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首页> 外文期刊>Organic process research & development >Rapid Analysis of Residual Palladium in Pharmaceutical Development Using a Catalysis-Based Fluorometric Method
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Rapid Analysis of Residual Palladium in Pharmaceutical Development Using a Catalysis-Based Fluorometric Method

机译:基于催化荧光法的药物开发中残留钯的快速分析

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摘要

Measurement of residual metals in pharmaceutical intermediates is routinely performed using inductively coupled plasma-optical emission spectroscopy (ICP-OES) or inductively coupled plasma-mass spectrometry (iCP-MS). However, these techniques suffer from drawbacks that limit their utility in pharmaceutical process development, including the requirement for expensive instrumentation, complex sample preparation, slow turnaround time, limited sample throughput, and the difficulty of performing the required measurements on the 'spot' within pilot plants or manufacturing environments. We investigate the use of a fast and inexpensive high-throughput approach for detection of residual palladium (Pd), based on the Pd-catalyzed Tsuji— Trost deallylation of an allylic ether substrate to produce a highly fluorescent product, We demonstrate the effectiveness of this fluorescence assay for accurate quantitation of Pd levels in a variety of Veal world' samples, including mixed oxidation-state samples containing strong Pd ligands.
机译:药物中间体中残留金属的测定通常使用电感耦合等离子体发射光谱法(ICP-OES)或电感耦合等离子体质谱法(iCP-MS)进行。但是,这些技术的缺点在于限制了它们在制药工艺开发中的实用性,包括对昂贵仪器的要求,复杂的样品制备,周转时间慢,样品通量有限以及难以在试点内的“现场”进行所需的测量工厂或制造环境。我们研究了基于Pd催化的Tsuji的快速廉价的高通量方法来检测残留的钯(Pd)的用途-烯丙基醚底物的Trost脱羧生成高荧光产物,我们证明了这种方法的有效性荧光测定法可准确定量各种小牛肉世界样品中的Pd水平,包括含有强Pd配体的混合氧化态样品。

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