CELLULAR BINDING OF HEMATOPORPHYRIN DERIVATIVE IN HUMAN BLADDER CANCER CELL LINES: KK-47

Abstract— The fluorescence lifetime and degree of fluorescence polarization of hematoporphyrin derivative (HpD) have been investigated using different solutions: organic and micellar solutions. Ham's F12 medium, and KK-47 cell suspension. The lifetime and polarization degree in organic and micellar solutions did not change with increasing incubation time, but the polarization degree in the cell suspensions temporarily increased at the initial incubation time and then decreased 4 h after incubation. The lifetime in the cell suspensions exhibited a bi-phasic exponential decay. The results obtained suggested that mainly dimeric HpD may bind weakly to the cell membrane, and then slowly be distributed throughout the cytoplasm. The polarity and viscosity of the intracellular loci containing HpD were evaluated from the fluorescence polarizations of HpD in MeOH-H₂O mixtures and ethylene glycol(EG)-MeOH mixtures. The dielectric constant and viscosity of the loci containing HpD were 35 and 11 cp, respectively. Accordingly, the intracellular location of HpD were considered relatively hydrophilic loci of the cells.     

Magnetic-field-induced deformation of lipid membranes

The substantial effects of relatively low, steady magnetic fields less than 0.5 T up to high magnetic fields up to 30 T on the membrane potential and resistance of black lipid membranes of didodecyl phosphite and dipalmitoylphosphatidylcholine (DPPC) are presented. Also, the magnetic-field-induced fusion and division of DPPC liposomes are demonstrated. Such significant magnetoresponses should result in the magnetic orientation of the lipid molecules and associated undulation of the membranes. Thus, the addition to membranes of diamagnetic aromatics having a large magnetic anisotropy enhanced the magnetoresponses: larger changes in membrane potential and resistance and a lower shift of the onset magnetic-field, with abrupt changes in liposome sizes and membrane potential.     

A laser flash photolysis study of the dynamic behaviour of radical pairs in micellar solutions under ultrahigh magnetic fields of up to 30 T

The photo-induced hydrogen abstraction reactions of benzophenone in aqueous micellar SDS and Brij 35 solutions, decafluorobenzophenone in an aqueous micellar Brij 35 solution and naphthoquinone in an aqueous micellar SDS solution were investigated at room temperature under pulsed magnetic fields of 0–29.6T. In each of these reactions, the radical pair decay rate is found to decrease with increasing field from 0 to about 3 T and to increase with increasing field above 3 T. The escape radical yield is found to increase with increasing field from 0 to about 3 T and to decrease with increasing field above 3 T. These magnetic field effects are explained in terms of the relaxation mechanism. In each of the Brij 35 micellar solution systems, the anisotropy in the g tensor of the ketyl radical and its correlation time are evaluated from the observed effects.