Electrospun chitosan modified montmorillonite/polyvinyl alcohol nanofibers as suitable coating for fiber-in-tube solid-phase microextraction of trace amounts of tricyclic antidepressants in biological fluids

IF 6.5 Q1 CHEMISTRY, ANALYTICAL
Saeed Pourhosseini, Yadollah Yamini, Seyedeh Sara Nasrollahi
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Abstract

Chitosan intercalated montmorillonite and polyvinyl alcohol-citric acid (PVA/CA) nanofibers were electrospun onto stainless steel wires. The fibers were placed inside a stainless steel tube and utilized for fiber-in-tube solid phase microextraction (FIT-SPME) to detect trace levels of tricyclic antidepressant drugs (TCAs) in biological samples. The analytes were separated and quantified using gas chromatography coupled with mass spectrometric detection (GC–MS). The effects of various parameters on the extraction efficiency, including pH (9), extraction time (25 min), extraction flow rate (3 mL min-1), salt addition (0 % w/v), type of eluent (ethanol 99 %), eluent volume (300 µL), and desorption flow rate (70 µL min-1), were investigated and optimized. Under optimal conditions, the linear dynamic range for doxepin, and sertraline was found to be 0.08–750.0 ng mL-1; for amitriptyline, desipramine, and trimipramine, it was 10.0–750.0 ng mL-1; and for carbamazepine and maprotiline, it was 50.0–750.0 ng mL-1. The proposed method exhibited low limits of detections in the range of 0.02–15.2 ng mL-1. Additionally, coefficients of determination (R²) exceeding 0.9911 were achieved, indicating excellent linearity for the calibration curves. To assess the feasibility of the FIT-SPME-GC–MS method, extraction and analysis of TCAs were performed on plasma and urine samples. Relative recovery percentages (RR%) ranged from 90.3 % to 117.6 %.

Abstract Image

静电纺壳聚糖改性蒙脱土/聚乙烯醇纳米纤维涂层用于管中纤维固相微萃取生物体液中微量三环类抗抑郁药
将壳聚糖嵌层蒙脱土和聚乙烯醇-柠檬酸(PVA/CA)纳米纤维电纺成不锈钢丝。这些纤维被放置在一个不锈钢管中,用于纤维管固相微萃取(FIT-SPME),以检测生物样品中痕量的三环抗抑郁药物(TCAs)。采用气相色谱-质谱联用检测(GC-MS)对分析物进行分离和定量。考察了pH(9)、提取时间(25 min)、提取流量(3 mL min-1)、盐添加量(0% w/v)、洗脱液类型(99%乙醇)、洗脱液体积(300µL)、解吸流量(70µL min-1)等参数对提取效率的影响,并进行了优化。在最佳条件下,多塞平和舍曲林的线性动态范围为0.08 ~ 750.0 ng mL-1;阿米替林、地西帕明和三嗪帕明为10.0 ~ 750.0 ng mL-1;卡马西平和马普替林为50.0 ~ 750.0 ng mL-1。该方法的低检出限为0.02 ~ 15.2 ng mL-1。测定系数(R²)均大于0.9911,表明标定曲线线性良好。为了评估FIT-SPME-GC-MS方法的可行性,对血浆和尿液样本进行了TCAs的提取和分析。相对回收率(RR%)为90.3% ~ 117.6%。
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