TY - JOUR
T1 - Efficient dispersive micro solid-phase extraction of antidepressant drugs by a robust molybdenum-based coordination polymer
AU - Bazargan, Maryam
AU - Mirzaei, Masoud
AU - Amiri, Amirhassan
AU - Ritchie, Chris
N1 - Funding Information:
M.M. gratefully acknowledges financial support from the Ferdowsi University of Mashhad(Grant No. 3/42202), the Iran Science Elites Federation (ISEF), Zeolite and Porous MaterialsCommittee of Iranian Chemical Society and the Iran National Science Foundation (INSF). M.M. also acknowledges the Cambridge Crystallographic Data Centre (CCDC) for access to the Cambridge Structural Database.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH, AT part of Springer Nature.
PY - 2021/4
Y1 - 2021/4
N2 - A molybdenum-based coordination polymer {[Mo(PDA)(NO)(μ-O)MoO3]·1.42H2O·0.58C2H5OH}n (1) (PDA is 1,10-phenanthroline-2,9-dicarboxylate) was synthesized using solvothermal reaction conditions and characterized using a suite of analytical techniques. Single-crystal X-ray diffraction studies reveal a 1D chain structure, with close contacts expanding the structure into 3D including π-interactions and hydrogen bonding. The utility of 1 as a sorbent for dispersive micro solid-phase extraction (D-μSPE) of basic organic compounds such as antidepressants is supported by the presence of many functional groups on the surface of 1 (such as pendant carboxylates, Mo=O, Mo–NO, and CH groups) as well as extensive electrostatic interactions. Therefore, 1 can be a suitable choice as sorbent in the D-μSPE of antidepressant drugs from human plasma samples via appreciable adsorbate-adsorbent interactions. Determination of the extracted antidepressant drugs was conducted using high-performance liquid chromatography-ultraviolet (HPLC-UV), with calibration plots being linear in the concentration range 0.1–500 ng mL−1 for amitriptyline and nortriptyline, 0.2–500 ng mL−1 for imipramine, and 0.5–300 ng mL−1 for sertraline. The relative standard deviation (RSD) values were calculated for both intra-day and inter-day precision, and the RSD% values were in the range 3.9 to 5.2% and 4.6–5.4%, respectively. The limits of detection (LODs) was determined as 0.03–0.2 ng mL−1. Due to the good stability and reusability of the sorbent, the adsorption capacity had no obvious decrease after being used 20 times. Finally, the D-μSPE-HPLC-UV method was applied for the determination of antidepressant drugs in human plasma samples with recoveries of the analytes in the range 94.9 to 102%. Graphical abstract: [Figure not available: see fulltext.]
AB - A molybdenum-based coordination polymer {[Mo(PDA)(NO)(μ-O)MoO3]·1.42H2O·0.58C2H5OH}n (1) (PDA is 1,10-phenanthroline-2,9-dicarboxylate) was synthesized using solvothermal reaction conditions and characterized using a suite of analytical techniques. Single-crystal X-ray diffraction studies reveal a 1D chain structure, with close contacts expanding the structure into 3D including π-interactions and hydrogen bonding. The utility of 1 as a sorbent for dispersive micro solid-phase extraction (D-μSPE) of basic organic compounds such as antidepressants is supported by the presence of many functional groups on the surface of 1 (such as pendant carboxylates, Mo=O, Mo–NO, and CH groups) as well as extensive electrostatic interactions. Therefore, 1 can be a suitable choice as sorbent in the D-μSPE of antidepressant drugs from human plasma samples via appreciable adsorbate-adsorbent interactions. Determination of the extracted antidepressant drugs was conducted using high-performance liquid chromatography-ultraviolet (HPLC-UV), with calibration plots being linear in the concentration range 0.1–500 ng mL−1 for amitriptyline and nortriptyline, 0.2–500 ng mL−1 for imipramine, and 0.5–300 ng mL−1 for sertraline. The relative standard deviation (RSD) values were calculated for both intra-day and inter-day precision, and the RSD% values were in the range 3.9 to 5.2% and 4.6–5.4%, respectively. The limits of detection (LODs) was determined as 0.03–0.2 ng mL−1. Due to the good stability and reusability of the sorbent, the adsorption capacity had no obvious decrease after being used 20 times. Finally, the D-μSPE-HPLC-UV method was applied for the determination of antidepressant drugs in human plasma samples with recoveries of the analytes in the range 94.9 to 102%. Graphical abstract: [Figure not available: see fulltext.]
KW - Adsorbate-adsorbent interactions
KW - Coordination polymer
KW - HPLC
KW - Plasma analysis
KW - Powder X-ray diffraction
UR - http://www.scopus.com/inward/record.url?scp=85102199391&partnerID=8YFLogxK
U2 - 10.1007/s00604-021-04767-4
DO - 10.1007/s00604-021-04767-4
M3 - Article
C2 - 33660036
AN - SCOPUS:85102199391
SN - 0026-3672
VL - 188
JO - Microchimica Acta
JF - Microchimica Acta
IS - 4
M1 - 108
ER -