NUCLEIC ACID BASED THERAPEUTIC DELIVERY SYSTEM: A REVIEW
Prachi Thakur, Pranshu Tangri*, Manish Kumar Mishra and Shaffi Khurana Tangri
Abstract
Nucleic acids have not been widely considered as an optimal material
for drug delivery. The development of nucleic acid-based therapeutics
has garnered tremendous interest in the past two decades as a new
category of biologic. Gene therapy using nucleic acids has many
clinical applications for the treatment of diseases with a genetic origin
as well as for the development of innovative vaccine formulations.
Targeted gene therapies have emerged as potential strategies for
treatment of such diseases. These therapies depend upon rare-cutting
endonucleases to cleave at specific sites in or near disease genes. Gene
expression is the process by which information from a gene is used in the synthesis of a
functional gene product. Among several talented new drug delivery systems, liposomes
characterized an advance technology to deliver active molecules to the site of action, and at
present, several formulations are in clinical use. This review focuses on the properties of
nucleic acid based therapeutics, also focuses on potential target disease for gene therapies,
gene therapies, gene expression, liposomal gene delivery system. We discuss recent progress
in nucleic acid based drug delivery strategies, their potential, unique use cases, and risks that
must be overcome or avoided.
Keywords: Nucleic acid, drug targeting, gene therapy.
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