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紫杉醇的电化学行为及直接定量测定

Electrochemical Behavior and Direct Quantitative Determination of Paclitaxel.

作者信息

Lang Jiaqi, Wang Wenting, Zhou You, Guo Dongqin, Shi Rujie, Zhou Nong

机构信息

The Chongqing Engineering Laboratory for Green Cultivation and Deep Processing of Three Gorges Reservoir Area's Medicinal Herbs, College of Food and Biology Engineering, Chongqing Three Gorges University, Chongqing, China.

Wanzhou Institute for Food and Drug Control, Chongqing, China.

出版信息

Front Chem. 2022 Apr 26;10:834154. doi: 10.3389/fchem.2022.834154. eCollection 2022.

Abstract

The electrochemical behavior and direct quantitative determination of paclitaxel, a poorly soluble drug made into microemulsion, were researched by cyclic voltammetry in acetate buffer solutions (pH = 4.0) at a glassy carbon electrode. The results show that the oxidation process is irreversible and controlled by diffusion. Moreover, the effects of anodic peak current (Ipa), anodic peak potential, scan rate, pH, and the electrochemical redox mechanism have been studied. The anodic peak current varied linearly with paclitaxel concentration in the range of 5 × 10 mol/L to 5 × 10 mol/L, and the detection limit was 9.15 × 10 mol/L. The results of RSD (0.90%) and recovery (99.22%-101.69%) were obtained. Additionally, it has been proved that one electron and one proton are involved in the electrochemical redox process. The present research has been successfully used to determine paclitaxel in pure and real samples, which further supported the electrochemical behavior investigation of paclitaxel and direct determination of micro-emulsion.

摘要

采用循环伏安法在pH = 4.0的醋酸盐缓冲溶液中于玻碳电极上研究了制成微乳液的难溶性药物紫杉醇的电化学行为及直接定量测定。结果表明,氧化过程是不可逆的且受扩散控制。此外,还研究了阳极峰电流(Ipa)、阳极峰电位、扫描速率、pH以及电化学氧化还原机理的影响。阳极峰电流在5×10⁻⁶mol/L至5×10⁻⁵mol/L范围内与紫杉醇浓度呈线性关系,检测限为9.15×10⁻⁷mol/L。获得了相对标准偏差(RSD)为0.90%和回收率为99.22% - 101.69%的结果。此外,已证明在电化学氧化还原过程中有一个电子和一个质子参与。本研究已成功用于纯样品和实际样品中紫杉醇的测定,这进一步支持了紫杉醇的电化学行为研究及微乳液的直接测定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be6a/9090486/c51d962f7665/fchem-10-834154-g001.jpg

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