Journal
PHARMACEUTICAL RESEARCH
Volume 34, Issue 1, Pages 84-100Publisher
SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-016-2041-y
Keywords
O-18-labeling; free lauric acid; hydrolysis; mass spectrometry; oxidation; polysorbate 20
Funding
- Genentech
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To investigate the mechanisms of polysorbate (PS) degradation with the added objective of differentiating the hydrolysis and oxidation pathways. Ultra-performance liquid chromatography mass spectrometry (UPLC-MS) was utilized to characterize all-laurate polysorbate 20 (PS20) and its degradants. O-18 stable isotope labeling was implemented to produce O-18-labeled degradation products of all-laurate PS20 in H-2 O-18, with subsequent UPLC-MS analysis for location of the cleavage site on the fatty acid-containing side chain of PS20. The analysis reveals that hydrolysis of all-laurate PS20 leads to a breakdown of the ester linkage to liberate free lauric acid, showing a distinct dependence on pH. Using a hydrophilic free radical initiator, 2,2-azobis(2-amidinopropane) dihydrochloride (AAPH) to study the oxidative degradation of all-laurate PS20, we demonstrate that free lauric acid and polyoxyethylene (POE) laurate are two major decomposition products. Measurement of O-18 incorporation into free lauric acid indicated that hydrolysis primarily led to O-18 incorporation into free lauric acid via acyl-cleavage of the fatty acid ester bond. In contrast, AAPH-exposure of all-laurate PS20 produced free lauric acid without O-18-incorporation. The O-18-labeling technique and unique degradant patterns of all-laurate PS20 described here provide a direct approach to differentiate the types of PS degradation.
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