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Development of an anti-methoxy poly(ethylene glycol) (α-mPEG) cell-based capture system to measure mPEG and mPEGylated molecules

  • Kuo Hsiang Chuang
  • , Chien Han Kao
  • , Steve R. Roffler
  • , Ssu Jung Lu
  • , Ta Chun Cheng
  • , Yun Ming Wang
  • , Chih Hung Chuang
  • , Yuan Chin Hsieh
  • , Yeng Tseng Wang
  • , Jaw Yuan Wang
  • , Kuo Yi Weng
  • , Tian Lu Cheng

研究成果: 雜誌貢獻文章同行評審

11   連結會在新分頁中打開 引文 斯高帕斯(Scopus)

摘要

Quantitative pharmacokinetic analysis of methoxy-poly(ethylene glycol) (mPEG) and mPEGylated molecules is important for clinical drug development. Here we developed sensitive sandwich and competitive ELISAs by expressing an anti-mPEG antibody on the surface of fibroblasts for effective capture of mPEG molecules in biological samples. α-mPEG sandwich ELISA could quantify the higher-molecular-weight of mPEG (2, 5, and 20 kDa) and mPEGylated molecules. α-mPEG cell-based competitive ELISA was developed to measure the lower-molecular-weight of mPEG molecules (559, 750, and 1000 Da) at nanomolar levels. In addition, α-mPEG cell-based ELISA was unaffected by the presence of 10% human serum or murine serum. We further demonstrate that the α-mPEG cell-based ELISA determined similar pharmacokinetics of mPEG5K as traditional gamma counting of 131I-mPEG5K. The α-mPEG cell-based ELISA may provide an accurate, high sensitivity and easy-to-use tool for directly measuring mPEG and mPEGylated molecules in complex biological samples to accelerate the clinical development of mPEG drugs.

原文英語
頁(從 - 到)6880-6888
頁數9
期刊Macromolecules
47
發行號19
DOIs
出版狀態已發佈 - 10月 14 2014

ASJC Scopus subject areas

  • 材料化學
  • 聚合物和塑料
  • 無機化學
  • 有機化學

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