Quantitative analysis of therapeutic peptides by CZE using multiple sample injection in hydrodynamically closed separation system.
Stefanik. Ondrej O; Mikus. Peter P; Piestansky. Juraj J
Key Findings
- First HCS‑based capillary electrophoresis method for measuring triptorelin
- Detection limits as low as 0.25 µg/mL in water and 0.5 µg/mL in synthetic urine
- Calibration linearity (R² > 0.99) with precision (2.2‑9.6% intraday, 5.2‑14.9% interday) and accuracy (91‑108%)
Practical Outcomes
- If you have access to capillary electrophoresis equipment, this protocol lets you verify the purity and concentration of triptorelin in powders or urine samples. For most biohackers, the main takeaway is that commercial triptorelin products are analytically measurable, but you’ll likely need to rely on reputable suppliers rather than DIY testing.
Summary
Scientists created a new lab test that can accurately measure tiny amounts of the peptide drug triptorelin (and lanreotide) using a technique called capillary zone electrophoresis. The test works well in water and fake urine, showing good precision and accuracy, and it was proven on a commercial injection powder. However, the method requires specialized equipment and isn’t something most DIY health enthusiasts can use directly.
Abstract
Therapeutic 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 (r<sup>2</sup> 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.
Study Information
pubmed
2024
2024-05-13T00:00:00.000Z
10.1002/elps.202400039
3
35