4.8 Article

Chemical Identity and Mechanism of Action and Formation of a Cell Growth Inhibitory Compound from Polycarbonate Flasks

Journal

ANALYTICAL CHEMISTRY
Volume 90, Issue 7, Pages 4603-4610

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.7b05102

Keywords

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Funding

  1. State Key Program of National Natural Science of China [U1508221]
  2. External Cooperation Program of BIC, Chinese Academy of Science [121421KYSB20130013]

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This paper reports the chemical identity and mechanism of action and formation of a cell growth inhibitory compound leached from some single-use Erlenmeyer polycarbonate shaker flasks under routine cell culture conditions. Single-use cell culture vessels have been increasingly used for the production of biopharmaceuticals; however, they often suffer from issues associated with leachables that may interfere with cell growth and protein stability. Here, high-performance liquid-chromatography preparations and cell proliferation assays led to identification of a compound from the water extracts of some polycarbonate flasks, which exhibited subline- and seeding density-dependent growth inhibition of CHO cells in suspension culture. Mass spectroscopy, nuclear magnetic resonance spectroscopy, and chemical synthesis confirmed that this compound is 3,S-dinitro-bisphenol A. Cell cycle analysis suggests that 3,5-dinitro-bisphenol A arrests CHO-S cells at the G(1)/G(0) phase. Dynamic mass redistribution assays showed that 3,5-dinitro-bisphenol A is a weak GPR3S agonist. Analysis of the flask manufacturing process suggests that 3,5-dinitro-bisphenol A is formed via the combination of molding process with gamma-sterilization. This is the first report of a cell culture/assay interfering leachable compound that is formed through gamma-irradiation-mediated nitric oxide free radical reaction.

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