news

Nanobombs – the future of cancer drug delivery?

Posted: 3 December 2015 | Victoria White | No comments yet

Researchers say nanobombs might overcome a biological barrier that has blocked development of agents that work by altering the expression of genes in cancer cells…

Researchers have developed ‘nanobombs’ – nanoparticles that swell and burst when exposed to near-infrared laser light.

The researchers, from The Ohio State University Comprehensive Cancer Centre – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC – James), say the nanobombs might overcome a biological barrier that has blocked development of agents that work by altering the expression of genes in cancer cells. The agents might kill cancer cells outright or stall their growth.

The kinds of agents that change gene expression are generally forms of RNA (ribonucleic acid), and they are notoriously difficult to use as drugs. First, they are readily degraded when free in the bloodstream. In this study, packaging them in nanoparticles that target tumour cells solved that problem.

 

Reserve your FREE place

 


Are you looking to optimise antibody leads in your drug discovery? Register for this webinar to find out how!

30 July 2025 | 10:00 AM BST | FREE Webinar

Join this webinar to hear from Dr. Lei Guo as she shares how early insights into liability, PK, stability, and manufacturability can help you optimise antibody leads in early drug discovery – and mitigate downstream risks later in development.

What You’ll Learn:

  • How to assess key developability risks early
  • How in silico modelling and in vitro testing can be combined to predict CMC risks earlier in discovery stage
  • How micro-developability strategies are tailored for complex or novel formats

Don’t miss your chance to learn from real-world leaders

Register Now – It’s Free!

 

This study suggests that the nanobombs might also solve the second problem. When cancer cells take up ordinary nanoparticles, they often enclose them in endosomes. This prevents the drug molecules from reaching their target, and they are soon degraded. However, nanobombs contain a chemical that vaporises, causing them to swell three times or more in size when exposed to near-infrared laser light. The endosomes burst, dispersing the RNA agent into the cell.

“A major challenge to using nanoparticles to deliver gene-regulating agents such as microRNAs is the inability of the nanoparticles to escape the compartments, the endosomes, that they are encased in when cells take up the particles,” says principal investigator Xiaoming (Shawn) He, PhD, associate professor of Biomedical Engineering and member of the OSUCCC – James Translational Therapeutics Programme.

“We believe we’ve overcome this challenge by developing nanoparticles that include ammonium bicarbonate, a small molecule that vaporises when exposing the nanoparticles to near-infrared laser light, causing the nanoparticle and endosome to burst, releasing the therapeutic RNA,” He explains.

The nanobombs encapsulate a leavening agent used in baking

For their study, He and colleagues used human prostate-cancer cells and human prostate tumours in an animal model. The nanoparticles were equipped to target cancer stem-like cells (CSCs). CSCs often resist therapy and are thought to play an important role in cancer development and recurrence.

The therapeutic agent in the nanoparticles was a form of microRNA called miR-34a. The researchers chose this molecule because it can lower the levels of a protein that is crucial for CSC survival and may be involved in chemotherapy and radiation therapy resistance.

The nanoparticles also encapsulate ammonium bicarbonate, which is a leavening agent sometimes used in baking. Near-infrared laser light, which induces vaporisation of the ammonium bicarbonate, can penetrate tissue to a depth of one centimetre. For deeper tumours, the light would be delivered using minimally invasive surgery.

Related topics
,

Related organisations

Leave a Reply

Your email address will not be published. Required fields are marked *