A novel fluorescent "turn-on" chemosensor for nanomolar detection of Fe(III) from aqueous solution and its application in living cells imaging

Biosensors and Bioelectronics

Volumn 61, Issue , 2014, Pages 612-617

  Nandre, Jitendra ^a   Patil, Samadhan ^a   Patil, Vijay ^a   Yu, Fabiao ^b   Chen, Lingxin ^b   Sahoo, Suban ^c   Prior, Timothy ^d   Redshaw, Carl ^d   Mahulikar, Pramod ^a   Patil, Umesh ^a  

^a NORTH MAHARASHTRA UNIVERSITY   (India)

^b YANTAI INSTITUTE OF COASTAL ZONE RESEARCH   (China)

^c SARDAR VALLABHBHAI NATIONAL INSTITUTE OF TECHNOLOGY   (India)

^d UNIVERSITY OF HULL   (United Kingdom)

Author keywords

Benzo thiazolo pyrimidine; Fluorescent "turn on" sensor; ICT; Live cells imaging; PET

Indexed keywords

AROMATIC COMPOUNDS; CELL CULTURE; CELLS; FLUORESCENCE; IMAGING TECHNIQUES; PHYSIOLOGY; POLYETHYLENE TEREPHTHALATES; SENSORS;

BENZO-THIAZOLO-PYRIMIDINE; CARCINOMA CELL LINES; FLUORESCENCE ENHANCEMENT; HOST GUEST COMPLEXES; ICT; LIVE CELL; PHOTO-INDUCED ELECTRON TRANSFER; TURN-ON SENSORS;

IRON COMPOUNDS;

BENZO THIAZOLO PYRIMIDINE; FERRIC ION; GLYCOSIDASE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG; FLUORESCENT DYE; IRON; THIAZOLE DERIVATIVE; THIAZOLO(3,2-A)PERIMIDINE;

ARTICLE; CONFOCAL MICROSCOPY; CONTROLLED STUDY; ELECTRON TRANSPORT; ENZYME INHIBITION; FLAME PHOTOMETRY; FLUORESCENCE ANALYSIS; HEPG2 CELL LINE; HL 7701 CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; INHIBITION KINETICS; LIMIT OF DETECTION; LIMIT OF QUANTITATION; LIVER CELL; QUALITATIVE ANALYSIS; QUANTITATIVE ANALYSIS; SENSITIVITY ANALYSIS; STOICHIOMETRY; STRUCTURE ANALYSIS; ULTRAVIOLET RADIATION; CELL LINE; CELL SURVIVAL; CHEMISTRY; CYTOLOGY; FLUORESCENCE IMAGING; FLUORESCENCE MICROSCOPY; LIVER; PROCEDURES; SPECTROFLUOROMETRY;

CELL LINE; CELL SURVIVAL; FERRIC COMPOUNDS; FLUORESCENT DYES; HEP G2 CELLS; HUMANS; IRON; LIMIT OF DETECTION; LIVER; MICROSCOPY, FLUORESCENCE; OPTICAL IMAGING; SPECTROMETRY, FLUORESCENCE; THIAZOLES;

EID: 84902972848     PISSN: 09565663     EISSN: 18734235     Source Type: Journal    
DOI: 10.1016/j.bios.2014.06.017     Document Type: Article

References (19)

1. Au-Yeung H.Y., Chan J., Chantarojsiri T., Chang C.J. J. Am. Chem. Soc. 2013, 135:15165-15173.
2. Cairo G., Pietrangelo A. Biochem. J. 2000, 352:241-250.
3. Callan J.F., Silva A.P., Magri D.C. Tetrahedron 2005, 61:8551-8588.
4. Chen X., Pradhan T., Wang F., Kim J.S., Yoon J. Chem. Rev. 2012, 112:1910-1956.
5. Crabtree H.H. Science 1994, 266:1591-1592.
6. Dutta M., Das D. Trends Anal. Chem. 2012, 32:113-132.
7. Fan L.F., Wayne J., Jones E. J. Am. Chem. Soc. 2006, 128:6784-6785.
8. Formica M., Fusi V., Giorgi L., Micheloni M. Coord. Chem. Rev. 2012, 256:170-192.
9. ® 2009, Gaussian Inc., Wallingford, USA.
10. Jain R., Mathur M., Sikarwar S., Mittal A. J. Environ. Manag. 2007, 85:956-964.
11. Kim H.N., Ren W.X., Kim J.S., Yoon J. Chem. Soc. Rev. 2012, 41:3210-3244.
12. Li N., Xu Q., Xia X., Wang L., Lu J., Men X. Mater. Chem. Phys. 2009, 114:339-343.
13. Li Z.-X., Zhang L.-F., Zhao W.-Y., Li X.-Y., Guo Y.-K., Yu M.-M., Liu J.-X. Inorg. Chem. Commun. 2011, 14:1656-1658.
14. Lin W., Yuan L., Cao X. Tetrahedron Lett. 2008, 49:6585-6588.
15. Lohani C.R., Kim J.-M., Lee K.-H. Bioorgan. Med. Chem. Lett. 2009, 19:6069-6073.
16. Patil V.S., Nandre K.P., Ghosh S., Rao V.J., Chopade B.A., Bhosale S.V., Bhosale S.V. Bioorgan. Med. Chem. Lett. 2012, 22:7011-7014.
17. Rochat J., Demenge P., Rerat J.C. Toxicol. Eur. Res. 1978, 1:23-26.
18. Sahoo S.K., Sharma D., Bera R.K., Crisponic G., Callan J.F. Chem. Soc. Rev. 2012, 41:7195-7227.
19. Tominaga Y., Ushirogochi A., Matsuda Y., Kobayashi G. Chem. Pharm. Bull. 1984, 32:3384-3395.