首页> 美国卫生研究院文献>Springer Open Choice >Fluorescence-suppressed time-resolved Raman spectroscopy of pharmaceuticals using complementary metal-oxide semiconductor (CMOS) single-photon avalanche diode (SPAD) detector
【2h】

Fluorescence-suppressed time-resolved Raman spectroscopy of pharmaceuticals using complementary metal-oxide semiconductor (CMOS) single-photon avalanche diode (SPAD) detector

机译:使用互补金属氧化物半导体(CMOS)单光子雪崩二极管(SPAD)检测器的药物的荧光抑制时间分辨拉曼光谱

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

In this work, we utilize a short-wavelength, 532-nm picosecond pulsed laser coupled with a time-gated complementary metal-oxide semiconductor (CMOS) single-photon avalanche diode (SPAD) detector to acquire Raman spectra of several drugs of interest. With this approach, we are able to reveal previously unseen Raman features and suppress the fluorescence background of these drugs. Compared to traditional Raman setups, the present time-resolved technique has two major improvements. First, it is possible to overcome the strong fluorescence background that usually interferes with the much weaker Raman spectra. Second, using the high photon energy excitation light source, we are able to generate a stronger Raman signal compared to traditional instruments. In addition, observations in the time domain can be performed, thus enabling new capabilities in the field of Raman and fluorescence spectroscopy. With this system, we demonstrate for the first time the possibility of recording fluorescence-suppressed Raman spectra of solid, amorphous and crystalline, and non-photoluminescent and photoluminescent drugs such as caffeine, ranitidine hydrochloride, and indomethacin (amorphous and crystalline forms). The raw data acquired by utilizing only the picosecond pulsed laser and a CMOS SPAD detector could be used for identifying the compounds directly without any data processing. Moreover, to validate the accuracy of this time-resolved technique, we present density functional theory (DFT) calculations for a widely used gastric acid inhibitor, ranitidine hydrochloride. The obtained time-resolved Raman peaks were identified based on the calculations and existing literature. Raman spectra using non-time-resolved setups with continuous-wave 785- and 532-nm excitation lasers were used as reference data. Overall, this demonstration of time-resolved Raman and fluorescence measurements with a CMOS SPAD detector shows promise in diverse areas, including fundamental chemical research, the pharmaceutical setting, process analytical technology (PAT), and the life sciences.>Graphical abstractTime-resolved Raman measurement of a pharmaceutical sample using the complementary metal-oxide semiconductor (CMOS) single photon avalanche diode (SPAD) detector technology
机译:在这项工作中,我们利用短波长532 nm皮秒脉冲激光与时间选通互补金属氧化物半导体(CMOS)单光子雪崩二极管(SPAD)检测器相结合,以获取几种目标药物的拉曼光谱。通过这种方法,我们能够揭示以前看不见的拉曼特征,并抑制这些药物的荧光背景。与传统的拉曼装置相比,目前的时间分辨技术有两个主要改进。首先,可以克服通常干扰弱得多的拉曼光谱的强荧光背景。其次,与传统仪器相比,使用高光子能量激发光源,我们能够产生更强的拉曼信号。此外,可以进行时域观察,从而在拉曼光谱和荧光光谱学领域实现新功能。利用该系统,我们首次证明了记录固体,无定形和结晶以及非光致发光和光致发光药物(例如咖啡因,雷尼替丁盐酸盐和吲哚美辛(无定形和结晶形式))的荧光抑制拉曼光谱的可能性。仅使用皮秒脉冲激光和CMOS SPAD检测器获得的原始数据无需任何数据处理即可直接用于鉴定化合物。此外,为验证这种时间分辨技术的准确性,我们提出了一种针对广泛使用的胃酸抑制剂盐酸雷尼替丁的密度泛函理论(DFT)计算。根据计算结果和现有文献对获得的时间分辨拉曼峰进行鉴定。使用非时间分辨设置并带有连续波785和532 nm激发激光器的拉曼光谱作为参考数据。总体而言,使用CMOS SPAD检测器进行的时间分辨拉曼光谱和荧光测量的演示展示了在各个领域的前景,包括基础化学研究,药物环境,过程分析技术(PAT)和生命科学。<!-fig ft0 -> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchored” f5-> >图形摘要<!-fig / graphic | fig /替代方案/图形模式=“锚定” m1-> <!-标题a7->使用互补金属氧化物半导体(CMOS)单光子雪崩二极管(SPAD)检测器技术对药物样品进行时间分辨拉曼测量

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