenyl)benzothiazole (HBT) moiety is more feasible than the imine nitrogen of chitosan. The fluorescence lifetime of BTHBC is found to increase remarkably in gel phase compared to its aqueous solution. Both the cellular uptake and cell imaging efficiency suggest that the biocompatible nature of the hydrogel permits easy access of maximum number of molecules into the cells which causes enhancement of the fluorescence intensity of the cells.
机译:使用3-(Benzo [D]噻唑-2-基)-2-羟基苯甲甲醛和壳聚糖的生物聚凝胶纳米管(BTHBC)已合成,在凝胶和溶液相中都表现出激发态态分子内质子转移(ESIPT)。发现具有较低能量的BTHBC单体的优化空间结构(能量:-1085688.464 kcal/mol)是平面。 FE-SEM分析表明,球形组件(20-100 nm)先于凝胶化。衰老后,由于这些球形聚集体融合到纳米管(200-500 nm)中,因此可以观察到凝胶化。 BTHBC的DFT研究表明,H原子从酚-OH基团到2-(2'羟基苯基)苯甲唑(HBT)部分的氮迁移比壳聚糖的亚胺氮更可行。与其水溶液相比,发现BTHBC的荧光寿命在凝胶相中显着增加。细胞摄取和细胞成像效率都表明,水凝胶的生物相容性性质允许轻松进入最大数量的分子进入细胞,从而导致细胞的荧光强度增强。

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