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
[81]   ANTISENSE OLIGONUCLEOTIDES ADSORBED TO POLYALKYLCYANOACRYLATE NANOPARTICLES SPECIFICALLY INHIBIT MUTATED HA-RAS-MEDIATED CELL-PROLIFERATION AND TUMORIGENICITY IN NUDE-MICE [J].
SCHWAB, G ;
CHAVANY, C ;
DUROUX, I ;
GOUBIN, G ;
LEBEAU, J ;
HELENE, C ;
SAISONBEHMOARAS, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (22) :10460-10464
[82]   In vivo protein transduction: Delivery of a biologically active protein into the mouse [J].
Schwarze, SR ;
Ho, A ;
Vocero-Akbani, A ;
Dowdy, SF .
SCIENCE, 1999, 285 (5433) :1569-1572
[83]   In vivo protein transduction:: intracellular delivery of biologically active proteins, compounds and DNA [J].
Schwarze, SR ;
Dowdy, SF .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2000, 21 (02) :45-48
[84]   DNA enzymes [J].
Sen, D ;
Geyer, CR .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1998, 2 (06) :680-687
[85]  
SENIOR JH, 1987, CRC CR REV THER DRUG, V3, P123
[86]  
Sioud M, 1999, INT J MOL MED, V3, P381
[87]   pH-sensitive liposomes for receptor-mediated delivery to chicken hepatoma (LMH) cells [J].
Skalko, N ;
Peschka, R ;
Altenschmidt, U ;
Lung, A ;
Schubert, R .
FEBS LETTERS, 1998, 434 (03) :351-356
[88]   TRANSPORT OF [I-125] TRANSFERRIN THROUGH THE RAT BLOOD-BRAIN-BARRIER [J].
SKARLATOS, S ;
YOSHIKAWA, T ;
PARDRIDGE, WM .
BRAIN RESEARCH, 1995, 683 (02) :164-171
[89]  
SOHAIL M, 2000, IN PRESS ADV DRUG DE
[90]   The spread and uptake pattern of intracerebrally administered oligonucleotides in nerve and glial cell populations of the rat brain [J].
Sommer, W ;
Cui, X ;
Erdmann, B ;
Wiklund, L ;
Bricca, G ;
Heilig, M ;
Fuxe, K .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1998, 8 (02) :75-85