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. Author manuscript; available in PMC: 2014 Nov 25.
Published in final edited form as: Eur J Pharm Biopharm. 2013 Dec 19;86(3):514–523. doi: 10.1016/j.ejpb.2013.12.009

Table 2.

Stability of gemcitabine and gemcitabine prodrugs in pH 7.4 Buffer and biological media (mean ± SD, n = 3).

Prodrug SGF t1/2 (min) SIF (pH 6.5) t1/2 (min) Buffer pH 7.4 t1/2 (min) Caco-2 cell homogenates t1/2 (min) Human liver microsome t1/2 (min) Thymidine phosphorylase t1/2 (min) AsPC-1 cell homogenates t1/2 (min)
Gemcitabine >120 >120 >120 105.0 ± 6.1 45.3 ± 3.3 6.0 ± 1.8 33.7 ± 14.5
5′-L-Phenylalanyl-gemcitabine >120 >120 >120 2.0 ± 0.3 1.8 ± 0.2 31.9 ± 5.0 6.8 ± 2.0
5′-D-Phenylalanyl-gemcitabine >120 >120 >120 21.7 ± 0.2 6.6 ± 1.3 >120 63.9 ± 11.2
5′-L-Valyl-gemcitabine >120 >120 >120 19.5 ± 1.9 27.8 ± 13.6 >120 13.8 ± 3.3
5′-D-Valyl-gemcitabine >120 >120 >120 42.0 ± 17.5 19.5 ± 4.4 >120 87.2 ± 13.5