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作 者:朱建喜[1] 庄波阳[2] 曾凡湘[3] 林敏[2]
机构地区:[1]南京军区福州总医院九五临床部药械科,福建莆田351100 [2]福建省药品检验所,福州350001 [3]福建省妇幼保健院,福州350001
出 处:《中国现代应用药学》2015年第2期185-189,共5页Chinese Journal of Modern Applied Pharmacy
摘 要:目的建立高效液相色谱法测定盐酸西那卡塞有关物质。方法采用Waters C18色谱柱(250 mm×4.6 mm,5μm),以乙腈-10 mmol·L^-1磷酸二氢钾(用2 mol·L^-1氢氧化钾调p H值至6.5)为流动相进行梯度洗脱,流速为1.0 m L·min^-1,检测波长为210 nm。结果各杂质与主峰之间的分离度良好。4个已知杂质:R-1-(1-萘基)乙胺(Imp1)浓度在0.228 6-4.572μg·m L?1内与峰面积呈良好的线性关系,r为1.000;3-(三氟甲基)苯丙醇(Imp2)浓度在0.239 6-4.791μg·m L?1内与峰面积呈良好的线性关系,r为1.000;3-(3-(三氟甲基)苯基)丙基甲磺酸酯(Imp3)浓度在0.274 1-5.481μg·m L^-1内与峰面积呈良好的线性关系,r为1.000;R-N-(1-(萘-1-基)乙基)-3-(3-(三氟甲基)苯基)-N-(3-(三氟甲基)苯基)丙基-1-胺(Imp4)浓度在0.102 9-2.059μg·m L^-1内与峰面积呈良好的线性关系,r为0.999 8;Imp1、Imp2、Imp3和Imp4加样回收率的平均值分别为99.3%,98.9%,99.0%和100.4%;RSD分别为1.8%,2.9%,1.7%和1.7%。结论本方法简便、准确可靠,适用于盐酸西那卡塞中有关物质的控制。OBJECTIVE To establish an HPLC method for determining the contents of the related substances of cinacalcet hydrochloride. METHODS The condition of detection were: Waters C18 column (250 mm×4.6 mm,5μm), the gradient mobile phase consisted of acetonitrile and 10 mmol·L^-1 potassium dihydrogen phosphate (adjust with 2 mol·L^-1 potassium hydroxide to pH 6.5) with a flow rate of 1.0 mL·min^-1, the UV detection wavelength was 210 nm. RESULTS The resolution of cinacalcet hydrochloride and relate substances was good. The calibration curves were linear in the range of 0.228 6-4.572 μg·mL^-1 for Impl(r=1.000); the calibration curves were linear in the range of 0.239 6-4.791 μg.mL-l for Imp2(r=1.000); the calibration curves were linear in the range of 0.274 1-5.481μg·mL^-1 for Imp3(r=1.000); the calibration curves were linear in the range of 0.102 9-2.059 μg·mL^-1 for Imp4(r=0.999 8). The average recoveries of Impl, Imp2, Imp3 and Imp4 were 99.3%, 98.9%, 99.0% and 100.4% respectively; the RSD were 1.8%, 2.9%, 1.7% and 1.7% respectively. CONCLUSION The method is simple, accurate, reliable and can be used for the quality control of the related substances of cinacalcet hydrochloride.
分 类 号:R917.101[医药卫生—药物分析学]
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