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RP-HPLC法测定格列吡嗪缓释片的释放度

屠思远 蒋海松 朱德志 王建明

哈尔滨商业大学学报(自然科学版)2012,Vol.28Issue(6):644-646,3.
哈尔滨商业大学学报(自然科学版)2012,Vol.28Issue(6):644-646,3.

RP-HPLC法测定格列吡嗪缓释片的释放度

RP-HPLC determination of drug release of glipizide sustained release tablets

屠思远 1蒋海松 2朱德志 2王建明1

作者信息

  • 1. 黑龙江中医药大学,哈尔滨150040
  • 2. 哈尔滨科信必成医药科技发展有限公司,哈尔滨150040
  • 折叠

摘要

Abstract

This paper established an RP - HPLC method for the determination of the drug release of glipizide sustained release tablets. The RP - HPLC was on a ODS C18 column (5 μm, 4. 6 mm × 250 mm) at room temperature, using the mobile phase of methanol - buffer solution(0. 1 mol/L sodium dihydrogen phosphate, adjusted to pH (6. 00 ±0. 05) with 2 mol/L sodium hydroxide) (55∶45) , at a flow rate of 1. 0 mL/min and the detection wavelength of 225 nm. Glipizide was detected by the apparatus Ⅲ of dissolution, using as the medium 250 mL of 0. 5% lauryl sodium sulfate solution, at 50 r/min. 5 mL sample of the medium in turn at 2, 6 and 10 h to determine following the above method. The calibration curve was linear in the range of 1. 019 ~ 26. 49 μg/mL. The method was accurate for the drug release determination of glipizide sustained release tablets. The analysis was out of interference of excipients.

关键词

格列吡嗪缓释片/释放度/高效液相色谱法

Key words

glipizide sustained release tablets/ release/ RP - HPLC

分类

医药卫生

引用本文复制引用

屠思远,蒋海松,朱德志,王建明..RP-HPLC法测定格列吡嗪缓释片的释放度[J].哈尔滨商业大学学报(自然科学版),2012,28(6):644-646,3.

哈尔滨商业大学学报(自然科学版)

OACSTPCD

1672-0946

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