Table 2.
Autofluorescence decay data analysis by the FLIMfit software tool74 glycated and unreacted control collagen before and after quenching with triiodide.
| Collagen | Collagen + I3− | Glycated collagen | Glycated collagen + I3− | |
|---|---|---|---|---|
| Mean τ/ns | 1.99 ± 0.10 | 0.26 ± 0.06 | 1.09 ± 0.04 | 0.86 ± 0.04 |
| τ1/ns | 5.41 ± 0.22 | 3.59 ± 2.92* | 3.37 ± 0.25 | 3.7 ± 0.27 |
| τ2/ps | 670 ± 30 | 240 ± 15 | 510 ± 35 | 440 ± 25 |
| β1 | 0.28 ± 0.01 | 0.01 ± 0.01 | 0.20 ± 0.02 | 0.13 ± 0.02 |
| β2 | 0.72 ± 0.01 | 0.99 ± 0.01 | 0.80 ± 0.02 | 0.87 ± 0.02 |
Pre-exponential coefficients (β1 and β2) and fluorescence lifetime values (τ1 and τ2) are described by the decay law . Data is presented as mean of 6–9 independent samples ± SD. Differences between τ1, τ2, β1, β2 and mean τ were found statistically significant in paired t-test for each of the four experimental conditions (except *). See also Fig. S3.