Suppr超能文献

用于递送阿霉素的聚乙二醇功能化的刺激响应性可自愈合可注射动态亚氨基硼酸根G-四链体水凝胶

PEG Functionalized Stimuli Responsive Self-Healable Injectable Dynamic Imino-boronate G-quadruplex Hydrogel for the Delivery of Doxorubicin.

作者信息

Biswas Ankan, Ghosh Tapas, Gavel Pramod K, Das Apurba K

机构信息

Department of Chemistry, Indian Institute of Technology Indore, Khandwa Road, Indore 453552, India.

出版信息

ACS Appl Bio Mater. 2020 Feb 17;3(2):1052-1060. doi: 10.1021/acsabm.9b01034. Epub 2020 Jan 24.

Abstract

Dynamic G-quadruplex hydrogel is engineered by using guanosine, 2-formylphenylboronic acid, and 4-Arm PEG-NH. The gelation conditions are optimized by varying concentrations of the gelators, pH, and different alkali metal ions. The formation of imino-boronate bonds during the gelation process is fully characterized with FT-IR, H NMR, and B NMR spectroscopy. The secondary supramolecular G-quadruplex structure and the formation of nanofibrillar morphology are well examined using several spectroscopic and microscopic techniques. The mechanical strength of the hydrogel is investigated by rheological experiments. The hydrogel is injectable and self-healable due to the dynamic nature of the imono-boronate bonds. The dynamic bonds provide distinct shear-thinning and thixotropic properties to the resulting hydrogel with almost 90% recovery of its mechanical strength after four cycles. The pH responsive behavior of the hydrogel is achieved by pH sensitive imino-boronate bonds, which are unstable at acidic pH. To investigate the biocompatibility of the hydrogel, a wide range of hydrogel concentrations are examined by in vitro cell culture experiments using the MCF-7 cell line. After a biocompatibility test of the hydrogel, the anticancer drug doxorubicin is incorporated inside the gel to analyze the drug release profile at different pHs. The release rate of the loaded drug is observed faster in lower pH (pH 4.8) than in physiological pH (pH 7.4). Different release rate of the drug from the drug loaded hydrogel in different pHs is driven by the pH sensitive imino-boronate bonds. The release profile of the drug is slow, sustain and steady.

摘要

动态G-四链体水凝胶是通过使用鸟苷、2-甲酰基苯硼酸和四臂聚乙二醇胺合成的。通过改变凝胶剂浓度、pH值和不同碱金属离子来优化凝胶化条件。利用傅里叶变换红外光谱(FT-IR)、氢核磁共振(H NMR)和硼核磁共振(B NMR)光谱对凝胶化过程中亚氨基硼酸酯键的形成进行了全面表征。使用多种光谱和显微镜技术对二级超分子G-四链体结构和纳米纤维形态的形成进行了充分研究。通过流变学实验研究了水凝胶的机械强度。由于亚氨基硼酸酯键的动态性质,该水凝胶具有可注射性和自愈性。这些动态键为所得水凝胶提供了独特的剪切变稀和触变性,在四个循环后其机械强度几乎恢复90%。水凝胶的pH响应行为是通过对pH敏感的亚氨基硼酸酯键实现的,这些键在酸性pH下不稳定。为了研究水凝胶的生物相容性,使用MCF-7细胞系通过体外细胞培养实验检测了多种水凝胶浓度。在对水凝胶进行生物相容性测试后,将抗癌药物阿霉素掺入凝胶中,以分析其在不同pH值下的药物释放曲线。观察到负载药物在较低pH(pH 4.8)下的释放速率比在生理pH(pH 7.4)下更快。药物从载药水凝胶在不同pH值下的不同释放速率是由对pH敏感的亚氨基硼酸酯键驱动的。药物的释放曲线缓慢、持续且稳定。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验