Liposomal drug delivery systems: from concept to clinical applications

TM Allen, PR Cullis - Advanced drug delivery reviews, 2013 - Elsevier
The first closed bilayer phospholipid systems, called liposomes, were described in 1965 and
soon were proposed as drug delivery systems. The pioneering work of countless liposome …

P-glycoprotein inhibition as a therapeutic approach for overcoming multidrug resistance in cancer: current status and future perspectives

Z Binkhathlan, A Lavasanifar - Current cancer drug targets, 2013 - ingentaconnect.com
One of the major causes of failure in cancer chemotherapy is multidrug resistance (MDR),
where cancer cells simultaneously become resistant to different anticancer drugs. Over …

Prospects for cationic polymers in gene and oligonucleotide therapy against cancer

T Merdan, J Kopec̆ek, T Kissel - Advanced drug delivery reviews, 2002 - Elsevier
Gene and antisense/ribozyme therapy possesses tremendous potential for the successful
treatment of genetically based diseases, such as cancer. Several cancer gene therapy …

Chemotherapy-induced resistance by ATP-binding cassette transporter genes

JP Gillet, T Efferth, J Remacle - … et Biophysica Acta (BBA)-Reviews on …, 2007 - Elsevier
A key issue in the treatment of many cancers is the development of resistance to
chemotherapeutic drugs. Resistance mechanisms are numerous and complex. One of them …

Pharmacological strategies for overcoming multidrug resistance

S Nobili, I Landini, B Giglioni, E Mini - Current drug targets, 2006 - ingentaconnect.com
Multidrug resistance (MDR) is a major obstacle to the effective treatment of cancer. One of
the underlying mechanisms of MDR is cellular overproduction of P-glycoprotein (P-gp) …

Role of ATP-binding cassette transporters in cancer initiation and progression

S Nobili, A Lapucci, I Landini, M Coronnello… - Seminars in cancer …, 2020 - Elsevier
Abstract ATP Binding Cassette (ABC) transporters, widely studied in cancer for their role in
drug resistance, have been more recently also considered for their contribution to cancer …

Tat-conjugated PAMAM dendrimers as delivery agents for antisense and siRNA oligonucleotides

H Kang, R DeLong, MH Fisher, RL Juliano - Pharmaceutical research, 2005 - Springer
Purpose PAMAM G5 dendrimer (P) was conjugated to Tat peptide (T), a cell penetrating
peptide, in search of an efficient cellular delivery vehicle for antisense and siRNA …

High-generation polycationic dendrimers are unusually effective at disrupting anionic vesicles: membrane bending model

ZY Zhang, BD Smith - Bioconjugate chemistry, 2000 - ACS Publications
The membrane disruption properties of high generation (G4 to G7) poly
(amidoamine)(PAMAM) dendrimers are evaluated and compared to linear poly (lysine). The …

Molecular targeting of drug delivery systems to cancer

T Minko, SS Dharap, RI Pakunlu… - Current drug targets, 2004 - ingentaconnect.com
This review presents molecular targeting approaches in anticancer drug delivery systems
(DDS) and identifies new developments in these systems. Targeting approaches include …

Enhanced delivery of antisense oligonucleotides with fluorophore-conjugated PAMAM dendrimers

H Yoo, RL Juliano - Nucleic Acids Research, 2000 - academic.oup.com
PAMAM dendrimers are cationic polymers that have been used for the delivery of genes and
oligonucleotides to cells. However, little is known about the behavior of dendrimer–nucleic …