A concentrated and stable aerosol formulation of cationic Lipid: DNA complexes giving high-level gene expression in mouse lung

被引:74
作者
Eastman, SJ
Lukason, MJ
Tousignant, JD
Murray, H
Lane, MD
StGeorge, JA
Akita, GY
Cherry, M
Cheng, SH
Scheule, RK
机构
[1] Genzyme Corporation, Framingham
[2] Genzyme Corporation, Framingham, MA 01701-9322, One Mountain Road
关键词
D O I
10.1089/hum.1997.8.6-765
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Advances in gene therapy vectors and techniques hold promise for treatment of many inherited and acquired diseases, For lung indications, especially those involving the epithelium, delivery of the gene therapy vehicle ideally will involve the use of an aerosol, Aerosol delivery of transgenes using cationic lipids is currently limited by the ability to generate highly concentrated formulations of lipid:DNA complexes that are stable and retain their activity following aerosolization, We have examined many of the variables inherent in aerosolizing cationic lipid gene delivery vehicles and have devised a new formulation that incorporates small amounts of a polyethylene glycol-containing lipid, This formulation has allowed the preparation of concentrated dispersions of cationic lipid:plasmid DNA (pDNA) complexes (>20 mM pDNA) at approximately 10-fold higher concentrations than previously reported, Most of the pDNA in these formulations was bound to the lipid component and thereby protected from nebulizer-induced shearing; the pDNA also maintained full biological activity both in vitro and in vivo, This new formulation thus represents a significant improvement over current methods to prepare concentrated, active cationic lipid gene delivery vectors, and provides a new tool with which to test gene transfer to the lung.
引用
收藏
页码:765 / 773
页数:9
相关论文
共 17 条
[1]
NONINVASIVE LIPOSOME-MEDIATED GENE DELIVERY CAN CORRECT THE ION-TRANSPORT DEFECT IN CYSTIC-FIBROSIS MUTANT MICE [J].
ALTON, EWFW ;
MIDDLETON, PG ;
CAPLEN, NJ ;
SMITH, SN ;
STEEL, DM ;
MUNKONGE, FM ;
JEFFERY, PK ;
GEDDES, DM ;
HART, SL ;
WILLIAMSON, R ;
FASOLD, KI ;
MILLER, AD ;
DICKINSON, P ;
STEVENSON, BJ ;
MCLACHLAN, G ;
DORIN, JR ;
PORTEOUS, DJ .
NATURE GENETICS, 1993, 5 (02) :135-142
[2]
INVIVO TRANSFECTION OF MURINE LUNGS WITH A FUNCTIONING PROKARYOTIC GENE USING A LIPOSOME VEHICLE [J].
BRIGHAM, KL ;
MEYRICK, B ;
CHRISTMAN, B ;
MAGNUSON, M ;
KING, G ;
BERRY, LC .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1989, 298 (04) :278-281
[3]
AEROSOL AND INTRAVENOUS TRANSFECTION OF HUMAN ALPHA-1-ANTITRYPSIN GENE TO LUNGS OF RABBITS [J].
CANONICO, AE ;
CONARY, JT ;
MEYRICK, BO ;
BRIGHAM, KL .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (01) :24-29
[4]
THE PHARMACOKINETICS OF PULMONARY-DELIVERED INSULIN - A COMPARISON OF INTRATRACHEAL AND AEROSOL ADMINISTRATION TO THE RABBIT [J].
COLTHORPE, P ;
FARR, SJ ;
TAYLOR, G ;
SMITH, IJ ;
WYATT, D .
PHARMACEUTICAL RESEARCH, 1992, 9 (06) :764-768
[5]
Optimization of formulations and conditions for the aerosol delivery of functional cationic lipid:DNA complexes [J].
Eastman, SJ ;
Tousignant, JD ;
Lukason, MJ ;
Murray, H ;
Siegel, CS ;
Constantino, P ;
Harris, DJ ;
Cheng, SH ;
Scheule, RK .
HUMAN GENE THERAPY, 1997, 8 (03) :313-322
[6]
LIPOFECTION - A HIGHLY EFFICIENT, LIPID-MEDIATED DNA-TRANSFECTION PROCEDURE [J].
FELGNER, PL ;
GADEK, TR ;
HOLM, M ;
ROMAN, R ;
CHAN, HW ;
WENZ, M ;
NORTHROP, JP ;
RINGOLD, GM ;
DANIELSEN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7413-7417
[7]
RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS [J].
GORMAN, CM ;
MOFFAT, LF ;
HOWARD, BH .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) :1044-1051
[8]
LOCALIZATION AND INDUCED EXPRESSION OF FUSION GENES IN THE RAT LUNG [J].
HAZINSKI, TA ;
LADD, PA ;
DEMATTEO, CA .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 4 (03) :206-209
[9]
PRELIMINARY-STUDY OF THE EFFICACY OF INSULIN AEROSOL DELIVERED BY ORAL INHALATION IN DIABETIC-PATIENTS [J].
LAUBE, BL ;
GEORGOPOULOS, A ;
ADAMS, GK .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 269 (16) :2106-2109
[10]
Detailed analysis of structures and formulations of cationic lipids for efficient gene transfer to the lung [J].
Lee, ER ;
Marshall, J ;
Siegel, CS ;
Jiang, CW ;
Yew, NS ;
Nichols, MR ;
Nietupski, JB ;
Ziegler, RJ ;
Lane, MB ;
Wang, KX ;
Wan, NC ;
Scheule, RK ;
Harris, DJ ;
Smith, AE ;
Cheng, SH .
HUMAN GENE THERAPY, 1996, 7 (14) :1701-1717