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Multi-wavelength deep-ultraviolet absorbance detector based upon program-controlled pulsing light-emitting diodes

journal contribution
posted on 2024-11-03, 23:11 authored by Ibraam MikhailIbraam Mikhail, Mohamed Hemida, Leo LebanovLeo Lebanov, Snezhana Astrakhantseva, Vipul GuptaVipul Gupta, Philip Hortin, John ParryJohn Parry, Miroslav MackaMiroslav Macka, Brett PaullBrett Paull
A novel approach for multi-wavelength ultraviolet (UV) absorbance detection has been introduced employing a single board computer (SBC) with a field programmable gate array (FPGA), Red Pitaya SBC, to generate separated micro pulses for three deep-ultraviolet light-emitting diodes (DUV-LEDs), λmax = 235, 250, and 280 nm, along with data acquisition and processing via a custom-made program. The pulse set generation and data acquisition were synchronized using the SBC. The outputs of the three pulsing DUV-LEDs were combined and transmitted to the flow cell via a solarisation resistant trifurcated optical fiber (OF). An ultra-fast responding photodiode was connected to the optical-fiber-compatible flow cell to record the intensity of the DUV pulses. Upper limit of detector linearity (A95 %) was found to be 1917 mAU, 2189 mAU, and 1768 mAU at 235 nm, 250 nm, and 280 nm, respectively, with stray light ≤0.9 %. In addition, the effective path length (Leff) was estimated to be ≥98.0 % of the length of the used flow cell (50 mm). The new pulsed multi-LEDs absorbance detector (PMLAD) has been successfully coupled with a standard liquid chromatograph and utilized for the analysis of pharmaceuticals. Paracetamol, caffeine, and aspirin were simultaneously determined at 250, 280, and 235 nm, respectively, using the PMLAD. The absorbance ratios between the different wavelengths were applied to further confirm the identity of the studied compounds. Excellent linearity was achieved over a range of 0.1-3.2 µg/mL for paracetamol, 0.4-6.4 µg/mL for caffeine, and 0.8-12.8 µg/mL for aspirin with a regression correlation coefficient (r2) ≥ 0.99996. The quantitation limits (LOQs) were 0.10 µg/mL, 0.38 µg/mL, and 0.66 µg/mL for paracetamol, caffeine, and aspirin, respectively.

History

Sub-type

  • Article

Publication title

JOURNAL OF CHROMATOGRAPHY A

Medium

Print-Electronic

Volume

1709

Article number

ARTN 464382

Pagination

9

eISSN

1873-3778

ISSN

0021-9673

Department/School

Chemistry, Geography, Planning, and Spatial Sciences

Publisher

ELSEVIER

Publication status

  • Published

Place of publication

Netherlands

Event Venue

Australian Centre for Research on Separation Science (ACROSS), School of Natural Sciences (Chemistry), University of Tasmania, Hobart, Tasmania 7001, Australia.

Rights statement

© 2023 The Author(s). Published by Elsevier B.V. This is an open access article distributed under the terms of the Creative Commons CC-BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.