首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >High-performance liquid chromatography electrospray ionization mass spectrometry determination of tulobuterol in rabbit's plasma.
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High-performance liquid chromatography electrospray ionization mass spectrometry determination of tulobuterol in rabbit's plasma.

机译:高效液相色谱电喷雾电离质谱法测定兔血浆中妥洛特罗。

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摘要

A sensitive and specific liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS) method has been developed and validated for the identification and quantification of tulobuterol in rabbits' plasma. After the addition of clenbuterol-HCl, the internal standard (IS) and 1.0 M sodium hydroxide solution, plasma samples were extracted using a solvent mixture comprised of 5% isopropanol in n-hexane. The compounds were separated on a prepacked Lichrospher CN (5 microm, 150 mm x 2.0 mm) column using a mixture of methanol-water (10 mM CH3COONH4, pH 4.0) as mobile phase. A Shimadzu LCMS-2010A mass spectrometer connected to a Shimadzu high performance liquid chromatograph (HPLC) was used to develop and validate the method. The method has shown to be sensitive and specific by testing six different blank plasma batches. Linearity was established for the range of concentrations 0.50-40.0 ng/mL with a coefficient of determination (r) of 0.9998. The intra-day precision was better than 15%. The lowerlimit of quantification (LLOQ) was identifiable and reproducible at 0.50 ng/mL. The proposed method enables the unambiguous identification and quantification of tulobuterol for pharmacokinetic, bioavailability or bioequivalence studies.
机译:已经开发了灵敏的液相色谱电喷雾电离质谱(LC-ESI-MS)方法,并已用于鉴定和定量兔血浆中的妥洛特罗。加入盐酸克仑特罗-盐酸,内标(IS)和1.0 M氢氧化钠溶液后,使用包含5%异丙醇的正己烷混合溶剂萃取血浆样品。使用甲醇-水(10 mM CH3COONH4,pH 4.0)的混合物作为流动相,在预装的Lichrospher CN(5 microm,150 mm x 2.0 mm)色谱柱上分离化合物。使用Shimadzu LCMS-2010A质谱仪连接Shimadzu高效液相色谱仪(HPLC)来开发和验证该方法。通过测试六种不同的空白血浆批次,该方法已显示出灵敏性和特异性。建立浓度范围为0.50-40.0 ng / mL的线性,测定系数(r)为0.9998。日内精确度优于15%。定量的下限(LLOQ)是可识别的,可重现为0.50 ng / mL。所提出的方法能够对药效学,生物利用度或生物等效性研究的妥洛特罗进行明确的鉴定和定量。

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