5 A), however this difference did not reach statistical significance.
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Characterisation of the roles of ABCB1, ABCC1, ABCC2 and ABCG2 in the transport and pharmacokinetics of actinomycin D in vitro and in vivo.
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A small trend of increased accumulation, compared to the absence of inhibitor (1.2-fold in MDCKII-ABCC1 and 1.4-fold in MDCKII-ABCC2) was seen when co-incubating Act D with MK571, but was not statistically significant ( Fig. 3 C).