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HPLC法测定来氟米特片中来氟米特的含量及含量均匀度 被引量:2

Determination of Content and Content Uniformity of Dosage Units of Leflunomide in Leflunomide Tablets by HPLC
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摘要 目的:建立来氟米特片中来氟米特的含量及其含量均匀度的HPLC测定法。方法:色谱柱:Waters SunfireTM C18(4.6mm×150mm,5μm);流动相:乙腈-水-三乙胺(35∶65∶5)(用磷酸调节pH至4.0);检测波长为254nm。结果:来氟米特在20.044~200.44mg·L-1范围内线性良好,相关系数r=0.99999(n=6);平均回收率为99.6%(n=9,RSD为0.3%)。结论:本法灵敏度高,重现性好,结果准确。 Objective: To establish a method using HPLC for determination of the content and content uniformity of dosage units of Le- flunomidc in Leflunomide Tablets. Methods: A Waters SunfireTM Cls (4. 6 mm × 150 mm,5 μm, ) column was used with mobile phase of acetonitrile-water-triethylamine(35:65:5 ) ,adjusted to pH4. 0 with phosphoric acid, The detected wavelength was 254nm. Results: The calibration curve was linear in the concentration range of 20. 044 - 200. 44 mg. L - 1 , r = 0. 999 99 ; The average recovery was 99. 6% with a relative standard deviation of 0. 3%. Conclusion: The method is sensitive, precise and accurate.
出处 《中国药品标准》 CAS 2010年第3期216-219,共4页 Drug Standards of China
关键词 来氟米特片 来氟米特 高效液相色谱法 Leflunomide Tablets Leflunomide HPLC
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  • 1Kalden J R,Schattenkirchner M,Sorensen H,et al.The efficacy and safety of leflunomide in patients with active rheumatoid arthritis: a five-year followup study[J].Arthritis Rheum,2003,48 (6): 1513.
  • 2Siva C,Eisen S A,Shepherd R,et al.Leflunomide use during the first 33 months after food and drug administration approval: experience with a national cohort of 3,325 patients[J].Arthritis Rheum,2003,49(6): 745.
  • 3Li J,Yao H W,Jin Y,et al.Pharmacokinetics of leflunomide in Chinese healthy volunteers[J].Acta Pharmacol Sin,2002,23(6): 551.
  • 4Schmidt A,Schwind B,Gillich M,et al.Simultaneous determination of leflunomide and its active metabolite,A77 1726,in human plasma by high-performance liquid chromatography[J].Biomed Chromatogr,2003,17(4): 276.

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