» Articles » PMID: 7680982

Liposomes in Drug Delivery. Clinical, Diagnostic and Ophthalmic Potential

Overview
Journal Drugs
Specialty Pharmacology
Date 1993 Jan 1
PMID 7680982
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

Liposomes (phospholipid-based vesicles) have been investigated since 1970 as a system for the delivery or targeting of drugs to specific sites in the body. Because of their structural versatility in terms of size, composition, surface charge, bilayer fluidity and ability to incorporate almost any drug regardless of solubility, or to carry on their surface cell-specific ligands, liposomes have the potential to be tailored in a variety of ways to ensure the production of formulations that are optimal for clinical use. This includes controlled retention of entrapped drugs in the presence of biological fluids, controlled vesicle residence in the blood circulation or other compartments in the body, and enhanced vesicle uptake by target cells. Accumulated in vivo evidence, particularly in areas such as cancer chemotherapy, antimicrobial therapy, vaccines, diagnostic imaging and the treatment of ophthalmic disorders has indicated clearly that some liposome-entrapped drugs and vaccines exhibit superior pharmacological properties to those observed with conventional formulations. Such work has encouraged the application of liposomes in the treatment of diseases in humans. A large number of trials in patients with cancer or infections suggest that certain liposomal drug formulations are likely to prove clinically useful.

Citing Articles

Improving dexamethasone drug loading and efficacy in treating rheumatoid arthritis via liposome: Focusing on inflammation and molecular mechanisms.

Zamanian M, Zafari H, Osminina M, Skakodub A, Aboqader Al-Aouadi R, Golmohammadi M Animal Model Exp Med. 2024; 8(1):5-19.

PMID: 39627850 PMC: 11798740. DOI: 10.1002/ame2.12518.


Hypocrellin: A Natural Photosensitizer and Nano-Formulation for Enhanced Molecular Targeting of PDT of Melanoma.

Gugu Nkosi P, Chandran R, Abrahamse H Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2024; 16(6):e1997.

PMID: 39568119 PMC: 11579242. DOI: 10.1002/wnan.1997.


Transepithelial transport of nanoparticles in oral drug delivery: From the perspective of surface and holistic property modulation.

Zheng Y, Luo S, Xu M, He Q, Xie J, Wu J Acta Pharm Sin B. 2024; 14(9):3876-3900.

PMID: 39309496 PMC: 11413706. DOI: 10.1016/j.apsb.2024.06.015.


Principle, application and challenges of development siRNA-based therapeutics against bacterial and viral infections: a comprehensive review.

Motamedi H, Mahdizade Ari M, Alvandi A, Abiri R Front Microbiol. 2024; 15:1393646.

PMID: 38939184 PMC: 11208694. DOI: 10.3389/fmicb.2024.1393646.


Histological findings for the absorption of small and large liposomes - the basis of future drug delivery and contrast media systems.

Sufaru R, Stan C, Peptu C, Gavril L, Chiran D, Crauciuc D Rom J Morphol Embryol. 2024; 64(4):535-542.

PMID: 38184834 PMC: 10863683. DOI: 10.47162/RJME.64.4.10.


References
1.
Caride V, Sostman H, Twickler J, Zacharis H, Orphanoudakis S, Jaffe C . Brominated radiopaque liposomes: contrast agent for computed tomography of liver and spleen: a preliminary report. Invest Radiol. 1982; 17(4):381-5. View

2.
Taylor R, Williams D, Craven P, Graybill J, Drutz D, Magee W . Amphotericin B in liposomes: a novel therapy for histoplasmosis. Am Rev Respir Dis. 1982; 125(5):610-1. DOI: 10.1164/arrd.1982.125.5.610. View

3.
Schaeffer H, KROHN D . Liposomes in topical drug delivery. Invest Ophthalmol Vis Sci. 1982; 22(2):220-7. View

4.
Karlik S, Florio E, Grant C . Comparative evaluation of two membrane-based liposomal MRI contrast agents. Magn Reson Med. 1991; 19(1):56-66. DOI: 10.1002/mrm.1910190106. View

5.
Fishman P, Peyman G, Hendricks R, Hui S . Liposome-encapsulated 3H-5FU in rabbits. Int Ophthalmol. 1989; 13(5):361-5. DOI: 10.1007/BF02279874. View