Liposomes are microscopic spheres made from the same material as the cell membranes in the human body. They have attracted a lot of attention due to their amazing properties. They can be used to carry drugs, nutrients and other agents to specific destinations in the body. There are various different preparation methods and techniques for liposome manufacturing and those used depend on on various factors.
When phosphlipids such as lecithin come into contact with water, an interesting effect occurs. The molecules consist of a head which loves water and two tails that repel it. This means that the heads all face one side and the tails the other. Another layer is formed with tails all facing the tails of the first later and the heads facing the other way. These layers form the membranes around and inside every cell of the human body.
Liposomes can be used as delivery vehicles for a wide variety of drugs, vaccines, enzymes, genetic material and for some nutritional supplements as well. They not only allow for release of encapsulated materials but are beneficial in themselves for cells. The lipids used to construct the fatty part of the molecule is used by the cell wall for repair and construction of new membranes.
The tiny size of liposomes means they are quickly assimilated into the bloodstream for delivery throughout the body. The payload is biologically inert until it is delivered to needy cells. They are all basically the same but the differences between them occur in the way they are released, how long this takes as well as where and why this occurs.
All the methods for preparation of liposomes have the same basic stages. Lipid vesicles are formed when thin lipid films are hydrated. The liquid bilayers become fluid, detach and self-close to form large vesicles. Once these large particles have formed, their size is reduced by energy input. This may be in the form of sonic energy called sonication or mechanical energy called extrusion.
So, the general elements consist of lipid preparation for hydration, hydration with agitation and then sizing of vesicles. Each different method used has certain advantages and disadvantages. Liquid hydration methods usually result in low dose loading. Sonication can affect the structure of an encapsulated drug.
Some of the problems that have to be faced are structural instability, inconsistency in size and expensive production costs. Liposomal delivery systems are still in the experimental stage. The precise ways in which they act within the body are being carefully studied as well as ways in which they can be made to target diseased tissue or a specific organ.
A great benefit involved in using liposomes is that they can be customized for different applications by varying the method of preparation, size, lipid content and surface charge. Many conventional techniques for preparing them and reducing their size are fairly simple to implement and equipment does not have to be too sophisticated. However, novel routes are being discovered for preparation due to motivation to scale-down for point-of-care applications or or to scale-up for industrial applications.
When phosphlipids such as lecithin come into contact with water, an interesting effect occurs. The molecules consist of a head which loves water and two tails that repel it. This means that the heads all face one side and the tails the other. Another layer is formed with tails all facing the tails of the first later and the heads facing the other way. These layers form the membranes around and inside every cell of the human body.
Liposomes can be used as delivery vehicles for a wide variety of drugs, vaccines, enzymes, genetic material and for some nutritional supplements as well. They not only allow for release of encapsulated materials but are beneficial in themselves for cells. The lipids used to construct the fatty part of the molecule is used by the cell wall for repair and construction of new membranes.
The tiny size of liposomes means they are quickly assimilated into the bloodstream for delivery throughout the body. The payload is biologically inert until it is delivered to needy cells. They are all basically the same but the differences between them occur in the way they are released, how long this takes as well as where and why this occurs.
All the methods for preparation of liposomes have the same basic stages. Lipid vesicles are formed when thin lipid films are hydrated. The liquid bilayers become fluid, detach and self-close to form large vesicles. Once these large particles have formed, their size is reduced by energy input. This may be in the form of sonic energy called sonication or mechanical energy called extrusion.
So, the general elements consist of lipid preparation for hydration, hydration with agitation and then sizing of vesicles. Each different method used has certain advantages and disadvantages. Liquid hydration methods usually result in low dose loading. Sonication can affect the structure of an encapsulated drug.
Some of the problems that have to be faced are structural instability, inconsistency in size and expensive production costs. Liposomal delivery systems are still in the experimental stage. The precise ways in which they act within the body are being carefully studied as well as ways in which they can be made to target diseased tissue or a specific organ.
A great benefit involved in using liposomes is that they can be customized for different applications by varying the method of preparation, size, lipid content and surface charge. Many conventional techniques for preparing them and reducing their size are fairly simple to implement and equipment does not have to be too sophisticated. However, novel routes are being discovered for preparation due to motivation to scale-down for point-of-care applications or or to scale-up for industrial applications.
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