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Correlation analysis based on the hydropathy properties of non-steroidal anti-inflammatory drugs in solid-phase extraction (SPE) and reversed-phase high performance liquid chromatography (HPLC) with photodiode array detection and their applications to biological samples. | LitMetric

AI Article Synopsis

  • The study examines the hydrophobic and hydrophilic properties of NSAIDs to predict their extraction recovery from biological fluids using solid phase extraction (SPE).
  • It established a strong correlation (Pearson correlation 0.95) between theoretical descriptors and experimental data, enabling accurate predictions.
  • High performance liquid chromatography (HPLC-PDA) was used to analyze NSAIDs in human plasma, achieving an extraction recovery of 81.9% to 86.6% and validating the method according to ICH guidelines.

Article 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 C (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.

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Source
http://dx.doi.org/10.1016/j.chroma.2019.07.005DOI Listing

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