首页> 外文期刊>Analytical and Bioanalytical Chemistry Research >Development of AgNPs-tragacanth Conjugated Gel as a Novel Green Membrane in Electro-membrane Extraction: Tenofovir Disoproxil Fumarate Assay in Human Plasma Samples
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Development of AgNPs-tragacanth Conjugated Gel as a Novel Green Membrane in Electro-membrane Extraction: Tenofovir Disoproxil Fumarate Assay in Human Plasma Samples

机译:agnps-tragacanth缀合的凝胶作为电膜提取中的新型绿膜:人血浆样品中的替诺福韦解毒富马酸核测定

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AgNPs-Tragacanth conjugate gel as an eco friendly and low cost membrane was applied for the effective electromembrane extraction (EME) of Tenofovir disproxil fumarate, an important acidic and high polar (log p=1.25) antiviral drug, followed by HPLC-UV determination. The effect of various parameters on the extraction efficiency including the presence of AgNPs, tragacanth gum concentration, gel thickness, pH values of the donor and acceptor phases, applied voltage, extraction time and agitation rate were investigated and optimized. The best extraction efficiency was obtained with: 2.5% w/v of tragacanth gum, 4.0 mm gel thickness, donor phase pH = 7.0, acceptor phase pH = 8.0, applied voltage: 30 V, extraction time: 15 min and agitation rate: 500 rpm. During method validation under the optimized conditions good linearity dynamic range (LDR) between 10-750 ngmL-1 with coefficient of determination (R2) =0.999 was obtained. Limit of detection (LOD) and Limit of quantitation (LOQ) were estimated to be 5.55 ng mL-1 and 10 ng mL-1, respectively. According to the validation results, the RSD values for intra and inter-day precisions were in the range of 0.53 to 10.04% and the relative error (RE %) ranged between -2.31 to 8.20% Finally the applicability of this method in real samples was confirmed by an acceptable performance in extraction and determination of TDF in human plasma samples.
机译:Agnps-TragaCanth缀合物凝胶作为ECO友好型和低成本膜应用于替诺福韦不掺富富马酸的有效电磁萃取(EME),重要的酸性和高极性(LOM P = 1.25)抗病毒药物,其次是HPLC-UV测定。研究了各种参数对提取效率的影响,包括AgNPS,曲囊胶浓度,凝胶厚度,供体和受体相的pH值,施加的电压,提取时间和搅拌速率,并进行优化。获得最佳的提取效率:2.5%w / v曲蓍胶,4.0mm凝胶厚度,供体相pH = 7.0,受体相pH = 8.0,施加电压:30 V,提取时间:15分钟和搅拌速度:500 rpm。在方法验证期间,优化条件下的良好线性度动态范围(LDR)在10-750ngml-1之间,获得了判定系数(R2)= 0.999。检测极限(LOD)和定量限制(LOQ)分别估计为5.55ng -1和10ng mL-1。根据验证结果,用于帧内和日间诊断的RSD值在0.53至10.04%的范围内,相对误差(RE%)在-2.31至8.20%之间,最终在真实样本中的这种方法的适用性是通过萃取和测定人血浆样品中TDF的可接受性能证实。

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