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. Author manuscript; available in PMC: 2010 Jul 2.
Published in final edited form as: J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Sep 5;808(2):141–152. doi: 10.1016/j.jchromb.2004.04.030

Table 4.

Extraction efficiency, linearity and sensitivity of assay in rat tissues

Sample Tissue concentration Linear range (nM) In vivo sample range (nM) Extraction efficiency (%) LOQ (nM) Sensitivity (pg)
Plasma DXR 20% (v/v) 0.343–10,000 0–5000 87.2 0.343 1.87
DXR-ol 20% (v/v) 0.945–10,000 0–2000 ND 1.89 10.3
Brain/tumor DXR 5% (w/v)# 0.125–1000 0.6–126 91.4 0.25 1.36
DXR-ol 5% (w/v)# 0.500–1000 0.4–92 ND 0.5 2.73
Liver DXR 0.5% (w/v) 0.686–1000 43–240 88.9 2.06 11.2
DXR-ol 0.5% (w/v) 2.06–1000 4–18 ND 2.1 11.2
Spleen DXR 1% (w/v) 2.06–1000 91–846 91.8 2.06 11.2
DXR-ol 1% (w/v) 2.06–1000 18–246 ND 2.1 11.2
Heart DXR 2.5% (w/v) 1.37–1000 60–680 112 2.06 11.2
DXR-ol 2.5% (w/v) 2.06–1000 11–55 ND 2.1 11.2
Lung DXR 2.5% (w/v) 2.06–1000 267–931 84.2 2.5 13.6
DXR-ol 2.5% (w/v) 2.06–1000 4–42 ND 2.1 11.2

Standard solutions of DXR or DXR-ol were prepared in blank plasma or tissue homogenates at known concentrations ((v/v) or (w/v)), extracted, and analyzed by LC–MS/MS. The extraction efficiency, linearity, and sensitivity of the method were determined. The in vivo sample range was determined after analysis of plasma and tissue samples from rats (n ≥ 12) treated intravenously with 5.67 mg/kg SSL–DXR. LOQ: limit of quantification; ND: not determined;

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concentration of brain tumor homogenate ranged from 3–7% (w/v).