Eco-friendly magnetic Solid-Phase extraction and deep eutectic solvent for the separation and detection of parabens from the environmental water and urine samples

被引:18
|
作者
Pasupuleti, Raghavendra Rao [1 ]
Hsieh, Jing-Ru [1 ]
Pasupuleti, Visweswara Rao [2 ,3 ,4 ]
Huang, Yeou-Lih [1 ,5 ,6 ,7 ]
机构
[1] Kaohsiung Med Univ, Dept Med Lab Sci & Biotechnol, 100 Shih Chuan 1st Rd, Kaohsiung 807, Taiwan
[2] Univ Malaysia Sabah, Fac Med & Hlth Sci, Dept Biomed Sci & Therapeut, Kota Kinabalu, Sabah, Malaysia
[3] Abdurrab Univ, Fac Med & Hlth Sci, Dept Biochem, Pekanbaru, Riau, Indonesia
[4] Reva Univ, Ctr Int Collaborat & Res, Rukmini Knowledge Pk, Bangalore, Karnataka, India
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Lab Med, Kaohsiung 807, Taiwan
[6] Kaohsiung Med Univ, Res Ctr Environm Med, Kaohsiung 807, Taiwan
[7] Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 807, Taiwan
关键词
Magnetic activated carbon; Deep eutectic solvents; Parabens; Urine; Water; HPLC-UV; ACTIVATED CARBON;
D O I
10.1016/j.microc.2022.107330
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work reports an eco-friendly, cheap, and sensitive magnetic solid-phase extraction (MSPE) and deep eutectic solvent (DES) for the isolation and detection of parabens from water and urine. The parabens were determined by liquid chromatography equipped with an ultraviolet detector (HPLC-UV). The magnetic-activated carbon (MAC) was synthesized from coffee waste was used as an adsorbent. DL-menthol and acetic acid-based deep eutectic solvent (DES) were synthesized and applied as a less toxic solvent in the parabens desorption. The ideal conditions which increase the efficiencies are 10 mg of adsorbent amount, adsorption time 8 min, DL -menthol and acetic acid-based DES used as eluent, eluent volume 200 mu L, desorption time 3 min. The parabens exhibited superior linearity between the 0.3 1000 ng mL(-1). The regression coefficient (R-2) values among 0.9962 0.9990. The developed MSPE-DES-HPLC-UV exhibited excellent sensitivity. The detection limit (LOD) ranged from 0.1 0.3 ng mL(-1) and the quantification limit (LOQ) between 0.3 0.5 ng mL(-1). The precision of the method expressed as RSDs was over the range of 3.49 9.15%, correspondingly. This technique was employed for the analysis of the real sample (swimming pool, river, and urine samples). The attained recoveries are 82.60 114.40% with RSD < 9.67% for water samples, 81.80 118.20% with RSD < 9.28% for urine samples. All the method validation results are in the acceptable range. This method claims its practical solicitation in the analytical sector in the near future.
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页数:9
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