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. 2025 Mar 31;150(10):2047–2057. doi: 10.1039/d4an00800f

Fig. 4. Identification plots for the PLS-DA model constructed using Raman spectra acquired from individual, living (a) CHO, (b) CHO-T, and (c) MDCK cells encapsulated in gelMA hydrogels. Cells located above the classification threshold denoted by the red dashed line were identified as (a) CHO cells (Inline graphic and Inline graphic, nmodel = 62, ntest = 61), (b) CHO-T cells (Inline graphic and Inline graphic, nmodel = 62, ntest = 61), and (c) MDCK cells (Inline graphic and Inline graphic, nmodel = 60, ntest = 59). Variable importance for prediction (VIP) plots for (d) CHO cells, (e) CHO-T cells, and (f) MDCK cells show which peaks have high (>1) scores that denote importance for identifying that cell type. Assignment of labeled peaks: 664 cm−1 (DNA bases), 680 cm−1 (DNA bases), 700 cm−1 (methionine), 716 cm−1 (lipids), 733 cm−1 (phosphatidylserine), 782 cm−1 (DNA/RNA), 789 cm−1 (phosphodiester bands), 956 cm−1 (cholesterol), 1015 cm−1 (carbohydrates), 1022 cm−1 (glycogen), 1442 cm−1 (fatty acids and collagen), and 1585 cm−1 (phenylalanine and hydroxyproline).

Fig. 4