Development of a disposable hollow fibre-solid phase microextraction device using chitosan functionalised MWCNTs and a polyoxometalate for the simultaneous extraction of angiotensin II receptor blocker drugs

IF 2.3 4区 化学 Q3 CHEMISTRY, ANALYTICAL
Aref Ansari Mohseni, Mahmoud Ebrahimi, Safarali Beyramabadi
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引用次数: 0

Abstract

ABSTRACTValsartan and Losartan are two angiotensin II receptor blocker drugs used to treat heart failure and high blood pressure. A straightforward and disposable hollow fibre-solid phase microextraction device was developed to extract these drugs from real water and urine samples. A green sorbent was synthesised by functionalised MWCNTs with chitosan through a chemical route method. Besides, a polyoxometalate (Ni-CoWO4 nanoparticles) was prepared as a modifier using the hydrothermal procedure. Using the sol-gel strategy, the sorbent and modifier were reinforced in the hollow fibre pores and lumen. The approach leads to an increase in the sorbent coating stability on/in hollow fibre. The influential factors were optimised with an experimental design, indicating that pH, extraction time, and desorption time significantly affect the Valsartan and Losartan extraction. The linearity of the method to determine Valsartan and Losartan was 3.4–1850 and 3.1–1800 ng mL−1, with R squared of 0.9929 and 0.9947, respectively. The detection and quantification limits were lower than 0.9 ng mL−1 and 3.4 ng mL−1, respectively. The pre-concentration factors for determining Valsartan and Losartan with a concentration of 20 ng mL−1 were 654.2 and 546.3, respectively. The intra-day and inter-day RSDs were lower than 3.11% and 3.87% for measuring Valsartan and Losartan. The recoveries and RSDs for analysing spiked eal water and urine samples were between 91.8–97.8% and 3.16–4.10%, respectively.KEYWORDS: ValsartanLosartanhollow fibre-solid phase microextractionMWCNTsPolyoxometalateschitosan AcknowledgmentsThe authors express their appreciation to the Research Council of Islamic Azad University of Mashhad, Iran, for financial support.Disclosure statementThe authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.Compliance with ethical standardsThe study has been carried out under the institutional and/or national research committee’s ethical standards and with the 1964 Helsinki declaration and its later amendments or comparable. Ethical standards.CRediT authorship contribution statementAref Ansari Mohseni: Conceptualization, Writing e original draft, Investigation, Methodology, Data curation, Formal analysis, Resources.Mahmoud Ebrahimi: Supervisor, Investigation, Writing e review & editing.Safarali Beyramabadi: Advisor, Investigation, Writing e review & editing.Supplementary dataSupplemental data for this article can be accessed online at https://doi.org/10.1080/03067319.2023.2253736.
利用壳聚糖功能化MWCNTs和多金属氧酸盐制备一次性中空纤维-固相微萃取装置,用于同时提取血管紧张素II受体阻断剂药物
摘要缬沙坦和氯沙坦是两种用于治疗心力衰竭和高血压的血管紧张素受体阻滞剂。开发了一种简单、一次性的中空纤维固相微萃取装置,用于从真实的水和尿液样品中提取这些药物。以壳聚糖为原料,通过化学途径合成了功能化MWCNTs的绿色吸附剂。此外,采用水热法制备了多金属氧酸盐(Ni-CoWO4纳米颗粒)作为改性剂。采用溶胶-凝胶策略,将吸附剂和改性剂在中空纤维孔隙和管腔中进行增强。该方法提高了中空纤维表面/内部吸附剂涂层的稳定性。通过实验设计对影响因素进行优化,结果表明pH、提取时间和解吸时间对缬沙坦和氯沙坦的提取有显著影响。缬沙坦和氯沙坦测定的线性关系分别为3.4 ~ 1850和3.1 ~ 1800 ng mL−1,R²分别为0.9929和0.9947。检测限和定量限分别低于0.9 ng mL−1和3.4 ng mL−1。缬沙坦和氯沙坦浓度为20 ng mL−1时的预浓度因子分别为654.2和546.3。缬沙坦和氯沙坦测定的日内、日间rsd分别低于3.11%和3.87%。加标水和尿液的加标回收率和rsd分别为91.8 ~ 97.8%和3.16 ~ 4.10%。关键词:缬沙坦-氯沙坦中空纤维-固相微萃取- mwcnt聚金属氧酸盐壳聚糖感谢伊朗马什哈德伊斯兰阿扎德大学研究委员会的资助。披露声明作者声明,他们没有已知的竞争经济利益或个人关系,可能会影响本文所报道的工作。遵守伦理标准本研究是在机构和/或国家研究委员会的伦理标准下进行的,并遵循1964年赫尔辛基宣言及其后来的修正案或可比文件。道德标准。作者署名声明aref Ansari Mohseni:概念化,撰写原稿,调查,方法论,数据管理,形式分析,资源。马哈茂德·易卜拉希米:主管,调查,写作,审查和编辑。Safarali Beyramabadi:调查、写作、评论和编辑顾问。本文的补充数据可以在线访问https://doi.org/10.1080/03067319.2023.2253736。
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来源期刊
CiteScore
5.90
自引率
7.70%
发文量
373
审稿时长
4.4 months
期刊介绍: International Journal of Environmental Analytical Chemistry comprises original research on all aspects of analytical work related to environmental problems. This includes analysis of organic, inorganic and radioactive pollutants in air, water, sediments and biota; and determination of harmful substances, including analytical methods for the investigation of chemical or metabolic breakdown patterns in the environment and in biological samples. The journal also covers the development of new analytical methods or improvement of existing ones useful for the control and investigation of pollutants or trace amounts of naturally occurring active chemicals in all environmental compartments. Development, modification and automation of instruments and techniques with potential in environment sciences are also part of the journal. Case studies are also considered, particularly for areas where information is scarce or lacking, providing that reported data is significant and representative, either spatially or temporally, and quality assured. Owing to the interdisciplinary nature of this journal, it will also include topics of interest to researchers in the fields of medical science (health sciences), toxicology, forensic sciences, oceanography, food sciences, biological sciences and other fields that, in one way or another, contribute to the knowledge of our environment and have to make use of analytical chemistry for this purpose.
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