Biomedical Engineering and Bioengineering Commons^™

Interaction Of Ciprofloxacin Loaded Liposomes With Pseudomonas Aeruginosa Cells, R. Nicholov, A. E. Khoury, A. W. Bruce, F. Dicosmo

Cells and Materials

An antibiotic delivery system has been developed using ciprotloxacin (CIPRO) encapsulated within sonicated unilamellar vesicles (SUV) of different lipid compositions composed of dipalmitoylphospatidylcholine (DPPC), L-aphosphatidylcholine (PC), phosphatidylethanolamine (PEA) and cholesterol (CHOL). The interaction of SUV (i.e. liposomes) with Pseudomonas aeruginosa (Tl 2977) cells was studied and the effect of the liposome encapsulated antibiotic was tested. Encapsulation of CIPRO apparently increased the amount of antibiotic resident in the vicinity of bacteria in aqueous solution at neutral pH.

Electrophoretic mobility measurements showed that P. aeruginosa cells were negatively charged. The zeta potential of P. aeruginosa was -11.4 ± 2.9 m V in …

Interaction Of Liposomal Drug Delivery Systems With Cells And Tissues: Microscopic Studies, M. Foldvari, G. T. Faulkner, C. Mezei, M. Mezei

Cells and Materials

Liposomes , as drug carriers, can be administered into the body by several routes e.g. intravenously, intraperitoneally, intramuscularly, intratracheally and topically among others. Radiolabelled markers are suitable to monitor the distribution and elimination of liposomes, but the tissue deposition of intact liposomes, the mode and sites of drug release from the liposomes and liposome-cell interactions cannot be investigated morphologically. Microscopic techniques could provide information regarding the intact state of liposomes and possibly the dynamics of liposomes in tissues provided that they can be identified with certainty in vivo. This is a formidable problem and in spite of several attempts, there …