Validation of a simple spectrophotometric method for the rapid determination of salicylates in plasma

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Younes Zebbiche , Abderrahmane Kori Yahia , Nour El Yakine Keraghel , Fiala Sarah , Chebli Akli Islam , Achouri Mohammed Yacine
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引用次数: 0

Abstract

Introduction

The determination of salicylate concentrations constitutes a critical aspect of medical diagnostics, particularly in emergency settings. High-performance liquid chromatography (HPLC) and spectrophotometry are efficient methods commonly utilized for this purpose. In emergency laboratories with limited resources, the validation of a cost-effective and reliable spectrophotometric method for salicylates in plasma becomes imperative. The present study aims to validate such a method, ensuring its applicability in toxicological emergencies within resource-constrained laboratories.

Materials and methods

The proposed spectrophotometric analysis relies on detecting salicylic ions amidst the presence of ferric salts, resulting in the formation of a distinct purple chelate complex. To ascertain the method's credibility, the validation guidelines established by the European Medicines Agency (EMA) were employed as a benchmark. A comprehensive validation process was conducted over a three-day period, with three levels of validation standards being considered.

Results

Following the EMA protocol, the spectrophotometric method demonstrated commendable fidelity, accuracy, and linearity over a concentration range of 50 to 500 mg/L. The limit of detection and quantification was found to be 10 and 50 mg/L, respectively, and the correlation coefficient was determined to be R2 = 0.998. However, it is essential to acknowledge that interference with phenothiazines occurred at concentrations ranging from 50 to 100 mg/L. Despite this, the method's average sensitivity remains viable for practical use in cases of poisoning. The accuracy per concentration level proved satisfactory, with relative biases remaining below 15%, and the confidence intervals of mean recovery closely approximating the desired target value of 100%.

Conclusion

In conclusion, the presented spectrophotometric method stands out as an economical, straightforward, and user-friendly approach, ideally suited for toxicological emergencies when resources are limited. The method delivers satisfying results, establishing its practical utility in critical medical scenarios. This validated method holds immense promise for emergency laboratories facing resource constraints.

快速测定血浆中水杨酸酯的简单分光光度法的验证。
简介:水杨酸盐浓度的测定是医学诊断的一个重要方面,特别是在紧急情况下。高效液相色谱法(HPLC)和分光光度法是用于此目的的有效方法。在资源有限的应急实验室中,验证一种具有成本效益和可靠的血浆中水杨酸酯分光光度法变得势在必行。本研究旨在验证这种方法,确保其在资源有限的实验室中适用于毒理学紧急情况。材料和方法:提出的分光光度分析依赖于在铁盐存在的情况下检测水杨酸离子,导致形成独特的紫色螯合物。为了确定方法的可信度,采用欧洲药品管理局(EMA)制定的验证指南作为基准。在为期三天的时间内进行了全面的验证过程,考虑了三个级别的验证标准。结果:在EMA方案下,分光光度法在50至500 mg/L的浓度范围内表现出值得称赞的保真度,准确性和线性。检测限和定量限分别为10和50 mg/L,相关系数为R2 = 0.998。然而,必须承认,在50至100 mg/L的浓度范围内,对吩噻嗪的干扰发生。尽管如此,该方法的平均灵敏度在实际中毒情况下仍然可行。每个浓度水平的准确度证明是令人满意的,相对偏差保持在15%以下,平均回收率的置信区间非常接近期望的目标值100%。结论:本文提出的分光光度法是一种经济、简单、用户友好的方法,非常适合资源有限的毒理学紧急情况。该方法取得了令人满意的效果,在关键医疗场景中具有实际应用价值。这种经过验证的方法为面临资源限制的应急实验室带来了巨大的希望。
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来源期刊
Journal of pharmacological and toxicological methods
Journal of pharmacological and toxicological methods PHARMACOLOGY & PHARMACY-TOXICOLOGY
CiteScore
3.60
自引率
10.50%
发文量
56
审稿时长
26 days
期刊介绍: Journal of Pharmacological and Toxicological Methods publishes original articles on current methods of investigation used in pharmacology and toxicology. Pharmacology and toxicology are defined in the broadest sense, referring to actions of drugs and chemicals on all living systems. With its international editorial board and noted contributors, Journal of Pharmacological and Toxicological Methods is the leading journal devoted exclusively to experimental procedures used by pharmacologists and toxicologists.
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