Studies of serum protein adsorption at phospholipid surfaces in relation to intravenous drug delivery

Abstract The adsorption of serum proteins at phospholipid surfaces was investigated in relation to the uptake of intravenously administered colloidal drug carriers. In particular, an approach based on the use of surface-modified flat substrates for investigations of the adsorption pattern by in situ ellipsometry and surface plasmon resonance (SPR) is discussed. Similar results regarding protein adsorption were obtained for phospholipid layers prepared through spin-coating, Langmuir–Blodgett deposition, and liposome adsorption. Furthermore, a good agreement was found between the adsorption at the model surfaces, on one hand, and at oil-in-water emulsion droplets, on the other, suggesting that curvature effects on the adsorption are minor. By using this approach, the adsorption of a number of proteins at a range of surfaces was investigated. Also, mixed (phospho)lipid layers were studied, as was the adsorption from diluted serum and plasma. The results obtained are discussed in relation to the effects of the surface properties on the performance of colloidal drug carriers.

[1]  M. Malmsten,et al.  Electrostatic Effects on Interfacial Film Formation in Emulsion Systems , 1996 .

[2]  M. Malmsten,et al.  Competitive protein adsorption at phospholipid surfaces , 1995 .

[3]  G Blume,et al.  Liposomes for the sustained drug release in vivo. , 1990, Biochimica et biophysica acta.

[4]  G. Whitesides,et al.  Formation of monolayer films by the spontaneous assembly of organic thiols from solution onto gold , 1989 .

[5]  W. Norde,et al.  Adsorption of proteins from solution at the solid-liquid interface. , 1986, Advances in colloid and interface science.

[6]  V. Torchilin,et al.  Coating liposomes with protein decreases their capture by macrophages , 1980, FEBS letters.

[7]  S. Davis,et al.  The influence of emulsifying agents on the phagocytosis of lipid emulsions by macrophages , 1985 .

[8]  M. Malmsten Protein adsorption at phospholipid surfaces , 1995 .

[9]  M. Malmsten Ellipsometry Studies of Protein Adsorption at Lipid Surfaces , 1994 .

[10]  H. Hemker,et al.  The adsorption of prothrombin to phospholipid monolayers quantitated by ellipsometry. , 1984, The Journal of biological chemistry.

[11]  Y. Ikada,et al.  Phagocytosis of polymer microspheres by macrophages , 1990 .

[12]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[13]  P. Cullis,et al.  Influence of cholesterol on the association of plasma proteins with liposomes. , 1996, Biochemistry.

[14]  M. Malmsten,et al.  Adsorption of Complement Proteins C3 and C1q , 1996 .

[15]  H. Gresham,et al.  Large scale isolation of functionally active components of the human complement system. , 1981, The Journal of biological chemistry.

[16]  M. Malmsten,et al.  Adsorption of Poly(Ethylene Glycol) Amphiphiles to Form Coatings Which Inhibit Protein Adsorption , 1996 .

[17]  T M Allen,et al.  Liposomes containing synthetic lipid derivatives of poly(ethylene glycol) show prolonged circulation half-lives in vivo. , 1991, Biochimica et biophysica acta.

[18]  S. Semple,et al.  Liposome-Blood Protein Interactions in Relation to Liposome Clearance , 1996 .

[19]  H. Hemker,et al.  Membrane-mediated assembly of the prothrombinase complex. , 1991, The Journal of biological chemistry.

[20]  Martin Malmsten,et al.  Ellipsometry Studies of Protein Layers Adsorbed at Hydrophobic Surfaces , 1994 .

[21]  D. Papahadjopoulos,et al.  Recognition of liposomes by cells: in vitro binding and endocytosis mediated by specific lipid headgroups and surface charge density. , 1992, Biochimica et biophysica acta.

[22]  F. Veer,et al.  Ellipsometry as a tool to study the adsorption behavior of synthetic and biopolymers at the air–water interface , 1978 .

[23]  P. Cullis,et al.  Association of blood proteins with large unilamellar liposomes in vivo. Relation to circulation lifetimes. , 1992, The Journal of biological chemistry.

[24]  M. Malmsten,et al.  Ellipsometry Studies of Interfacial Film Formation in Emulsion Systems , 1995 .

[25]  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.

[26]  D. Small The Physical Chemistry of Lipids , 1986 .

[27]  P. Cullis,et al.  β2-Glycoprotein I Is a Major Protein Associated with Very Rapidly Cleared Liposomes in Vivo, Suggesting a Significant Role in the Immune Clearance of "Non-self" Particles (*) , 1995, The Journal of Biological Chemistry.

[28]  T. Allen The use of glycolipids and hydrophilic polymers in avoiding rapid uptake of liposomes by the mononuclear phagocyte system , 1994 .

[29]  V. Torchilin,et al.  Influence of the steric barrier activity of amphipathic poly(ethyleneglycol) and ganglioside GM1 on the circulation time of liposomes and on the target binding of immunoliposomes in vivo , 1991, FEBS letters.

[30]  G. Gregoriadis,et al.  Tissue distribution of liposomes exhibiting long half-lives in the circulation after intravenous injection. , 1985, Biochimica et biophysica acta.

[31]  H M Patel,et al.  Serum opsonins and liposomes: their interaction and opsonophagocytosis. , 1992, Critical reviews in therapeutic drug carrier systems.

[32]  P. Cullis,et al.  Separation of large unilamellar liposomes from blood components by a spin column procedure: towards identifying plasma proteins which mediate liposome clearance in vivo. , 1991, Biochimica et biophysica acta.

[33]  Muller,et al.  Sequential Adsorption of Human Serum Albumin (HSA), Immunoglobulin G (IgG), and Fibrinogen (Fgn) at HMDSO Plasma Polymer Surfaces , 1997, Journal of colloid and interface science.

[34]  H. Hemker,et al.  Monitoring of unbound protein in vesicle suspensions with off-null ellipsometry. , 1993, Biochimica et biophysica acta.

[35]  P. Cullis,et al.  Ganglioside GM1 and Hydrophilic Polymers Increase Liposome Circulation Times by Inhibiting the Association of Blood Proteins , 1992 .

[36]  C. Haynes,et al.  Globular proteins at solid/liquid interfaces , 1994 .

[37]  D. Papahadjopoulos Fate of Liposomes In Vivo: A Brief Introductory Review , 1996 .

[38]  Michel Veillard,et al.  Non-stealth (poly(lactic acid/albumin)) and stealth (poly(lactic acid-polyethylene glycol)) nanoparticles as injectable drug carriers , 1995 .

[39]  B. Liedberg,et al.  Surface plasmon resonance for gas detection and biosensing , 1983 .

[40]  J. M. Harris,et al.  Poly(Ethylene Glycol) Chemistry , 1992 .

[41]  M. Malmsten,et al.  Adsorption of Apolipoprotein B at Phospholipid Model Surfaces , 1995 .

[42]  J. M. Harris,et al.  Poly(Ethylene Glycol) Chemistry Biotechnical and Biomedical Applications , 1992 .

[43]  M. Malmsten,et al.  Competitive Adsorption at Hydrophobic Surfaces from Binary Protein Systems , 1994 .

[44]  J. Israelachvili Intermolecular and surface forces , 1985 .

[45]  Kazuo Maruyama,et al.  Amphipathic polyethyleneglycols effectively prolong the circulation time of liposomes , 1990, FEBS letters.

[46]  M. Malmsten,et al.  Formation of Adsorbed Protein Layers. , 1998, Journal of colloid and interface science.