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Determination of o-phthalaldehyde for dose verification of the clinical disinfectant by fluorescent sequential injection analysis

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Abstract

A new automated, generic analytical approach for determining the clinical disinfectant o-phthalaldehyde (OPA) is reported in this study. The proposed sequential injection analysis (SIA) is based on the online reaction of the OPA with glycine/N-acetylcysteine (NAC) in a neutral medium (pH = 7.0) to form a highly fluorescent isoindole derivative. All critical flow and reaction variables were investigated, while validation was carried out in the linearity detection range (0.0075–0.02%). As a result, excellent linearity (R2 > 0.99) and precision (1.5–2.4% for repeatability and 0.7–2.2% for reproducibility) were achieved for the reference OPA solutions. Furthermore, reasonable concentration verification of OPA disinfection (0.2–0.6%) in healthcare institutes can be achieved using the developed fluorescent SIA due to its good sensitivity (0.111 V/%) and precision (1.0–2.3% for intermediate precision) around the minimum effective concentration (MEC) of 0.3% for Cidex-OPA disinfectant.

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Acknowledgements

The authors would like to thank the Ministry of Science and Technology of Taiwan, for financially supporting this research under Contract Nos. MOST-107-2313-B-002-015 and MOST-105-2313-B-002-022.

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Correspondence to Tzong-Jih Cheng.

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Chen, HY., Chen, R.L.C., Hsieh, BC. et al. Determination of o-phthalaldehyde for dose verification of the clinical disinfectant by fluorescent sequential injection analysis. ANAL. SCI. 39, 2007–2017 (2023). https://doi.org/10.1007/s44211-023-00415-4

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