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Engineered Zn(II)-Dipicolylamine-Gold Nanorod Provides Effective Prostate Cancer Treatment by Combining siRNA Delivery and Photothermal Therapy. | LitMetric

AI Article Synopsis

  • Combination cancer treatment utilizing a novel theranostic nanoformulation has shown significant effectiveness in anticancer therapies, integrating photoacoustic imaging with gene and photothermal therapy.
  • The study focuses on gold nanorods (GNR) coated with dipicolyl amine (DPA) that interact with zinc ions, creating stable nanoparticles capable of recognizing and delivering anti-polo-like kinase 1 siRNA (siPLK) to cancer cells.
  • In a mouse model with PC-3 tumors, the combination of siPLK with the Zn(II)/DPA-GNRs led to impressive tumor suppression, suggesting potential for further advancements in cancer treatment strategies involving other polynucleotides.

Article Abstract

Combination cancer treatment has emerged as a critical approach to achieve remarkable anticancer effect. In this study, we prepared a theranostic nanoformulation that allows for photoacoustic imaging as well as combination gene and photothermal therapy. Gold nanorods (GNR) were coated with dipicolyl amine (DPA), which forms stable complexes with Zn cations. The resulting nanoparticles, Zn(II)/DPA-GNR, recognize phosphate-containing molecules, including siRNA, because of the specific interaction between Zn(II) and the phosphates. We chose anti-polo-like kinase 1 siRNA (siPLK) as our example for gene silencing. The strong complexation between Zn(II)/DPA-GNR and siPLK provided high stability to the nano-complexes, which efficiently delivered siRNA into the targeted cancer cells and . The particle served as a theranostic agent because the GNRs of nano-complexes permitted effective photothermal therapy as well as photoacoustic imaging upon laser irradiation. This gene/photothermal combination therapy using siPLK/Zn(II)DPA-GNRs exhibited significant antitumor activity in a PC-3 tumor mouse model. The concept described in this work may be extended to the development of efficient delivery strategies for other polynucleotides as well as advanced anticancer therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695010PMC
http://dx.doi.org/10.7150/thno.22435DOI Listing

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