期刊文献+

HPLC法测定盐酸二甲双胍缓释片中盐酸二甲双胍的含量 被引量:10

Content Determination of Metformin Hydrochloride Sustained-release Tablets by HPLC
原文传递
导出
摘要 目的:建立测定盐酸二甲双胍缓释片中盐酸二甲双胍含量的方法。方法:采用高效液相色谱法。色谱柱为HypersilODS2柱为,2流0μ动L相,柱为温0为.053%0庚℃烷。磺结酸果钠:盐溶酸液二(用甲磷双酸胍溶检液测调浓节度p在H0至.114~.0)1-0乙.7腈0(μg8·4m∶1L6-)(1,r检=测0.波99长97为)范23围3内nm与,流峰速面为积1积.0分m值L·呈mi良n-好1,线进性样量关系;平均加样回收率为98.17%、99.69%、100.19%,RSD=0.60%。结论:本方法简便、准确,可用于二甲双胍缓释片的质量控制。 OBJECTIVE: To establish the method for the content determination of main component of Metformin hydrochloride sustained- release tablets. METHODS:HPLC was conducted on a Hypersil ODS2 with mobile phase consisted of 0.05% sodium heptanesulfonate solution (pH adjusted to 4.0)-acetonitrile (84 ∶ 16) at a flow rate of 1.0 mL·min-1. The UV detection wavelength was set at 233 nm. The injection volume was 20 μL and the column temperature was 30℃. RESULTS: The linear range of metformin hydrochloride was 0.11~10.70 μg·mL-1 (r=0.999 7) with an average recovery of 98.17%, 99.69%, 100.19%(RSD=0.60%). CONCLUSION: The method is simple and accurate for the content determination of Metformin hydrochloride sustained-release tablets.
出处 《中国药房》 CAS CSCD 北大核心 2011年第24期2296-2297,共2页 China Pharmacy
关键词 高效液相色谱法 盐酸二甲双胍缓释片 含量测定 HPLC Metformin hydrochloride sustained-release tablets Content determination
  • 相关文献

参考文献8

二级参考文献11

  • 1贺国芳,郭小梅,丁玉峰,闵敏.氢氯噻嗪缓释片的制备及体外释放考察[J].中国医院药学杂志,2004,24(9):526-527. 被引量:9
  • 2杨青,展霞.高效液相色谱法测定卡托普利片的含量[J].中国药业,2006,15(19):43-43. 被引量:4
  • 3奚念珠主编.药剂学[M].第3版.北京:人民卫生出版社,1996:456.
  • 4Fonseca V, Rosenstock J, Patwardhan R,et al. Effect of metformin and rosiglitazone combination therapy in patients with type 2 diabetes mellitus[J ] .JAMA, 2000, 283(13) : 1 695.
  • 5Fonseca V, Biswas N, Salzman A. Once - daily rosiglitazone (RSG) in combination with metformin (MET) effectively reduces hyperglycemia in patients with Type 2 diabetes [ J ]. Diabetes, 1999,48(Suppl 1):A95.
  • 6Smith AR, Shenvi SV, WidlanskyM, et al.Lipoic acid as a potential therapy for chronic diseases associated with oxidative stress[J].CurrentMedicinal Chemistry, 2004,11(9):1132.
  • 7Teichert J, Preiss R .Determination of lipoic acid in human plasma by high- performance liquid chromatography with electrochemical detection[J] .J Chromatogr B Biomed Appl, 1995,672(2) : 277.
  • 8Teichert J, Preiss R. High matographic assay for a- -performance liquid chrolipoic acid and five of its metabolites in human plasma and urine[J] .J Chromat ogr B Biomed Appl, 2002,769(2) : 269.
  • 9Bernkop - Schnurch A, Reich M, et al. Development of a - Rohrwig E, Marschutz sustained release dosage form for a- Lipoic Acid. Ⅱ. evaluation in human vol unteers [J] . Drug Dew Ind Pharm , 2004,30( 1 ) : 35.
  • 10钟明康,施晓金,王宏图,张静华.复方卡托普利片中卡托普利在人体内的药物动力学[J].中国医院药学杂志,1997,17(8):339-341. 被引量:7

共引文献15

同被引文献96

引证文献10

二级引证文献22

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部