Chitosan nanocarriers for non-coding RNA therapeutics: A review
Non-coding RNA (ncRNA)-based therapies entail delivering ncRNAs to cells to regulate gene expression and produce proteins that combat infections, cancer, neurological diseases, and bone abnormalities. Nevertheless, the therapeutic potential of these ncRNAs has been limited due to the difficulties in...
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Published in | International journal of biological macromolecules Vol. 263; no. Pt 1; p. 130361 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.04.2024
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Subjects | |
Online Access | Get full text |
ISSN | 0141-8130 1879-0003 1879-0003 |
DOI | 10.1016/j.ijbiomac.2024.130361 |
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Abstract | Non-coding RNA (ncRNA)-based therapies entail delivering ncRNAs to cells to regulate gene expression and produce proteins that combat infections, cancer, neurological diseases, and bone abnormalities. Nevertheless, the therapeutic potential of these ncRNAs has been limited due to the difficulties in delivering them to specific cellular targets within the body. Chitosan (CS), a biocompatible cationic polymer, interacts with negatively charged RNA molecules to form stable complexes. It is a promising biomaterial to develop nanocarriers for ncRNA delivery, overcoming several disadvantages of traditional delivery systems. CS-based nanocarriers can protect ncRNAs from degradation and target-specific delivery by surface modifications and intracellular release profiles over an extended period. This review briefly summarizes the recent developments in CS nanocarriers' synthesis and design considerations and their applications in ncRNA therapeutics for treating various diseases. We also discuss the challenges and limitations of CS-based nanocarriers for ncRNA therapeutics and potential strategies for overcoming these challenges. |
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AbstractList | Non-coding RNA (ncRNA)-based therapies entail delivering ncRNAs to cells to regulate gene expression and produce proteins that combat infections, cancer, neurological diseases, and bone abnormalities. Nevertheless, the therapeutic potential of these ncRNAs has been limited due to the difficulties in delivering them to specific cellular targets within the body. Chitosan (CS), a biocompatible cationic polymer, interacts with negatively charged RNA molecules to form stable complexes. It is a promising biomaterial to develop nanocarriers for ncRNA delivery, overcoming several disadvantages of traditional delivery systems. CS-based nanocarriers can protect ncRNAs from degradation and target-specific delivery by surface modifications and intracellular release profiles over an extended period. This review briefly summarizes the recent developments in CS nanocarriers' synthesis and design considerations and their applications in ncRNA therapeutics for treating various diseases. We also discuss the challenges and limitations of CS-based nanocarriers for ncRNA therapeutics and potential strategies for overcoming these challenges. Non-coding RNA (ncRNA)-based therapies entail delivering ncRNAs to cells to regulate gene expression and produce proteins that combat infections, cancer, neurological diseases, and bone abnormalities. Nevertheless, the therapeutic potential of these ncRNAs has been limited due to the difficulties in delivering them to specific cellular targets within the body. Chitosan (CS), a biocompatible cationic polymer, interacts with negatively charged RNA molecules to form stable complexes. It is a promising biomaterial to develop nanocarriers for ncRNA delivery, overcoming several disadvantages of traditional delivery systems. CS-based nanocarriers can protect ncRNAs from degradation and target-specific delivery by surface modifications and intracellular release profiles over an extended period. This review briefly summarizes the recent developments in CS nanocarriers' synthesis and design considerations and their applications in ncRNA therapeutics for treating various diseases. We also discuss the challenges and limitations of CS-based nanocarriers for ncRNA therapeutics and potential strategies for overcoming these challenges.Non-coding RNA (ncRNA)-based therapies entail delivering ncRNAs to cells to regulate gene expression and produce proteins that combat infections, cancer, neurological diseases, and bone abnormalities. Nevertheless, the therapeutic potential of these ncRNAs has been limited due to the difficulties in delivering them to specific cellular targets within the body. Chitosan (CS), a biocompatible cationic polymer, interacts with negatively charged RNA molecules to form stable complexes. It is a promising biomaterial to develop nanocarriers for ncRNA delivery, overcoming several disadvantages of traditional delivery systems. CS-based nanocarriers can protect ncRNAs from degradation and target-specific delivery by surface modifications and intracellular release profiles over an extended period. This review briefly summarizes the recent developments in CS nanocarriers' synthesis and design considerations and their applications in ncRNA therapeutics for treating various diseases. We also discuss the challenges and limitations of CS-based nanocarriers for ncRNA therapeutics and potential strategies for overcoming these challenges. |
ArticleNumber | 130361 |
Author | Karthik, S. Ganesamoorthi, Srinidhi Gurunathan, Raghav Selvamurugan, N. Kolipaka, Rushil Mohan, Sahithya Magesh, Induja Sathiya, K. Bharathy, Ashok Shanmugavadivu, Abinaya |
Author_xml | – sequence: 1 givenname: S. surname: Karthik fullname: Karthik, S. – sequence: 2 givenname: Sahithya surname: Mohan fullname: Mohan, Sahithya – sequence: 3 givenname: Induja surname: Magesh fullname: Magesh, Induja – sequence: 4 givenname: Ashok surname: Bharathy fullname: Bharathy, Ashok – sequence: 5 givenname: Rushil surname: Kolipaka fullname: Kolipaka, Rushil – sequence: 6 givenname: Srinidhi surname: Ganesamoorthi fullname: Ganesamoorthi, Srinidhi – sequence: 7 givenname: K. surname: Sathiya fullname: Sathiya, K. – sequence: 8 givenname: Abinaya surname: Shanmugavadivu fullname: Shanmugavadivu, Abinaya – sequence: 9 givenname: Raghav surname: Gurunathan fullname: Gurunathan, Raghav – sequence: 10 givenname: N. surname: Selvamurugan fullname: Selvamurugan, N. email: selvamun@srmist.edu.in |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38395284$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_3390_biom15030359 crossref_primary_10_1016_j_ijbiomac_2024_137764 crossref_primary_10_1016_j_colsurfb_2024_114221 crossref_primary_10_1016_j_ijbiomac_2024_131493 crossref_primary_10_3390_polym16213101 |
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