“…As can be seen, the detection limits of BPA, DES and E2 obtained by ODS-PAN-TFME and PEP-PAN-TFME coupled with HPLC-UV are competitive to those obtained by SBA-C18-SPE-HPLC-DAD (Gañán, Pérez-Quintanilla, Morante-Zarcero, & Sierra, 2013), SPE-derivatization-HPLC-FLD (Mao, Sun, Zhang, Li, & Wu, 2004) and MIP-polypropylene hollow fibre tuber (HFT)-HPLC-UV (Liu, Li, Qiu, Chen, & Chen, 2010). But they are higher than those obtained by other approaches including HF-LLLME-HPLC-UV (Chen et al, 2013), C18-SPE-HPLC-FLD (Zhang et al, 2012), Table 2 Comparison of detection limits (ng mL À1 ) with different sample preparations for the determination of estrogens in water samples followed by HPLC analysis. HF-LLLME: hollow fiber liquid-liquid-liquid microextraction; MM: magnetic-mediated; MP: micro-particle; MIP-HFT: molecularly imprinted polymer-coated polypropylene hollow fiber tuber; SBSE-LD: stir bar sorptive extraction and liquid desorption; SDME: single-drop microextraction.…”