Osborne P G, Niwa O, Kato T, Yamamoto K
BioelectroAnalytical Science Inc, Department of Research and Development, Tokyo, Japan.
J Neurosci Methods. 1997 Dec 1;77(2):143-50. doi: 10.1016/s0165-0270(97)00119-2.
A sensitive, enzymatic glucose electrode was coupled with the microdialysis sampling technique to enable the continuous, on-line measurement of dialysate glucose. The glucose sensitive electrode was fabricated by immobilizing glucose oxidase onto the surface of an osmium-polyvinylpyrridine horse radish peroxidase gel (Os-gel-HRP) which had been cast coated onto a glassy carbon electrode. This 'bilayer' electrode generated a reductive current to glucose at a potential of 0 mV thereby minimizing faradic oxidative interferences. The system utilized the continuous mixing of two fluids immediately prior to the 'bilayer' electrode. One fluid was the dialysate. The other was an oxygenated, low pH phosphate buffer which minimized oxidative interference, buffered the electrode from variations of pH and maximized enzyme efficiency. In practical terms, the 'bilayer' electrode was simple to manufacture, quick to reach stable basal currents (less than 60 min), sensitive (2.5 microM glucose could be detected in the dialysate) and durable (usable for up to 3 days). In vivo experiments, used the smallest commercially available microdialysis probes to demonstrate that on-line, continuous measurements of EC striatal glucose in the dialysate were receptive to pharmacological (local perfusion with veratridine (50 microM), systemic hyperglycemia (1.5 ml of 0.55 M glucose intraperitoneal (i.p.)) and anesthesia (Nembutal 40 mg/kg i.p.)) and behavioral (restraint) manipulations. This technique allows for greater temporal resolution than conventional HPLC procedures whilst requiring significantly less technical outlay or analytical expertise. The high sensitivity of the analytical technique could facilitate the study of EC glucose levels in very localized regions of the brain if coupled to microdialysis probes of small dimensions.
一种灵敏的酶促葡萄糖电极与微透析采样技术相结合,实现了对透析液葡萄糖的连续在线测量。葡萄糖敏感电极是通过将葡萄糖氧化酶固定在已浇铸涂覆在玻碳电极上的锇 - 聚乙烯吡啶辣根过氧化物酶凝胶(Os - 凝胶 - HRP)表面制成的。这种“双层”电极在0 mV电位下对葡萄糖产生还原电流,从而将法拉第氧化干扰降至最低。该系统在“双层”电极之前立即利用两种流体的连续混合。一种流体是透析液。另一种是含氧的低pH磷酸盐缓冲液,它能最大限度地减少氧化干扰,缓冲电极免受pH变化的影响,并使酶效率最大化。实际上,“双层”电极制造简单,能快速达到稳定的基线电流(少于60分钟),灵敏度高(透析液中可检测到2.5微摩尔葡萄糖)且耐用(可使用长达3天)。体内实验使用了市售最小的微透析探针,以证明对透析液中纹状体细胞外葡萄糖的在线连续测量对药理学(用藜芦碱(50微摩尔)局部灌注、全身性高血糖(腹腔注射(i.p.)1.5毫升0.55 M葡萄糖)和麻醉(腹腔注射戊巴比妥40毫克/千克))和行为(约束)操作有反应。与传统的高效液相色谱法相比,该技术具有更高的时间分辨率,同时所需的技术投入和分析专业知识显著减少。如果与小尺寸的微透析探针结合使用,这种分析技术的高灵敏度有助于研究大脑非常局部区域的细胞外葡萄糖水平。