AOAC Guidelines for Single Laboratory
ثبت نشده
چکیده
CONTENTS 1.0 Introduction 1.1 Definitions 1.1.1 Validation 1.1.2 Method of analysis 1.1.3 Performance characteristics of a method of analysis 2.0 Single-Laboratory Validation Work 2.1 Preparation of the Laboratory Sample 2.2 Identification 2.3 Method of Analysis or Protocol 2.3.1 Optimization 2.3.2 Reference standard 2.3.3 Ruggedness Trial 2.3.4 Specific variables a. Analyte addition b. Reextraction of the extracted residue c. Comparison with different solvents d. Comparison with results from a different procedure e. System Suitability Checks 3.0 Performance Characteristics 3.1 Applicability 3.2 Selectivity 3.3 Calibration 3.3.1 External Standard Method 3.3.2 Internal Standard Method 3.3.3 Standard Addition Method 3.4 Reliability Characteristics 3.4.1 Accuracy 3.4.2 Repeatability Precision (sr, RSDr) 3.4.3 Measurement Uncertainty 3.4.4 Reproducibility Precision (sR, RSDR) 3.4.5 Intermediate Precision 3.4.6 Limit of Determination 3.4.7 Reporting Low-level Values 3.4.8 Dichotomous Reporting 3.5 Controls 3.5.1 Control Charts 3.5.2 Injection Controls 3.5.3 Duplicate Controls 3.6 Confirmation of Analyte
منابع مشابه
Determination of phytase activity in feed by a colorimetric enzymatic method: collaborative interlaboratory study.
Fourteen laboratories participated in a collaborative study (coded fyt9404) and 13 laboratories participated in a study (coded fyt9410) to validate a colorimetric assay for determination of microbial phytase activity in feed. For each study, all laboratories received 6 laboratory samples provided by one commercial supplier (phytase activity levels within the range of 200-400 per kg) to be analy...
متن کاملAnalysis of 5'-mononucleotides in infant formula and adult/pediatric nutritional formula by liquid chromatography: First Action 2011.20.
A method for the routine determination of 5'-mononucleotides (uridine 5'-monophosphate, inosine 5'-monophosphate, adenosine 5'-monophosphate, guanosine 5'-monophosphate, and cytidine 5'-monophosphate) in infant formula and adult nutritionals is described. After sample dissolution and addition of internal standard, potential interferences were removed by anion-exchange SPE followed by HPLC-UV an...
متن کاملInternational Union of Pure and Applied Chemistry Analytical, Applied, Clinical, Inorganic and Physical Chemistry Divisions Interdivisional Working Party for Harmonization of Quality Assurance Schemes for Analytical Laboratories* Harmonised Guidelines for the Use of Recovery Information in Analytical Measurement
ISO, IUPAC and AOAC International have co-operated to produce agreed protocols or guidelines on the ‘Design, Conduct and Interpretation of Method Performance Studies’ [1] on the ‘Proficiency Testing of (Chemical) Analytical Laboratories’ [2] and on ‘Internal Quality Control in Analytical Chemistry Laboratories’ [3]. The Working Group that produced these protocols/guidelines was asked to prepare...
متن کاملProbability of Detection (POD) as a statistical model for the validation of qualitative methods.
A statistical model is presented for use in validation of qualitative methods. This model, termed Probability of Detection (POD), harmonizes the statistical concepts and parameters between quantitative and qualitative method validation. POD characterizes method response with respect to concentration as a continuous variable. The POD model provides a tool for graphical representation of response...
متن کاملDetermination of nitrogen solubility in dilute pepsin hydrochloric acid solution of fishmeal: interlaboratory study.
A revised method to determine solubility of nitrogen in dilute pepsin, using 0.0002% pepsin in place of 0.2% in AOAC Official Method 971.09, was tested in 16 laboratories with 12 samples of fishmeal. Results were calculated according to 2 procedures: AOAC Official Method 971.09 and a method described in 1964 by researchers at the Torry Research Station (Aberdeen, Scotland), and generally referr...
متن کامل