1. Academic Validation
  2. Chemical Identity and Mechanism of Action and Formation of a Cell Growth Inhibitory Compound from Polycarbonate Flasks

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

  • Anal Chem. 2018 Apr 3;90(7):4603-4610. doi: 10.1021/acs.analchem.7b05102.
Jinlin Peng Yaopeng Zhao 1 Yulong Hong Robert S Burkhalter Carrie L Hogue Elizabeth Tran Lai Wei 1 Lori Romeo Paula Dolley-Sonneville Zara Melkoumian Xinmiao Liang 1 Ye Fang
Affiliations

Affiliation

  • 1 Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics , Chinese Academy of Sciences , Dalian , Liaoning , China.
Abstract

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 3,5-dinitro-bisphenol A. Cell cycle analysis suggests that 3,5-dinitro-bisphenol A arrests CHO-S cells at the G1/Go phase. Dynamic mass redistribution assays showed that 3,5-dinitro-bisphenol A is a weak GPR35 Agonist. Analysis of the flask manufacturing process suggests that 3,5-dinitro-bisphenol A is formed via the combination of molding process with γ-sterilization. This is the first report of a Cell Culture/assay interfering leachable compound that is formed through γ-irradiation-mediated nitric oxide free radical reaction.

Figures
Products