首页> 外文期刊>Current Analytical Chemistry >Quantitative Determination of Paliperidone in OROS Tablets by Derivative Spectrophotometric Method - Application in Extraction and Comparison to HPLC
【24h】

Quantitative Determination of Paliperidone in OROS Tablets by Derivative Spectrophotometric Method - Application in Extraction and Comparison to HPLC

机译:分光光度法定量测定OROS片剂中帕潘立酮的应用-在HPLC提取和比较中的应用。

获取原文
获取原文并翻译 | 示例
           

摘要

A derivative UV spectrophotometric method for determination of paliperidone in OROS tablets was validated and compared to a previously validated HPLC. The parameters specificity, linearity, precision, accuracy, LOD and LOQ were studied according to official guidelines. The first-order derivative spectra were obtained at N = 5, Δλ = 1.0 nm, and determinations were made at 288 nm. The drug was extracted from osmotic tablets by using 0.1 M HCl as solvent, and ultrasonic bath. The proposed method showed specificity and linearity in the concentration range of 40.0 to 80.0 μg mL~(-1). The intra and interday precision data demonstrated that the method has good reproducibility. The drug content on the formulation was ranged from 101.84 to 102.76%. Accuracy was also evaluated and results were found to be satisfactory. The detection and quantitation limits were 0.85 and 2.59 μg mL~(-1), respectively. When compared to HPLC, both methods proved to be adequate for determination of paliperidone in tablets.
机译:验证了用于测定OROS片剂中帕潘立酮的衍生紫外分光光度法,并将其与先前验证的HPLC进行了比较。根据官方指南研究了参数特异性,线性,精度,准确度,LOD和LOQ。一阶导数光谱是在N = 5,Δλ= 1.0 nm处获得的,并在288 nm处进行了测定。通过使用0.1 M HCl作为溶剂从渗透片中提​​取药物,并进行超声波浴。该方法在40.0〜80.0μgmL〜(-1)的浓度范围内具有特异性和线性。日内和日间精度数据表明该方法具有良好的重现性。制剂上的药物含量为101.84至102.76%。还评估了准确性,发现结果令人满意。检出限和定量限分别为0.85和2.59μgmL〜(-1)。与HPLC相比,两种方法都证明足以测定片剂中的帕潘立酮。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号