Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, April 18, 2016

NTU scientists invent bubble technology which can shoot drugs deep into tumours

Our researchers should look into this possibility for delivering tPA. I'm sure a much smaller and less dangerous bolus might be able to be delivered this way. Maybe way past the 4.5 hour current timeframe. But this is a BHAG(Big Hairy Audacious Goal) that will never be attempted because we don't have persons willing to take risks.
http://www.alphagalileo.org/ViewItem.aspx?ItemId=163208&CultureCode=en
Using ultrasound, drug particles can be directed to a specific area
Scientists at Nanyang Technological University (NTU Singapore) have invented a new way to deliver cancer drugs deep into tumour cells.
The NTU scientists create micro-sized gas bubbles coated with cancer drug particles and iron oxide nanoparticles, and then use magnets to direct these bubbles to gather around a specific tumour.
Ultrasound is then used to vibrate the microbubbles, providing the energy to direct the drug particles into a targeted area.
This innovative technique was developed by a multidisciplinary team of scientists, led by Asst Prof Xu Chenjiefrom the School of Chemical and Biomedical Engineering and Assoc Prof Claus-Dieter Ohl from the School of Physical and Mathematical Sciences.
NTU’s microbubbles were successfully tested in mice and the study has been published by the Nature Publishing Group in Asia Materials, the top journal for materials sciences in the Asia-Pacific region.
Overcoming limitations of chemotherapy
Asst Prof Xu, who is also a researcher at the NTU-Northwestern Institute for Nanomedicine, said their new method may solve some of the most pressing problems faced in chemotherapy used to treat cancer.
The main issue is that current chemotherapy drugs are largely non-targeted. The drug particles flow in the bloodstream, damaging both healthy and cancerous cells. Typically, these drugs are flushed away quickly in organs such as the lungs and liver, limiting their effectiveness.
The remaining drugs are also unable to penetrate deep into the core of the tumour, leaving some cancer cells alive, which could lead to a resurgence in tumour growth.
“The first unique characteristic of our microbubbles is that they are magnetic. After injecting them into the bloodstream, we are able to gather them around the tumour using magnets and ensure that they don’t kill the healthy cells,” explains Asst Prof Xu, who has been working on cancer diagnosis and drug delivery systems since 2004.
“More importantly, our invention is the first of its kind that allows drug particles to be directed deep into a tumour in a few milliseconds. They can penetrate a depth of 50 cell layers or more – which is about 200 micrometres, twice the width of a human hair. This helps to ensure that the drugs can reach the cancer cells on the surface and also inside the core of the tumour.”
Clinical Associate Professor Chia Sing Joo, a Senior Consultant at the Tan Tock Seng Hospital’s Endoscopy Centre and the Urology & Continence Clinic, was one of the consultants for this study.
A trained robotic surgeon experienced in the treatment of prostate, bladder and kidney cancer, Assoc Prof Chia said, “For anticancer drugs to achieve their best effectiveness, they need to penetrate into the tumour efficiently in order to reach the cystoplasm of all the cancer cells that are being targeted without affecting the normal cells.
“Currently, these can be achieved by means of a direct injection into the tumour or by administering a large dosage of anticancer drugs, which can be painful, expensive, impractical and might have various side effects.”
The specialist in Uro-oncology added that if NTU’s technology proves to be viable, clinicians might be able to localise and concentrate the anticancer drugs around a tumour, and introduce the drugs deep into tumour tissues in just a few seconds using a clinical ultrasound system.
“If successful, I envisage it can be a good alternative treatment in the future, one which is low cost and yet effective for the treatment of cancers involving solid tumours, as it might minimise the side effects of drugs.”
New drug delivery system
The motivation for this research project is to find alternative solutions for drug delivery systems that are non-invasive and safe.
Ultrasound uses soundwaves with frequencies higher than those heard by the human ear. It is commonly used for medical imaging such as to get diagnostic images.
Magnets, which can draw and attract the microbubbles, are already in use in diagnostic machines such the Magnetic Resonance Imaging (MRI).
“We are looking at developing novel drug carriers – essentially better ways of delivering drugs with minimum side effects,” explained Prof Ohl, an expert in biophysics who had published previous studies involving drug delivery systems and bubble dynamics.
“Most prototype drug delivery systems on the market face three main challenges before they can be commercially successful: they have to be non-invasive, patient-friendly and yet cost-effective.
“Using the theory of microbubbles and how their surface vibrates under ultrasound, we were able to come up with our solution that addresses these three challenges.”
Interdisciplinary team
This study, which took two and a half years, involved a 12-man international interdisciplinary team consisting of NTU scientists as well as scientists from City University of Hong Kong and Tel Aviv University in Israel. Two NTU undergraduates doing their Final Year Project and one student in Summer Research Internship Programme (NTU) were also part of the team.
Moving forward, the team will be adopting this new drug delivery system in studies on lung and liver cancer using animal models, and eventually clinical studies.
They estimate that it will take another eight to ten years before it reaches human clinical trials.
http://media.ntu.edu.sg/NewsReleases/Pages/newsdetail.aspx?news=581d56b4-84d3-46a9-a155-3a68431d615d

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