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HPLC法测定盐酸尼卡地平缓释片的含量 被引量:3

Determination of Nicardipine Hydrochloride Sustained-release Tablets by HPLC
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摘要 建立高效液相色谱法测定盐酸尼卡地平缓释片的含量。采用高效液相色谱法,色谱柱为Waters XTerra^TM RP18柱;以甲醇-0.01mol·L^-1磷酸二氢钾溶液(72:28)为流动相,流速为1.0mL·min^-1;检测波长为236nm;柱温为35℃。浓度在5.008-95.152μg·mL^-1(r=0.9999)范围内具有良好线性关系,平均回收率为99.28%,RSD为0.46%(n=9)。方法可靠、简单可行,可用于测定盐酸尼卡地平缓释片的含量。 A method for determination of Nicardipine Hydrochloride Sustained--release Tablets was developed. HPLC method was carried out on a Waters XTerraTM RP18 column with UV detection at 236nm. The mobile phase was methanol-0. 01mol · L^-1 potassium dihydrogen phosphate (72 : 28) with a flow rate of 1.0 mL · min^-1 and the column temperture was 35℃. The content of nicardipine hydrochloride was calculated by external standardization method. There was a good linear relationship for nicardipine hydrochloride within the range of 5. 008 - 95. 152μg · mL^-1 (r = 0. 9999). The average recovery was 99. 28% and RSD was 0. 46% (n=9). The method is simple, specific and not interfered by excipients. It is accurate for quality control of Nicardipine Hydrochloride Sustained-release Tablets.
出处 《中国药事》 CAS 2008年第7期576-577,共2页 Chinese Pharmaceutical Affairs
关键词 盐酸尼卡地平缓释片 HPLC 含量测定 Nicardipine Hydrochloride Sustained-release Tablets HPLC determination
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  • 1.中国药典[S]二部[M].,2005年版.844.

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