TY - JOUR
TI - A new Chimeric Drug Delivery nano System (chi-aDDnS) composed of PAMAM G 3.5 dendrimer and liposomes as Doxorubicin's carrier. In vitro pharmacological studies
AU - Gardikis, K.
AU - Fessas, D.
AU - Signorelli, M.
AU - Dimas, K.
AU - Tsimplouli, C.
AU - Ionov, M.
AU - Demetzos, C.
JO - Journal of Nanoscience and Nanotechnology
PY - 2011
VL - 11
TODO - 5
SP - 3764-3772
PB - 
SN - 1533-4880, 1533-4899
TODO - 10.1166/jnn.2011.3847
TODO - Cancer cell lines;  Chimeric advanced Drug Delivery NanoSystem (chi-aDDnS);  Combination process;  Dendrimer molecules;  Doxorubicin;  Drug carrier;  In vitro cytotoxicity;  In-vitro;  In-vivo;  Liposomal membranes;  Nanobiomaterials;  PAMAM;  Pharmacological properties;  Release rate;  Strong interaction, Cell culture;  Dendrimers;  Differential scanning calorimetry;  Drug delivery;  Fluorescence spectroscopy;  Liposomes;  Phospholipids, Nanosystems, antineoplastic agent;  dendrimer;  doxorubicin;  liposome, article;  drug delivery system;  human;  membrane fluidity;  nanotechnology;  tumor cell line, Antineoplastic Agents;  Cell Line, Tumor;  Dendrimers;  Doxorubicin;  Drug Delivery Systems;  Humans;  Liposomes;  Membrane Fluidity;  Nanotechnology
TODO - Chimeric advanced Drug Delivery nano Systems (chi-aDDnSs) could be defined as mixed nanosystems due to the combination process of nanobiomaterials and can offer advantages as drug carriers. The role of the release modulator from the liposomal system is undertaken by the dendrimer molecules leading to new pharmacokinetic and, probably, pharmacological properties of the chimeric system. In this work, a conventional DOPC/DPPG liposomal system and a new chiaDDnS composed of liposomes (DOPC/DPPG) incorporating PAMAM G3,5 has been developed, Doxorubicin (Dox) was loaded in the systems and the final formulations were lyophilized. The physicochemical (spectroscopic and calorimetric) investigation concerning the chi-aDDnS, revealed a strong interaction between both lipophilic and hydrophilic parts of the liposomal membrane and the dendrimer, with the induction of multiple energetic states. These states are probably the basis of higher Dox encapsulation and slower release rate compared to the respective conventional liposome. These results, in conjunction with the increase in TI observed in two investigated cancer cell lines (i.e., MB231 and MCF7), compared to the respective conventional liposomal system and to the free Dox, make this new chi-aDDnS the basic candidate for further in vivo investigations. Copyright © 2011 American Scientific Publishers All rights reserved.
ER -