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[[File:Gene_delivery_liposome_with_phospholipid_bilayers.png|thumb|250px|right|Gene delivery liposome with phospholipid bilayers]] | [[File:Gene_delivery_liposome_with_phospholipid_bilayers.png|thumb|250px|right|Gene delivery liposome with phospholipid bilayers]] | ||
'''Liposome extruders''' are mainly used for the liposome formulation and achieving uniform size distributions. It is an ideal instrument to generate nanoscale liposome formulations, and to prepare exosomes and artificial cell membranes. By utilizing the tracked-etched filter membranes, the liposome extruders are capable of capturing large particles, precipitation and achieving sterile filtration. | '''Liposome extruders''' are mainly used for the liposome formulation and achieving uniform size distributions. It is an ideal instrument to generate nanoscale liposome formulations, and to prepare exosomes and artificial cell membranes. By utilizing the tracked-etched filter membranes, the liposome extruders are capable of capturing large particles, precipitation and achieving sterile filtration. | ||
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A liposome is a spherical-shaped vesicle composed of phospholipid bilayers. Phospholipid bilayers are critical components of cell membranes, with hydrophilic and hydrophobic properties. In an aqueous solution, the hydrophobic ends tend to bind to each other, and spontaneously form small spherical liposomes. The liposome extruder is designed for the preparation of liposomes. It is easy to use, and has high precision particle size control ability with narrow distributions and satisfactory repeatability. So far it has been widely used in the preparations of complex injectable products, such as paclitaxel liposomes, adriamycin liposomes, amphotericin B liposomes, doxorubicin liposomes, cytarabine liposomes, and irinotecan liposomes. | A liposome is a spherical-shaped vesicle composed of phospholipid bilayers. Phospholipid bilayers are critical components of cell membranes, with hydrophilic and hydrophobic properties. In an aqueous solution, the hydrophobic ends tend to bind to each other, and spontaneously form small spherical liposomes. The liposome extruder is designed for the preparation of liposomes. It is easy to use, and has high precision particle size control ability with narrow distributions and satisfactory repeatability. So far it has been widely used in the preparations of complex injectable products, such as paclitaxel liposomes, adriamycin liposomes, amphotericin B liposomes, doxorubicin liposomes, cytarabine liposomes, and irinotecan liposomes. | ||
[[File:Schematic_diagram_depicting_the_liposome_extrusion.png|thumb|250px|right|Schematic diagram depicting the liposome extrusion]] | |||
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Liposome extrusion technology is employing the structural and performance characteristics of liposomal phospholipid bilayers. When the operational temperature is slightly above the phase transition temperature of phospholipids, the large vesicles of liposomes will pass through polycarbonate membranes with specific pore sizes by a certain external extrusion force. The large particle size liposome or multiple compartments liposomes are rapidly repolymerized into smaller-size liposomes after being ruptured by the shear of membrane pores. Since the pore size of polycarbonate membrane is fixed (e.g., 50nm, 100nm, 200nm, 400nm, 1um, etc.), and the polycarbonate extrusion membrane features vertical and uniform nano pore distributions on the membrane surface, when the large vesicles pass through the membrane with a specific nano pore size several times, the sample is extruded to the uniform size decided by the pore. | |||
=Application= | |||
Research and Development for the liposomal drug delivery system, vaccine, gene delivery, and cosmetics. Liposome extruders are mainly used for the liposome formulation and achieving uniform size distributions. It is an ideal instrument to generate nanoscale liposome formulations, and to prepare exosomes and artificial cell membranes. By utilizing the tracked-etched filter membranes, the liposome extruders are capable of capturing large particles, precipitation and achieving sterile filtration. | |||
=Key Principles= | =Key Principles= |
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