Biomedical Engineering Graduate Interdisciplinary Program, The University of Arizona, Tucson, AZ 85721, USA.
Biomedical Engineering Graduate Interdisciplinary Program, The University of Arizona, Tucson, AZ 85721, USA; Department of Agricultural and Biosystems Engineering, The University of Arizona, Tucson, AZ 85721, USA.
Biosens Bioelectron. 2015 May 15;67:560-9. doi: 10.1016/j.bios.2014.09.040. Epub 2014 Oct 3.
We have developed a rapid, sensitive, and specific droplet-based immunoassay for the detection of Escherichia coli and Salmonella within a single-pipetted sample. Polycaprolactone (PCL) electrospun fibers on indium-tin-oxide (ITO) glass provide a sufficient surface to render a non-slip droplet condition, and while the PCL fibers lend a local hydrophilicity (contact angle θ=74°) for sufficient sub-micron particle adhesion, air pockets within the fibers lend an apparent hydrophobicity. Overall, the contact angle of water on this electrospun surface is 119°, and the air pockets cause the droplet to be completely immobile and resistant to movement, protecting it from external vibration. By using both anti-E. coli conjugated, 510 nm diameter green fluorescent particles (480 nm excitation and 520 nm emission) and anti-Salmonella conjugated, 400 nm diameter red fluorescent particles (640 nm excitation and 690 nm emission), we can detect multiple targets in a single droplet. Using appropriate light sources guided by fiber optics, we determined a detection limit of 10(2) CFU mL(-1). Immunoagglutination can be observed under a fluorescence microscope. Fluorescence detection (at the emission wavelength) of immunoagglutination was maximum at 90° from the incident light, while light scattering (at the excitation wavelength) was still present and behaved similarly, indicating the ability of double detection, greatly improving credibility and reproducibility of the assay. A power function (light intensity) simulation of elastic Mie scatter confirmed that both fluorescence and light scattering were present. Due to the size of the fluorescent particles relative to their incident excitation wavelengths, Mie scatter conditions were observed, and fluorescence signals show a similar trend to light scattering signals. Smartphone detection was included for true portable detection, in which the high contact angle pinning of the droplet makes this format re-usable and re-configurable.
我们开发了一种快速、灵敏、特异的基于液滴的免疫分析方法,可在单个移液样本中检测大肠杆菌和沙门氏菌。聚己内酯(PCL)在氧化铟锡(ITO)玻璃上的静电纺丝纤维提供了足够的表面,形成不易滑动的液滴状态,而 PCL 纤维具有局部亲水性(接触角θ=74°),足以使亚微米颗粒附着,同时纤维内的气穴赋予明显的疏水性。总的来说,水在这种静电纺丝表面上的接触角为 119°,气穴使液滴完全固定且不易移动,从而防止其受到外部振动的影响。通过使用抗大肠杆菌共轭的、510nm 直径的绿色荧光颗粒(480nm 激发和 520nm 发射)和抗沙门氏菌共轭的、400nm 直径的红色荧光颗粒(640nm 激发和 690nm 发射),我们可以在单个液滴中检测多个目标。通过使用光纤引导的适当光源,我们确定了 10(2)CFU mL(-1)的检测限。免疫凝集可以在荧光显微镜下观察到。在荧光显微镜下,免疫凝集的荧光检测(在发射波长下)在与入射光成 90°时达到最大值,而光散射(在激发波长下)仍然存在且行为相似,表明可以进行双检测,这极大地提高了该检测方法的可信度和重现性。弹性米氏散射的幂函数(光强)模拟证实,荧光和光散射都存在。由于荧光颗粒的尺寸相对于其入射激发波长,观察到米氏散射条件,荧光信号的趋势与光散射信号相似。包括智能手机检测,用于真正的便携式检测,其中液滴的高接触角固定使得这种格式可重复使用和重新配置。