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. 2007 Jun 29;104(28):11760–11765. doi: 10.1073/pnas.0703875104

Table 1.

Comparison of nonconfocal, confocal, and multiphoton fluorescence scanning microscopy for in vivo sensing of DiIC18(3)-labeled RBCs

Parameter measured Nonconfocal Confocal Multiphoton
Output power, mW* 1 1 35
Background intensity, a.u. 492–651 47–108 15–47
Signal intensity, a.u. 786–3,895 337–1,588 204–3,895
S/B ratio 1.30–6.98 3.46–21.90 5.51–108.90
S/B mean 2.36 ± 0.96† 9.37 ± 4.37† 22.38 ± 14.52†
Number detected, cells/min‡ 124.0 ± 13.2† 54.8 ± 8.8† 100.0 ± 11.1†

S/B, signal-to-background ratio.

*Output power was measured as the laser power out of objective lens.

†Values are expressed ± SD.

‡Number detected represents the number of cells detected by two-photon fluorescence microscopy.