Liposomal Drug Delivery: A Versatile Platform for Challenging Clinical Applications

被引:118
作者
Madni, Asadullah [1 ]
Sarfraz, Muhammad [2 ]
Rehman, Mubashar [1 ]
Ahmad, Mahmood [1 ]
Akhtar, Naveed [1 ]
Ahmad, Saeed
Tahir, Nayab [1 ]
Ijaz, Shakeel [1 ]
Al-Kassas, Raida [3 ]
Loebenberg, Raimar [2 ]
机构
[1] Islamia Univ Bahawalpur, Fac Pharm & Alternat Med, Dept Pharm, Bahawalpur, Pakistan
[2] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB T6G 2N8, Canada
[3] Univ Auckland, Fac Med & Hlth Sci, Sch Pharm, Auckland 1, New Zealand
来源
JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES | 2014年 / 17卷 / 03期
关键词
liposomes; cancer treatment; drug targeting; micelle systems; drug delivery; clinical applications; PH-SENSITIVE LIPOSOMES; IN-VITRO CHARACTERIZATION; TOPICAL DELIVERY; GENE DELIVERY; POLYMERIZED LIPOSOMES; VESICULAR SYSTEMS; AMPHOTERICIN-B; SERUM-ALBUMIN; CANCER CELLS; PROLIPOSOMES;
D O I
10.18433/J3CP55
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liposomes are lipid based vesicular systems that offer novel platform for versatile drug delivery to target cell. Liposomes were first reported by Bangham and his co-workers in 1964 (1). Since then, liposomes have undergone extensive research with the prime aim to optimize encapsulation, stability, circulation time and target specific drug delivery. Manipulation of a liposome's lipid bilayer and surface decoration with selective ligands has transformed conventional liposomes into adaptable and multifunctional liposomes. Development of liposomes with target specificity provide the prospect of safe and effective therapy for challenging clinical applications. Bioresponsive liposomes offer the opportunity to release payload in response to tissue specific microenvironment. Incorporation of novel natural and synthetic materials has extended their application from stable formulations to controlled release targeted drug delivery systems. Integration and optimization of multiple features into one system revolutionized research in the field of cancer, gene therapy, immunotherapy and infectious diseases. After 50 years since the first publication, this review is aimed to highlight next generation of liposomes, their preparation methods and progress in clinical applications.
引用
收藏
页码:401 / 426
页数:26
相关论文
共 230 条
[1]  
AHMAD I, 1992, CANCER RES, V52, P4817
[2]   Combination radiofrequency ablation with intratumoral liposomal doxorubicin: Effect on drug accumulation and coagulation in multiple tissues and tumor types in animals [J].
Ahmed, M ;
Liu, ZJ ;
Lukyanov, AN ;
Signoretti, S ;
Horkan, C ;
Monsky, WL ;
Torchilin, VP ;
Goldberg, SN .
RADIOLOGY, 2005, 235 (02) :469-477
[3]   PROLIPOSOMES AS AN INTRANASAL DOSAGE FORM FOR THE SUSTAINED DELIVERY OF PROPRANOLOL [J].
AHN, BN ;
KIM, SK ;
SHIM, CK .
JOURNAL OF CONTROLLED RELEASE, 1995, 34 (03) :203-210
[4]   Pharmacokinetics & tissue distribution of temperature-sensitive liposomal doxorubicin in tumor-bearing mice triggered with mild hyperthermia [J].
Al-Jamal, Wafa' T. ;
Al-Ahmady, Zahraa S. ;
Kostarelos, Kostas .
BIOMATERIALS, 2012, 33 (18) :4608-4617
[5]  
Amram M, 2012, U.S. Patents, Patent No. [US 20120237562, 20120237562]
[6]   Triggered Release from Liposomes through Magnetic Actuation of Iron Oxide Nanoparticle Containing Membranes [J].
Amstad, Esther ;
Kohlbrecher, Joachim ;
Mueller, Elisabeth ;
Schweizer, Thomas ;
Textor, Marcus ;
Reimhult, Erik .
NANO LETTERS, 2011, 11 (04) :1664-1670
[7]   Earliest Stage of the Tetrahedral Nanochannel Formation in Cubosome Particles from Unilamellar Nanovesicles [J].
Angelov, Borislav ;
Angelova, Angelina ;
Garamus, Vasil M. ;
Drechsler, Markus ;
Willumeit, Regine ;
Mutafchieva, Rada ;
Stepanek, Petr ;
Lesieur, Sylviane .
LANGMUIR, 2012, 28 (48) :16647-16655
[8]  
Anitha P., 2011, Int J Rev Life Sci, V1, P17
[9]   Preparation and in vitro in vivo evaluation of luteinizing hormone releasing hormone (LHRH)-loaded polyhedral and spherical tubular niosomes [J].
Arunothayanun, P ;
Turton, JA ;
Uchegbu, IF ;
Florence, AT .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1999, 88 (01) :34-38
[10]   Cationic lipid-mediated transfection in vitro and in vivo [J].
Audouy, S ;
Hoekstra, D .
MOLECULAR MEMBRANE BIOLOGY, 2001, 18 (02) :129-143