DOES ADSORPTION ON THE SURFACE OF A SILVER COLLOID PERTURB DRUG-DNA INTERACTIONS - COMPARATIVE SERS, FT-SERS, AND RESONANCE RAMAN-STUDY OF MITOXANTRONE AND ITS DERIVATIVES

Citation
I. Nabiev et al., DOES ADSORPTION ON THE SURFACE OF A SILVER COLLOID PERTURB DRUG-DNA INTERACTIONS - COMPARATIVE SERS, FT-SERS, AND RESONANCE RAMAN-STUDY OF MITOXANTRONE AND ITS DERIVATIVES, Journal of physical chemistry, 99(5), 1995, pp. 1608-1613
Citations number
25
Categorie Soggetti
Chemistry Physical
ISSN journal
00223654
Volume
99
Issue
5
Year of publication
1995
Pages
1608 - 1613
Database
ISI
SICI code
0022-3654(1995)99:5<1608:DAOTSO>2.0.ZU;2-L
Abstract
SERS spectra of the potent antitumour agent mitoxantrone in aqueous hy drosol and in the hydrosol prepared from deuterium oxide and of its co mplexes with DNA have been recorded and compared with the correspondin g preresonance Raman (pre-RR) and FT-SERS spectra of the same species. SERS and pre-RR spectra obtained at the same excitation wavelength an d at concentrations of 5 x 10(-8) and 5 x 10(-5) M, respectively, were found to be nearly identical both in the frequencies and the relative intensities of the bands. Moreover, interactions between the drug and calf thymus DNA induced identical effects in the pre-resonance Raman, surface-enhanced Raman scattering (SERS), and Fourier transform SERS spectra of the drugs. An analysis of these spectral changes showed tha t an interaction involves preferential intercalation of the ring A and , in part, ring B of the chromophore inside the DNA double-stranded he lix. The structural specificity of the mitoxantrone intercalation has been studied by SERS analysis of the complexes between the drug and DN A duplexes [d(CpG)(9)](2) and [d(ApT)(9)](2). Mitoxantrone was found t o be intercalated preferentially within the CG-rich regions of the dou ble-stranded helix. The data show that the adsorption of the drug/DNA complex on the surface of silver hydrosol does not induce detectable p erturbations of the molecular interactions within the complex and thus demonstrate the applicability of SERS for the analysis of drug/DNA in teractions under conditions preserving the structure of the complexes and at extremely low concentrations.