Volume 6 Issue 2
Apr.  2016
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Pei Zhang a, Yu-Qiang Gou b, Xia Gao a, Rui-Bin Bai a, Wen-Xia Chen a, Bo-Lu Sun a, Fang-Di Hu a, n, Wang-Hong Zhao c. The pharmacokinetic study of rutin in rat plasma based on an electrochemically reduced graphene oxide modified sensor$[J]. Journal of Pharmaceutical Analysis, 2016, 6(2): 80-86. doi: 10.1016/j.jpha.2015.12.003
Citation: Pei Zhang a, Yu-Qiang Gou b, Xia Gao a, Rui-Bin Bai a, Wen-Xia Chen a, Bo-Lu Sun a, Fang-Di Hu a, n, Wang-Hong Zhao c. The pharmacokinetic study of rutin in rat plasma based on an electrochemically reduced graphene oxide modified sensor$[J]. Journal of Pharmaceutical Analysis, 2016, 6(2): 80-86. doi: 10.1016/j.jpha.2015.12.003

The pharmacokinetic study of rutin in rat plasma based on an electrochemically reduced graphene oxide modified sensor$

doi: 10.1016/j.jpha.2015.12.003
  • Publish Date: Apr. 10, 2016
  • An electrochemical method based on a directly electrochemically reduced graphene oxide (ERGO) film coated on a glassy carbon electrode (GCE) was developed for the rapid and convenient determination of rutin in plasma. ERGO was modified on the surface of GCE by one-step electro-deposition method. Electrochemical behavior of rutin on ERGO/GCE indicated that rutin underwent a surface-controlled quasi-reversible process and the electrochemical parameters such as charge transfer coefficient (α), electron transfer number (n) and electrode reaction standard rate constant (ks) were 0.53, 2 and 3.4 s?1, respectively. The electrochemical sensor for rutin in plasma provided a wide linear response range of 4.70 ? 10 ? 7 ? 1.25 ? 10 ? 5 M with the detection limit (s/n ? 3) of 1.84 ? 10 ? 8 M. The assay was success-fully used to the pharmacokinetic study of rutin. The pharmacokinetic parameters such as elimination rate half-life (t1/2), area under curve (AUC), and plasma clearance (CL) were calculated to be 3.345 7 0.647 min, 5750 7 656.0 mg min/mL, and 5.891 7 0.458 mL/min/kg, respectively. The proposed method utilized a small sample volume of 10μL and had no complicated sample pretreatment (without deproteinization), which was simple, eco-friendly, and time-and cost-efficient for rutin pharmacokinetic studies.
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