Detection of diethylene glycol adulteration in propylene glycol-Method validation through a multi-instrument collaborative study

被引:11
作者
Li, Xiang [1 ,2 ]
Arzhantsev, Sergey [1 ]
Kauffman, John F. [1 ]
Spencer, John A. [1 ]
机构
[1] US FDA, Div Pharmaceut Anal, Ctr Drug Evaluat & Res, St Louis, MO 63101 USA
[2] Penn State Univ, University Pk, PA 16802 USA
关键词
Near infrared transmission; Propylene glycol; Diethylene glycol; Partial least squares; Hand-held instruments;
D O I
10.1016/j.jpba.2010.11.042
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Four portable NIR instruments from the same manufacturer that were nominally identical were programmed with a PLS model for the detection of diethylene glycol (DEG) contamination in propylene glycol (PG)-water mixtures. The model was developed on one spectrometer and used on other units after a calibration transfer procedure that used piecewise direct standardization. Although quantitative results were produced, in practice the instrument interface was programmed to report in Pass/Fail mode. The Pass/Fail determinations were made within 10 s and were based on a threshold that passed a blank sample with 95% confidence. The detection limit was then established as the concentration at which a sample would fail with 95% confidence. For a 1% DEG threshold one false negative (Type II) and eight false positive (Type I) errors were found in over 500 samples measured. A representative test set produced standard errors of less than 2%. Since the range of diethylene glycol for economically motivated adulteration (EMA) is expected to be above 1%, the sensitivity of field calibrated portable NIR instruments is sufficient to rapidly screen out potentially problematic materials. Following method development, the instruments were shipped to different sites around the country for a collaborative study with a fixed protocol to be carried out by different analysts. NIR spectra of replicate sets of calibration transfer, system suitability and test samples were all processed with the same chemometric model on multiple instruments to determine the overall analytical precision of the method. The combined results collected for all participants were statistically analyzed to determine a limit of detection (2.0% DEG) and limit of quantitation (6.5%) that can be expected for a method distributed to multiple field laboratories. Published by Elsevier B.V.
引用
收藏
页码:1001 / 1006
页数:6
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