Microorganisms, molecules, or viruses in the fluidic environment are usually at considerably low Reynolds numbers because of small diameters. The viscous forces of molecules and viruses dominate at considerably low Reynolds numbers. This study developed three microfluidic devices, that is, T type, U type, and W type devices, to control the flow movement, which can increase the adhesion density of viruses on the surface of the sensor. The linker 11-mercaptoundecanoic acid (11-MUA) and Turnip yellow mosaic virus (TYMV) were used in this study and measured by a confocal microscope. Fluorescent intensity and coverage of 11-MUA and TYMV were used to identify the adhesion density quantitatively. Results indicate that 11-MUA layers and TYMV disperse randomly by the dipping method. Attachment tests for T-, U-, and W-type devices demonstrated average fluorescence intensities of 1.56, 2.18, and 2.67, respectively, and average fluorescence coverage of 1.31, 1.87, and 2.55 times those of dipping techniques, respectively. The T-type device produced the lowest fluorescence coverage uniformity (10%-80%), whereas the W-type device produced the highest fluorescence coverage uniformity (80%-90%). Fluorescence intensity correlates positively with flow within a specified flow range; however, the exact relationship between fluorescence intensity and flow requires further study. Attachment tests for TYMV virus samples indicated that the W-type device produced an average fluorescence intensity of 3.59 and average fluorescence coverage of 19.13 times greater than those achieved through dipping techniques. Traditional immersion methods achieved fluorescence coverage of 0%-10%, whereas that of the W-type device reached 70%-90%. V C 2012 American Institute of Physics. [http://dx
Recently, there has been an increasing interest to develop rapid, reliable and low-concentration detection methods of micro-organisms involved in bioterrorism, food poisoning, and clinical problems. How to detect virus at concentration below the threshold will be challenging with respect to specificity, selectivity, and sensitivity. Among all parameters, sensitivity is probably the most critical consideration. If the sensitivity is not satisfied for real-time detection, researchers need to duplicate numerous numbers of viruses. However, it will substantially increase processing times and experimental hazard. To increase the sensitivity of virus sensors, this paper discusses how to increase the density of linkers and viruses on sensor’s surface in the microfluidic channels. In the future, researcher could use emerging technology, such as PT-PCR, QCM, C-V and I-V measurements, etc, to detect viruses on sensor’s surface. Usually microorganisms, molecules, or viruses in the fluidic environment are at very low Reynolds numbers because of tiny diameters. At very low Reynolds numbers, viscous forces of molecules and viruses will dominate. Those micro- or nanoparticles will stop moving immediately when flows cease and drag forces disappear. Of course, molecules and viruses are still subject to Brownian motion and move randomly. In order to increase the adhesion density of micro- and nanoparticles on sensor’s surface, designs of the flow movements in microfluidic channel is proposed. Adhesion density of linker 11-mercaptoundecanoic acid (MUA) and turnip yellow mosaic virus (TYMV) with specific quantum dots were measured by confocal microscope. Results show that TYMV and MUA layers disperse randomly by dipping method. Infusion rate, flow rate, and transverse flow could affect the adhesion densities of recognition layers on sensors’ surface. Adhesion densities of MUA and TYMV can be reached 70∼80% by microfluidic method to contrast just 10% by dipping method.
Usually microorganisms, molecules, or viruses in the fluidic environment are at very low Reynolds numbers because of tiny diameters. At very low Reynolds numbers, viscous forces of molecules and viruses will dominate. Those micro- or nanoparticles will stop moving immediately when flows cease and drag forces disappear, those phenomena were discovered by the fluorescent particle experiment. Of course, molecules and viruses are still subject to Brownian motion and move randomly. In order to increase the adhesion density of micro- and nanoparticles on sensor’s surface, designs of the flow movements in microfluidic channel is proposed. Adhesion density of linker 11-mercaptoundecanoic acid (MUA) and Turnip yellow mosaic virus (TYMV) with specific quantum dots were measured by confocal microscope. Fluorescent intensity and coverage of quantum dots are used to identify the adhesion density quantitatively. Results show that TYMV and MUA layers disperse randomly by dipping method. Fluorescent intensity of quantum dots; i.e. relative to the amount of MUA and TYMV; were 2.67A.U. and 19.13A.U., respectively, in W-type microfluidic devices to contrast just 1.00A.U. and 1.00A.U., respectively, by dipping method. Coverage of MUA and TYMV were 80∼90% and 70∼90%, respectively, in W-type microfluidic channel to contrast just 20∼50% and 0∼10%, respectively, by dipping method.
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