DocumentCode
3045350
Title
SERS and micro-SERS analysis of doxorubicin interaction in vitro and in living human cancer cells
Author
Norjani, Hamid ; Sharonov, Sergei ; Manfait, Michel ; Sokolov, Kostantin ; Nabiev, Igor
Author_Institution
Lab. de Spectrosc. Biomoleculaire, UFR de Pharmacie, Reims, France
Volume
1
fYear
1992
fDate
Oct. 29 1992-Nov. 1 1992
Firstpage
330
Lastpage
331
Abstract
A new technique for selective measurement of small amounts of antitumor drugs in the nucleus and cytoplasm of a living cancer cell, based on surface-enhanced Raman spectroscopy (SERS), is proposed. The ability to detect SERS signals from very diluted (up to 10-10 N) solutions of doxorubicin (DOX) as well as from its complex with DNA in vitro and in living cells, has been demonstrated. SERS spectra were obtained from a population as well as. from single living erythroleukemia K562 cells treated with DOX. The SERS spectrum obtained from nucleus of living cells correlated well with the spectrum of the in vitro complex of DOX with Calf thymus DNA. The spectrum obtained from cytoplasm is different from the spectrum of free DOX. This means that DOX in the cytoplasm has some kind of target different from its target (DNA) in the cell nucleus.
Keywords
DNA; biochemistry; biomedical measurement; cancer; cellular biophysics; drugs; molecular biophysics; surface enhanced Raman scattering; tumours; Calf thymus DNA; DNA in vitro; SERS signals; SERS spectrum; antitumor drugs; cell nucleus; cytoplasm; diluted solutions; doxorubicin interaction; in vitro complex; living human cancer cells; microSERS analysis; selective measurement; single living erythroleukemia K562 cells; surface-enhanced Raman spectroscopy; DNA; Drugs; Fluorescence; In vitro; Silver; Surface treatment;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology Society, 1992 14th Annual International Conference of the IEEE
Conference_Location
Paris
Print_ISBN
0-7803-0785-2
Electronic_ISBN
0-7803-0816-6
Type
conf
DOI
10.1109/IEMBS.1992.5760989
Filename
5760989
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