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Quantifying glucose and lipid components in human serum by Raman spectroscopy and multivariate statistics
Landulfo Silveira1,2, Rita de Cássia Fernandes Borges3, Ricardo Scarparo Navarro3
1Biomedical Engineering Center, Universidade Anhembi Morumbi - UAM, Parque Tecnológico de São José dos Campos, Estr. Dr. Altino Bondensan, 500, São José dos Campos, 12247-016, SP, Brazil. landulfo.silveira@gmail.com.
Raman spectroscopy can accurately measure glucose and lipid levels in human serum using a partial least squares (PLS) model. This technique shows promise for routine clinical diagnosis and biochemical analysis.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Spectroscopy
Background:
- Quantitative analysis of human serum biochemical components is crucial for clinical diagnosis.
- Raman spectroscopy offers a non-invasive method for biochemical analysis.
- Developing accurate spectral models is key to leveraging Raman spectroscopy for diagnostics.
Purpose of the Study:
- To develop a spectral model for estimating glucose and lipid fractions in human serum.
- To evaluate the feasibility of Raman spectroscopy for diagnostic purposes.
- To correlate Raman spectral data with established colorimetric assay results.
Main Methods:
- Collected 44 human blood serum samples.
- Performed Raman spectroscopy (830 nm, 250 mW, 50-s accumulation).
- Developed a quantitative model using partial least squares (PLS) regression with leave-one-out cross-validation.
Main Results:
- The PLS model accurately estimated triglyceride (r=0.98) and cholesterol (r=0.96) concentrations.
- Root mean square errors for triglycerides and cholesterol were 35.4 and 15.9 mg/dL, respectively.
- Correlation coefficients (r) for other biochemicals ranged from 0.75 to 0.86.
Conclusions:
- Raman spectroscopy combined with PLS regression can effectively perform biochemical assays in human serum.
- This technique demonstrates potential for routine clinical analysis and diagnosis.
- The study validates Raman spectroscopy as a viable tool for quantitative biochemical analysis.
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