Coacervate microspheres as carriers of recombinant adenoviruses

被引:28
作者
Kalyanasundaram, S
Feinstein, S
Nicholson, JP
Leong, KW
Garver, RI
机构
[1] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21205 USA
[2] Univ Alabama, Sch Med, Div Pulm & Crit Care Med, Birmingham, AL 35294 USA
[3] Birmingham Vet Affiars Med Ctr, Birmingham, AL 35294 USA
关键词
gene therapy; adenoviridae; microspheres;
D O I
10.1038/sj.cgt.7700025
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 ; 0836 ; 090102 ; 100705 ;
摘要
The therapeutic utility of recombinant adenoviruses (rAds) is limited in part by difficulties in directing the Viruses to specific sites and by the requirement for bolus administration, both of which limit the efficiency of target tissue infection. As a first step toward overcoming these limitations, rAds were encapsulated in coacervate microspheres comprised of gelatin and alginate followed by stabilization with calcium ions. Ultrastructural evaluation showed that the microspheres formed in this manner were 0.8-10 mu M in diameter, with viruses evenly distributed. The microspheres achieved a sustained release of adenovirus with a nominal loss of bioactivity. The pattern of release and the total amount of virus released was modified by changes in microsphere formulation. Administration of the adenovirus-containing microspheres to human tumor nodules engrafted in mice showed that the viral transgene was transferred to the tumor cells. It is concluded that coacervate microspheres can be used to encapsulate bioactive rAd and release it in a time-dependent manner.
引用
收藏
页码:107 / 112
页数:6
相关论文
共 8 条
[1]   INVIVO GENE-TRANSFER WITH RETROVIRAL VECTOR PRODUCER CELLS FOR TREATMENT OF EXPERIMENTAL BRAIN-TUMORS [J].
CULVER, KW ;
RAM, Z ;
WALLBRIDGE, S ;
ISHII, H ;
OLDFIELD, EH ;
BLAESE, RM .
SCIENCE, 1992, 256 (5063) :1550-1552
[2]  
CURIEL DT, 1997, GENE THERAPY DIS LUN, P29
[3]   Amplification of recombinant adenoviral transgene products occurs by inhibition of histone deacetylase [J].
Dion, LD ;
Goldsmith, KT ;
Tang, DC ;
Engler, JA ;
Yoshida, M ;
Garver, RI .
VIROLOGY, 1997, 231 (02) :201-209
[4]  
Dion LD, 1996, GENE THER, V3, P1021
[5]  
Dion LD, 1996, CANCER GENE THER, V3, P230
[6]   TRANS COMPLEMENTATION OF AN E1A-DELETED ADENOVIRUS WITH CODELIVERED E1A SEQUENCES TO MAKE RECOMBINANT ADENOVIRAL PRODUCER CELLS [J].
GOLDSMITH, KT ;
CURIEL, DT ;
ENGLER, JA ;
GARVER, RI .
HUMAN GENE THERAPY, 1994, 5 (11) :1341-1348
[7]   ADENOVIRUS-MEDIATED TRANSFER OF LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE ACUTELY ACCELERATES CHOLESTEROL CLEARANCE IN NORMAL MICE [J].
HERZ, J ;
GERARD, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2812-2816
[8]  
TRUONG VL, 1995, DRUG DELIV, V2, P166