We studied the interactions of tetracycline antibiotics, TCs, with phospholipid monolayers with the two-fold aim of elucidating the mechanism of action of TCs and to provide a first step for the realization of bio-mimetic sensor for such drugs by means of the Langmuir-Blodgett technique. Preliminary surface tension studies demonstrated that surface activity of tetracycline is moderate and dependent on the pH of the subphase. We selected three phospholipids having hydrophobic chains of the same length but differing in the polar head structures, i.e. dipalmitoylphosphatidylcholine, dipalmitoylphosphatidylethanolamine, and dipalmitoylphosphatidic acid. Surface pressure- and surface potential- area isotherms were employed to investigate the behavior of the phospholipid monolayers at the water-air interface when tetracycline was added to the aqueous subphase. Analysis of the results indicated that the electrostatic interaction is the driving force for migration of tetracycline towards the interface where localized adsorption to the head groups occurs. Nevertheless, such interactions appear to be insufficient to promote penetration of tetracycline through the hydrophobic layer.

Gambinossi, F., Mecheri, B., Nocentini, M., Puggelli, M., Caminati, G. (2004). Effect of the phospholipid head group in antibiotic-phospholipid association at water-air interface. BIOPHYSICAL CHEMISTRY, 110(1-2), 101-117 [10.1016/j.bpc.2004.01.008].

Effect of the phospholipid head group in antibiotic-phospholipid association at water-air interface

Mecheri B.;
2004-01-01

Abstract

We studied the interactions of tetracycline antibiotics, TCs, with phospholipid monolayers with the two-fold aim of elucidating the mechanism of action of TCs and to provide a first step for the realization of bio-mimetic sensor for such drugs by means of the Langmuir-Blodgett technique. Preliminary surface tension studies demonstrated that surface activity of tetracycline is moderate and dependent on the pH of the subphase. We selected three phospholipids having hydrophobic chains of the same length but differing in the polar head structures, i.e. dipalmitoylphosphatidylcholine, dipalmitoylphosphatidylethanolamine, and dipalmitoylphosphatidic acid. Surface pressure- and surface potential- area isotherms were employed to investigate the behavior of the phospholipid monolayers at the water-air interface when tetracycline was added to the aqueous subphase. Analysis of the results indicated that the electrostatic interaction is the driving force for migration of tetracycline towards the interface where localized adsorption to the head groups occurs. Nevertheless, such interactions appear to be insufficient to promote penetration of tetracycline through the hydrophobic layer.
2004
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/07 - FONDAMENTI CHIMICI DELLE TECNOLOGIE
Settore CHIM/02 - CHIMICA FISICA
English
Con Impact Factor ISI
1,2-Dipalmitoylphosphatidylcholine; Anti-Bacterial Agents; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Phosphatidic Acids; Phosphatidylethanolamines; Phospholipids; Pressure; Surface Tension; Tetracycline; Air; Water
Gambinossi, F., Mecheri, B., Nocentini, M., Puggelli, M., Caminati, G. (2004). Effect of the phospholipid head group in antibiotic-phospholipid association at water-air interface. BIOPHYSICAL CHEMISTRY, 110(1-2), 101-117 [10.1016/j.bpc.2004.01.008].
Gambinossi, F; Mecheri, B; Nocentini, M; Puggelli, M; Caminati, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/215642
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