Department of Chemistry and Biochemistry, Auburn University, Auburn, AL, USA.
Analyst. 2023 Sep 25;148(19):4810-4819. doi: 10.1039/d3an01149f.
The development of microfluidic systems for biological assays presents challenges, particularly in adapting traditional optical absorbance assays to smaller volumes or to microfluidic formats. This often requires assay modification or translation to a fluorescence version, which can be impractical. To address this issue, our group has developed the μChopper device, which uses microfluidic droplet formation as a surrogate for an optical beam chopper, allowing for lock-in analysis and improved limits of detection with both absorbance and fluorescence optics without modifying the optical path length. Here, we have adapted the μChopper to low-cost optics using a light-emitting diode (LED) source and photodiode detector, and we have fabricated the pnuematically valved devices entirely by 3D printing instead of traditional photolithography. Using a hybrid device structure, fluidic channels were made in polydimethylsiloxane (PDMS) by moulding onto a 3D-printed master then bonding to a prefabricated thin layer, and the pneumatic layer was directly made of 3D-printed resin. This hybrid structure allowed an optical slit to be fabricated directly under fluidic channels, with the LED interfaced closely above the channel. Vacuum-operated, normally closed valves provided precise temporal control of droplet formation from 0.6 to 2.0 Hz. The system was validated against the standard plate reader format using a colorimetric fructosamine assay and by quantifying fructosamine in human serum from normal and diabetic patients, where strong correlation was shown. Showing a standard benefit of microfluidics in analysis, the device required 6.4-fold less serum volume for each assay. This μChopper device and lower cost optical system should be applicable to various absorbance based assays in low volumes, and the reliance on inexpensive 3D printers makes it more accessible to users without cleanroom facilities.
用于生物分析的微流控系统的发展带来了挑战,特别是在将传统的光吸收分析方法应用于较小体积或微流控格式时。这通常需要对分析方法进行修改或转换为荧光版本,但这可能不切实际。为了解决这个问题,我们小组开发了 μChopper 设备,该设备使用微流控液滴形成作为光斩波器的替代物,允许进行锁相分析,并在不改变光程长度的情况下,提高吸收和荧光光学的检测限。在这里,我们使用发光二极管 (LED) 光源和光电二极管探测器,对 μChopper 进行了低成本光学元件的适配,并完全通过 3D 打印制造了气动阀设备,而不是传统的光刻技术。使用混合设备结构,通过在 3D 打印母模上成型然后与预制的薄层键合,在聚二甲基硅氧烷 (PDMS) 中制造了流体通道,而气动层则直接由 3D 打印树脂制成。这种混合结构允许在流体通道下方直接制造光学狭缝,并且 LED 紧密地位于通道上方。真空操作的常闭阀提供了从 0.6 到 2.0 Hz 的精确时间控制液滴形成。该系统通过使用比色法果糖胺分析以及通过定量分析正常和糖尿病患者血清中的果糖胺,与标准平板读数器格式进行了验证。结果显示,该设备在分析中显示了微流控的标准优势,每个分析所需的血清量减少了 6.4 倍。这种 μChopper 设备和低成本光学系统应该适用于各种低体积的基于吸收的分析方法,并且对廉价 3D 打印机的依赖使得没有洁净室设施的用户更容易获得。