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使用超滤和带紫外检测的液相色谱法测定牛血浆中未结合蛋白的苯基布他松

Determination of non-protein bound phenylbutazone in bovine plasma using ultrafiltration and liquid chromatography with ultraviolet detection.

作者信息

De Veau E J

机构信息

U.S. Food and Drug Administration, Center for Veterinary Medicine, Laurel, MD 20708, USA.

出版信息

J Chromatogr B Biomed Sci Appl. 1999 Jan 8;721(1):141-5. doi: 10.1016/s0378-4347(98)00487-3.

Abstract

A liquid chromatographic procedure using UV detection was coupled with ultrafiltration for the quantitation of free phenylbutazone in bovine plasma, in the range of 20 ng/ml to 2.0 microg/ml. Whole plasma samples (0.5 to 1 ml) were placed in a 2-ml centrifugal concentrator with a molecular-mass cut-off membrane of 10000 and centrifuged at 4500 g for 2 h at 4 degrees C using a fixed angle rotor. The ultrafiltrate was transferred to an LC vial with a 200-microl insert and 100 microl was injected into an LC system. The chromatographic system used a C18 reversed-phase column connected to a UV detector set at 264 nm. The mobile phase was 0.2 M sodium phosphate buffer (pH 7)-methanol (1:1). Recoveries of phenylbutazone from protein-free plasma water fortified at levels of 20 ng/ml to 2 microg/ml ranged from 91 to 93%, with relative standard deviations (R.S.D.s) ranging from 1 to 4%. The concentration of incurred non-protein bound phenylbutazone obtained from a cow intravenously dosed twice with 2 g phenylbutazone, 8 h apart, was 111, 26 and 11 ng/ml for 2, 72 and 104 h post first phenylbutazone dose, respectively.

摘要

采用紫外检测的液相色谱法与超滤相结合,用于定量测定牛血浆中游离苯基布他松,测定范围为20 ng/ml至2.0 μg/ml。将全血样品(0.5至1 ml)置于一个带有截留分子量为10000的膜的2 ml离心浓缩器中,使用固定角度转头在4℃下以4500 g离心2小时。将超滤物转移至带有200 μl内衬的液相色谱小瓶中,并将100 μl注入液相色谱系统。色谱系统使用连接到设置在264 nm的紫外检测器的C18反相柱。流动相为0.2 M磷酸钠缓冲液(pH 7)-甲醇(1:1)。从添加了20 ng/ml至2 μg/ml苯基布他松的无蛋白血浆水中回收苯基布他松的回收率在91%至93%之间,相对标准偏差(R.S.D.s)在1%至4%之间。对一头牛静脉注射两次2 g苯基布他松(间隔8小时),在首次注射苯基布他松后2、72和104小时测得的非蛋白结合苯基布他松浓度分别为111、26和11 ng/ml。

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