This study proposes and demonstrates the use of thermal desorption in on-line solid phase extraction coupled with reversed-phase liquid chromatography (on-line SPE-LC) for the desorption of analytes strongly retained by multiple interaction polymeric sorbents. In detail, this analytical strategy was applied to the on-line SPE-LC targeted analysis of a model set of 34 human gut metabolites characterized by heterogeneous physicochemical properties (i.e., octanol–water partition coefficient in the range -0.3 – 3.4). The novel thermally assisted on-line SPE approach was investigated in comparison to conventional room temperature desorption strategies based on the use of (i) an optimized elution gradient or (ii) organic desorption followed by post-cartridge dilution. The thermally assisted desorption strategy has been shown to be better performing and suitable for the development of a reliable and sensitive method for the analysis of the model group of analytes in urine and serum. In more detail, under the optimized experimental conditions, the proposed method provided negligible matrix effects in both biofluids for almost all target analytes. Moreover, method quantification limits were in the ranges 0.026-7.2 µg L-1 and 0.033-23 µg L-1 for urine and serum, respectively, i.e., comparable to or lower than those reported in methods previously published.

Novel Thermally Assisted On-Line Solid Phase Extraction-Reversed Phase Liquid Chromatography to Perform High Throughput Targeted Nutrimetabolomics in Human Biofluids / Lapo RENAI, Luca MARZULLO, Giulia BONACCORSO, Serena ORLANDINI, Massimo DEL BUBBA. - ELETTRONICO. - (2023), pp. 143-143. (Intervento presentato al convegno 27th International Symposium on Separation Sciences tenutosi a Cluj-Napoca nel 24-27 Settembre 2023).

Novel Thermally Assisted On-Line Solid Phase Extraction-Reversed Phase Liquid Chromatography to Perform High Throughput Targeted Nutrimetabolomics in Human Biofluids

Lapo RENAI
Investigation
;
Luca MARZULLO
Investigation
;
Giulia BONACCORSO
Investigation
;
Serena ORLANDINI
Writing – Review & Editing
;
Massimo DEL BUBBA
Conceptualization
2023

Abstract

This study proposes and demonstrates the use of thermal desorption in on-line solid phase extraction coupled with reversed-phase liquid chromatography (on-line SPE-LC) for the desorption of analytes strongly retained by multiple interaction polymeric sorbents. In detail, this analytical strategy was applied to the on-line SPE-LC targeted analysis of a model set of 34 human gut metabolites characterized by heterogeneous physicochemical properties (i.e., octanol–water partition coefficient in the range -0.3 – 3.4). The novel thermally assisted on-line SPE approach was investigated in comparison to conventional room temperature desorption strategies based on the use of (i) an optimized elution gradient or (ii) organic desorption followed by post-cartridge dilution. The thermally assisted desorption strategy has been shown to be better performing and suitable for the development of a reliable and sensitive method for the analysis of the model group of analytes in urine and serum. In more detail, under the optimized experimental conditions, the proposed method provided negligible matrix effects in both biofluids for almost all target analytes. Moreover, method quantification limits were in the ranges 0.026-7.2 µg L-1 and 0.033-23 µg L-1 for urine and serum, respectively, i.e., comparable to or lower than those reported in methods previously published.
2023
Book of Abstracts 27th International Symposium on Separation Sciences
27th International Symposium on Separation Sciences
Cluj-Napoca
Lapo RENAI, Luca MARZULLO, Giulia BONACCORSO, Serena ORLANDINI, Massimo DEL BUBBA
File in questo prodotto:
File Dimensione Formato  
ABSTRACT.pdf

accesso aperto

Descrizione: Abstract contributo
Tipologia: Pdf editoriale (Version of record)
Licenza: Open Access
Dimensione 215.47 kB
Formato Adobe PDF
215.47 kB Adobe PDF

I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1330578
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact