Recent developments in lipid-based pharmaceutical nanocarriers

被引:77
作者
Musacchio, Tiziana [1 ]
Torchilin, Vladimir P. [1 ]
机构
[1] Northeastern Univ, Ctr Pharmaceut Biotechnol & Nanomed, Boston, MA 02115 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2011年 / 16卷
关键词
Micelles; Liposomes; Phospholipids; Polymers; Nanomedicine; Anticancer drugs; siRNA; DNA; Targeted delivery of therapeutics; Review; BLOCK-COPOLYMER MICELLES; PEGYLATED LIPOSOMAL DOXORUBICIN; DRUG-DELIVERY SYSTEMS; LONG-CIRCULATING LIPOSOMES; POLYELECTROLYTE COMPLEX MICELLES; BIODEGRADABLE POLYMERIC MICELLES; PH-SENSITIVE LIPOSOMES; POORLY SOLUBLE DRUGS; STERICALLY STABILIZED LIPOSOMES; POLYETHYLENE-GLYCOL-LIPOSOMES;
D O I
10.2741/3795
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Within the broad spectrum of nanoparticulate carriers, polymeric and lipid-core micelles, liposomes, solid nanoparticles and many others have demonstrated great biological properties which make them excellent pharmaceutical delivery systems. In particular, micelles and liposomes have been shown to have good longevity in the blood that allows their accumulation in pathological areas with a compromised vasculature; can possess specific targeting to disease sites when various targeting ligands are attached to the surface of the nanocarriers or to surface-attached cell-penetrating molecules (like TAT peptide) to enhance intracellular penetration; possess stimulus-sensitivity allowing for drug release from the carriers under certain pathological conditions; and show contrast properties with carrier loading of various contrast materials that allow for direct carrier visualization in vivo. The engineering of "multifunctional pharmaceutical nanocarriers" based on the combination of several useful properties in the same system can significantly enhance the efficacy of many therapeutic and diagnostic protocols. This review considers the current status and next future directions in the emerging area of nanomedicine with particular attention to two lipid-based nanoparticulate systems: liposomes and micelles.
引用
收藏
页码:1388 / 1412
页数:25
相关论文
共 276 条
[1]  
ABUCHOWSKI A, 1979, CANCER TREAT REP, V63, P1127
[2]   Controlled destabilization of a liposomal drug delivery system enhances mitoxantrone antitumor activity [J].
Adlakha-Hutcheon, G ;
Bally, MB ;
Shew, CR ;
Madden, TD .
NATURE BIOTECHNOLOGY, 1999, 17 (08) :775-779
[3]   Biodegradable polymersomes loaded with both paclitaxel and doxorubicin permeate and shrink tumors, inducing apoptosis in proportion to accumulated drug [J].
Ahmed, Fariyal ;
Pakunlu, Refika I. ;
Brannan, Aaron ;
Bates, Frank ;
Minko, Tamara ;
Discher, Dennis E. .
JOURNAL OF CONTROLLED RELEASE, 2006, 116 (02) :150-158
[4]  
Alakhov V Y, 1998, Expert Opin Investig Drugs, V7, P1453, DOI 10.1517/13543784.7.9.1453
[5]   Efficacy and safety of liposomal anthracyclines in phase I/II clinical trials [J].
Alberts, DS ;
Muggia, FM ;
Carmichael, J ;
Winer, EP ;
Jahanzeb, M ;
Venook, AP ;
Skubitz, KM ;
Rivera, E ;
Sparano, JA ;
Dibella, NJ ;
Stewart, SJ ;
Kavanagh, JJ ;
Gabizon, AA .
SEMINARS IN ONCOLOGY, 2004, 31 (06) :53-90
[6]  
Aliabadi Hamidreza Montazeri, 2006, Expert Opin Drug Deliv, V3, P139
[7]   Micelles of methoxy poly(ethylene oxide)-b-poly(ε-caprolactone) as vehicles for the solubilization and controlled delivery of Cyclosporine A [J].
Aliabadi, HM ;
Mahmud, A ;
Sharifabadi, AD ;
Lavasanifar, A .
JOURNAL OF CONTROLLED RELEASE, 2005, 104 (02) :301-311
[8]   Polycaprolactone-b-poly(ethylene oxide) copolymer micelles as a delivery vehicle for dihydrotestosterone [J].
Allen, C ;
Han, JN ;
Yu, YS ;
Maysinger, D ;
Eisenberg, A .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (03) :275-286
[9]   Nano-engineering block copolymer aggregates for drug delivery [J].
Allen, C ;
Maysinger, D ;
Eisenberg, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :3-27
[10]   PHARMACOKINETICS OF STEALTH VERSUS CONVENTIONAL LIPOSOMES - EFFECT OF DOSE [J].
ALLEN, TM ;
HANSEN, C .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1068 (02) :133-141