Yaqi Wu , Lin Zhang , Steve W. Dodd , Christian Schöneich
{"title":"Metal-induced oxidation of polysorbate 80 in the presence of hydrogen peroxide: mechanistic studies","authors":"Yaqi Wu , Lin Zhang , Steve W. Dodd , Christian Schöneich","doi":"10.1016/j.xphs.2025.103799","DOIUrl":null,"url":null,"abstract":"<div><div>Polysorbate 80 (PS80) is a commonly used surfactant in protein formulations and is highly susceptible to oxidative degradation. Here, we present mechanistic studies on metal-induced PS80 oxidation in the presence of hydrogen peroxide in acetate buffer. A total of 12 pharmaceutically relevant metal ions were tested, including Mn(II), Cu(II), Cu(I), Mg(II), Zn(II), Ca(II), Al(III), Pb(II), Sn(II), Co(II), Fe(III), Ni(II) and W(IV). The overall PS80 degradation was monitored by a fluorescence micelle assay (FMA) and the oxidation products were characterized by mass spectrometry (MS). Three metal ions, Cu(II), Co(II), and Fe(III), induced significant PS80 degradation and solutions containing these ions were subjected to further mechanistic studies. The extent of oxidation was dependent on both metal and peroxide concentrations. PS80 degradation catalyzed by Cu(II) and Co(II) was completely prevented by 250 µM and 500 µM ethylenediaminetetraacetic acid (EDTA), but only partially inhibited when catalyzed by Fe(III). The role for superoxide radical anion in the initiation of PS80 oxidation was examined by addition of Cu,Zn superoxide dismutase (SOD). The potential of the metal ions to generate free radicals was monitored with the spin trap 5,5-dimethyl-1-pyrroline N-oxide (DMPO), followed by LC-MS analysis. Degradation mechanisms, particularly the initiation of the oxidation chain reactions, are discussed for each metal.</div></div>","PeriodicalId":16741,"journal":{"name":"Journal of pharmaceutical sciences","volume":"114 7","pages":"Article 103799"},"PeriodicalIF":3.7000,"publicationDate":"2025-04-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmaceutical sciences","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022354925002564","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Polysorbate 80 (PS80) is a commonly used surfactant in protein formulations and is highly susceptible to oxidative degradation. Here, we present mechanistic studies on metal-induced PS80 oxidation in the presence of hydrogen peroxide in acetate buffer. A total of 12 pharmaceutically relevant metal ions were tested, including Mn(II), Cu(II), Cu(I), Mg(II), Zn(II), Ca(II), Al(III), Pb(II), Sn(II), Co(II), Fe(III), Ni(II) and W(IV). The overall PS80 degradation was monitored by a fluorescence micelle assay (FMA) and the oxidation products were characterized by mass spectrometry (MS). Three metal ions, Cu(II), Co(II), and Fe(III), induced significant PS80 degradation and solutions containing these ions were subjected to further mechanistic studies. The extent of oxidation was dependent on both metal and peroxide concentrations. PS80 degradation catalyzed by Cu(II) and Co(II) was completely prevented by 250 µM and 500 µM ethylenediaminetetraacetic acid (EDTA), but only partially inhibited when catalyzed by Fe(III). The role for superoxide radical anion in the initiation of PS80 oxidation was examined by addition of Cu,Zn superoxide dismutase (SOD). The potential of the metal ions to generate free radicals was monitored with the spin trap 5,5-dimethyl-1-pyrroline N-oxide (DMPO), followed by LC-MS analysis. Degradation mechanisms, particularly the initiation of the oxidation chain reactions, are discussed for each metal.
期刊介绍:
The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.