Department of Chemistry, Oklahoma State University, Stillwater, OK 74078, USA.
Analyst. 2018 Mar 26;143(7):1544-1555. doi: 10.1039/c7an01872j.
Diabetes is a complex immune disorder that requires extensive medical care beyond glycemic control. Recently, the prevalence of diabetes, particularly type 1 diabetes (T1D), has significantly increased from 5% to 10%, and this has affected the health-associated complication incidences in children and adults. The 2012 statistics by the American Diabetes Association reported that 29.1 million Americans (9.3% of the population) had diabetes, and 86 million Americans (age ≥20 years, an increase from 79 million in 2010) had prediabetes. Personalized glucometers allow diabetes management by easy monitoring of the high millimolar blood glucose levels. In contrast, non-glucose diabetes biomarkers, which have gained considerable attention for early prediction and provide insights about diabetes metabolic pathways, are difficult to measure because of their ultra-low levels in blood. Similarly, insulin pumps, sensors, and insulin monitoring systems are of considerable biomedical significance due to their ever-increasing need for managing diabetic, prediabetic, and pancreatic disorders. Our laboratory focuses on developing electrochemical immunosensors and surface plasmon microarrays for minimally invasive insulin measurements in clinical sample matrices. By utilizing antibodies or aptamers as the insulin-selective biorecognition elements in combination with nanomaterials, we demonstrated a series of selective and clinically sensitive electrochemical and surface plasmon immunoassays. This review provides an overview of different electrochemical and surface plasmon immunoassays for insulin. Considering the paramount importance of diabetes diagnosis, treatment, and management and insulin pumps and monitoring devices with focus on both T1D (insulin-deficient condition) and type 2 diabetes (insulin-resistant condition), this review on insulin bioassays is timely and significant.
糖尿病是一种复杂的免疫紊乱疾病,需要广泛的医疗护理,不仅仅是血糖控制。最近,糖尿病的患病率,特别是 1 型糖尿病(T1D),已经从 5%显著增加到 10%,这影响了儿童和成人的健康相关并发症发生率。美国糖尿病协会 2012 年的统计数据显示,有 2910 万美国人(占人口的 9.3%)患有糖尿病,有 8600 万美国人(年龄≥20 岁,比 2010 年的 7900 万有所增加)患有糖尿病前期。个性化血糖仪可以通过轻松监测高毫摩尔血糖水平来进行糖尿病管理。相比之下,非葡萄糖糖尿病生物标志物由于其在血液中的超低水平,已引起人们对早期预测的极大关注,并为糖尿病代谢途径提供了深入的了解,但这些标志物很难测量。同样,胰岛素泵、传感器和胰岛素监测系统由于对管理糖尿病、糖尿病前期和胰腺疾病的需求不断增加,具有相当大的生物医学意义。我们的实验室专注于开发电化学免疫传感器和表面等离子体微阵列,用于在临床样本基质中进行微创胰岛素测量。通过将抗体或适体用作胰岛素选择性生物识别元件,并结合纳米材料,我们展示了一系列选择性和临床敏感的电化学和表面等离子体免疫分析。本综述介绍了不同的电化学和表面等离子体免疫分析方法用于胰岛素的测量。考虑到糖尿病诊断、治疗和管理的重要性,以及胰岛素泵和监测设备的重要性,重点关注 1 型糖尿病(胰岛素缺乏症)和 2 型糖尿病(胰岛素抵抗),因此,这篇关于胰岛素生物分析的综述是及时且有意义的。