2020
DOI: 10.1007/s00216-020-02504-z
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Comparative study on quantitation of human myoglobin by both isotope dilution mass spectrometry and surface plasmon resonance based on calibration-free analysis

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Cited by 4 publications
(2 citation statements)
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“…CFCA was also used to evaluate the potency of TNF-α before and after temperature stress, proving an alternative to a traditional EC 50 analysis [37]. Absolute CFCA was recently used to quantify human myoglobin with good agreement with isotope dilution mass spectrometry measurements [99], and a mathematical framework was developed to quantify analytes prone to self-association [100]. CFCA, especially in a relative framework, has already been proven to be efficient and accurate, and we predict its use will increase in the near future.…”
Section: Spr To Measure Concentrationsmentioning
confidence: 99%
“…CFCA was also used to evaluate the potency of TNF-α before and after temperature stress, proving an alternative to a traditional EC 50 analysis [37]. Absolute CFCA was recently used to quantify human myoglobin with good agreement with isotope dilution mass spectrometry measurements [99], and a mathematical framework was developed to quantify analytes prone to self-association [100]. CFCA, especially in a relative framework, has already been proven to be efficient and accurate, and we predict its use will increase in the near future.…”
Section: Spr To Measure Concentrationsmentioning
confidence: 99%
“…However, the SA method is time-consuming, complex, and costly due to the need for additional reagents and steps, often involving a full calibration curve with several successive standard additions for each sample to be analyzed . In practice, when a SA-based analytical method is used routinely and high efficiency is required in terms of time, workload, and resources, this approach is reduced to one- or two-point calibrations, along with a reduced number of replicas at each level, as long as the calibration curve has been previously well-characterized by proper statistical treatment and method validation to ensure the reliability and quality of the analytical results. Recent efforts have pursued reducing the extent of the calibration step , or even its elimination through implementation of calibration-free sensors. , Calibration-free sensors have been demonstrated to be feasible but not without requiring a highly robust development process involving the optimization of sensing materials, fabrication and assay protocols, and the use of the most adequate readout methodologies . The use of SA is particularly time-consuming in the case of immunoassays because each measurement typically requires 20–30 min (primarily as incubation time for capturing the target antigen), leading to complete assay times of over 60 or 90 min (along with the corresponding related labor and reagent costs).…”
mentioning
confidence: 99%