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In analytical chemistry, the detection limit, lower limit of detection, also termed LOD for limit of detection or analytical sensitivity (not to be confused with statistical sensitivity), is the lowest quantity of a substance that can be distinguished from the absence of that substance (a blank value) with a stated confidence level (generally 99%).
A calibration curve plot showing limit of detection (LOD), limit of quantification (LOQ), dynamic range, and limit of linearity (LOL).. In analytical chemistry, a calibration curve, also known as a standard curve, is a general method for determining the concentration of a substance in an unknown sample by comparing the unknown to a set of standard samples of known concentration. [1]
An example of a Levey–Jennings chart with upper and lower limits of one and two times the standard deviation. A Levey–Jennings chart is a graph that quality control data is plotted on to give a visual indication whether a laboratory test is working well. The distance from the mean is measured in standard deviations.
The triple quadrupole mass spectrometer allows for increased sensitivity and specificity yielding lower detection and quantitation limits. [8] For these reasons, employment of the TQMS is a vital asset in the fields of drug metabolism, pharmacokinetics, environmental studies, and biological analyses.
All analytical procedures should be validated. Identification tests are conducted to ensure the identity of an analyte in a sample through comparison of the sample to a reference standard through methods such as spectrum, chromatographic behavior, and chemical reactivity. [5] Impurity testing can either be a quantitative test or a limit test.
In selective ion monitoring (SIM) certain ion fragments are entered into the instrument method and only those mass fragments are detected by the mass spectrometer. The advantages of SIM are that the detection limit is lower since the instrument is only looking at a small number of fragments (e.g. three fragments) during each scan.
Typical amplitudes of these pulses range between 10 and 50 mV, whereas pulse duration is 20 to 50 ms. The difference between both current values is the analytical signal. This technique results in a 100 to 1000-fold improvement of the detection limit, because the capacitive component is effectively subtracted.
The detection limit for electron capture detectors is 5 femtograms per second (fg/s) and the detector commonly exhibits a 10,000-fold linear range. [ citation needed ] This made it possible to detect halogenated compounds such as pesticides and CFCs , even at levels of only one part per trillion ( ppt ), thus revolutionizing our understanding ...