DETERMINATION OF PRILOCAINE HCl IN BULK DRUG AND PHARMACEUTICAL FORMULATION BY GC-NPD METHOD

被引:4
作者
Atila, Alptug [1 ]
Kadioglu, Yucel [1 ]
机构
[1] Ataturk Univ, Dept Analyt Chem, Fac Pharm, TR-25240 Erzurum, Turkey
关键词
GC-NPD; prilocaine HCl; pharmaceutical formulation; validation; PERFORMANCE LIQUID-CHROMATOGRAPHY; LOCAL-ANESTHETICS; HUMAN PLASMA; HUMAN SERUM; STEREOSELECTIVE DETERMINATION; O-TOLUIDINE; LIDOCAINE; IMPURITIES; PHASE;
D O I
10.2298/CICEQ120124064A
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel analytical method was developed and validated for determination of prilocaine HCl in bulk drug and pharmaceutical formulation by gas chromatography-nitrogen phosphorus detection (GC-NPD). The chromatographic separation was performed using a HP-5MS column. The calibration curve was linear over the concentration range of 40-1000 ng ml(-1) with a correlation coefficient of 0.9998. The limits of detection (LOD) and quantification (LOQ) of the method were 10 and 35 ng m(-1), respectively. The within-day and between-day precision, expressed as the percent relative standard deviation (RSD%) were less than 5.0%, and the accuracy (percent relative error) was better than 4.0%. The developed method can be directly and easily applied for determination of prilocaine HCl in bulk drug and pharmaceutical formulation using internal standard methodology.
引用
收藏
页码:313 / 319
页数:7
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