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Determination of o-phthalaldehyde for dose verification of the clinical disinfectant by fluorescent sequential injection analysis.
Analytical Sciences ( IF 1.6 ) Pub Date : 2023-08-26 , DOI: 10.1007/s44211-023-00415-4
Hung-Yu Chen,Richie L C Chen,Bo-Chuan Hsieh,Tzong-Jih Cheng

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.

中文翻译:

荧光连续进样分析法测定邻苯二甲醛,用于临床消毒剂剂量验证。

本研究报告了一种新的自动化通用分析方法,用于测定临床消毒剂邻苯二甲醛 (OPA)。所提出的顺序注射分析 (SIA) 基于 OPA 与甘氨酸/N-乙酰半胱氨酸 (NAC) 在中性介质 (pH = 7.0) 中的在线反应,形成高荧光异吲哚衍生物。研究了所有关键流量和反应变量,同时在线性检测范围 (0.0075-0.02%) 内进行验证。结果,参考 OPA 解决方案实现了出色的线性度(R2 > 0.99)和精度(重复性为 1.5-2.4%,再现性为 0.7-2.2%)。此外,利用所开发的荧光SIA,由于其良好的灵敏度(0.111 V/%)和精度(中间精度为1.0-2.3%),可以在医疗机构中实现OPA消毒的合理浓度验证(0.2-0.6%)。 Cidex-OPA 消毒剂的有效浓度 (MEC) 为 0.3%。
更新日期:2023-08-26
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