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建立并验证犬血浆中米尔贝肟的 HPLC-FLD 定量分析方法。

Development and validation of an HPLC-FLD method for milbemectin quantification in dog plasma.

机构信息

College of Veterinary, Northeast Agricultural University, 59 Mucai Street, Xiangfang District, 150030 Harbin, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Jul 15;878(22):2013-7. doi: 10.1016/j.jchromb.2010.05.037. Epub 2010 May 31.

Abstract

Milbemectin is a widely used veterinary antiparasitic agent. A high-performance liquid chromatography with fluorescent detection (HPLC-FLD) method is described for the determination of milbemectin in dog plasma. The derivative procedure included mixing 1-methylimizole [MI, MI-ACN (1:1, v/v), 100 microL], trifluoroacetic anhydride [TFAA, TFAA-ACN (1:2, v/v), 150 microL] with a subsequent incubation for 3s at the room temperature to obtain a fluorescent derivative, which is reproducible in different blood samples and the derivatives proved to be stable for at least 80 h at room temperature. HPLC method was developed on C18 column with FLD detection at an excitation wavelength of 365 nm and emission wavelength of 475 nm, with the mobile phase consisting of methanol and water in the ratio of 98:2 (v/v). The assay lower limit of quantification was 1 ng/mL. The calibration curve was linear over concentration range of 1-200 ng/mL. The intra- and inter-day accuracy was >94% and precision expressed as % coefficient of variation was <5%. This method is specific, simple, accurate, precise and easily adaptable to measure milbemycin in blood of other animals.

摘要

米尔贝肟是一种广泛应用于兽医驱虫的药物。本文描述了一种采用荧光检测的高效液相色谱法(HPLC-FLD)来测定犬血浆中的米尔贝肟。衍生步骤包括将 1-甲基咪唑[MI,MI-ACN(1:1,v/v),100μL]和三氟乙酐[TFAA,TFAA-ACN(1:2,v/v),150μL]混合,随后在室温下孵育 3 秒,以获得可在不同血样中重现的荧光衍生物,该衍生物在室温下至少稳定 80 小时。在 C18 柱上采用 FLD 检测,激发波长为 365nm,发射波长为 475nm,流动相由甲醇和水以 98:2(v/v)的比例组成,建立了 HPLC 方法。定量下限为 1ng/mL。校准曲线在 1-200ng/mL 浓度范围内呈线性。日内和日间精密度大于 94%,以变异系数表示的精密度小于 5%。该方法特异性强,简单,准确,精密,易于适应其他动物血液中米尔贝霉素的测定。

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