Application of two-phase hollow fiber liquid phase microextraction coupled with high-performance liquid chromatography for the study of the echinacoside pharmacokinetics in Parkinson's disease rat plasma

Typical chromatograms of determination of echinacoside (50ngmL−1) and IS in plasma samples; (A) plasma sample 1h after oral administration with liquid–liquid extraction; (B) plasma sample 1h after oral administration with two-phase hollow fiber liquid phase microextraction. •Based on HF-LPME techniq...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2013-07, Vol.81-82, p.27-33
Hauptverfasser: Zhou, Jun, Zeng, Ping, Sun, Jiang Bing, Wang, Feng Qiao, Zhang, Qiong
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Sprache:eng
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Zusammenfassung:Typical chromatograms of determination of echinacoside (50ngmL−1) and IS in plasma samples; (A) plasma sample 1h after oral administration with liquid–liquid extraction; (B) plasma sample 1h after oral administration with two-phase hollow fiber liquid phase microextraction. •Based on HF-LPME technique has been developed.•The HF-LPME was investigated detailedly.•The first report HP-LPME for the analysis of ECH in Parkinson's disease rat plasma. A simple and solvent-minimized sample preparation technique based on two-phase hollow fiber liquid phase microextraction (HF-LPME) was developed and used to quantify the echinacoside in Parkinson's disease rat plasma following oral administration. Analysis was accomplished by reversed-phase high performance liquid chromatography (HPLC) with ultraviolet detection. The influence factors relevant to the HF-LPME processes were optimized. Under the optimized conditions, the preconcentration factor for echinacoside was 337. Calibration curves with reasonable linearity (r2≥0.9998) were obtained in the range of 5–750ngmL−1. Intra-day and inter-day precision (RSD) were ≤5.43% and the limit of detection (LOD) for the analyte was 2.0ngmL−1 (S/N=3). The validated method has been successfully applied for pharmacokinetic studies of echinacoside in Parkinson's disease (PD) rat plasma after oral administration.
ISSN:0731-7085
1873-264X
DOI:10.1016/j.jpba.2013.03.020