4.7 Article

Hydrazine selective dual signaling chemodosimetric probe in physiological conditions and its application in live cells

Journal

ANALYTICA CHIMICA ACTA
Volume 893, Issue -, Pages 84-90

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2015.08.041

Keywords

Chemodosimetric probe; Hydrazine; Rhodamine; Turn-on fluorescence; Cell imaging

Funding

  1. Marie Curie actions of the European Commission
  2. DST (Gov. of WB)
  3. FNRS (Belgium)
  4. Fonds Speciaux de Recherche (UCL)
  5. CSIR, New Delhi
  6. UGC, New Delhi

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A rhodamineecyanobenzene conjugate, (E)-4-((2-(3',6'-bis(diethylamino)-3-oxospiro[ isoindoline-1,9'-xanthene]- 2-yl) ethylimino) methyl) benzonitrile (1), which structure has been elucidated by single crystal X-ray diffraction, was synthesized for selective fluorescent turn-on and colorimetric recognition of hydrazine at physiological pH 7.4. It was established that 1 detects hydrazine up to 58 nM. The probe is useful for the detection of intracellular hydrazine in the human breast cancer cells MCF-7 using a fluorescence microscope. Spirolactam ring opening of 1, followed by its hydrolysis, was established as a probable mechanism for the selective sensing of hydrazine. (C) 2015 Elsevier B.V. All rights reserved.

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