Pros and Cons of Using Correlation versus Multivariate Algorithms for Material Identification via Handheld Spectroscopy
Technical notes | 2019 | MetrohmInstrumentation
Handheld Raman spectroscopy has emerged as a pivotal tool for rapid, non-destructive identification of raw materials in pharmaceutical quality control and manufacturing. By enabling on-site analysis—often in warehouses—these portable instruments reduce laboratory turnaround times and support robust supply-chain traceability. Advances in detector sensitivity, laser stability, and onboard data processing now allow many handheld units to approach the performance of bench-top analyzers, making them indispensable for both exploratory screening and formal material verification.
This work compares two primary statistical approaches embedded in handheld Raman instruments for material identification:
Illustrative examples include discrimination of amino acids and differentiation of potassium carbonate from its sesquihydrate.
All experiments employed the NanoRam handheld Raman spectrometer (Model BWS456-785, B&W Tek, USA). For library matching, measured spectra were cross-correlated against reference libraries. For identity verification, the Soft Independent Modeling of Class Analogy (SIMCA) workflow was used, involving:
The two analytical strategies show complementary strengths:
In a three-amino-acid study (L-alanine, L-aspartic acid, L-cysteine HCl), HQI clearly separated all three (scores >98). SIMCA models likewise clustered each amino acid distinctly in PCA space, with test samples correctly passing only their respective models (p-values >0.05) and failing others (p<<0.05).
For potassium carbonate versus its sesquihydrate, HQI values exceeded 96 for both, failing to discriminate. The SIMCA approach, however, produced p-values >0.95 for correct matches and p-values <10^-3 for mismatches, demonstrating unambiguous identification.
The dual-algorithm framework in handheld Raman systems supports:
Adopting the appropriate algorithm optimizes workflow efficiency and minimizes false positives in both warehouse and production settings.
Ongoing developments in chemometric software, machine learning-augmented classification, and expanded spectral libraries will further enhance handheld spectroscopy. Integration with cloud-based data management and real-time regulatory reporting promises streamlined compliance. Emerging applications include counterfeit drug detection, in-process monitoring, and field-deployable forensic analysis.
Handheld Raman spectrometers equipped with both HQI correlation and SIMCA-based p-value analysis offer complementary capabilities. HQI is ideal for swift investigation of unknowns, while multivariate p-value testing provides robust confirmation of known materials and resolves closely related compounds. Understanding each method’s strengths ensures reliable, efficient material identification in pharmaceutical and industrial environments.
RAMAN Spectroscopy
IndustriesMaterials Testing
ManufacturerMetrohm
Summary
Significance of the topic
Handheld Raman spectroscopy has emerged as a pivotal tool for rapid, non-destructive identification of raw materials in pharmaceutical quality control and manufacturing. By enabling on-site analysis—often in warehouses—these portable instruments reduce laboratory turnaround times and support robust supply-chain traceability. Advances in detector sensitivity, laser stability, and onboard data processing now allow many handheld units to approach the performance of bench-top analyzers, making them indispensable for both exploratory screening and formal material verification.
Objectives and study overview
This work compares two primary statistical approaches embedded in handheld Raman instruments for material identification:
- Hit Quality Index (HQI): a correlation-based metric for library matching of unknown samples.
- Significance level (p-value) from multivariate classification (SIMCA): a confidence-driven test for verifying known materials.
Illustrative examples include discrimination of amino acids and differentiation of potassium carbonate from its sesquihydrate.
Methodology and instrumentation
All experiments employed the NanoRam handheld Raman spectrometer (Model BWS456-785, B&W Tek, USA). For library matching, measured spectra were cross-correlated against reference libraries. For identity verification, the Soft Independent Modeling of Class Analogy (SIMCA) workflow was used, involving:
- Acquisition of at least 20 spectra from authenticated material for model training.
- PCA model construction with a 95% confidence interval defining class membership limits.
- Projection of unknown spectra onto the PCA space, calculation of Hotelling’s T2 statistic, conversion to an F-value, and derivation of a p-value.
Main results and discussion
The two analytical strategies show complementary strengths:
- HQI library matching rapidly compares an unknown spectrum against large libraries, with scaled scores 0–100. A threshold (typically ≥95) automates match/no-match calls. It excels in exploratory screening but does not provide match probability nor sensitivity to subtle spectral differences.
- SIMCA-based p-value testing yields a statistical pass/fail decision at a chosen significance level (commonly p≥0.05 for acceptance). It requires prior model development but offers rigorous confidence metrics and reliably distinguishes structurally similar compounds.
In a three-amino-acid study (L-alanine, L-aspartic acid, L-cysteine HCl), HQI clearly separated all three (scores >98). SIMCA models likewise clustered each amino acid distinctly in PCA space, with test samples correctly passing only their respective models (p-values >0.05) and failing others (p<<0.05).
For potassium carbonate versus its sesquihydrate, HQI values exceeded 96 for both, failing to discriminate. The SIMCA approach, however, produced p-values >0.95 for correct matches and p-values <10^-3 for mismatches, demonstrating unambiguous identification.
Benefits and practical applications
The dual-algorithm framework in handheld Raman systems supports:
- Rapid screening of unknown raw materials against extensive spectral libraries (HQI).
- Regulated identity verification of known batches with defined statistical confidence (p-value/SIMCA).
- Discrimination of subtle compositional or polymorphic differences not captured by simple correlation.
Adopting the appropriate algorithm optimizes workflow efficiency and minimizes false positives in both warehouse and production settings.
Future trends and applications
Ongoing developments in chemometric software, machine learning-augmented classification, and expanded spectral libraries will further enhance handheld spectroscopy. Integration with cloud-based data management and real-time regulatory reporting promises streamlined compliance. Emerging applications include counterfeit drug detection, in-process monitoring, and field-deployable forensic analysis.
Conclusion
Handheld Raman spectrometers equipped with both HQI correlation and SIMCA-based p-value analysis offer complementary capabilities. HQI is ideal for swift investigation of unknowns, while multivariate p-value testing provides robust confirmation of known materials and resolves closely related compounds. Understanding each method’s strengths ensures reliable, efficient material identification in pharmaceutical and industrial environments.
References
- Üstün B. Raw Material Identity Verification in the Pharmaceutical Industry. European Pharmaceutical Review. 2013;13(3).
- Diehl B, Chen CS, Grout B, et al. An implementation perspective on handheld Raman spectrometers for raw material verification. European Pharmaceutical Review. 2012;17(5).
- Kalyanaraman R, Ribick M, Dobler G. Portable Raman spectroscopy for pharmaceutical counterfeit detection. European Pharmaceutical Review. 2012;17(5).
- The Economist. Fake Pharmaceuticals: Bad Medicine. October 2012.
- Lozano Diz E, Thomas RJ. Portable Raman for raw material QC: What’s the ROI? Pharmaceutical Manufacturing. 2013.
- Yang D, Thomas RJ. The benefits of a high-performance handheld Raman spectrometer for rapid identification of pharmaceutical raw materials. American Pharmaceutical Review. 2012.
- Lowry SR. Automated spectral searching in infrared, Raman and near-infrared spectroscopy. In: Handbook of Vibrational Spectroscopy. Wiley; 2002:1948–1960.
- Kauffman J, Rodriguez JD, Buhse LF. Spectral preprocessing for Raman library searching. American Pharmaceutical Review. 2011;14(4).
- Gryniewicz-Ruzicka CM, Rodriguez J, Arzhantsev S, Buhse LF, Kauffman J. Comparison of chemometric methods for analysis of Raman spectra of contaminated pharmaceuticals. J Pharm Biomed Anal. 2013;61:191–198.
- McCreery RL, Horn AJ, Spencer J, Jefferson E. Noninvasive identification of materials inside USP vials with Raman spectroscopy. J Pharm Sci. 1998;87:1–8.
- Champagne AB, Emmel KV. Rapid screening test for adulteration in dietary supplement raw materials. Vibrational Spectroscopy. 2011;55:216–223.
- Wold S. Pattern recognition by means of disjoint principal component models. Pattern Recognition. 1976;8:127–139.
- Svensson O, Josefson M, Langkilde FW. Classification of chemically modified celluloses using NIR and SIMCA. Appl Spectrosc. 1997;51(12):1826–1835.
- Brereton RG. Chemometrics for Pattern Recognition. Wiley; 2009.
- Brown SD. Chemical systems under indirect observation: Latent properties and chemometrics. Appl Spectrosc. 1995;49(12):14A–31A.
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