Affiliation:
1. Nano-Gene and Drug Delivery Laboratory, Discipline of Biochemistry, School of Life Sciences, University of KwaZulu-
Natal, Private Bag X54001, Durban, South Africa
Abstract
Background:
Nucleic acid-mediated therapy holds immense potential in treating recalcitrant
human diseases such as cancer. This is underscored by advances in understanding the mechanisms
of gene regulation. In particular, the endogenous protective mechanism of gene silencing known
as RNA interference (RNAi) has been extensively exploited.
Methods:
We review the developments from 2011 to 2021 using nano-graphene oxide, carbon nanotubes,
fullerenes, carbon nanohorns, carbon nanodots and nanodiamonds for the delivery of therapeutic
small RNA molecules.
Results:
Appropriately designed effector molecules such as small interfering RNA (siRNA) can, in
theory, silence the expression of any disease-causing gene. Alternatively, siRNA can be generated in
vivo by introducing plasmid-based short hairpin RNA (shRNA) expression vectors. Other small
RNAs, such as micro RNA (miRNA), also function in post-transcriptional gene regulation and are
aberrantly expressed under disease conditions. The miRNA-based therapy involves either restoration
of miRNA function through the introduction of miRNA mimics; or the inhibition of miRNA function
by delivering anti-miRNA oligomers. However, the large size, hydrophilicity, negative charge and
nuclease-sensitivity of nucleic acids necessitate an appropriate carrier for their introduction as medicine
into cells.
Conclusion:
While numerous organic and inorganic materials have been investigated for this purpose,
the perfect carrier agent remains elusive. Carbon-based nanomaterials have received widespread attention
in biotechnology recently due to their tunable surface characteristics and mechanical, electrical,
optical and chemical properties.
Funder
National Research Foundation, South Africa
Publisher
Bentham Science Publishers Ltd.
Subject
Biomedical Engineering,Pharmaceutical Science
Cited by
3 articles.
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