“…Separation of highly hydrophobic structurally related corticosteroids 3.6% w/w SDS, 6.6% w/w 1-butanol, 0.8% w/w n-octane and 89% w/w 40 mM sodium dihydrogen phosphate buffer pH 8.0 [49] Enantioseparation of ephedrine and pseudoephedrine 2% R/S DDCV, 1.65% v/v 2-hexanol, 1.23% v/v diethyl tartrate and 50 mM sodium phosphate buffer pH 7.0 [59] Detection and separation of ephedrine and pseudoephedrine employing laser-induced fluorescence detection 3.24% w/w n-heptane, 3.24% w/w SDS, 26.44% w/w 1-butanol and 95% 50 mM sodium borate buffer containing 16% ACN pH 7 [69] Separation and determination of flavonoids employing electrochemical detection 0.9% w/v SDS, 0.9% w/v SC, 0.9% w/v 1-butanol, 0.6% w/v ethyl acetate and 98.2% v/v 10 mM sodium tetraborate buffer pH 7.5 [70] Determination of the coenzyme Q10 (2,3-dimethoxy-5-methyl-6-decaprenyl-1,4-benzoquinone) in human plasma 1.4% w/w sodium bis(2-ethylhexyl) sulphosuccinate (AOT), 4% w/w cholic acid, 8.5% w/w butanol, 1% w/w octane, 0.1% w/w PVA and 85% w/w 10 mM Tris buffer pH 9.0 [51] Fingerprint analysis and extraction of resina draconis 3.3% w/v SDS, 6.6% w/v 1-butanol, 0.8% w/v n-octane and 10 mM sodium tetraborate buffer pH 9.2 [79] Separation and determination of NF antibiotics in fish 3.48% w/w SDS, 6.48% w/w 1-butanol, 0.82% w/w octane and 10 mM sodium tetraborate buffer pH 9.70 [80] Separation of phenolic acids and diterpenoids using W/O MEEKC 48% w/v 1-butanol, 18% w/v SDS, 8.0% w/v 2-propanol and 26% v/v sodium acetate buffer pH 6.0 [82] Electrophoresis 2010, 31,[755][756][757][758][759][760][761][762][763][764][765][766][767] have been shown to be both mutagenic and carcinogenic. The ME was optimised in terms of surfactant, co-surfactant and oil concentration with the optimum buffer being composed of 0.82% w/w octane, 3.48% w/w SDS and 6.48% w/w butanol in a 10 mM sodium borate buffer pH 9.70.…”