Evidence of lipoplex dissociation in liquid formulations

被引:22
作者
Lai, E
van Zanten, JH [1 ]
机构
[1] N Carolina State Univ, Dept Chem Engn, Raleigh, NC 27695 USA
[2] Johns Hopkins Univ, Dept Chem Engn, Baltimore, MD 21218 USA
基金
美国国家科学基金会;
关键词
gene therapy; light scattering; lipoplex; liposome; stability;
D O I
10.1002/jps.10108
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aggregation is typically cited as the root cause of lipoplex transfection efficacy loss in liquid formulations. Typically, this conclusion is based on observed increases in lipoplex hydrodynamic size. A more detailed physical characterization of the lipoplex transfection efficacy diminution has previously never been conducted. As a result, most research has focused on either methods of forming more stable lipoplex formulations or preservation methods such as lyophilization. These studies typically consider the use of stabilizing additives, such as polymer, and sugar molecules, to enhance the efficacy of lipoplex dispersions. This report details a recent multiangle laser light scattering study of the temporal evolution of lipoplex geometric size (i.e., radius of gyration) and molar mass in liquid-based formulations over several months. The results indicate that for the lipoplex systems considered, the primary factor underlying the long-term loss of lipoplex transfection efficiency is actually lipoplex dissociation caused by a decrease in the observed molar mass of some lipoplex formulations. The increasing geometric sizes observed are actually the result of lipoplex dissociation combined with an increase in volume. That is, the lipoplexes lose mass and expand in volume, leading to a less dense lipoplex structure over time. (C) 2002 Wiley-Liss, Inc. and the American Pharmaceutical Association.
引用
收藏
页码:1225 / 1232
页数:8
相关论文
共 17 条
[1]  
Allison SD, 2000, J PHARM SCI, V89, P682, DOI 10.1002/(SICI)1520-6017(200005)89:5<682::AID-JPS14>3.3.CO
[2]  
2-R
[3]   Stability of lipid/DNA complexes during agitation and freeze-thawing [J].
Anchordoquy, TJ ;
Girouard, LG ;
Carpenter, JF ;
Kroll, DJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (09) :1046-1051
[4]   Maintenance of transfection rates and physical characterization of lipid/DNA complexes after freeze-drying and rehydration [J].
Anchordoquy, TJ ;
Carpenter, JF ;
Kroll, DJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 348 (01) :199-206
[5]   LIPOSOME-MEDIATED CFTR GENE-TRANSFER TO THE NASAL EPITHELIUM OF PATIENTS WITH CYSTIC-FIBROSIS [J].
CAPLEN, NJ ;
ALTON, EWFW ;
MIDDLETON, PG ;
DORIN, JR ;
STEVENSON, BJ ;
GAO, X ;
DURHAM, SR ;
JEFFERY, PK ;
HODSON, ME ;
COUTELLE, C ;
HUANG, L ;
PORTEOUS, DJ ;
WILLIAMSON, R ;
GEDDES, DM .
NATURE MEDICINE, 1995, 1 (01) :39-46
[6]   Potentiation of cationic liposome-mediated gene delivery by polycations [J].
Gao, X ;
Huang, L .
BIOCHEMISTRY, 1996, 35 (03) :1027-1036
[7]   Formation of stable cationic lipid/DNA complexes for gene transfer [J].
Hofland, HEJ ;
Shephard, L ;
Sullivan, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7305-7309
[8]   Stabilization of cationic liposome-plasmid DNA complexes by polyamines and poly(ethylene glycol)-phospholipid conjugates for efficient in vivo gene delivery [J].
Hong, KL ;
Zheng, WW ;
Baker, A ;
Papahadjopoulos, D .
FEBS LETTERS, 1997, 400 (02) :233-237
[9]   Monitoring DNA/poly-L-lysine polyplex formation with time-resolved multiangle laser light scattering [J].
Lai, E ;
van Zanten, JH .
BIOPHYSICAL JOURNAL, 2001, 80 (02) :864-873
[10]  
Li B, 2000, J PHARM SCI-US, V89, P355, DOI 10.1002/(SICI)1520-6017(200003)89:3<355::AID-JPS7>3.0.CO