Literature DB >> 2672806

Use of liposomes as injectable-drug delivery systems.

M J Ostro1, P R Cullis.   

Abstract

The formation of liposomes and their application as delivery systems for injectable drugs are described. Liposomes are microscopic vesicles composed of one or more lipid membranes surrounding discrete aqueous compartments. These vesicles can encapsulate water-soluble drugs in their aqueous spaces and lipid-soluble drugs within the membrane itself. Liposomes release their contents by interacting with cells in one of four ways: adsorption, endocytosis, lipid exchange, or fusion. Liposome-entrapped drugs are distributed within the body much differently than free drugs; when administered intravenously to healthy animals and humans, most of the injected vesicles accumulate in the liver, spleen, lungs, bone marrow, and lymph nodes. Liposomes also accumulate preferentially at the sites of inflammation and infection and in some solid tumors; however, the reason for this accumulation is not clear. Four major factors influence liposomes' in vivo behavior and biodistribution: (1) liposomes tend to leak if cholesterol is not included in the vesicle membrane, (2) small liposomes are cleared more slowly than large liposomes, (3) the half-life of a liposome increases as the lipid dose increases, and (4) charged liposomal systems are cleared more rapidly than uncharged systems. The most advanced application of liposome-based therapy is in the treatment of systemic fungal infections, especially with amphotericin B. Liposomes are also under investigation for treatment of neoplastic disorders. Liposomes' uses in cancer therapy include encapsulation of known antineoplastic agents such as doxorubicin and methotrexate, delivery of immune modulators such as N-acetylmuramyl-L-alanine-D-isoglutamine, and encapsulation of new chemical entities that are synthesized with lipophilic segments tailored for insertion into lipid bilayers. Liposomal formulations of injectable antimicrobial agents and antineoplastic agents already are undergoing clinical testing, and most probably will receive approval for marketing in the early 1990s. Liposomal encapsulation of drugs represents a new drug delivery system that appears to offer important therapeutic advantages over existing methods of drug delivery.

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Year:  1989        PMID: 2672806

Source DB:  PubMed          Journal:  Am J Hosp Pharm        ISSN: 0002-9289


  33 in total

1.  Delivery of macromolecules into living cells: a method that exploits folate receptor endocytosis.

Authors:  C P Leamon; P S Low
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

2.  Distribution of lipid formulations of amphotericin B into bone marrow and fat tissue in rabbits.

Authors:  A H Groll; D Mickiene; S C Piscitelli; T J Walsh
Journal:  Antimicrob Agents Chemother       Date:  2000-02       Impact factor: 5.191

3.  Preparation and properties of nanoscale containers for biomedical application in drug delivery: preliminary studies with kynurenic acid.

Authors:  V Hornok; T Bujdosó; J Toldi; K Nagy; I Demeter; C Fazakas; I Krizbai; L Vécsei; I Dékány
Journal:  J Neural Transm (Vienna)       Date:  2011-11-08       Impact factor: 3.575

Review 4.  Toward a cure for osteoporosis: reversal of excessive bone fragility.

Authors:  C H Turner
Journal:  Osteoporos Int       Date:  1991-10       Impact factor: 4.507

5.  Microencapsulation technology by nature: Cell derived extracellular vesicles with therapeutic potential.

Authors:  A Kittel; A Falus; E Buzás
Journal:  Eur J Microbiol Immunol (Bp)       Date:  2013-06-05

Review 6.  Newer antifungal agents.

Authors:  Walid Abuhammour; Eyassu Habte-Gaber
Journal:  Indian J Pediatr       Date:  2004-03       Impact factor: 1.967

7.  Spectrofluorimetric determination of second critical micellar concentration of SDS and SDS/Brij 30 systems.

Authors:  Ana Paula Romani; Antonio Eduardo da Hora Machado; Noboru Hioka; Divinomar Severino; Mauricio S Baptista; Lúcia Codognoto; Maira R Rodrigues; Hueder Paulo Moisés de Oliveira
Journal:  J Fluoresc       Date:  2008-09-25       Impact factor: 2.217

8.  Acyl chain orientational order in large unilamellar vesicles: comparison with multilamellar liposomes: a 2H and 31P nuclear magnetic resonance study.

Authors:  D B Fenske; P R Cullis
Journal:  Biophys J       Date:  1993-05       Impact factor: 4.033

Review 9.  Liposomal formulations of cytotoxic drugs.

Authors:  R Janknegt
Journal:  Support Care Cancer       Date:  1996-07       Impact factor: 3.603

10.  Indium-111-labelled liposomes: dosimetry and tumour detection in patients with cancer.

Authors:  A Kubo; K Nakamura; T Sammiya; M Katayama; T Hashimoto; S Hashimoto; H Kobayashi; T Teramoto
Journal:  Eur J Nucl Med       Date:  1993-02
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