Biomedical application of chitosan-based nanoscale delivery systems: Potential usefulness in siRNA delivery for

Milad Ashrafizadeh1, Masoud Delfi2, Farid Hashemi3

  • 1Sabanci University Nanotechnology Research and Application Center (SUNUM), Tuzla, 34956 Istanbul, Turkey; Faculty of Engineering and Natural Sciences, Sabanci University, Orta Mahalle, Üniversite Caddesi No. 27, Orhanlı, Tuzla, 34956 Istanbul, Turkey.

Carbohydrate Polymers
|March 13, 2021
PubMed

Insights

Chitosan nanoparticles effectively deliver small interfering RNA (siRNA) for cancer therapy, suppressing tumor growth and metastasis. These biocompatible nanoparticles show promise for clinical applications in cancer treatment.

Area of Science:

  • Biotechnology
  • Nanomedicine
  • Cancer Therapy

Background:

  • Gene therapy using small interfering RNA (siRNA) shows promise for cancer treatment by down-regulating target genes.
  • Challenges with siRNA include off-targeting and enzymatic degradation, limiting its therapeutic efficacy.
  • Nanoparticles offer a solution for siRNA delivery, enhancing gene silencing capabilities.

Purpose of the Study:

  • To explore the potential of chitosan (CS) nanoparticles for delivering siRNA in cancer therapy.
  • To evaluate the efficacy of CS nanoparticles in suppressing cancer proliferation, metastasis, and chemoresistance.
  • To discuss the advantages of CS nanoparticles, including their biocompatibility, biodegradability, and potential for co-delivery.

Main Methods:

  • Utilizing chitosan (CS) nanoparticles for the encapsulation and delivery of siRNA.
  • Investigating the use of pH-sensitive CS nanoparticles for enhanced therapeutic effects.
  • Exploring chemical modifications of CS nanoparticles for improved stability and co-delivery of anti-tumor agents.

Main Results:

  • siRNA-loaded CS nanoparticles demonstrated suppression of cancer cell proliferation and metastasis.
  • pH-sensitive CS nanoparticles showed particular efficacy in inhibiting cancer progression.
  • CS nanoparticles facilitated the co-delivery of siRNA and other anti-tumor agents, enhancing stability.

Conclusions:

  • CS nanoparticles represent a promising and safe platform for siRNA delivery in cancer gene therapy.
  • Pre-clinical studies support the potential of CS-based nanoparticles for effective cancer treatment.
  • Further clinical investigations are warranted to evaluate the therapeutic application of these nanoparticles in cancer patients.