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Nucleic Acid Aptamers as a Potential Nucleus Targeted Drug Delivery System.
- Source :
-
Current drug delivery [Curr Drug Deliv] 2020; Vol. 17 (2), pp. 101-111. - Publication Year :
- 2020
-
Abstract
- Background: Nucleus targeted drug delivery provides several opportunities for the treatment of fatal diseases such as cancer. However, the complex nucleocytoplasmic barriers pose significant challenges for delivering a drug directly and efficiently into the nucleus. Aptamers representing singlestranded DNA and RNA qualify as next-generation highly advanced and personalized medicinal agents that successfully inhibit the expression of certain proteins; possess extraordinary gene-expression for manoeuvring the diseased cell's fate with negligible toxicity. In addition, the precisely directed aptamers to the site of action present a tremendous potential to reach the nucleus by escaping the ensuing barriers to exhibit a better drug activity and gene expression.<br />Objective: This review epigrammatically highlights the significance of targeted drug delivery and presents a comprehensive description of the principal barriers faced by the nucleus targeted drug delivery paradigm and ensuing complexities thereof. Eventually, the progress of nucleus targeting with nucleic acid aptamers and success achieved so far have also been reviewed.<br />Methods: Systematic literature search was conducted of research published to date in the field of nucleic acid aptamers.<br />Conclusion: The review specifically points out the contribution of individual aptamers as the nucleustargeting agent rather than aptamers in conjugated form.<br /> (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
- Subjects :
- Animals
Humans
Aptamers, Nucleotide
Cell Nucleus metabolism
Drug Delivery Systems
Subjects
Details
- Language :
- English
- ISSN :
- 1875-5704
- Volume :
- 17
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Current drug delivery
- Publication Type :
- Academic Journal
- Accession number :
- 31906837
- Full Text :
- https://doi.org/10.2174/1567201817666200106104332