Posted in | News | Nanomaterials

Researchers Observe Improved Therapeutic Results on Tumors Treated With Communicating Nanoparticles

Researchers of the University of California at San Diego (UCSD), the Sanford-Burnham Medical Research Institute, and MIT have developed a new drug delivery system which can release a first batch of nanoparticles that selectively attaches on the tumor, and then emits a second batch of nanoparticles that gives out the cancer drug.

In a mouse study, the link between nanoparticles improved drug delivery to tumors by almost 40-times. Researchers claim that this new technique could improve effectiveness of drugs to cure cancer and other diseases. The details of the research are published in the Nature Materials journal.

Sangeeta Bhatia, a member of the MIT-Harvard Center of Cancer Nanotechnology Excellence and her colleagues developed their delivery system based on complicated biological systems in which numerous components function in unison to attain a common objective.

The team's method is dependent on a series of reactions known as the blood coagulation cascade that begins when a blood vessel is injured. Clotting substances in the blood react in a complicated manner to generate fibrin strands, which help in the loss of blood. The researchers require two types of nanoparticle for receiving and signaling in order to control the communication capabilities of the cascade.

Signaling particles, comprising the first batch, gets out of the bloodstream and reaches the tumor area through minute holes in the blood vessels that envelop the tumors. The first wave of nanoparticles gives signals to the body that an injury has taken place at a tumor site. This is achieved either by releasing heat or by attaching to a protein that begins the cascade. Proteins attached to fibrin coats the receiving particles. The second batch of receiving particles carries a drug payload, which is released at the tumor site.

Researchers conducted a study of mice; one group of nanoparticle systems released 40 times the amount of anticancer agent doxorubicin than possible with non-communicating nanoparticles. They witnessed a good therapeutic outcome on the tumors of mice undergoing treatment using communicating nanoparticles. Dr. Bhatia and her co-workers aim to change the cooperative nanosystem’s components with drugs to treat patients.

Source: http://www.cancer.gov/

Citations

Please use one of the following formats to cite this article in your essay, paper or report:

  • APA

    Chai, Cameron. (2019, February 12). Researchers Observe Improved Therapeutic Results on Tumors Treated With Communicating Nanoparticles. AZoNano. Retrieved on April 20, 2024 from https://www.azonano.com/news.aspx?newsID=23021.

  • MLA

    Chai, Cameron. "Researchers Observe Improved Therapeutic Results on Tumors Treated With Communicating Nanoparticles". AZoNano. 20 April 2024. <https://www.azonano.com/news.aspx?newsID=23021>.

  • Chicago

    Chai, Cameron. "Researchers Observe Improved Therapeutic Results on Tumors Treated With Communicating Nanoparticles". AZoNano. https://www.azonano.com/news.aspx?newsID=23021. (accessed April 20, 2024).

  • Harvard

    Chai, Cameron. 2019. Researchers Observe Improved Therapeutic Results on Tumors Treated With Communicating Nanoparticles. AZoNano, viewed 20 April 2024, https://www.azonano.com/news.aspx?newsID=23021.

Tell Us What You Think

Do you have a review, update or anything you would like to add to this news story?

Leave your feedback
Your comment type
Submit

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.