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本文引用的文献

1
The role of dysregulated glucagon secretion in type 2 diabetes.胰高血糖素分泌失调在 2 型糖尿病中的作用。
Diabetes Obes Metab. 2011 Oct;13 Suppl 1:126-32. doi: 10.1111/j.1463-1326.2011.01449.x.
2
Regulation of glucagon secretion by glucose: paracrine, intrinsic or both?葡萄糖对胰高血糖素分泌的调节作用:旁分泌、固有还是两者兼有?
Diabetes Obes Metab. 2011 Oct;13 Suppl 1:95-105. doi: 10.1111/j.1463-1326.2011.01450.x.
3
Circulating glucagon is associated with inflammatory mediators in metabolically compromised subjects.循环胰高血糖素与代谢受损患者的炎症介质有关。
Eur J Endocrinol. 2011 Oct;165(4):639-45. doi: 10.1530/EJE-11-0384. Epub 2011 Jul 28.
4
Minimizing the number of voltage sources and fluid reservoirs for electrokinetic valving in microfluidic devices.最小化微流控设备中电动阀的电压源和流体储液器的数量。
Anal Chem. 1999 Aug 1;71(15):3273-6. doi: 10.1021/ac990059s.
5
Simultaneous capillary electrophoresis competitive immunoassay for insulin, glucagon, and islet amyloid polypeptide secretion from mouse islets of Langerhans.同时毛细管电泳竞争免疫分析法检测胰岛分泌的胰岛素、胰高血糖素和胰岛淀粉样多肽。
J Chromatogr A. 2011 Jul 1;1218(26):4059-64. doi: 10.1016/j.chroma.2011.05.006. Epub 2011 May 13.
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Glucagon antagonism as a potential therapeutic target in type 2 diabetes.胰高血糖素拮抗作用作为 2 型糖尿病的潜在治疗靶点。
Diabetes Obes Metab. 2011 Nov;13(11):965-71. doi: 10.1111/j.1463-1326.2011.01427.x.
7
Tumors on chips: oncology meets microfluidics.芯片上的肿瘤:肿瘤学与微流控技术的结合。
Curr Opin Chem Biol. 2010 Oct;14(5):556-67. doi: 10.1016/j.cbpa.2010.08.016. Epub 2010 Sep 9.
8
Microfluidic system for generation of sinusoidal glucose waveforms for entrainment of islets of Langerhans.用于产生正弦葡萄糖波形以 entraɪn 胰岛的微流控系统。
Anal Chem. 2010 Aug 1;82(15):6704-11. doi: 10.1021/ac101461x.
9
Reversibly sealed multilayer microfluidic device for integrated cell perfusion and on-line chemical analysis of cultured adipocyte secretions.用于集成细胞灌注和培养脂肪细胞分泌物在线化学分析的可反复密封的多层微流控装置。
Anal Bioanal Chem. 2010 Aug;397(7):2939-47. doi: 10.1007/s00216-010-3897-z. Epub 2010 Jun 12.
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Latest developments in microfluidic cell biology and analysis systems.微流控细胞生物学与分析系统的最新进展。
Anal Chem. 2010 Jun 15;82(12):4848-64. doi: 10.1021/ac1009707.

在微流控芯片上对活细胞分泌的胰高血糖素进行动态监测。

Dynamic monitoring of glucagon secretion from living cells on a microfluidic chip.

机构信息

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

出版信息

Anal Bioanal Chem. 2012 Mar;402(9):2797-803. doi: 10.1007/s00216-012-5755-7.

DOI:10.1007/s00216-012-5755-7
PMID:22286080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3324330/
Abstract

A rapid microfluidic based capillary electrophoresis immunoassay (CEIA) was developed for on-line monitoring of glucagon secretion from pancreatic islets of Langerhans. In the device, a cell chamber containing living islets was perfused with buffers containing either high or low glucose concentration. Perfusate was continuously sampled by electroosmosis through a separate channel on the chip. The perfusate was mixed on-line with fluorescein isothiocyanate-labeled glucagon (FITC-glucagon) and monoclonal anti-glucagon antibody. To minimize sample dilution, the on-chip mixing ratio of sampled perfusate to reagents was maximized by allowing reagents to only be added by diffusion. Every 6 s, the reaction mixture was injected onto a 1.5-cm separation channel where free FITC-glucagon and the FITC-glucagon-antibody complex were separated under an electric field of 700 V cm(-1). The immunoassay had a detection limit of 1 nM. Groups of islets were quantitatively monitored for changes in glucagon secretion as the glucose concentration was decreased from 15 to 1 mM in the perfusate revealing a pulse of glucagon secretion during a step change. The highly automated system should be enable studies of the regulation of glucagon and its potential role in diabetes and obesity. The method also further demonstrates the potential of rapid CEIA on microfluidic systems for monitoring cellular function.

摘要

一种基于快速微流控的毛细管电泳免疫分析(CEIA)被开发出来,用于在线监测胰岛细胞中胰高血糖素的分泌。在该装置中,含有活胰岛的细胞室用含有高或低葡萄糖浓度的缓冲液灌注。通过芯片上的单独通道,电渗流连续地对灌流液进行采样。灌流液与荧光素异硫氰酸酯标记的胰高血糖素(FITC-胰高血糖素)和单克隆抗胰高血糖素抗体在线混合。为了最大限度地减少样品稀释,通过允许试剂仅通过扩散添加来最大化芯片上采样灌流液与试剂的混合比例。每 6 秒,将反应混合物注入 1.5 厘米长的分离通道中,在 700 V cm(-1) 的电场下分离游离的 FITC-胰高血糖素和 FITC-胰高血糖素-抗体复合物。免疫分析的检测限为 1 nM。当灌流液中的葡萄糖浓度从 15 降至 1 mM 时,对胰岛进行定量监测,以观察到胰高血糖素分泌的脉冲,这表明在阶跃变化期间存在胰高血糖素分泌。该高度自动化的系统应能够研究胰高血糖素的调节及其在糖尿病和肥胖症中的潜在作用。该方法还进一步证明了快速 CEIA 在微流控系统中用于监测细胞功能的潜力。