Mussel inspired polydopamine functionalized poly(ether ether ketone) tube for online solid-phase microextraction–high performance liquid chromatography and its application in analysis of protoberberine alkaloids in rat plasma

A novel and simple poly(ether ether ketone) (PEEK) tube-based solid-phase microextraction (SPME)-HPLC method was developed in this work. A mussel inspired polydopamine method was used to functionalize the chemically resistant surface of PEEK tube and a poly(acrylamide–ethylene glycol dimethacrylate) monolith was synthesized inside the PEEK tube and chemically bonded with its surface. The stability of the polydopamine layer was investigated and found to be well enduring to most of commonly used organic solvents and strong acidic conditions. The PEEK tube-based monolith was coupled with HPLC system through a six-port valve, and the performance of the online SPME–HPLC system was demonstrated by analyzing three protoberberine alkaloids in aqueous samples, namely jatrorrhizine (Jat), palmatine (Pal) and berberine (Ber). These analytes were well extracted and separated within 10 min, and enrichment factors of about 400 were obtained. The limit of detection of the proposed method was decreased to 0.01 ng/mL by using UV detection. Finally, the online SPME–HPLC method was applied for determining Jat, Pal and Ber in rat plasma samples. Reproducibility was obtained by evaluating the intra- and inter-day precisions with RSDs less than 6.1% and 8.5%, respectively, and recoveries of the analytes in spiked plasma samples ranged from 89.8% to 96.7%. The proposed method was also applied to determine the concentration of Jat, Pal and Ber in rat plasma after oral administration of Cortex Phellodendri Chinensis.

► A new approach for functionalization of PEEK tube was developed.
► Poly(AA–EGDMA) sorbents was connected with PEEK surface covalently.
► PEEK tube was used for SPME and online coupling with HPLC.
► Online SPME–HPLC-UV for analysis of protoberberine alkaloids with LOD of 0.01 ng/mL.
► Monitoring drug concentration in rat plasma after oral administration of herbs.