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An in situ Measurement of Extracellular Cysteamine Homocysteine and Cysteine Concentrations in Organotypic Hippocampal Slice Cultures by Integration of Electroosmotic Sampling and Microfluidic Analysis

机译:一个在海马脑切片培养由电渗取样和微流控分析的集成外半胱胺同型半胱氨酸和半胱氨酸浓度的测量现场

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摘要

We demonstrate an all-electric sampling/derivatization/separation/detection system for the quantitation of thiols in tissue cultures. Extracellular fluid collected from rat organotypic hippocampal slice cultures (OHSCs) by electroosmotic flow through an11 cm (length) × 50 μm (ID) sampling capillary is introduced to a simple microfluidic chip for derivatization, continuous flow-gated injection, separation and detection.With the help of a fluorogenic, thiol-specific reagent, ThioGlo-1, we have successfully separated and detected the extracellular levels of free reduced cysteamine, homocysteineand cysteinefrom OHSCs within 25 s in a 23 mm separation channel with a confocal laser induced fluorescence (LIF) detector. Attention to the conductivities of the fluids being transported is required for successful flow-gated injections.When the sample conductivity is much higher than the run buffer conductivities, the electroosmotic velocities are such that there is less fluid coming by electroosmosis into the cross from the sample/reagent channel than is leaving by electroosmosis into the separation and waste channels. The resulting decrease in the internal fluid pressure in the injection cross pulls flow from the gated channel. This process may completely shut down the gated injection. Using a glycylglycine buffer with physiological osmolarity but only 62% of physiological conductivity and augmenting the conductivity of the run buffers solved this problem. Quantitation is by standard additions. Concentrations of cysteamine, homocysteine and cysteine in the extracellular space of OHSCs are10.6±1.0 nM (n=70), 0.18±0.01 μM (n=53) and 11.1±1.2 μM (n=70), respectively. This is the first in situquantitative estimation of endogenous cysteamine in brain. Extracellular levels of homocysteine and cysteine are comparable with other reported values.
机译:我们展示了用于组织培养物中硫醇定量的全电动采样/衍生化/分离/检测系统。通过电渗流通过11厘米(长)×50μm(ID)采样毛细管从大鼠器官型海马切片培养物(OHSC)收集的细胞外液引入到简单的微流控芯片中,以进行衍生化,连续流控注射,分离和检测。在荧光的,硫醇特异性试剂ThioGlo-1的帮助下,我们已经通过共聚焦激光诱导荧光(LIF)在23毫米分离通道中在25 s内成功地分离并检测了OHSC中游离还原型半胱胺,高半胱氨酸和半胱氨酸的细胞外水平。探测器。成功进行流控进样时需要注意所输送流体的电导率。当样品电导率比运行缓冲液电导率高得多时,电渗速率应使电渗入样品中的流体较少。 /试剂通道比通过电渗离开分离通道和废物通道要多。注射交叉口中内部流体压力的下降导致了来自门控通道的流动。此过程可能会完全关闭门控进样。使用具有生理渗透压但只有62%的生理电导率的甘氨酰甘氨酸缓冲液并增加电泳缓冲液的电导率解决了这个问题。通过标准添加进行定量。 OHSCs细胞外空间中半胱胺,高半胱氨酸和半胱氨酸的浓度分别为10.6±1.0 nM(n = 70),0.18±0.01μM(n = 53)和11.1±1.2μM(n = 70)。这是大脑中内源性半胱胺的第一个原位定量估计。同型半胱氨酸和半胱氨酸的细胞外水平与其他报道的值相当。

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