HPLC
TESTING
High-Performance Liquid Chromatography for purity determination, potency verification, and degradation profiling. The workhorse of pharmaceutical and peptide quality control. UV/VIS and PDA detection for comprehensive characterization.
- 01Purity determination
- 02Potency verification
- 03Stability testing
- 04Degradation profiling
- 05Content uniformity
HPLC at Standard Analytica is the cornerstone of our analytical services. Our systems are equipped with UV/VIS and photodiode array (PDA) detectors, enabling simultaneous multi-wavelength monitoring for comprehensive peak characterization.
The method is ideally suited for purity assessment of synthetic peptides, active pharmaceutical ingredients, and formulated products. Reverse-phase, normal-phase, and size-exclusion column chemistries are available to address diverse analytical challenges.
All HPLC methods are developed and validated in accordance with ICH guidelines. System suitability criteria are verified at the start of each analytical sequence to ensure data integrity and reproducibility.
SAMPLE INTAKE
Your sample is received, logged into our LIMS system, and assigned a unique tracking identifier. Sample integrity is verified and documented upon receipt.
PREPARATION
Samples are weighed, dissolved, and diluted according to validated preparation protocols. Reference standards are prepared concurrently for accurate quantification.
ANALYSIS
Prepared samples are injected into the HPLC system equipped with UV/VIS or PDA detection. Separation is achieved using optimized column chemistry and mobile phase gradients.
REPORTING
Chromatographic data is integrated and reviewed by senior analysts. A comprehensive report including purity calculations, peak identification, and raw chromatograms is delivered.
SUBMIT A SAMPLE
Ready to submit a sample for HPLC testing? Contact our team to discuss your requirements, receive sample preparation guidelines, and initiate testing.