TY - JOUR
T1 - In vitro evaluation of ion-exchange microspheres for the sustained release of liposomal-adenoviral conjugates.
AU - Steel, Jason
AU - Cavanagh, Heather
AU - Burton, Mark
AU - Dingwall, Daniel
AU - Kalle, Wouter
N1 - Imported on 12 Apr 2017 - DigiTool details were: Journal title (773t) = Journal of Controlled Release. ISSNs: 0168-3659;
PY - 2004
Y1 - 2004
N2 - This study looks at the development of a novel combination vector consisting of adenovirus conjugated to liposomes (AL complexes) bound to cation-exchanging microspheres (MAL complexes). With adenovirus having a net negative charge and the liposomes a net positive charge it was possible to modify the net charge of the AL complexes by varying the concentrations of adenovirus to liposomes. The modification of the net charge resulted in altered binding and release characteristics. Of the complexes tested, the 5:1 and 2:1 ratio AL complexes were able to be efficiently bound by the microspheres and exhibited sustained release over 24 h. The 1:1 and 1:2 AL complexes, however, bound poorly to the microspheres and were rapidly released. In addition the MAL complexes also were able to reduce the toxicity of the AL complexes, which was seen with the 10:1 ratio. The AL complexes showed considerably more toxicity alone than in combination with microspheres, highlighting a potential benefit of this vector.
AB - This study looks at the development of a novel combination vector consisting of adenovirus conjugated to liposomes (AL complexes) bound to cation-exchanging microspheres (MAL complexes). With adenovirus having a net negative charge and the liposomes a net positive charge it was possible to modify the net charge of the AL complexes by varying the concentrations of adenovirus to liposomes. The modification of the net charge resulted in altered binding and release characteristics. Of the complexes tested, the 5:1 and 2:1 ratio AL complexes were able to be efficiently bound by the microspheres and exhibited sustained release over 24 h. The 1:1 and 1:2 AL complexes, however, bound poorly to the microspheres and were rapidly released. In addition the MAL complexes also were able to reduce the toxicity of the AL complexes, which was seen with the 10:1 ratio. The AL complexes showed considerably more toxicity alone than in combination with microspheres, highlighting a potential benefit of this vector.
U2 - 10.1016/j.jconrel.2004.01.001
DO - 10.1016/j.jconrel.2004.01.001
M3 - Article
SN - 0168-3659
VL - 95
SP - 601
EP - 611
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 3
ER -