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Power-free polydimethylsiloxane femtoliter-sized arrays for bead-based digital immunoassays

机译:用于珠子的数字免疫测定的无功聚二甲基硅氧烷Femtoliter大小的阵列

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A novel microfluidic chip employing power-free polydimethylsiloxane (PDMS) femtoliter-sized arrays was developed for the detection of low concentrations of protein biomakers by isolating individual paramagnetic beads in single wells. Arrays of femtoliter-sized wells were fabricated with PDMS using well-developed molding techniques. Paramagnetic beads were functionalized with specific antibodies to capture the antigens. These antigens were labeled with enzymes via conventional multistep immunosandwich approach. After suspending in aqueous solutions of enzyme substrate, the solutions were delivered to the arrays using a conventional micropipette. The aqueous solutions were introduced into the microwells by capillarity and the beads were loaded into microwells by gravity. A fluorocarbon oil was then flowed into the chip to remove excess beads from the surface of the array and meanwhile isolated the femtoliter-sized wells. All processes were achieved by conventional micropipette, without external pumping systems and valves. Finally, the arrays were imaged using standard fluorescence imaging after incubation 30 min for digital counting enzyme molecules. It was demonstrated that the chip platform possessed the performance of digital counting with a linear dynamic range from 1 aM to 1 fM for the detection of biotinylated beta-galactosidase (B beta G), achieving a limit of detection (LOD) of 930 zM. Using this chip, a digital immunoassay to detect Tumor Necrosis Factor alpha (TNF - alpha) was developed. Since the chip fabrication is low-cost and circumvents the surface modification, we expect it can become a new chip-based digital immunoassay platform for ultrasensitive diagnostic of biomarkers.
机译:通过在单孔中隔离单独的顺磁珠,开发了一种采用无功聚二甲基硅氧烷(PDMS)Femtoliter尺寸阵列的新型微流体芯片用于检测低浓度的蛋白质生物干草剂。使用良好开发的模制技术用PDMS制造了Femtoliter大小的井阵列。用特异性抗体官能化的顺磁珠捕获抗原。这些抗原通过常规多中的MultiSep免疫系统和酶用酶标记。悬浮在酶底物的水溶液后,使用常规的微量纤维液将溶液递送至阵列。通过毛细管分流将水溶液引入微孔中,并通过重力将珠子装入微孔中。然后将碳碳油流入芯片中以从阵列的表面上除去过量的珠子,同时分离毫无升性的井。所有过程均通过传统的微型电池实现,无需外部泵送系统和阀门。最后,在孵育30分钟后,使用标准荧光成像进行成像,用于数字计数酶分子。据证明,芯片平台具有从1Ab的线性动态范围的数字计数的性能,用于检测生物素化的β-半乳糖苷酶(BβG),实现930 ZM的检测极限(LOD)。使用该芯片,开发了一种数字免疫测定以检测肿瘤坏死因子α(TNF-α)。由于芯片制造是低成本并避免表面改性,因此我们预计它可以成为一种新的基于芯片的数字免疫测定平台,用于对生物标志物的超声诊断。

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