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Optimization of PTFE Coating on PDMS Surfaces for Inhibition of Hydrophobic Molecule Absorption for Increased Optical Detection Sensitivity

机译:PDMS表面PTFE涂层的优化抑制光学检测灵敏度增加的疏水分子吸收

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摘要

Polydimethylsiloxane (PDMS) is a polymer widely used for fabrication and prototyping of microfluidic chips. The porous matrix structure of PDMS allows small hydrophobic molecules including some fluorescent dyes to be readily absorbed to PDMS and results in high fluorescent background signals, thereby significantly decreasing the optical detection sensitivity. This makes it challenging to accurately detect the fluorescent signals from samples using PDMS devices. Here, we have utilized polytetrafluoroethylene (PTFE) to inhibit absorption of hydrophobic small molecules on PDMS. Nile red was used to analyze the effectiveness of the inhibition and the absorbed fluorescence intensities for 3% and 6% PTFE coating (7.7 ± 1.0 and 6.6 ± 0.2) was twofold lower compared to 1% and 2% PTFE coating results (17.2 ± 0.5 and 15.4 ± 0.5). When compared to the control (55.3 ± 1.6), it was sevenfold lower in background fluorescent intensity. Furthermore, we validated the optimized PTFE coating condition using a PDMS bioreactor capable of locally stimulating cells during culture to quantitatively analyze the lipid production using Chlamydomonas reinhardtii CC-125. Three percent PTFE coating was selected as the optimal concentration as there was no significant difference between 3% and 6% PTFE coating. Intracellular lipid contents of the cells were successfully stained with Nile Red inside the bioreactor and 3% PTFE coating successfully minimized the background fluorescence noise, allowing strong optical lipid signal to be detected within the PDMS bioreactor comparable to that of off-chip, less than 1% difference.
机译:聚二甲基硅氧烷(PDMS)是广泛用于微流体芯片的制造和原型的聚合物。 PDMS的多孔基质结构允许包括一些荧光染料的小型疏水分子容易地吸收到PDMS并导致高荧光背景信号,从而显着降低光学检测灵敏度。这使得可以使用PDMS器件准确地检测来自样品的荧光信号的挑战。这里,我们利用聚四氟乙烯(PTFE)来抑制PDMS上疏水性小分子的吸收。尼罗红用于分析抑制的有效性和3%和6%PTFE涂层的吸收荧光强度(7.7±1.0和6.6±0.2),而2%和2%PTFE涂层结果(17.2±0.5 15.4±0.5)。与控制相比(55.3±1.6)相比,背景荧光强度下降了七倍。此外,我们使用能够在培养过程中局部刺激细胞的PDMS生物反应器验证了优化的PTFE涂覆条件,以定量使用衣原体ReinhardtII CC-125定量分析脂质生产。选择三种PTFE涂层作为最佳浓度,因为3%至6%PTFE涂层之间没有显着差异。细胞的细胞内脂质含量与生物反应器内的尼罗红色成功染色,3%PTFE涂层成功地最小化了背景荧光噪声,允许在PDMS生物反应器内检测强光脂质信号,比片上的PDMS生物反应器相当,小于1 % 区别。

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