Li Chao, Huang Zheng, Gao Ning, Sui Yang, Niu Hong, Guan Jianjun
Department of Materials Science and Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
Department of Mechanical Engineering and Materials Science, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
ACS Biomater Sci Eng. 2019 May 13;5(5):2173-2179. doi: 10.1021/acsbiomaterials.9b00106. Epub 2019 Apr 17.
Various therapeutic approaches have been developed for vascularization of diseased tissues. To quickly and accurately evaluate efficacy of a therapy, reproducible monitoring of tissue oxygen concentration changes at the same tissue location by a minimally invasive or noninvasive spectroscopic approach represents a compelling strategy. Yet this cannot be achieved by any clinically available approaches. Magnetic-resonance-based method, electron paramagnetic resonance (EPR), has the potential to accomplish the goal. However, the existing small molecule EPR probes cannot maintain a consistent concentration at the same tissue location during vascularization period to acquire a stable EPR signal, and they cannot be implanted and/or retrieved by a minimally invasive approach such as injection. Herein, a polymeric, injectable, and degradable EPR probe was developed. The probe was based on the complex of chitosan and tetrathiatriarylmethyl (TAM) radical. The probe had high oxygen sensitivity and reproducibility. It was more stable than free TAM radical when exposed to oxidoreductants that commonly appear in diseased tissues. The probe maintained EPR signal intensity for 4 weeks in vitro and in vivo without changing oxygen sensitivity. It also exhibited excellent biocompatibility. The developed TAM/chitosan complex may be used for long-term detection of tissue oxygen content during therapies.
针对病变组织的血管生成,已经开发了多种治疗方法。为了快速准确地评估一种治疗方法的疗效,通过微创或无创光谱方法在同一组织位置对组织氧浓度变化进行可重复监测是一种极具吸引力的策略。然而,目前任何临床可用的方法都无法实现这一点。基于磁共振的方法,即电子顺磁共振(EPR),有潜力实现这一目标。然而,现有的小分子EPR探针在血管生成期间无法在同一组织位置保持一致的浓度以获取稳定的EPR信号,并且它们不能通过诸如注射等微创方法进行植入和/或取出。在此,开发了一种聚合物、可注射且可降解的EPR探针。该探针基于壳聚糖和四硫代三芳基甲基(TAM)自由基的复合物。该探针具有高氧敏感性和可重复性。当暴露于病变组织中常见的氧化还原物质时,它比游离TAM自由基更稳定。该探针在体外和体内4周内保持EPR信号强度不变,且氧敏感性也不变。它还表现出优异的生物相容性。所开发的TAM/壳聚糖复合物可用于治疗期间组织氧含量的长期检测。