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

• Published in: Analytical and bioanalytical chemistry 2016-01, Vol.408 (3), p.761-774
• Main Authors: Rojalin, Tatu, Kurki, Lauri, Laaksonen, Timo, Viitala, Tapani, Kostamovaara, Juha, Gordon, Keith C, Galvis, Leonardo, Wachsmann-Hogiu, Sebastian, Strachan, Clare J, Yliperttula, Marjo
• Format: Article
• Language: English
• Subjects: Analytical Chemistry; Biochemistry; Biofilms; Caffeine; Characterization and Evaluation of Materials; Chemical research; Chemistry; Chemistry and Materials Science; CMOS; Data processing; Detectors; Drugs; Electrical engineering; energy; Fluorescence; fluorescence emission spectroscopy; Food Science; Fractionation; gastric acid; indomethacin; Laboratory Medicine; Lasers; Life sciences; Light sources; Mathematical analysis; Metal oxide semiconductors; Metals - chemistry; Monitoring/Environmental Analysis; Nanospectroscopy; Oxides - chemistry; Pharmaceutical Preparations - chemistry; Pharmaceuticals; photoluminescence; R&D; Raman spectra; Raman spectroscopy; Research & development; Research Paper; Semiconductors; Sensors; Spectroscopy; Spectrum Analysis, Raman - instrumentation; Spectrum Analysis, Raman - methods
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-015-9156-6

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 abstract Time-resolved Raman measurement of a pharmaceutical sample using the complementary metal-oxide semiconductor (CMOS) single photon avalanche diode (SPAD) detector technology