Title of article :
Interaction of cationic phosphorus dendrimers (CPD) with charged and neutral lipid membranes
Author/Authors :
Ionov، نويسنده , , Maksim and Gardikis، نويسنده , , Konstantinos and Wrَbel، نويسنده , , Dominika and Hatziantoniou، نويسنده , , Sophia and Mourelatou، نويسنده , , Helena and Majoral، نويسنده , , Jean-Pierre and Klajnert، نويسنده , , Barbara and Bryszewska، نويسنده , , Maria and Demetzos، نويسنده , , Costas، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
5
From page :
8
To page :
12
Abstract :
Despite the rapid development of modern pharmaceutics, delivery of drugs to sites of action is not always effective. The research on new targeting delivery systems of pharmacologically active molecules is of great importance. e properties such as surface charge of drug delivery particles frequently define their pharmacokinetic profile; hence the efficiency of drugs can be increased by application of nanoparticles having appropriate surface properties. m of the present work was to study the interactions of cationic phosphorus-containing dendrimers (CPD) with model lipid membranes with no charge or bearing surface charge. The interactions of two generations of phosphorus dendrimers on the thermotropic behavior of model lipid membranes composed of DMPC (uncharged) or DMPC/DPPG (negatively charged) were studied using differential scanning calorimetry (DSC). The results of this study showed that CPDs can alter the thermotropic behaviour of the bilayer by reducing the cooperativity of phospholipids and this effect strongly depends on membrane surface charge. The information resulting from this study may be applied to the rational design of new drug carriers combining liposomal and dendrimeric technology.
Keywords :
DSC , Surface charge , Phosphorus-containing dendrimers , Model lipid membranes , Liposome–dendrimer interactions
Journal title :
Colloids and Surfaces B Biointerfaces
Serial Year :
2011
Journal title :
Colloids and Surfaces B Biointerfaces
Record number :
1972145
Link To Document :
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