The cellular uptake of liposomes is generally believed to be mediated by adsorption of liposomes onto the cell surface and subsequent endocytosis. This report examines the effect of liposome surface charge on liposomal binding and endocytosis in two different cell lines: a human ovarian carcinoma cell line (HeLa) and a murine derived mononuclear macrophage cell line (J774). The large unilamellar liposomes were composed of 1, 2-dioleolyl-sn-glycero-3-phosphatidylcholine with and without the addition of either a positively charged lipid, 1, 2-dioleoyl-3-dimethylammonium propanediol (DODAP), or a negatively charged lipid, 1,2-dioleolyl-sn-glycero-3-phosphatidylserine. In some experiments 5 mol % of the anionic PEG2000-PE or a neutral PEG lipid of the same molecular weight was added. HeLa cells were found to endocytose positively charged liposomes to a greater extent than either neutral or negatively charged liposomes. This preference was not lipid-specific since inclusion of a cationic cyanine dye, DiIC18(3), to impart positive charge in place of DODAP resulted in a similar extent of endocytosis. In contrast the extent of liposome interaction with J774 cells was greater for both cationic and anionic liposomes than for neutral liposomes. The greater uptake of positively charged liposomes by HeLa cells was also observed with sterically stabilized liposomes (PEG liposomes). Although the overall amount of endocytosis for all the PEG liposomes examined was attenuated relative to conventional liposomes, the extent of endocytosis was greatest for positively charged PEG liposomes, whereas negatively charged PEG2000-PE liposomes were hardly endocytosed by the HeLa cells. Incorporation of a neutral PEG lipid into liposomes permits the independent variation of liposome steric and electrostatic effects in a manner that may allow interactions with cells of the reticuloendothelial system to be minimized, yet permit strong interactions between liposomes and proliferating cells.

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in 1962. After spending nearly 25 years at the Eastman Kodak Research Laboratories, he joined the Department of Chemistry Faculty at the University of Arizona in early 1987. His research interests include polymerization of organized media for the triggered release of reagents and the preparation of novel materials.

Phthalocyanines (Pc) modified at eight positions with benzyloxyethoxy groups (CuPc(OC2OBz)8 and H2Pc(OC2OBz)8) form discotic mesophases in the bulk and self-assemble into cofacial rodlike aggregates in monolayers. These Pc aggregates form close packed arrays which are simple to process into highly coherent multilayer thin films. When these self-organizing molecular systems are compressed on the surface of an LB trough, the Pc columns align parallel to the compression barriers and form a rigid bilayer film (ca. 5.6 nm thick). Sections of these bilayer films can be mechanically removed from the trough surface with complete retention of integrity of the remaining film. This unprecedented behavior appears to arise from the multiple π−π interactions between adjacent Pcs, resulting in unusually strong noncovalent interactions. AFM and STM studies of monolayer and bilayer films show that they consist of Pc columns which are coherent over distances of 50−100 nm. Thin films consisting of up to 15 bilayers (ca. 84 nm) can be quickly built by a “mechanical stamping” process, and small-angle X-ray scattering characterization of these film materials confirms their unusual coherence. Large electrical and optical anisotropies are observed in multilayer films of CuPc(OC2OBz)8 and H2Pc(OC2OBz)8 which are comparable to those previously reported for thin film assemblies based on side-chain-modified silicon phthalocyanine polymers.

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