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Doping Poly (dimethylsiloxane) for Intentional Leaching of Small Molecules into Microdevices

机译:掺杂聚二甲基硅氧烷以将小分子有意浸入微器件

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The goal of this study is to show that diffusion of a dopant from poly(dimethylsiloxane) (PDMS) may be applied to deliver small molecules to a microfluidic channel. Native PDMS is hydrophobic and often requires surface modifications for biologically relevant applications. Surface modification is not permanent, as the surface reverts to a hydrophobic state via bulk diffusion of monomers to the surface. Likewise, solid substances can be added into PDMS prepolymer mixture prior to curing and these particles can diffuse from the cured polymer bulk to the surface and surrounding fluid media. This characteristic of PDMS has applications for drug delivery to cell culture, cell and analyte labeling, on chip live/dead assays, flow and diffusion visualization, gradient generation, and transport phenomena in microfluidic systems. We use fluorescein to quantify and model this small molecule diffusion out of PDMS thin films and microchannels into fluid flow. The results from microchannel leaching show steady state leaching into the fluid flow over 90 minutes at concentrations around 150 nM. Results from immersion of doped PDMS shows continued leaching of fluorescein from the polymer over 4 days. The results show promise to use PDMS substrates for administering small amounts of substances to microfluidic cell cultures, as well as developing systems for studying cellular behavior with minimal interference.
机译:这项研究的目的是表明可以应用掺杂剂从聚二甲基硅氧烷(PDMS)中扩散来将小分子传递至微流体通道。天然PDMS具有疏水性,通常需要对表面进行修饰以实现生物学相关的应用。表面改性不是永久性的,因为表面会通过单体大量扩散到表面而恢复为疏水状态。同样,可以在固化之前将固体物质添加到PDMS预聚物混合物中,并且这些颗粒可以从固化的聚合物主体扩散到表面和周围的流体介质中。 PDMS的这一特性可用于将药物递送至细胞培养,细胞和分析物标记,芯片活/死分析,流动和扩散可视化,梯度生成以及微流系统中的传输现象。我们使用荧光素来量化和建模这种小分子从PDMS薄膜和微通道向流体流动的扩散。微通道浸出的结果表明,在90分钟内,在150 nM左右的浓度下,稳态浸入流体流中。掺杂的PDMS的浸入结果显示,荧光素在4天内持续从聚合物中浸出。结果表明,有望将PDMS底物用于对微流细胞培养物施用少量物质,并开发出用于以最小干扰研究细胞行为的系统。

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