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. Author manuscript; available in PMC: 2018 Jun 12.
Published in final edited form as: Mol Pharm. 2016 Nov 7;14(5):1365–1372. doi: 10.1021/acs.molpharmaceut.6b00929

Table 2. Organ Pharmacokinetic Parameters of Gemcitabine (GEM) and Its Inactive Metabolite 2′,2′-Difluorodeoxyuridine (dFdU) after Single Intravenous Injection of Free GEM and mPEG-b-PCC-g-GEM-g-DC (Abbreviated as F-GEM and P-GEM) at GEM Equivalent Dose of 40 mg/kg in NSG Mice Bearing Orthotopic Pancreatic Tumors.

pharmacokinetic parameters

organs samples t1/2 (h) Cmax (ng/mL) AUC (ng/mL × h)
liver F-GEM 4.5 ± 0.3 43,406 ± 6249 347,329 ± 26,578
P-GEM 12.6 ± 0.9 31,598 ± 2636 564,977 ± 37,638
heart F-GEM 9.3 ± 0.7 3,879 ± 113 38,237 ± 3,494
P-GEM 11.7 ± 0.4 3,449 ± 129 121,475 ± 1,378
spleen F-GEM 8.2 ± 0.5 25,635 ± 1204 20,5084 ± 9,533
P-GEM 8.7 ± 0.3 25,366 ± 5435 59,3119 ± 8,122
lung F-GEM 10.3 ± 0.8 4,593 ± 395 80,216 ± 1,378
P-GEM 14.4 ± 1.7 3,720 ± 264 131,612 ± 6,115
tumor F-GEM 7.8 ± 0.05 3,009 ± 125 79,970 ± 7,715
P-GEM 8.5 ± 0.4 9,765 ± 1025 263,251 ± 9,148
kidney F-GEM 9.6 ± 0.3 6,811 ± 497 102,983 ± 6,557
P-GEM 11.8 ± 1.1 4,069 ± 226 105,975 ± 5,451