Recent approaches to intracellular delivery of drugs and DNA and organelle targeting

被引:434
作者
Torchilin, Vladimir P. [1 ]
机构
[1] Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
关键词
intracellular drug delivery; intracellular gene delivery; cell-penetrating proteins and peptides; liposomes; pH-sensitive liposomes; polymeric micelles; intracellular antigens; lysosomes; mitochondria; nuclei;
D O I
10.1146/annurev.bioeng.8.061505.095735
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Intracellular delivery of various drugs, including DNA, and drug carriers can sharply increase the efficiency of various treatment protocols. However, the receptor-mediated endocytosis of drugs, drug carriers, and DNA results in their lysosomal delivery and significant degradation. The problem can be solved and therapy efficacy still further increased if the approaches for direct intracytoplasmic delivery that bypass the endocytic pathway are developed. This is especially important for many anticancer drugs (proapoptotic drugs whose primary action site is the mitochondrial membrane) and gene therapy (nuclear or mitochondrial genomes should be targeted). This review considers several current approaches for intracellular drug delivery: the use of pH-selisitive liposomes, the use of cell-penetrating proteins and peptides, and the use of immunoliposomes targeting intracellular antigens. Among intracellular targets, nuclei (gene therapy), mitochondria (proapoptotic cancer therapy and targeting of the mitochondrial genome), and lysosomes (lysosomal targeting of enzymes for the therapy of the lysosomal storage diseases) are considered. Examples of successful intracellular and organelle-specific delivery of biologically active molecules, including DNA, are presented; unanswered questions, challenges, and future trends are also discussed.
引用
收藏
页码:343 / 375
页数:33
相关论文
共 187 条
[1]   Gene therapy of single-gene disorders:: Preface to the special section [J].
Aalto-Setälä, K ;
Vuorio, E .
ANNALS OF MEDICINE, 1997, 29 (06) :549-551
[2]   PHARMACOKINETICS AND ANTITUMOR-ACTIVITY OF VINCRISTINE ENCAPSULATED IN STERICALLY STABILIZED LIPOSOMES [J].
ALLEN, TM ;
NEWMAN, MS ;
WOODLE, MC ;
MAYHEW, E ;
USTER, PS .
INTERNATIONAL JOURNAL OF CANCER, 1995, 62 (02) :199-204
[3]   TUMOR-CELL RETENTION OF ANTIBODY FAB FRAGMENTS IS ENHANCED BY AN ATTACHED HIV TAT PROTEIN-DERIVED PEPTIDE [J].
ANDERSON, DC ;
NICHOLS, E ;
MANGER, R ;
WOODLE, D ;
BARRY, M ;
FRITZBERG, AR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 194 (02) :876-884
[4]  
[Anonymous], IMMOBILIZED ENZYMES
[5]  
[Anonymous], 1993, J LIPOSOME RES, DOI DOI 10.3109/08982109309148213]
[6]  
[Anonymous], ENZYME THERAPY
[7]  
[Anonymous], ENZYME THERAPY LYSOS
[8]   ANTIVIRAL STATE AGAINST INFLUENZA-VIRUS NEUTRALIZED BY MICROINJECTION OF ANTIBODIES TO INTERFERON-INDUCED MX PROTEINS [J].
ARNHEITER, H ;
HALLER, O .
EMBO JOURNAL, 1988, 7 (05) :1315-1320
[9]   Protection against ischemic brain injury by protein therapeutics [J].
Asoh, S ;
Ohsawa, I ;
Mori, T ;
Hiraide, T ;
Katayama, Y ;
Kimura, M ;
Ozaki, D ;
Yamagata, K ;
Ohta, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (26) :17107-17112
[10]   Cytosolic delivery of macromolecules - II. Mechanistic studies with pH-sensitive morpholine lipids [J].
Asokan, A ;
Cho, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1611 (1-2) :151-160