Evaluation of pegylated lipid nanocapsules versus complement system activation and macrophage uptake.
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J. Benoit | C. Passirani | A. Vonarbourg | J. Leroux | P. Saulnier | J P Benoit | C Passirani | P Simard | A Vonarbourg | P Saulnier | J C Leroux | P. Simard
[1] Lisbeth Illum,et al. Long circulating microparticulate drug carriers , 1995 .
[2] R. Müller,et al. Surface characteristics and the interaction of colloidal particles with mouse peritoneal macrophages. , 1987, Biomaterials.
[3] T. Kinoshita. Biology of complement: the overture. , 1991, Immunology today.
[4] J. Benoit,et al. The influence of lipid nanocapsule composition on their size distribution. , 2003, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[5] Devine,et al. The complement system in liposome clearance: Can complement deposition be inhibited? , 1998, Advanced drug delivery reviews.
[6] M. Papisov,et al. Why do Polyethylene Glycol-Coated Liposomes Circulate So Long?: Molecular Mechanism of Liposome Steric Protection with Polyethylene Glycol: Role of Polymer Chain Flexibility , 1994 .
[7] S. Moghimi,et al. Capture of stealth nanoparticles by the body's defences. , 2001, Critical reviews in therapeutic drug carrier systems.
[8] I. Rubinstein,et al. VIP receptors as molecular targets of breast cancer: implications for targeted imaging and drug delivery. , 2001, Journal of controlled release : official journal of the Controlled Release Society.
[9] J. Benoit,et al. Biodistribution of dual radiolabeled lipidic nanocapsules in the rat using scintigraphy and gamma counting. , 2002, International journal of pharmaceutics.
[10] J. Kreuter,et al. Colloidal Drug Delivery Systems , 1994 .
[11] D. Bazile,et al. Effect of PEO surface density on long-circulating PLA-PEO nanoparticles which are very low complement activators. , 1996, Biomaterials.
[12] Phagocytosis in vitro of polyethylene glycol-modified liposome-encapsulated hemoglobin by human peripheral blood monocytes plus macrophages through scavenger receptors. , 2001, Life sciences.
[13] S. Nagaoka,et al. Interaction Between Blood Components and Hydrogels With Poly(Oxyethylene) Chains , 1984 .
[14] J. Benoit,et al. A Novel Phase Inversion-Based Process for the Preparation of Lipid Nanocarriers , 2002, Pharmaceutical Research.
[15] Hideyoshi Harashima,et al. Enhanced Hepatic Uptake of Liposomes Through Complement Activation Depending on the Size of Liposomes , 1994, Pharmaceutical Research.
[16] Feng Liu,et al. Antibody Dependent, Complement Mediated Liver Uptake of Liposomes Containing GM1 , 2004, Pharmaceutical Research.
[17] J Szebeni,et al. Stealth liposomes and long circulating nanoparticles: critical issues in pharmacokinetics, opsonization and protein-binding properties. , 2003, Progress in lipid research.
[18] J. Benoit,et al. Complement Activation by Injectable Colloidal Drug Carriers , 2004 .
[19] P. Ralph,et al. Functional macrophage cell lines transformed by abelson leukemia virus , 1978, Cell.
[20] E. Roux,et al. Novel Long-Circulating Lipid Nanocapsules , 2004, Pharmaceutical Research.
[21] D. Fischer,et al. Surface-modified biodegradable albumin nano- and microspheres. II: effect of surface charges on in vitro phagocytosis and biodistribution in rats. , 1998, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[22] Joseph D. Andrade,et al. Protein—surface interactions in the presence of polyethylene oxide , 1991 .
[23] D. Devine,et al. Liposome-complement interactions in rat serum: implications for liposome survival studies. , 1994, Biochimica et biophysica acta.
[24] R L Juliano,et al. The effect of particle size and charge on the clearance rates of liposomes and liposome encapsulated drugs. , 1975, Biochemical and biophysical research communications.
[25] Papisov. Theoretical considerations of RES-avoiding liposomes: Molecular mechanics and chemistry of liposome interactions. , 1998, Advanced drug delivery reviews.
[26] S. Davis,et al. The effect of surface coverage and conformation of poly(ethylene oxide) (PEO) chains of poloxamer 407 on the biological fate of model colloidal drug carriers. , 2001, Biochimica et biophysica acta.
[27] M. Kazatchkine,et al. Specific antibodies enhance Sephadex-induced activation of the alternative complement pathway in human serum. , 1988, Biomaterials.
[28] Alving Cr,et al. Antibodies to cholesterol, cholesterol conjugates and liposomes: implications for atherosclerosis and autoimmunity. , 1991 .
[29] O. Bourdon,et al. Relationship between complement activation, cellular uptake and surface physicochemical aspects of novel PEG-modified nanocapsules. , 2001, Biomaterials.
[30] A. Hoffman,et al. Water Structure of PEG Solutions by Differential Scanning Calorimetry Measurements , 1992 .
[31] C. Passirani,et al. Interactions of nanoparticles bearing heparin or dextran covalently bound to poly(methyl methacrylate) with the complement system. , 1998, Life sciences.
[32] K. Goodrum,et al. Complement Component C3 Secretion by Mouse Macrophage‐Like Cell Lines , 1987, Journal of leukocyte biology.
[33] M. Bodó,et al. The interaction of liposomes with the complement system: in vitro and in vivo assays. , 2003, Methods in enzymology.
[34] J. Benoit,et al. Electrokinetic properties of noncharged lipid nanocapsules: Influence of the dipolar distribution at the interface , 2005, Electrophoresis.
[35] V. Kolb-Bachofen,et al. Coating particles with a block co-polymer (poloxamine-908) suppresses opsonization but permits the activity of dysopsonins in the serum. , 1993, Biochimica et biophysica acta.