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1.
Eur Phys J E Soft Matter ; 45(7): 57, 2022 Jul 04.
Article in English | MEDLINE | ID: mdl-35781758

ABSTRACT

This work presents a study of the reciprocal dispersive power, also known as constringence or Abbe number of an aqueous solution of NaCl in a wide range of concentrations. The constringence exhibited a distinct behavior in the region close to the phase transition between a phase containing exclusively brine and a phase containing brine+halite. Molecular dynamics simulations of this system indicated the existence of halite formation below the known saturation curve, which agreed with the experimental measurements, indicating a crystal growth in the unsaturated region.


Subject(s)
Molecular Dynamics Simulation , Salts , Crystallization , Salts/chemistry , Sodium Chloride/chemistry
2.
Lasers Med Sci ; 19(2): 119-26, 2004.
Article in English | MEDLINE | ID: mdl-15340863

ABSTRACT

The use of 5-aminolevulinic acid (5-ALA) ester derivatives as precursors of endogenous protoporphyrin IX (PpIX) has been proposed as a good strategy for improved drug diffusion across biological membranes. In the present work, the 5-ALA ester derivatives hexyl-ALA (h-ALA), octyl-ALA (o-ALA), and decyl-ALA (d-ALA) were synthesized, and their efficacy to induce endogenous PpIX was explored in a murine melanoma cell line (B-16) as compared with that of 5-ALA. The maximum level of PpIX induced in cells treated with 5-ALA, h-ALA, o-ALA, and d-ALA was reached at optimal concentrations of 0.3, 0.075, 0.1, and 0.075 mM, respectively. The derivatives h-ALA and o-ALA appear as the most efficient PpIX precursors in this cell line, since a higher or similar PpIX production could be achieved with a fourfold and threefold lower dose of these precursors compared with 5-ALA. The phototoxicity effect of h-ALA and o-ALA ester derivatives showed the same phototoxicity behavior detected for 5-ALA but at much lower drug doses. Our study suggests that h-ALA and o-ALA esters improve intracellular PpIX formation in B-16 cells at reduced concentrations. This should enable clinical applications at lower precursor doses with reduced effective costs.


Subject(s)
Aminolevulinic Acid/pharmacology , Melanoma/drug therapy , Photochemotherapy/methods , Photosensitizing Agents/pharmacology , Protoporphyrins/biosynthesis , Animals , Diffusion , Dose-Response Relationship, Drug , Magnetic Resonance Spectroscopy , Mice , Microscopy, Fluorescence , Tumor Cells, Cultured
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