首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Simultaneous determination of unbound ropivacaine in rat blood and brain using microdialysis
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Simultaneous determination of unbound ropivacaine in rat blood and brain using microdialysis

机译:微透析同时测定大鼠血液和大脑中未结合的罗哌卡因

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To investigate the pharmacokinetics of ropivacaine in rat blood and brain,a sensitive HPLC method and microdialysis were developed for the simultaneous determination of unbound ropivacaine in rat blood and brain.Adult,male Sprague-Dawley rats (290-350 g) were anesthetized with sodium pentobarbital (50 mg/kg, i.p.).Two microdialysis probes were inserted,one into the jugular vein toward right atrium,and one into the brain striatum of rats.Ropivacaine (5 mg/kg,i.v.) was then administered via the femoral vein.Blood and brain dialysates were collected and eluted with a mobile phase containing methanol-acetonitrite-20 mM monosodium phosphoric acid (pH 5.5) (10:40:50,v/v/v) in a liquid chromatographic system.Separation of ropivacaine was achieved by a CN column (Phenomenex Luna,250X4.6 mm,particle size 5 #mu#m;Torrance,CA,USA) within 10 min.The UV detector wavelength was set at 205 nm and the detection limit of ropivacaine was 20 ng/ml.The intra- and inter-day accuracy and precision of the analyses were less than 10% in the ranges of 0.02-5 #mu#g/ml.The pharmacokinetic data were calculated from the individual animal measurements of dialysate concentration versus time.This method exhibits no endogenous interference and its sensitivity is sufficient for the determination of biological samples.The present results confirm that microdialysis sampling followed by LC separation with UV detection represents a viable approach for the measurement of free ropivacaine in rat brain and plasma.
机译:为了研究罗哌卡因在大鼠血液和脑中的药代动力学,建立了灵敏的HPLC方法和微透析法同时测定大鼠血液和脑中未结合的罗哌卡因。成年雄性Sprague-Dawley大鼠(290-350 g)用钠麻醉戊巴比妥(50 mg / kg,ip)。将两种微透析探针插入大鼠的右心房颈静脉中,另一种插入大鼠脑纹状体中。然后通过股静脉施用罗哌卡因(5 mg / kg,iv)收集血液和脑透析液,并在液相色谱系统中用含甲醇-丙酮酸20 mM磷酸一钠(pH 5.5)(10:40:50,v / v / v)的流动相洗脱。用CN色谱柱(Phenomenex Luna,250X4.6 mm,粒径5#μ#m; Torrance,CA,USA)在10分钟内完成.UV检测器波长设置为205 nm,罗哌卡因的检出限为20 ng / ml。溶解度在0.02-5#mu#g / ml的范围内小于10%。根据动物透析液浓度随时间的变化计算药代动力学数据,该方法无内源性干扰,其灵敏度足以确定目前的结果证实,微透析采样,然后进行LC分离和紫外检测代表了一种测量大鼠脑和血浆中游离罗哌卡因的可行方法。

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