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1.
Photochem Photobiol ; 97(1): 71-79, 2021 01.
Article in English | MEDLINE | ID: mdl-32619275

ABSTRACT

Toluidine blue O (TBO) is a water-soluble photosensitizer that has been used in photodynamic antimicrobial and anticancer treatments, but suffers from limited solubility in hydrophobic media. In an effort to incrementally increase TBO's hydrophobicity, we describe the synthesis of hexanoic (TBOC6) and myristic (TBOC14) fatty acid derivatives of TBO formed in low to moderate percent yields by condensation with the free amine site. Covalently linking 6 and 14 carbon chains led to modifications of not only TBO's solubility, but also its photophysical and photochemical properties. TBOC6 and TBOC14 derivatives were more soluble in organic solvents and showed hypsochromic shifts in their absorption and emission bands. The solubility in phosphate buffer solution was low for both TBOC6 and TBOC14, but unexpectedly slightly greater in the latter. Both TBOC6 and TBOC14 showed decreased triplet excited-state lifetimes and singlet oxygen quantum yields in acetonitrile, which was attributed to heightened aggregation of these conjugates particularly at high concentrations due to the hydrophobic "tails." While in diluted aqueous buffer solution, indirect measurements showed similar efficiency in singlet oxygen generation for TBOC14 compared to TBO. This work demonstrates a facile synthesis of fatty acid TBO derivatives leading to amphiphilic compounds with a delocalized cationic "head" group and hydrophobic "tails" for potential to accumulate into biological membranes or membrane/aqueous interfaces in PDT applications.


Subject(s)
Fatty Acids/chemistry , Photosensitizing Agents/chemical synthesis , Photosensitizing Agents/pharmacology , Tolonium Chloride/analogs & derivatives , Molecular Structure , Photosensitizing Agents/chemistry , Singlet Oxygen/chemistry , Spectrometry, Fluorescence , Tolonium Chloride/chemical synthesis , Tolonium Chloride/pharmacology
2.
Carbohydr Polym ; 205: 533-539, 2019 Feb 01.
Article in English | MEDLINE | ID: mdl-30446137

ABSTRACT

Bacterial biofilms are widely associated with persistent infections and food contamination. High resistance to conventional antimicrobial agents resulted in an urgent need for novel formulation to eliminate these bacterial communities. Herein we fabricated light controllable chitosan micelles loading with thymol (T-TCP) for elimination of biofilm. Due to the exterior chitosan, T-TCP micelles easily bind to negative biofilm through electrostatic interaction and efficiently deliver the essential oil payloads. Under irradiation, T-TCP micelles generated ROS, which triggered simultaneous thymol release and also resulted in additional ROS-inducing bactericidal effects, both effectively eradicating biofilms of Listeria monocytogenes and Staphylococcus aureus. This formulation provided a platform for other water-insoluble antimicrobials and might be used as a potent and controllable solution to biofilm fighting.


Subject(s)
Biofilms/drug effects , Chitosan/analogs & derivatives , Chitosan/chemistry , Drug Carriers/chemistry , Micelles , Thymol/pharmacology , Chitosan/chemical synthesis , Chitosan/radiation effects , Drug Carriers/chemical synthesis , Drug Carriers/radiation effects , Drug Liberation/radiation effects , Hydrophobic and Hydrophilic Interactions , Light , Listeria monocytogenes/physiology , Oils, Volatile/pharmacology , Polymers/chemical synthesis , Polymers/chemistry , Polymers/radiation effects , Reactive Oxygen Species , Staphylococcus aureus/physiology , Sulfides/chemical synthesis , Sulfides/chemistry , Sulfides/radiation effects , Tolonium Chloride/chemical synthesis , Tolonium Chloride/chemistry , Tolonium Chloride/radiation effects
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