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用释放一氧化氮的聚(丙交酯-共-乙交酯)基涂层制备的血管内葡萄糖/乳酸传感器,以提高生物相容性。

Intravascular glucose/lactate sensors prepared with nitric oxide releasing poly(lactide-co-glycolide)-based coatings for enhanced biocompatibility.

机构信息

Department of Chemistry, The University of Michigan, Ann Arbor, MI 48109-1055, USA.

出版信息

Biosens Bioelectron. 2011 Jul 15;26(11):4276-82. doi: 10.1016/j.bios.2011.04.026. Epub 2011 Apr 22.

Abstract

Intravenous amperometric needle-type enzymatic glucose/lactate sensors intended for continuous monitoring are prepared with a novel nitric oxide (NO) releasing layer to improve device hemocompatibility. To create an underlying NO release coating, the sensors with immobilized enzymes (either glucose oxidase or lactate oxidase) are prepared with a thin layer of poly(lactide-co-glycolide) (PLGA) loaded with lipophilic diazeniumdiolate species that slowly release NO via a proton driven reaction. An outer thin layer (ca. 30 μm) of PurSil (polyurethane/dimethylsiloxane copolymer) limits the flux of glucose and lactate to the inner layer of enzyme, to provide the desired linear amperometric response. A 30 μm coating of PLGA containing 33 wt% of the appropriate NO donor (N-diazeniumdiolated dibutylhexanediamine, DBHD/N₂O₂) can release NO at a physiologically relevant rate > 1 × 10⁻¹⁰mol min⁻¹ cm⁻² for at least 7 days without influencing the analytical performance of the glucose/lactate sensors. In vitro, the sensors exhibit relatively stable amperometric response over a one-week period with high selectivity over interferences (e.g., ascorbic acid) required for blood monitoring applications. Glucose sensors implanted in the veins of rabbits for 8h exhibit significantly enhanced hemocompatibility for the NO release sensors vs. corresponding controls (without NO release in same animals), with greatly reduced thrombus formation on their surfaces. Further, the analytical performance of the NO release glucose sensors are superior to controls placed in the veins of the same animals, with a greater accuracy in measuring blood glucose levels as evaluated using a Clarke error grid type analysis.

摘要

用于连续监测的静脉安培型酶葡萄糖/乳酸传感器通过释放一氧化氮(NO)的新层来改善器件的血液相容性。为了创建基础 NO 释放涂层,将固定化酶(葡萄糖氧化酶或乳酸氧化酶)的传感器用负载亲脂性偶氮二硝酸盐物种的聚(丙交酯-共-乙交酯)(PLGA)的薄层制备,该物种通过质子驱动反应缓慢释放 NO。外层(约 30 μm)的 PurSil(聚氨酯/二甲基硅氧烷共聚物)限制葡萄糖和乳酸向酶内层的通量,以提供所需的线性安培响应。含有 33wt%适当 NO 供体(N-偶氮二硝丁基六亚胺,DBHD/N₂O₂)的 30 μm PLGA 涂层可以以生理相关的速率(> 1 × 10⁻¹⁰mol min⁻¹ cm⁻²)持续释放 NO 至少 7 天,而不会影响葡萄糖/乳酸传感器的分析性能。在体外,传感器在一周的时间内表现出相对稳定的安培响应,并且对血液监测应用所需的干扰(例如抗坏血酸)具有高选择性。与相同动物中没有 NO 释放的对照相比,在兔子静脉中植入 8 小时的葡萄糖传感器的 NO 释放传感器表现出显著增强的血液相容性,其表面上的血栓形成大大减少。此外,NO 释放葡萄糖传感器的分析性能优于放置在同一动物静脉中的对照,使用 Clarke 误差网格类型分析评估时,在测量血糖水平方面具有更高的准确性。

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