Nanovesicular Formulations for Cancer Gene Therapy

被引:4
作者
Tavano, Lorena [1 ]
Mazzotta, Elisabetta [1 ]
Muzzalupo, Rita [1 ]
机构
[1] Univ Calabria, Dept Pharm Hlth & Nutr Sci, Via Pietro Bucci,Ed Polifunz, I-87036 Arcavacata Di Rende, Italy
关键词
Liposomes; niosomes; gene therapy; cancer; liposomes; cationic nanocarriers; SURFACTANT VESICLES NIOSOMES; ETHANOL INJECTION METHOD; DRUG-DELIVERY SYSTEMS; SMALL INTERFERING RNA; CATIONIC LIPOSOMES; TRANSFECTION EFFICIENCY; PLASMID DNA; TOPICAL DELIVERY; VIRAL VECTORS; NANO-NIOSOMES;
D O I
10.2174/1381612823666170519115023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the last decades, gene therapy has become a novel therapeutic strategy for cancer treatment, including immunologic and molecular approaches. Among molecular avenue, the design of efficient and effective gene delivery systems, like cationic liposomes and niosomes, has been widely investigated and proposed as the most promising research area. The advantages of cationic vesicles rely on their natural ability to form complexes with anionic genetic molecules and deliver them into the cells via the endosomal pathway. Obviously, cationic vesicles-mediated gene delivery is affected by numerous factors, in particular composition, that strongly affects vesicle physical-chemistry characteristics and transfection effectiveness. This review will analyse the potential of cationic nanocarriers in cancer gene therapy, focusing on the role of liposomes and niosomes as vesicular devices and giving an exhaustive collection of the most representative investigations.
引用
收藏
页码:5327 / 5335
页数:9
相关论文
共 102 条
  • [1] Recent advances in non-ionic surfactant vesicles (niosomes): self-assembly, fabrication, characterization, drug delivery applications and limitations
    Abdelkader, Hamdy
    Alani, Adam W. G.
    Alany, Raid G.
    [J]. DRUG DELIVERY, 2014, 21 (02) : 87 - 100
  • [2] Targeting Anticancer Drugs to Tumor Vasculature Using Cationic Liposomes
    Abu Lila, Amr S.
    Ishida, Tatsuhiro
    Kiwada, Hiroshi
    [J]. PHARMACEUTICAL RESEARCH, 2010, 27 (07) : 1171 - 1183
  • [3] Oxaliplatin targeting to angiogenic vessels by PEGylated cationic liposomes suppresses the angiogenesis in a dorsal air sac mouse model
    Abu-Lila, Amr
    Suzuki, Takuya
    Doi, Yusuke
    Ishida, Tatsuhiro
    Kiwada, Hiroshi
    [J]. JOURNAL OF CONTROLLED RELEASE, 2009, 134 (01) : 18 - 25
  • [4] Liposomal drug delivery systems: From concept to clinical applications
    Allen, Theresa M.
    Cullis, Pieter R.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (01) : 36 - 48
  • [5] Amer Magid H, 2014, Mol Cell Ther, V2, P27
  • [6] Ausubel FM, 2001, CURR PROTOC MOL BIOL
  • [7] Bertram John S., 2000, Molecular Aspects of Medicine, V21, P167, DOI 10.1016/S0098-2997(00)00007-8
  • [8] Comparison of Methods for Accurate Quantification of DNA Mass Concentration with Traceability to the International System of Units
    Bhat, Somanath
    Curach, Natalie
    Mostyn, Thomas
    Bains, Gursharan Singh
    Griffiths, Kate R.
    Emslie, Kerry R.
    [J]. ANALYTICAL CHEMISTRY, 2010, 82 (17) : 7185 - 7192
  • [9] Gene delivery with synthetic (non viral) carriers
    Brown, MD
    Schätzlein, AG
    Uchegbu, IF
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 229 (1-2) : 1 - 21
  • [10] Fighting Cancer: From the Bench to Bedside Using Second Generation Cationic Liposomal Therapeutics
    Campbell, Robert B.
    Ying, Bo
    Kuesters, Geoffrey M.
    Hemphill, Ryan
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (02) : 411 - 429