Lipoplex-loaded microbubbles for gene delivery: A Trojan horse controlled by ultrasound

被引:54
作者
Lentacker, Ine
De Smedt, Stefaan C.
Demeester, Joseph
Van Marck, Veerle
Bracke, Marc
Sanders, Niek N.
机构
[1] Fac Pharmaceut Sci, Lab Gen Biochem & Phys Pharm, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Dept Radiotherapy & Nucl Med, Expt Cancerol Lab, B-9000 Ghent, Belgium
关键词
D O I
10.1002/adfm.200700106
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cationic poly(ethylene glycol)ylated (PEGylated) liposomes are one of the most important gene transfer reagents in non-viral gene therapy. However, the low transfection efficiencies of highly PEGylated lipoplexes currently hamper their clinical use. Recently, ultrasound has been used in combination with microbubbles to enhance the uptake of genes in different cell types. However, the gene transfer efficiency still remains low in these experiments. To overcome the limitations of both techniques, we present the attachment of PEGylated lipoplexes to microbubbles via biotin-avidin-biotin linkages. Exposure of these lipoplex-loaded microbubbles to ultrasound results in the release of unaltered lipoplexes. Furthermore, these lipoplex-loaded microbubbles exhibit much higher transfection efficiencies than "free" PEGylated lipoplexes or naked plasmid DNA (pDNA) when combined with microbubbles and ultrasound. Interestingly, the lipoplex-loaded microbubbles only transfect cells when exposed to ultrasound, which is promising for space- and time-controlled gene transfer. Finally, this novel Trojan-horse-like concept can also be exploited to achieve the ultrasound- triggered release of nanoparticles containing other therapeutic agents such as anticancer drugs.
引用
收藏
页码:1910 / 1916
页数:7
相关论文
共 34 条
[1]   Regulated secretion of conventional lysosomes [J].
Andrews, NW .
TRENDS IN CELL BIOLOGY, 2000, 10 (08) :316-321
[2]   Cationic lipid-mediated transfection in vitro and in vivo [J].
Audouy, S ;
Hoekstra, D .
MOLECULAR MEMBRANE BIOLOGY, 2001, 18 (02) :129-143
[3]   Ultrasound-targeted microbubble destruction can repeatedly direct highly specific plasmid expression to the heart [J].
Bekeredjian, R ;
Chen, SY ;
Frenkel, PA ;
Grayburn, PA ;
Shohet, RV .
CIRCULATION, 2003, 108 (08) :1022-1026
[4]   The effect of poly(ethylene glycol) molecular architecture on cellular interaction and uptake of DNA complexes [J].
Deshpande, MC ;
Davies, MC ;
Garnett, MC ;
Williams, PM ;
Armitage, D ;
Bailey, L ;
Vamvakaki, M ;
Armes, SP ;
Stolnik, S .
JOURNAL OF CONTROLLED RELEASE, 2004, 97 (01) :143-156
[5]   The effects of albumin-coated microbubbles in DNA delivery mediated by therapeutic ultrasound [J].
Duvshani-Eshet, Maayan ;
Adam, Dan ;
Machluf, Marcelle .
JOURNAL OF CONTROLLED RELEASE, 2006, 112 (02) :156-166
[6]   Lipoplex-induced hemagglutination: potential involvement in intravenous gene delivery [J].
Eliyahu, H ;
Servel, N ;
Domb, AJ ;
Barenholz, Y .
GENE THERAPY, 2002, 9 (13) :850-858
[7]   A novel method for the intracellular delivery of siRNA using microbubble-enhanced focused ultrasound [J].
Kinoshita, M ;
Hynynen, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 335 (02) :393-399
[8]   Microbubble contrast agents - Targeted ultrasound imaging and ultrasound-assisted drug-delivery applications [J].
Klibanov, AL .
INVESTIGATIVE RADIOLOGY, 2006, 41 (03) :354-362
[9]   Ultrasound-responsive polymer-coated microbubbles that bind and protect DNA [J].
Lentacker, Ine ;
De Geest, Bruno G. ;
Vandenbroucke, Roosmarijn E. ;
Peeters, Liesbeth ;
Demeester, Joseph ;
De Smedt, Stefaan C. ;
Sanders, Niek N. .
LANGMUIR, 2006, 22 (17) :7273-7278
[10]   Encapsulated ultrasound microbubbles: Therapeutic application in drug/gene delivery [J].
Liu, Yiyao ;
Miyoshi, Hirokazu ;
Nakamura, Michihiro .
JOURNAL OF CONTROLLED RELEASE, 2006, 114 (01) :89-99