TY - JOUR
T1 - Spectroscopic studies of anthracyclines
T2 - Structural characterization and in vitro tracking
AU - Szafraniec, Ewelina
AU - Majzner, Katarzyna
AU - Farhane, Zeineb
AU - Byrne, Hugh J.
AU - Lukawska, Malgorzata
AU - Oszczapowicz, Irena
AU - Chlopicki, Stefan
AU - Baranska, Malgorzata
N1 - Publisher Copyright:
© 2016
PY - 2016/12/5
Y1 - 2016/12/5
N2 - A broad spectroscopic characterization, using ultraviolet–visible (UV–vis) and Fourier transform infrared absorption as well as Raman scattering, of two commonly used anthracyclines antibiotics (DOX) daunorubicin (DNR), their epimers (EDOX, EDNR) and ten selected analogs is presented. The paper serves as a comprehensive spectral library of UV–vis, IR and Raman spectra of anthracyclines in the solid state and in solution. The particular advantage of Raman spectroscopy for the measurement and analysis of individual antibiotics is demonstrated. Raman spectroscopy can be used to monitor the in vitro uptake and distribution of the drug in cells, using both 488 nm and 785 nm as source wavelengths, with submicrometer spatial resolution, although the cellular accumulation of the drug is different in each case. The high information content of Raman spectra allows studies of the drug-cell interactions, and so the method seems very suitable for monitoring drug uptake and mechanisms of interaction with cellular compartments at the subcellular level.
AB - A broad spectroscopic characterization, using ultraviolet–visible (UV–vis) and Fourier transform infrared absorption as well as Raman scattering, of two commonly used anthracyclines antibiotics (DOX) daunorubicin (DNR), their epimers (EDOX, EDNR) and ten selected analogs is presented. The paper serves as a comprehensive spectral library of UV–vis, IR and Raman spectra of anthracyclines in the solid state and in solution. The particular advantage of Raman spectroscopy for the measurement and analysis of individual antibiotics is demonstrated. Raman spectroscopy can be used to monitor the in vitro uptake and distribution of the drug in cells, using both 488 nm and 785 nm as source wavelengths, with submicrometer spatial resolution, although the cellular accumulation of the drug is different in each case. The high information content of Raman spectra allows studies of the drug-cell interactions, and so the method seems very suitable for monitoring drug uptake and mechanisms of interaction with cellular compartments at the subcellular level.
KW - Anthracyclines
KW - Doxorubicin in vitro
KW - Drug-cell interactions
KW - FT-IR spectroscopy
KW - Raman spectroscopy
KW - UV–Vis spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=84976565699&partnerID=8YFLogxK
U2 - 10.1016/j.saa.2016.06.035
DO - 10.1016/j.saa.2016.06.035
M3 - Article
C2 - 27372511
AN - SCOPUS:84976565699
SN - 1386-1425
VL - 169
SP - 152
EP - 160
JO - Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
JF - Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
ER -