Long-circulating (sterically stabilized) liposomes for targeted drug delivery
TM Allen - Trends in pharmacological sciences, 1994 - cell.com
Since their description 30 years ago 1, liposomes (phospholipid bilayer vesicles) have found
widespread use as model membrane systems, and have been extensively investigated for …
widespread use as model membrane systems, and have been extensively investigated for …
On the formulation of pH-sensitive liposomes with long circulation times
S Simões, JN Moreira, C Fonseca, N Düzgüneş… - Advanced drug delivery …, 2004 - Elsevier
Strategies used to enhance liposome-mediated drug delivery in vivo include the
enhancement of stability and circulation time in the bloodstream, targeting to specific tissues …
enhancement of stability and circulation time in the bloodstream, targeting to specific tissues …
Pharmacokinetics of long-circulating liposomes
TM Allen, CB Hansen, DEL de Menezes - Advanced Drug Delivery …, 1995 - Elsevier
Association of drugs with carriers such as liposomes has marked effects on both the
pharmacokinetic profiles of the carrier and of the carrier-associated drug. In general …
pharmacokinetic profiles of the carrier and of the carrier-associated drug. In general …
Current status of pH-sensitive liposomes in drug delivery
DC Drummond, M Zignani, JC Leroux - Progress in lipid research, 2000 - Elsevier
Liposomes are being increasingly utilized to deliver drugs, enzymes, antisense
oligonucleotides, and genes to various therapeutic targets. Liposome-mediated delivery of …
oligonucleotides, and genes to various therapeutic targets. Liposome-mediated delivery of …
Liposomes for the sustained drug release in vivo
G Blume, G Cevc - Biochimica et Biophysica Acta (BBA)-Biomembranes, 1990 - Elsevier
New lipidic carriers suitable for the sustained drug release in vivo are presented. They
consist of middle sized, compact phospholipid vesicles with one or up to few lipid bilayers …
consist of middle sized, compact phospholipid vesicles with one or up to few lipid bilayers …
The use of glycolipids and hydrophilic polymers in avoiding rapid uptake of liposomes by the mononuclear phagocyte system
TM Allen - Advanced drug delivery reviews, 1994 - Elsevier
Sterically stabilized (Stealth®) liposomes, in which the surface of liposomes has been
altered, have been developed through the use of glycolipids (principally …
altered, have been developed through the use of glycolipids (principally …
Liposomes in drug delivery: clinical, diagnostic and ophthalmic potential
G Gregoriadis, AT Florence - Drugs, 1993 - Springer
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 …
for the delivery or targeting of drugs to specific sites in the body. Because of their structural …
Sterically stabilized liposomes: a hypothesis on the molecular origin of the extended circulation times
DD Lasic, FJ Martin, A Gabizon, SK Huang… - … et Biophysica Acta (BBA …, 1991 - Elsevier
Therapeutic applications of intravenously injected liposomes have been limited by their
rapid clearance from the bloodstream and their uptake by the macrophage cells of the liver …
rapid clearance from the bloodstream and their uptake by the macrophage cells of the liver …
Recent developments in medical applications of liposomes: sterically stabilized liposomes in cancer therapy and gene delivery in vivo
DD Lasic - Journal of controlled release, 1997 - Elsevier
In the first part, medical applications of liposomes loaded with small molecular weight drugs
is discussed and the use of sterically stabilized liposomes containing doxorubicin in cancer …
is discussed and the use of sterically stabilized liposomes containing doxorubicin in cancer …
pH‐sensitive, serum‐stable and long‐circulating liposomes as a new drug delivery system
The lack of stability in blood and the short blood circulation time of pH‐sensitive liposomes
are major drawbacks for their application in‐vivo. To develop pH‐sensitive, serum‐stable …
are major drawbacks for their application in‐vivo. To develop pH‐sensitive, serum‐stable …