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Strong binding and fluorescence sensing of bisphosphonates by guanidinium-modified calix[5]arene.
Gao, Jie; Zheng, Zhe; Shi, Lin; Wu, Si-Qi; Sun, Hongwei; Guo, Dong-Sheng.
Affiliation
  • Gao J; College of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China.
  • Zheng Z; College of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China.
  • Shi L; College of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China.
  • Wu SQ; College of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China.
  • Sun H; College of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China.
  • Guo DS; College of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China.
Beilstein J Org Chem ; 14: 1840-1845, 2018.
Article in En | MEDLINE | ID: mdl-30112088
ABSTRACT
Based on the indicator displacement assay (IDA) approach, we herein report the fluorescence "switch-on" sensing and quantitative detection of bisphosphonates (BPs), a class of drugs extensively used in the treatment of patients with various skeletal diseases. Guanidinium-modified calix[5]arene (GC5A) affords strong binding on the micromolar to nanomolar level towards BPs dominantly via multiple salt bridge interactions, which was evaluated by fluorescence competitive titrations. Fluorescent IDA enables the highly sensitive and label-free detection of BPs in buffer solution, and more importantly, in artificial urine. Calibration lines were therefore set up in untreated artificial urine, allowing for quantifying the concentrations of BPs in the biologically relevant low range.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Beilstein J Org Chem Year: 2018 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Beilstein J Org Chem Year: 2018 Document type: Article Affiliation country: China