| Literature DB >> 31307791 |
Edoardo Milanetti1, Giuseppe Carlucci2, Pier Paolo Olimpieri3, Paola Palumbo4, Maura Carlucci5, Vincenzo Ferrone6.
Abstract
In the present work we analyzed the hydrophobicity and hydrophilicity properties of several non-steroidal anti-inflammatory drugs (NSAIDs) by investigating the structural changes of the dynamic hydrogen bond network in order to predict the extraction recovery of NSAIDs from biological fluids set by solid phase extraction (SPE). This work allows investigating the relationship between theoretical descriptors and experimental data using a parameter free method with a strong correlation (Pearson correlation 0.95, p-value 0.0003). The identification and quantification of analytes in human plasma were carried out by high performance liquid chromatography coupled with photodiode array detection (HPLC-PDA) using a Kinetex Evo C18 (150 x 4.6 mm I.D) protected by a guard column and a mixture of acetonitrile and 10 mM phosphate buffer (pH 2.5) (50:50, v/v) as mobile phase at isocratic conditions. Accuracy (BIAS%) ranged within -2.33% and + 8.05% while precision (RSD%) was less than 5.73%.The mean extraction recovery of the carprofen (IS) was 84.1% and the recovery of NSAIDs from human plasma ranged between 81.9% to 86.6%. LODs and LOQs for all the investigated NSAIDs were 0.003 and 0.01 μg/mL, respectively. The method was validated according to the ICH guide line in the range 0.010-20.0 μg/mL.Entities:
Keywords: Bioanalytical method validation; Human plasma; Molecular dynamics; NSAIDs; PLFR; SPE-HPLC-PDA analysis
Year: 2019 PMID: 31307791 DOI: 10.1016/j.chroma.2019.07.005
Source DB: PubMed Journal: J Chromatogr A ISSN: 0021-9673 Impact factor: 4.759