Nanostructured Hyaluronic Acid-based Materials for the Delivery of siRNA

Keval Shah1, Sunita Chawla1, Anuradha Gadeval1

  • 1National Institute of Pharmaceutical Education and Research (NIPER)-Ahmedabad, An Institute of National Importance, Government of India), Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Palaj, Opposite Air Force Station, Gandhinagar, Gujarat-382355, India.

Abstract

Insights

Hyaluronic acid (HA) enhances silencing RNA (siRNA) delivery for cancer treatment, improving targeting and release. Further research is needed to address HA

Area of Science:

  • Biotechnology
  • Nanomedicine
  • Cancer Therapy

Background:

  • Cancer treatment requires effective strategies against abnormal cell growth.
  • Gene therapies, including RNA interference (RNAi) like siRNA, show promise for cancer pharmacotherapy.
  • siRNA offers expanded druggable targets and potential for treating various cancers.

Purpose of the Study:

  • To review hyaluronic acid (HA) and HA-hybridized nanoplatforms for siRNA delivery systems.
  • To discuss current reports on HA-based siRNA delivery for cancer treatment.
  • To address the future potential of HA-based treatment strategies.

Main Methods:

  • Review of existing literature on HA and HA-hybridized nanoplatforms for siRNA delivery.
  • Focus on studies demonstrating HA's role in modifying siRNA release and targeting.
  • Exploration of HA's properties and potential remedies for toxicity.

Main Results:

  • HA-modified siRNA delivery systems demonstrate enhanced targeting in various cancers.
  • HA influences the release kinetics of siRNA.
  • While HA exhibits favorable properties like biocompatibility, its toxicity requires further investigation and mitigation strategies.

Conclusions:

  • Glycosaminoglycan HA-based biopolymers are employed to overcome challenges with genetic tools like siRNA.
  • HA offers beneficial properties including biodegradability, biocompatibility, aqueous solubility, viscoelasticity, and non-immunogenicity.
  • Further research is necessary to fully exploit HA's potential in siRNA delivery for cancer therapy while managing its toxicity.

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