首页> 美国卫生研究院文献>Journal of Diabetes Science and Technology >Interstitial Fluid Physiology as It Relates to Glucose Monitoring Technologies: Modulation of the Foreign Body Reaction for Implants in the Subcutaneous Space: Microdialysis Probes as Localized Drug Delivery/Sampling Devices
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Interstitial Fluid Physiology as It Relates to Glucose Monitoring Technologies: Modulation of the Foreign Body Reaction for Implants in the Subcutaneous Space: Microdialysis Probes as Localized Drug Delivery/Sampling Devices

机译:与葡萄糖监测技术有关的组织液生理学:皮下空间植入物异物反应的调节:作为局部药物输送/采样装置的微透析探针

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摘要

Modulation of the foreign body reaction is considered to be an important step toward creation of implanted sensors with reliable long-term performance. In this work, microdialysis probes were implanted into the subcutaneous space of Sprague-Dawley rats. The probe performance was evaluated by comparing collected endogenous glucose concentrations with internal standard calibration (2-deoxyglucose, antipyrine, and vitamin B12). Probes were tested until failure, which for this work was defined as loss of fluid flow. In order to determine the effect of fibrous capsule formation on probe function, monocyte chemoattractant protein-1/CC chemokine ligand 2 (MCP-1/CCL2) was delivered locally via the probe to increase capsule thickness and dexamethasone 21-phosphate was delivered to reduce capsule thickness. Probes delivering MCP-1 had a capsule that was twice the thickness (500–600 μm) of control probes (200–225 μm) and typically failed 2 days earlier than control probes. Probes delivering dexamethasone 21-phosphate had more fragile capsules and the probes typically failed 2 days later than controls. Unexpectedly, extraction efficiency and collected glucose concentrations exhibited minor differences between groups. This is an interesting result in that the foreign body capsule formation was related to the duration of probe function but did not consistently relate to probe calibration.
机译:异物反应的调节被认为是朝着创建具有可靠长期性能的植入式传感器迈出的重要一步。在这项工作中,将微透析探针植入Sprague-Dawley大鼠的皮下空间。通过将收集的内源葡萄糖浓度与内部标准校准品(2-脱氧葡萄糖,安替比林和维生素B12)进行比较,可以评估探针的性能。探针一直进行测试直至失效,这被定义为流体流失。为了确定纤维状胶囊的形成对探针功能的影响,通过探针局部递送单核细胞趋化蛋白-1 / CC趋化因子配体2(MCP-1 / CCL2)以增加胶囊厚度,并递送地塞米松21-磷酸盐以减少胶囊厚度。输送MCP-1的探针的囊膜厚度是对照探针(200-225μm)的两倍(500-600μm),通常比对照探针早2天失效。传递21-磷酸地塞米松的探针的胶囊更易碎,通常比对照组晚2天失效。出乎意料的是,各组之间的提取效率和收集的葡萄糖浓度显示出微小的差异。这是一个有趣的结果,因为异物囊的形成与探针功能的持续时间有关,但与探针校准并不一致。

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