Moore P, Mai K, Lai C M
J Pharm Sci. 1986 Apr;75(4):424-6. doi: 10.1002/jps.2600750424.
A sensitive, specific, reproducible, and convenient high-performance liquid chromatographic (HPLC) assay was developed for quantitation of the new ultra short acting beta-adrenergic antagonist, flestolol (1), in whole blood. The instability of the compound in blood was overcome by the esterase inhibitor, NaF, and deproteinization of blood samples with CH3CN:CH2Cl2 (2:5). The internal standard was p-ethoxyphenethyl alcohol. The compounds were back extracted from the CH3CN:CH2Cl2 phase into a small volume of pH 3-4 phosphate buffer and then separated on a reversed-phase C18 column with 0.05 M phosphate buffer (pH 3-4) in acetonitrile (4.6:1) as the mobile phase, and detected with an UV detector at 229 nm. The assay was linear with a blood concentration range from 10 to 1270 ng/mL (r2 greater than 0.998, p greater than 0.01), and reproducible with an overall CV of 8%. The assay procedure was used to determine the blood levels of flestolol intravenously infused into a male dog for 105 min at 230 micrograms/kg/min. The steady-state unchanged drug concentration of 5 micrograms/mL in blood was achieved within 10-20 min and declined biexponentially to 0.02 microgram/mL at 6 h following termination of the infusion.
已开发出一种灵敏、特异、可重现且便捷的高效液相色谱(HPLC)分析法,用于定量全血中新型超短效β-肾上腺素能拮抗剂氟司洛尔(1)。通过酯酶抑制剂氟化钠以及用乙腈:二氯甲烷(2:5)对血样进行脱蛋白处理,克服了该化合物在血液中的不稳定性。内标为对乙氧基苯乙醇。化合物从乙腈:二氯甲烷相中反萃取到少量pH 3 - 4的磷酸盐缓冲液中,然后在反相C18柱上分离,以乙腈(4.6:1)中0.05 M磷酸盐缓冲液(pH 3 - 4)作为流动相,并用紫外检测器在229 nm处检测。该分析法在血液浓度范围为10至1270 ng/mL时呈线性(r2大于0.998,p大于0.01),且可重现,总体变异系数为8%。该分析方法用于测定以230微克/千克/分钟的速度静脉输注到一只雄性犬体内105分钟的氟司洛尔的血药浓度。输注终止后10 - 20分钟内血中稳态未变化药物浓度达到5微克/毫升,并在6小时时呈双指数下降至0.02微克/毫升。