Quantitative analysis of therapeutic peptides by CZE using multiple sample injection in hydrodynamically closed separation system

Author:

Stefanik Ondrej12,Mikus Peter12ORCID,Piestansky Juraj234ORCID

Affiliation:

1. Department of Pharmaceutical Analysis and Nuclear Pharmacy Faculty of Pharmacy Comenius University in Bratislava Bratislava Slovakia

2. Toxicological and Antidoping Center Faculty of Pharmacy Comenius University in Bratislava Bratislava Slovakia

3. Department of Galenic Pharmacy Faculty of Pharmacy Comenius University in Bratislava Bratislava Slovakia

4. Institute of Neuroimmunology Slovak Academy of Sciences Bratislava Slovakia

Abstract

AbstractTherapeutic peptides have emerged as an innovative and promising class of therapeutic compounds in modern medicine. Synthetic peptide analogs triptorelin and lanreotide are known for their pronounced clinical versatility and potency. In this study, we present the development and validation of novel methods based on capillary zone electrophoresis performed in hydrodynamically closed system (HCS) and paired with ultraviolet detection and repeated injection sample introduction. To the best of our knowledge, we developed the first capillary electrophoresis‐based method for the determination of lanreotide, and concurrently, the first HCS method for the determination of triptorelin. Maximal separation efficiency and signal intensity were achieved using background electrolytes composed of 50 mM formic acid with the addition of 0.05% (v/v) methyl‐hydroxyethyl cellulose. The proposed methods exhibit favorable performance characteristics, namely, calibration curve (r2 exceeding 0.99), low limits of detection (0.25 µg/mL in a water matrix and 0.5 µg/mL in synthetic urine), acceptable precision (relative standard deviation ranging from 2.2% to 9.6% for intraday repeatability and between 5.2% and 14.9% for interday reproducibility), and accuracy (relative errors falling within the 91.1%–107.8% range). The method for triptorelin determination was then used for its quantification in a commercially available drug dosage form (powder for injection) and in spiked synthetic urine samples. The developed methods were also evaluated according to the novel blue applicability grade index, revealing their superior applicability. The results collectively point out the potential of the proposed methods for both quality control and clinical investigations.

Funder

Vedecká Grantová Agentúra MŠVVaŠ SR a SAV

Publisher

Wiley

Reference35 articles.

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