Development, validation and application of a UHPLC-MS/MS method for quantification of the adiponectin-derived active peptide ADP355 in rat plasma.
Qiaoxi LiFulin JiangYanping GuanXianxing JiangJunyan WuMin HuangGuo-Ping ZhongPublished in: Biomedical chromatography : BMC (2022)
A UHPLC-MS/MS method for the quantification of ADP355, an adiponectin-derived active peptide, was developed and validated. The extraction method employed simple protein precipitation using methanol and chromatographic separation was achieved on anAccucore™ RP-MS C 18 column (100 × 2.1 mm, 2.6 μm, 80 Å), using 0.1% formic acid in both water and acetonitrile with gradient elution at the flow rate of 400 μl/min within 4.0 min. Detections were performed under positive ion mode with multiple reaction monitoring ion transitions m/z 1109.2 → 309.8 and 871.4 → 310.1 for ADP355 and Jt003 respectively at unit resolution. The linearity range of the calibration curve was 2-1,000 ng/ml with a lower limit detection of 0.5 ng/ml. The selectivity, linearity, precision, accuracy, recovery, matrix effect and stability were validated, and all items met the requirement of US Food and Drug Administration guidance. This method was successfully applied to an intravenous pharmacokinetic study of ADP355 in rats and the in-vitro stability in rat serum, plasma and whole blood was also assessed.
Keyphrases
- ms ms
- simultaneous determination
- drug administration
- liquid chromatography
- metabolic syndrome
- mass spectrometry
- high resolution mass spectrometry
- insulin resistance
- multiple sclerosis
- solid phase extraction
- oxidative stress
- type diabetes
- tyrosine kinase
- protein protein
- low dose
- risk assessment
- loop mediated isothermal amplification
- label free
- skeletal muscle
- gas chromatography