“…Cells were pre-incubated for 30 min with CBD 10 or 25 µM (working concentration previously published (Holland et al, 2006; Ligresti et al, 2006; Zhu et al, 2006; Holland et al, 2007; Holland, Allen & Arnold, 2008; De Filippis et al, 2011; Arnold et al, 2012; Harvey et al, 2012; Hill et al, 2012; Maor et al, 2012; Solinas et al, 2012; Dudášová et al, 2013; Juknat et al, 2013; Nabissi et al, 2013), and initially dissolved in DMSO) or CsA 20 µM (known P-gp inhibitor used as positive control (Mori et al, 2012)), dissolved in transport buffer (TB) (pH = 7.4) (Feinshtein et al, 2010), while “control cells” were pre-incubated in TB with the correlating concentration of DMSO. Following pre-incubation, P-gp substrates were added (Calcein-AM or DiOC2(3) or rh123) (Minderman et al, 1996; Martin et al, 2003) and cells were further incubated for 30 min.…”