首页> 美国卫生研究院文献>BioMed Research International >Two Spectrophotometric Assays for Dopamine Derivatives in Pharmaceutical Products and in Biological Samples of SchizophrenicPatients Using Copper Tetramine Complex and Triiodide Reagent
【2h】

Two Spectrophotometric Assays for Dopamine Derivatives in Pharmaceutical Products and in Biological Samples of SchizophrenicPatients Using Copper Tetramine Complex and Triiodide Reagent

机译:药品和精神分裂症生物样品中多巴胺衍生物的两种分光光度测定使用四氨合铜和三碘化物试剂的患者

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Two simple, rapid, and sensitive spectrophotometric methods are proposed for the determination of levodopa (LD). The first method is based on coupling of 4-aminoantipyrine (4-AAP) with one of the dopamine derivatives (LD, CD) to give a new ligand that reacts with copper tetramine complex to give intensely colored chelates. The colored products are quantified spectrophotometrically at 525 and 520 nm for LD and CD, respectively. The optimization of the experimental conditions is described. The method has been used for the determination of 19.7–69.0 and 18.1–54.3 μg mL−1 of LD and CD, respectively. The accuracy of the method is achieved by the values of recovery (100 ± 0.2%) and the precision is supported by the low standard deviation (SD = 0.17–0.59) and relative standard deviation (CV = 0.4%–1.54%) values. The second method is based on the formation of ion-pair iodinated inner sphere or outer sphere colored complexes between the LD and triiodide ions at pH 5 and room temperature (23 ± 3°C). This method has been used for the determination of LDwithin the concentration range 39.44–78.88 μgmL−1 with SD = 0.22–0.24 and recovery percent = 100 ± 0.3%.The sensitivity of the two methods is indicated bySandell's sensitivity of 0.014–0.019 g cm−2. Theresults of the two methods are compared with those of theofficial method. The interference of common drug additives,degradation products, and excipients was also studied. Theproposed methods were applied successfully to the determinationof the LD-CD synthetic mixture and Levocare drug. Thedetermination of LD in urine of some schizophrenic patients wasapplied with good precision and accuracy. The reliability of themethods was established by parallel determinations against theofficial British pharmacopoeia method.
机译:提出了两种简单,快速和灵敏的分光光度法测定左旋多巴(LD)的方法。第一种方法基于将4-氨基安替比林(4-AAP)与一种多巴胺衍生物(LD,CD)偶联,得到新的配体,该配体与四胺铜络合物反应,得到深色的螯合物。用LD和CD分别在525和520nm处用分光光度法对有色产物进行定量。描述了实验条件的优化。该方法分别用于测定LD和CD的19.7–69.0和18.1–54.3μg mL -1 。该方法的准确度由回收率值(100±0.2%)实现,而精密度由较低的标准偏差(SD = 0.17–0.59)和相对标准偏差(CV = 0.4%–1.54%)值所支持。第二种方法是基于在pH 5和室温(23±3 °C)下LD和三碘化物离子之间形成离子对碘化的内球或外球有色络合物。该方法已用于测定LD在39.44–78.88μg的浓度范围内mL −1 ,SD = 0.22-0.24,回收率= 100±0.3%。两种方法的灵敏度表示为Sandell的灵敏度为0.014–0.019 g cm −2 。的将两种方法的结果与官方方法。普通药物添加剂的干扰,还研究了降解产物和赋形剂。的提出的方法已成功应用于测定LD-CD合成混合物和Levocare药物。的精神分裂症患者尿液中LD的测定精度高,精度高。的可靠性方法是通过平行测定确定的英国官方药典方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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