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Xenobiotica
the fate of foreign compounds in biological systems
Volume 50, 2020 - Issue 5
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Clinical Pharmacokinetics and Metabolism

Plasma and cerebrospinal fluid pharmacokinetics of hydroxysafflor yellow A in patients with traumatic brain injury after intravenous administration of Xuebijing using LC-MS/MS method

, , & ORCID Icon
Pages 545-551 | Received 04 Aug 2019, Accepted 13 Sep 2019, Published online: 24 Sep 2019
 

Abstract

  1. Hydroxysafflor yellow A (HSYA) is the most pharmaceutically relevant compound in Xuebijing (XBJ) for traumatic brain injury (TBI) treatment. We aimed to investigate biofluids pharmacokinetics of HSYA from XBJ to ensure the drug safety and to guide the clinical use.

  2. A sensitive, rapid and reliable liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was applied to investigate pharmacokinetics of HSYA in TBI patients after intravenous administration of XBJ. Non-compartmental methods using DAS 3.0 software were applied to analyse the pharmacokinetic parameters.

  3. A similar half-life (Plasmat1/2: 14.55 ± 3.51 h vs. CSFt1/2: 15.73 ± 3.63) was observed. HSYA reached the peak level rapidly, but exhibited a strongly slow absorption phase from blood to cerebrospinal fluid (CSF, PlasmaTmax: 0.69 ± 0.26 h vs. CSFTmax: 4.0 ± 2.62 h). HSYA exhibited much higher Cmax (PlasmaCmax: 9342.76 ± 2489.23 μg/L vs. CSFCmax: 98.08 ± 14.51 μg/L) and AUC0-t (PlasmaAUC0-t: 57490.5 ± 5560.3 μg h/L vs. CSFAUC0-t: 1851.6 ± 269.1 μg h/L), yet a shorter CL (PlasmaCL: 0.02 ± 0.002 L/h/kg vs. CSFCL: 0.55 ± 0.01 L/h/kg) in plasma than in CSF. The AUCCSF/AUCplasma of HSYA was almost 3.37%.

  4. In summary, the results demonstrate that part of HSYA come across blood-brain barrier after XBJ administration. This study provides evidence for better understanding the pharmacokinetics and potential for clinical guidance of XBJ for TBI treatment.

Author contributions

Yang Wang designed the research; Chenxia Sheng, Weijun Peng, Yang Wang and Zian Xia performed the study; Yang Wang and Chenxia Sheng analysed the data; Chenxia Sheng and Yang Wang wrote and revised the paper.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This research was supported by supported by the National Natural Science Foundation of China (No. 81673719), and the Project funded by China Postdoctoral Science Foundation (Nos. 2017T100614 and 2016M600639).

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