An IUPAC-based approach to estimate the detection limit in co-extraction-based optical sensors for anions with sigmoidal response calibration curves

被引:28
作者
Fernandez-Ramos, M. D. [1 ]
Cuadros-Rodriguez, L. [1 ]
Arroyo-Guerrero, E. [2 ]
Capitan-Vallvey, L. F. [1 ]
机构
[1] Univ Granada, Dept Analyt Chem, E-18071 Granada, Spain
[2] Dept Environm Rural & Marine Affairs, Cent Lab Anim Hlth Serv, Granada 18320, Spain
关键词
Bulk optical sensors; Anion determination; Sigmoidal calibration curves; Detection limit methodology; SELECTIVE OPTODE MEMBRANES; BULK OPTODES; NEUTRAL IONOPHORES; TEST STRIP; CHLORIDE; COEXTRACTION; POTASSIUM;
D O I
10.1007/s00216-011-5366-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An approach based on IUPAC methodology to estimate the limit of detection of bulk optode-based analytical methods for anions has been developed. The traditional IUPAC methodology for calculating the detection limit was modified to be adapted to particular cases where the calibration curves have a sigmoidal profile. Starting from the different full theoretical models for every co-extraction mechanism of the analyte in the membrane in bulk optodes, several particular simplified models at low analyte concentration were obtained and validated. The slope of the calibration curve at low analyte concentration was calculated from the first derivative of the simplified equation and, subsequently, the detection limit was estimated. This fitted-for-purpose estimation strategy was applied to anion quantification for in-house bulk optode-based analytical methods, and the estimated limits of detection were compared with those obtained by applying classical geometrical methodology. This way of establishing the detection limit yields values that maintain their true statistical and probabilistic aspects. It can be easily applied to any analytical system which yields non-linear calibration curves at low analyte concentration.
引用
收藏
页码:2881 / 2889
页数:9
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