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PDMS-Glass bonding using grafted polymeric adhesive - Alternative process flow for compatibility with patterned biological molecules

机译:使用pDms-玻璃粘接接枝聚合物粘合剂 - 为相容的替代处理流程与图案化的生物分子

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摘要

We report a novel modification of silicone elastomer, polydimethylsiloxane (PDMS) with a polymer graft that allows interfacial bonding between elastomer and glass substrate to be performed without exposure of said substrate to harsh treatment conditions like oxygen plasma. Organic molecules can thus be patterned within microfluidic channels and still remain functional post-bonding. In addition, after polymer grafting the PDMS can be stored in a desiccator for at least 40 days, and activated upon exposure to acidic buffer for bonding. The bonded devices remain fully bonded in excess of 80 psi driving pressure, with no signs of compromise to the bond integrity. Finally, we demonstrate the compatibility of our method with biological molecules using a proof-of-concept DNA sensing device, in which fluorescently-labelled DNA targets are successfully captured by a patterned probe in a device sealed using our method, while the pattern on a plasma-treated device was completely destroyed. Therefore, this method provides a much-needed alternative bonding process for incorporation of biological molecules in microfluidic devices.
机译:我们报道了用聚合物接枝对有机硅弹性体,聚二甲基硅氧烷(PDMS)进行的新颖改性,其允许进行弹性体与玻璃基底之间的界面结合,而无需将所述基底暴露于苛刻的处理条件如氧等离子体下。因此,有机分子可以在微流体通道内形成图案,并在键合后仍然保持功能。另外,在接枝聚合物后,PDMS可以在干燥器中保存至少40天,并在暴露于酸性缓冲液中活化以进行键合。粘合设备在超过80 psi的驱动压力下仍保持完全粘合状态,而丝毫不影响粘合完整性。最后,我们使用概念验证的DNA传感设备展示了我们的方法与生物分子的兼容性,其中荧光标记的DNA目标通过使用我们的方法密封的设备中的图案化探针成功捕获,而等离子体处理过的装置被完全破坏。因此,该方法为将生物分子掺入微流体装置中提供了急需的替代键合方法。

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