Detection limit

About: Detection limit is a research topic. Over the lifetime, 34379 publications have been published within this topic receiving 644817 citations. The topic is also known as: limit of detection & lower detection limit.

Chemiluminescence detection for a microchip capillary electrophoresis system fabricated in poly(dimethylsiloxane).

Abstract: Chemiluminescence (CL) detection integrated with a microchip capillary electrophoresis (MCE) system that was fabricated in poly(dimethylsiloxane) was demonstrated for chemical and biochemical analyses. Two model CL systems were involved here: metal ion-catalyzed luminol-peroxide reaction and dansyl species conjugated peroxalate-peroxide reaction. Different strategies based on three chip patterns (cross, cross combining with Y, and cross combining with V) to perform on-line CL detection for MCE were evaluated and compared in terms of sensitivity, reproducibility, and peak symmetry. The chip pattern of cross combining with Y proved to be promising for the luminol-peroxide CL system, while the chip pattern of cross combining with V was preferred for the peroxalate-peroxide system where CL reagent could not be effectively transported by electroosmotic flow. A detection limit down to submicromolar concentrations (midattomole) was achieved with good reproducibility and symmetric peak shape. Successful separation of three metal cations such as Cr(III), Co(II), and Cu(II) and chiral recognition of dansyl phenylalanine enantiomers within 1 min revealed distinct advantages of combining MCE with CL detection for rapid and sensitive analyses.

Trace Metal Detection by Laser-Induced Breakdown Spectroscopy

Abstract: Laser-induced breakdown spectroscopy (LIBS) has been widely pursued for trace elemental determination in gases, solids, and liquids. Application to liquids has proved problematic due to high spatial confinement of the LIBS plasma and rapid quenching of the excited-state emission. This work presents an alternative approach to trace metal determination in liquids in which 1.0 mL of liquid is deposited onto a carbon planchet and then evaporated, thus transforming the liquid analysis to a solid surface analysis. Using optimized excitation and detection conditions, we have identified spectral regions for sensitive detection of 15 metals (Mg, Al, Si, Ca, Ti, Cr, Fe, Co, Ni, Cu, Zn, As, Cd, Hg, Pb). The limit of detection (LOD) for the technique ranged from 10 ppb to 10 ppm for these elements. A 100 ppb LOD represents detection of 130 picograms of metal (approximately 2 picomoles) in a single measurement calculated from the laser spot size on the sample. Scanning electron microscopy (SEM) images and energy-dispersive X-ray (EDX) spectra of the samples provide insight into the observed reproducibility and linearity of the technique for several of the metals studied.

Folding Analytical Devices for Electrochemical ELISA in Hydrophobic R H Paper

Abstract: This work describes a device for electrochemical enzyme-linked immunosorbent assay (ELISA) designed for low-resource settings and diagnostics at the point of care. The device is fabricated entirely in hydrophobic paper, produced by silanization of paper with decyl trichlorosilane, and comprises two zones separated by a central crease: an embossed microwell, on the surface of which the antigen or antibody immobilization and recognition events occur, and a detection zone where the electrodes are printed. The two zones are brought in contact by folding the device along this central crease; the analytical signal is recorded from the folded configuration. Two proof-of-concept applications, an electrochemical direct ELISA for the detection of rabbit IgG as a model antigen in buffer and an electrochemical sandwich ELISA for the detection of malarial histidine-rich protein from Plasmodium falciparum (Pf HRP2) in spiked human serum, show the versatility of this device. The limit of detection of the electrochemical sandwich ELISA for the quantification of Pf HRP2 in spiked human serum was 4 ng mL(-1) (10(2) pmol L(-1)), a value within the range of clinically relevant concentrations.

Pulsed amperometric detection of glucose in biological fluids at a surface-modified gold electrode.

Abstract: A nonenzymatic glucose sensor that utilizes permselective membranes to achieve the selectivity required for screening glucose in biological fluids has been described. Interference from endogenous oxidizable substances such as amino acids, urea, ascorbic acid, and uric acid, as well as the effect of chloride and proteins on glucose response, is studied by using flow injection analysis. A set of membranes made of Naflin perfluorinated membrane and collagen, when arranged in front of the working electrode (gold), result in significant improvement in the system selectivity. Even at physiological pH, which is far from being the optimum pH for pulsed amperometric detection of carbohydrates, the sensor shows a good limit of detection (4-5 micrograms of glucose injected).