The feasible, reliable and selective multi-template molecularly imprinted polymers (MT-MIPs) based on SBA-15 (SBA-15@MT-MIPs) for the selective separation and determination of the trace level of ginsenoside Rb₁ (Rb₁), ginsenoside Rg₁ (Rg₁) and notoginsenoside R₁ (R₁) simultaneously from biological samples were developed. The polymers were constructed by SBA-15 as support, Rb₁, Rg₁, R₁ as multi-template, acrylamide (AM) as functional monomer and ethylene glycol dimethacrylate (EGDMA) as cross-linker. The new synthetic SBA-15@MT-MIPs were satisfactorily applied to solid-phase extraction (SPE) coupled with high performance liquid chromatography (HPLC) for the separation and determination of trace Rb₁, Rg₁ and R₁ in plasma samples. Under the optimized conditions, the limits of detection (LODs) and quantitation (LOQs) of the proposed method for Rb₁, Rg₁ and R₁ were in the range of 0.63⁻0.75 ng·mL-1 and 2.1⁻2.5 ng·mL-1, respectively. The recoveries of R₁, Rb₁ and Rg₁ were obtained between 93.4% and 104.3% with relative standard deviations (RSDs) in the range of 3.3⁻4.2%. All results show that the obtained SBA-15@MT-MIPs could be a promising prospect for the practical application in the selective separation and enrichment of trace Panax notoginseng saponins (PNS) in the biological samples.
Keywords: Panax notoginseng saponins; SBA-15; multi-template molecularly imprinted polymers; separation and determination; solid-phase extraction.