The delivery of antisense therapeutics

被引:204
作者
Akhtar, S
Hughes, MD
Khan, A
Bibby, M
Hussain, M
Nawaz, Q
Double, J
Sayyed, P
机构
[1] Aston Univ, Pharmaceut Sci Res Inst, Aston Ctr Gene Based Therapeut, Birmingham B4 7ET, W Midlands, England
[2] Univ Bradford, Clin Oncol Unit, Bradford BD7 1DP, W Yorkshire, England
基金
英国生物技术与生命科学研究理事会;
关键词
antisense; ribozymes; DNAzymes; delivery; liposomes; biodegradable polymer; microspheres; receptor-mediated; brain delivery; oral delivery;
D O I
10.1016/S0169-409X(00)00080-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antisense oligonucleotides, ribozymes and DNAzymes have emerged as novel, highly selective inhibitors or modulators of gene expression. Indeed, their use in the treatment of diseases arising from genetic abnormalities has become a real possibility over the past few years. The first antisense drug molecule is now available for clinical use in Europe and USA. However, their successful application in the clinic will require improvements in cellular targeting and intracellular delivery. This review aims to look at recent advances in the in vitro and in vivo delivery of antisense oligodeoxynucleotides and ribozymes. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:3 / 21
页数:19
相关论文
共 105 条
[1]   Specific inhibition of influenza virus RNA polymerase and nucleoprotein gene expression by liposomally encapsulated antisense phosphorothioate oligonucleotides in MDCK cells [J].
Abe, T ;
Suzuki, S ;
Hatta, T ;
Takai, K ;
Yokota, T ;
Takaku, H .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1998, 9 (03) :253-262
[2]   Antisense therapeutics: is it as simple as complementary base recognition? [J].
Agrawal, S ;
Kandimalla, ER .
MOLECULAR MEDICINE TODAY, 2000, 6 (02) :72-81
[3]   Antisense therapeutics [J].
Agrawal, S ;
Zhao, QY .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1998, 2 (04) :519-528
[4]   ABSORPTION, TISSUE DISTRIBUTION AND IN-VIVO STABILITY IN RATS OF A HYBRID ANTISENSE OLIGONUCLEOTIDE FOLLOWING ORAL-ADMINISTRATION [J].
AGRAWAL, S ;
ZHANG, XS ;
LU, ZH ;
ZHAO, H ;
TAMBURIN, JM ;
YAN, YM ;
CAI, HY ;
DIASIO, RB ;
HABUS, I ;
JIANG, ZW ;
IYER, RP ;
YU, D ;
ZHANG, RW .
BIOCHEMICAL PHARMACOLOGY, 1995, 50 (04) :571-576
[5]   The influence of polarized epithelial (Caco-2) cell differentiation on the cellular binding of phosphodiester and phosphorothioate oligonucleotides [J].
Akhtar, S ;
Beck, GF ;
Hawley, P ;
Irwin, WJ ;
Gibson, I .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1996, 6 (03) :197-206
[6]   Antisense oligonucleotide delivery to cultured macrophages is improved by incorporation into sustained-release biodegradable polymer microspheres [J].
Akhtar, S ;
Lewis, KJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 151 (01) :57-67
[7]  
Akhtar S, 1992, Trends Cell Biol, V2, P139, DOI 10.1016/0962-8924(92)90100-2
[9]   In vivo studies with antisense oligonucleotides [J].
Akhtar, S ;
Agrawal, S .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1997, 18 (01) :12-18
[10]   STABILITY OF ANTISENSE DNA OLIGODEOXYNUCLEOTIDE ANALOGS IN CELLULAR-EXTRACTS AND SERA [J].
AKHTAR, S ;
KOLE, R ;
JULIANO, RL .
LIFE SCIENCES, 1991, 49 (24) :1793-1801