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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),用于将小分子的有意浸出到微生物中

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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:本研究的目的是表明,可以施加来自聚(二甲基硅氧烷)(PDMS)的掺杂剂的扩散以将小分子输送到微流体通道。本机PDMS是疏水性的,通常需要对生物相关应用的表面改性。表面改性不是永久性的,因为表面通过单体的块状扩散到表面上恢复到疏水状态。同样地,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体积扩散到表面和周围的流体介质。 PDMS的这种特性具有用于细胞培养,细胞和分析物标记的药物递送,对微流体系统中的芯片实时/死测地,流动和扩散可视化,梯度产生和运输现象进行药物递送。我们使用荧光素来量化,并将这种小分子扩散从PDMS薄膜和微通道中的扩散模拟成流体流动。微通道浸出的结果显示在150nm左右90分钟内进入流体流入的稳态浸出。浸没掺杂PDMS的结果显示,在4天内,荧光素的持续浸出荧光素。结果表明,希望使用PDMS底物用于向微流体细胞培养物中施用少量物质,以及用于研究具有最小干扰的细胞行为的显影系统。

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