Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
An effervescence tablet-assisted switchable solvent-based microextraction: On-site preconcentration of steroid hormones in water samples followed by HPLC-UV determination. / Shishov, Andrey; Sviridov, Ivan; Timofeeva, Irina; Chibisova, Natalia; Moskvin, Leonid; Bulatov, Andrey.
в: Journal of Molecular Liquids, Том 247, 2017, стр. 246-253.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - An effervescence tablet-assisted switchable solvent-based microextraction: On-site preconcentration of steroid hormones in water samples followed by HPLC-UV determination
AU - Shishov, Andrey
AU - Sviridov, Ivan
AU - Timofeeva, Irina
AU - Chibisova, Natalia
AU - Moskvin, Leonid
AU - Bulatov, Andrey
PY - 2017
Y1 - 2017
N2 - An effervescence tablet-assisted switchable solvent-based microextraction (ETA-SHS-ME) strategy for the on-site pretreatment of water samples was developed in this study. The performance of the suggested strategy was demonstrated by the HPLC-UV determination of steroid hormones (testosterone, progesterone, estradiol and hydrocortisone) in water samples. This analytical task was used as a proof-of-concept example. The ETA-SHS-ME procedure involves dissolution of two effervescent tablets containing a solid proton donor agent (oxalic acid) and an effervescency (NaHCO3) agent as well as a source of organic phase (sodium nonate) in water sample. The proton donor agent reacts with the effervescency agent and water-soluble source of organic phase in aqueous sample phase. The pH changing promotes conversion of sodium nonate into a water-insoluble nonanoic acid dispersed by carbon dioxide bubbles generated in situ. After phase separation an organic phase containing steroid hormones is collected and delivered to a laboratory, and HPLC-UV analysis is performed. The linear calibration ranges were from 5 to 500 ng L− 1 for testosterone, from 25 to 750 ng L− 1 for progesterone, from 10 to 1000 ng L− 1 for estradiol and from 50 to 500 ng L− 1 for hydrocortisone. The LODs, calculated from the blank tests based on 3σ, were 2, 8, 3 and 17 ng L− 1, respectively. The method was successfully applied to the analysis of river samples.Novelty Statement.In this research, for the first time, the effervescence tablet-assisted switchable solvent-based microextraction (ETA-SHS-ME) approach was developed and successfully applied for on-site sample pretreatment of water samples. The organic phase is generated in situ in the ETA-SHS-ME procedure compared to the reported in literature effervescence-assisted microextraction approaches. This feature allows to implement microextraction from a large volume of the aqueous sample phase with extremely high enrichment factors. The manufacturing of effervescence tablets for ETA-SHS-ME is simple due to all agents used are solid substances, which can be easily mixed and compressed.The ETA-SHS-ME was coupled with the HPLC-UV method for the first time and applied for the determination of testosterone, progesterone, estradiol and hydrocortisone in river samples. The effervescence-assisted microextraction procedure was implemented for the determination of steroid hormones in water samples for the first time.
AB - An effervescence tablet-assisted switchable solvent-based microextraction (ETA-SHS-ME) strategy for the on-site pretreatment of water samples was developed in this study. The performance of the suggested strategy was demonstrated by the HPLC-UV determination of steroid hormones (testosterone, progesterone, estradiol and hydrocortisone) in water samples. This analytical task was used as a proof-of-concept example. The ETA-SHS-ME procedure involves dissolution of two effervescent tablets containing a solid proton donor agent (oxalic acid) and an effervescency (NaHCO3) agent as well as a source of organic phase (sodium nonate) in water sample. The proton donor agent reacts with the effervescency agent and water-soluble source of organic phase in aqueous sample phase. The pH changing promotes conversion of sodium nonate into a water-insoluble nonanoic acid dispersed by carbon dioxide bubbles generated in situ. After phase separation an organic phase containing steroid hormones is collected and delivered to a laboratory, and HPLC-UV analysis is performed. The linear calibration ranges were from 5 to 500 ng L− 1 for testosterone, from 25 to 750 ng L− 1 for progesterone, from 10 to 1000 ng L− 1 for estradiol and from 50 to 500 ng L− 1 for hydrocortisone. The LODs, calculated from the blank tests based on 3σ, were 2, 8, 3 and 17 ng L− 1, respectively. The method was successfully applied to the analysis of river samples.Novelty Statement.In this research, for the first time, the effervescence tablet-assisted switchable solvent-based microextraction (ETA-SHS-ME) approach was developed and successfully applied for on-site sample pretreatment of water samples. The organic phase is generated in situ in the ETA-SHS-ME procedure compared to the reported in literature effervescence-assisted microextraction approaches. This feature allows to implement microextraction from a large volume of the aqueous sample phase with extremely high enrichment factors. The manufacturing of effervescence tablets for ETA-SHS-ME is simple due to all agents used are solid substances, which can be easily mixed and compressed.The ETA-SHS-ME was coupled with the HPLC-UV method for the first time and applied for the determination of testosterone, progesterone, estradiol and hydrocortisone in river samples. The effervescence-assisted microextraction procedure was implemented for the determination of steroid hormones in water samples for the first time.
KW - Effervescence tablet-assisted switchable solvent-based microextraction
KW - Fatty acids
KW - On-site preconcentration
KW - HPLC-UV
KW - Steroid hormones
KW - water
U2 - 10.1016/j.molliq.2017.09.120
DO - 10.1016/j.molliq.2017.09.120
M3 - Article
VL - 247
SP - 246
EP - 253
JO - Journal of Molecular Liquids
JF - Journal of Molecular Liquids
SN - 0167-7322
ER -
ID: 9160015