ALAMIN: a chemometric program to check analytical method performance and to assess the trueness by standard addition methodology

1997 ◽  
Vol 16 (7) ◽  
pp. 381-385 ◽  
Author(s):  
A.M.García Campaña ◽  
L.Cuadros Rodríguez ◽  
F.Alés Barrero ◽  
M.Román Ceba ◽  
J.L.Sierra Fernández
2008 ◽  
Vol 1 (3) ◽  
pp. 283-289
Author(s):  
G. Buttinger ◽  
S. Harbeck ◽  
R. Josephs

In the context of control activities contamination of food and feed with aflatoxins is a frequently observed non compliance. Pistachios, peanuts and products thereof are particularly affected. The Institute for Reference Materials and Measurements has therefore produced a peanut butter material certified for its aflatoxin mass fractions. This certified reference material (CRM) allows for the evaluation of analytical method performance and the assessment of the comparability of results from different laboratories. The CRM was produced using naturally contaminated raw materials to ensure equivalent behaviour compared to samples routinely encountered. The homogeneity and stability of the CRM were thoroughly tested and certified values were determined in an inter-laboratory study. Furthermore, uncertainties of the certified values were assessed including contributions of the homogeneity, stability and certification studies to the combined uncertainty. This newly prepared CRM allows an assessment of trueness of the analytical method at a concentration level corresponding to the legal limits enforced in the European Union. The material has the following certified properties: aflatoxin B1 1.77±0.29 µg/kg, aflatoxin B2 0.48±0.07 µg/kg, aflatoxin G1 0.9±0.4 µg/kg, aflatoxin G2 0.31±0.12 µg/kg and total aflatoxins, as sum of aflatoxins B1, B2, G1 and G2, 3.5±0.5 µg/kg.


AIHAJ ◽  
1996 ◽  
Vol 57 (11) ◽  
pp. 1035-1043 ◽  
Author(s):  
Paul C. Schlecht ◽  
Jensen H. Groff ◽  
Amy Feng ◽  
Ruiguang Song

1997 ◽  
Vol 80 (3) ◽  
pp. 676-680 ◽  
Author(s):  
Michael Thompson ◽  
Philip J Lowthian

Abstract A statistical test was made of the Horwitz function, an empirical relationship between the reproducibility precision of an analytical method and the concentration of the analyte regardless of the nature of the analyte, matrix, and the method. The large data set (7502 observations) was compiled by Horwitz from collaborative trials (method performance studies) spanning the period 1915 to 1995. The data followed the Horwitz function well down to concentrations of about 10-8 (10 ppb), but they followed a more stringent specification at lower concentrations. This discrepancy may be due to special circumstances prevailing in collaborative trials at very low concentrations. Deviations of individual observations from the function were in large part accounted for by random variations. No consequential improvement in precision with time was found.


1977 ◽  
Vol 60 (4) ◽  
pp. 940-945
Author(s):  
Thomas J Dols ◽  
Bernard H Armbrecht

Abstract A random review of the analytical literature shows the need to define more clearly the terms for techniques that are used to assess the merits of analytical methods for a particular purpose. One such performance characteristic is the systematic error or bias of a method. This term is defined and contrasted with other terms commonly used in method assessment. Components of the systematic error are described and techniques are given for their measurement.


2000 ◽  
Vol 41 (3) ◽  
pp. 224-227 ◽  
Author(s):  
Kumiko SASAKI ◽  
Takashi TATSUNO ◽  
Munetomo NAKAMURA ◽  
Akira ANAZAWA ◽  
Tsuyoshi IMAZAWA ◽  
...  

Author(s):  
Antonino Laudani ◽  
Deborah Sangregorio ◽  
Pietro Zuccarello ◽  
Teresa Licciardello ◽  
Stephanie Grasso ◽  
...  

Abstract Bone marrow is the tissue contained inside the bones and can be considered one of the potential alternative tissues in forensic toxicology. This matrix could be particularly useful in those cases where the routine sample is not available due to an advanced state of decomposition or skeletonization of the corpse. The aim of this study was to develop, validate and apply an analytical method of extraction and analysis of different antidepressants and antipsychotics, commonly used in therapy, from spiked pig ribs. Pig ribs, each of 5 g and 5 cm long, were spiked at 3 concentration levels (100, 200 and 500 ng/g). For each concentration, 10 pig ribs were prepared. The method involves the leaching by ethanol at different pHs of nine drugs from the inside of ribs, in particular from the bone marrow, without the fragmentation of bone tissue. Following a liquid–liquid purification and extraction, analysis was performed by gas chromatography coupled with mass spectrometry in selected ion monitoring mode. For method validation was assessed linearity, sensitivity, precision and accuracy, matrix interferences and, finally, carryover. Analytical method performance was acceptable respect to acceptance criteria for validation. No matrix interferences were detected; for this reason, it is possible to affirm that this method has a good selectivity. Moreover, the method was not affected by carryover. Considering that the study conducted on pig ribs has given encouraging results, it can be assumed that this method can be used in forensic toxicological protocols (human autopsy cases) as alternative to classic procedures.


2001 ◽  
Vol 42 (4) ◽  
pp. 278-282 ◽  
Author(s):  
Kumiko SASAKI ◽  
Takashi TATSUNO ◽  
Munetomo NAKAMURA ◽  
Tsuyoshi IMAZAWA ◽  
Osamu UTSUNOMIYA ◽  
...  

Author(s):  
G. Demire ◽  
D. Saray ◽  
B. Yaman, A. Turkyilmaz Yaman ◽  
A. Turkyilmaz

Quality by Design (QbD) is well established in the pharmaceutical industry for pharmaceutical development and manufacturing processes. The knowledge obtained during development may support the establishment of a design space and determines suitable process controls. This same QbD principle has been applied to the development of analytical methods and is termed “Analytical Quality by Design” (AQbD). Analogous to process QbD, the outcome of AQbD is well understood, fit for purpose, and robust method that consistently delivers the intended performance throughout its life cycle. The present work is aimed to develop an AQbD approach to analytical method development and validation based of Tadalafil and its impurities by the NP-HPLC method. The other objective of this work is to establish an in-depth understanding of the method and build in the quality during the method development to ensure optimum method performance over the lifetime of the product.


2000 ◽  
Vol 41 (3) ◽  
pp. 219-223 ◽  
Author(s):  
Kumiko SASAKI ◽  
Takashi TATSUNO ◽  
Munetomo NAKAMURA ◽  
Tsuyoshi IMAZAWA ◽  
Tatsuyuki OHSHIMA ◽  
...  

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