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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.


Papers
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Journal ArticleDOI
07 Jan 2014-Analyst
TL;DR: An effective fluorescent sensor based on adenosine capped CdSe/ZnS quantum dots (A-QDs) for highly sensitive detection of DA in human urine samples with quantitative recoveries is reported.
Abstract: Facile detection of dopamine (DA) in biological samples for diagnostics remains a challenge. This paper reported an effective fluorescent sensor based on adenosine capped CdSe/ZnS quantum dots (A-QDs) for highly sensitive detection of DA in human urine samples. In this assay, adenosine serves as a capping ligand or stabilizer for QDs to render high-quality QDs dispersed in water, and as a receptor for DA to attach DA onto the surface of A-QDs. DA molecules can bind to A-QDs via non-covalent bonding, leading to the fluorescence quenching of A-QDs due to electron transfer. The A-QDs based fluorescence probe showed a limit of detection (LOD) of ca. 29.3 nM for DA detection. This facile method exhibited high selectivity and anti-interference in the presence of amino acid, ascorbic acid (AA), uric acid (UA) and glucide with 100-fold higher concentration in PBS solution. Furthermore, it was also successfully used in the detection of DA in the human urine samples with quantitative recoveries (94.80–103.40%).

104 citations

Journal ArticleDOI
24 Jan 2000-Talanta
TL;DR: A rapid and sensitive method was proposed for the determination of hydrogen peroxide based on the catalytic effect of hemoglobin using o-phenylenediamine as the substrate using stopped-flow spectrophotometric method.

104 citations

Journal ArticleDOI
01 Jan 1990-Analyst
TL;DR: For all elements significantly above the detection limit and reagent blank concentrations, good agreement exists between ICP-MS and certified values.
Abstract: A procedure has been developed for the analysis of biological materials by inductively coupled plasma mass spectrometry (ICP-MS). Fast, efficient and complete sample digestion is achieved by a combined microwave-nitric acid/open beaker-nitric acid-hydrogen peroxide procedure. The ICP-MS analysis is performed with an on-line five-element internal standard to correct for matrix and instrumental drift effects. Results are presented for 24 elements in three biological reference materials (National Institute of Standards and Technology Standard Reference Materials 5277a Liver and 1566 Oyster and International Atomic Energy Agency Certified Reference Material H4 Animal Muscle). For all elements significantly above the detection limit and reagent blank concentrations, good agreement exists between ICP-MS and certified values.

104 citations

Journal ArticleDOI
TL;DR: The results indicated the proposed platform has potential utility for detection of microRNA, and a wide linear range of 10fM to 1000fM with a relatively low detection limit was obtained by visual detection.

104 citations

Journal ArticleDOI
TL;DR: In this paper, a simple multi-residue method is described for assaying 13 quinolones (QNs; pipemidic acid, rufloxacin, enoxacins, ofloxacincin, norfloxacsin, ciprofloxcin, danofloxacanthus, enroflocin, diflocacin etc.) in feeds and validated by spiking a feed sample at three different levels (5, 10 and 25 mg kg −1 ) and linearity,

104 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20241
20236,071
202212,796
20211,671
20201,442
20191,445