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Joint Research Centre the European Commission's in-house science service Chemometrics in method validation – why? Jone Omar 10 th May 2016, Gent Eurachem.

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Presentation on theme: "Joint Research Centre the European Commission's in-house science service Chemometrics in method validation – why? Jone Omar 10 th May 2016, Gent Eurachem."— Presentation transcript:

1 Joint Research Centre the European Commission's in-house science service Chemometrics in method validation – why? Jone Omar 10 th May 2016, Gent Eurachem 2016

2 2 PhD in analytical chemistry in 2013 ‘New analytical strategies for the characterization of bioactive compounds’ Early career scientist – Who am I? Bilbao

3 3 Early career scientist – Who am I? Since 2013 Research fellow in the JRC-IRMM Geel

4 4 Outline Chemometrics in method validation-why? Briefly, what is chemometrics Where can we apply chemometrics, how? Applicability of chemometrics, some examples Conclusions

5 5 Chemometrics in method validation – why? Method validation Accuracy Precision Specificity LOD/LOQ Linearity Etc… Sample preparation Instrumental setup Data treatment

6 6 What is chemometrics? The chemical discipline that uses mathematical and statistical methods, a)to design or select optimal measurement procedures and experiments and b) to provide maximum chemical information by analysing chemical data

7 7 Where can we apply chemometrics? Sample preparation Instrumental method Data treatment DoE for getting the best /optimum analyte disposition DoE for getting the best working conditions in our method & validate Multivariate data or image analysis

8 8 Design of Experiments = DoE Screening designs – Full Factorial Design (FFD) Information of the statistically significant parameters Optimisation Design – Central Composite Design (CCD) Optimum conditions of the system and the interactions among the parameters What is DoE? And what advantages does it have Maximum information - minimum Nº of experiments Interaction between parameters

9 9 DoE how to proceed: 1.Do you need a screening design or an optimisation design? 2.Decide the affecting/important parameters of your system / sample preparation 3.Decide the range in which the parameters will be studied, according to your knowledge / expertise.

10 10 Chemometrics useful in many fields/matrixes Characterisation of nanomaterials Extraction of volatiles Quantitative method development in olive oil Deterpenation of cannabis Authentication method for coccidiostats Extraction & digestion of allergens in cookies Applicability of chemometrics, some examples 1 2 34 5 6

11 11 Smallest particle size Example 1: characterisation of nanomaterials Focused Ultrasound Value of interest Optimise the dispersion of TiO 2 into minimum dispersible units Submitted to JCA, March 2016

12 12 Smallest particle size Example 1: characterisation of nanomaterials Focused Ultrasound Optimise the dispersion of TiO 2 into minimum dispersible units Raw material Optimised dispersion protocol Material in suspension Submitted to JCA, March 2016

13 13 Optimise an AF4 method that can separate a polydisperse TiO 2 material FFD - Pareto diagram with the significant variables Variables to be studied in a CCD Example 1: characterisation of nanomaterials Fractogram of TiO 2 under optimised conditions Particle size 200nm= Value of interest

14 14 Example 2: volatiles 1) Screening - FFD 2) Optimisation - CCD Develop & optimise a quantitative method for extracting aromas from plants by means of SFE or FUSE 15 volatiles Highest amount = Value of interest J.Omar, et al. Food Analytical Methods 6 (2013), 1611-1620, Optimization of FUSE and SFE of Volatile Compounds and Antioxidants from Aromatic Plants

15 15 Optimise a GCxGC-MS separation method that suits all volatiles GCxGC-MS microfluidic modulator Example 2: volatiles & antioxidants Highest intensity = Value of interest J.Omar, et al. Talanta 88 (2012) 145– 151, Optimization of comprehensive two-dimensional gas-chromatography (GC×GC) mass spectrometry for the determination of essential oils

16 16 Optimise the measuring conditions of a Raman method We look for the highest signal of the spectra Without burning the sample The shortest acquisition time with an acceptable signal/noise ratio Example 3: aromas in olive oil J.Omar, et al. Journal of Raman Spectroscopy 43 (2012) 1151-1156, Quantitative analysis of Essential oils from rosemary in virgin olive oil using Raman spectroscopy and chemometrics

17 17 630-660 cm -1 Spectral windows of interest Develop a quantitative Raman method for volatiles in olive oil Example 3: aromas in olive oil

18 18 RMSEP Number of principal components Develop a quantitative Raman method for volatiles in olive oil Example 3: aromas in olive oil

19 19 Validate the model Compare real sample concentrations between two techniques Example 3: aromas in olive oil

20 20 Example 4: deterpenation of cannabis 1)Screening to see feasibility - FFD 2)Optimisation to get quantitative conditions - CCD 2 fractions: aromas & cannabinoids Develop & optimise a deterpenation method for extracting aromas & cannabinoids from cannabis by means of SFE or FUSE Highest amount = Value of interest J.Omar, et al. Journal of Separation Science 36 (2013), 1397-1404, Optimisation and Characterisation of marihuana extracts obtained by SFE and FUSE and RTL-GC-MS

21 21 MCR-ALS to deconvolute the co-elutions by means of MS information Deconvolute co-eluting sesquiterpenes and cannabinoids in GCxGC-MS Example 4: deterpenation of cannabis J.Omar, et al. Talanta, 121 (2014) 273-280, Resolution of co-eluting compounds of Cannabis Sativa in GCxGC-MS detection with Multivariate Curve Resolution-Alternating Least Squares

22 22 Example 5: authentication of coccidiostats Difficult to distinguish with the naked eye, model created by PCA and validated NIR spectra of coccidiostats Develop a model for authentication of coccidiostats in NIR & MIR J.Omar, et al. Journal of Food Additives and Contaminants, Part A, 32 (2015) 1464-1474, Differentiation of coccidiostats-containing feed additives by Mid and Near Infra-Red Microscopy

23 23 Example 5: authentication of coccidiostats Difficult to distinguish with the naked eye, model created by PCA and validated NIR spectra of coccidiostats Develop a model for authentication of coccidiostats in NIR & MIR J.Omar, et al. Journal of Food Additives and Contaminants, Part A, 32 (2015) 1464-1474, Differentiation of coccidiostats-containing feed additives by Mid and Near Infra-Red Microscopy

24 24 Example 6: allergens in cookies Develop & optimise an extraction + digestion method for MS based quantification of milk & egg allergens in food products. DoE 1 Extraction DoE 2 Digestion Method validation (coming soon) Can one method suit all ? 18 peptides to monitor compromise needed

25 25 Conclusions -Time and money saving -Interactions of parameters visible -Applicability to many fields / matrixes -Optimised methods will lead to better figures of merit

26 26

27 27 Stay in touch JRC Science Hub: ec.europa.eu/jrc Jone.OMAR-ONAINDIA@ec.europa.eu @Jone_OO Acknowledgements University of the Basque Country Joint Research Centre Standards for Food Bioscience


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