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.

Showing posts with label regenerating nerves. Show all posts
Showing posts with label regenerating nerves. Show all posts

Tuesday, May 12, 2015

Bioprinting in 3D: Looks like candy, could regenerate nerve cells

And couldn't this be used for our needs to regenerate dead areas? What research team will figure that out? And who will provide them with the funds to do it?
http://www.rdmag.com/news/2015/05/bioprinting-3d-looks-candy-could-regenerate-nerve-cells?
The printer looks like a toaster oven with the front and sides removed. Its metal frame is built up around a stainless steel circle lit by an ultraviolet light. Stainless steel hydraulics and thin black tubes line the back edge, which lead to an inner, topside box made of red plastic. In front, the metal is etched with the red Bio Bot logo. All together, the gray metal frame is small enough to fit on top of an old-fashioned school desk, but nothing about this 3D printer is old school. In fact, the tissue-printing machine is more like a sci-fi future in the flesh—and it has very real medical applications.
Researchers at Michigan Technological University hope to use this newly acquired 3D bioprinter to make synthesized nerve tissue. The key is developing the right “bioink” or printable tissue. The nanotechnology-inspired material could help regenerate damaged nerves for patients with spinal cord injuries, says Tolou Shokuhfar, an assistant professor of mechanical engineering and biomedical engineering at Michigan Tech.
Shokuhfar directs the In-Situ Nanomedicine and Nanoelectronics Laboratory at Michigan Tech, and she is an adjunct assistant professor in the Bioengineering Department and the College of Dentistry at the University of Illinois at Chicago.
In the bioprinting research, Shokuhfar collaborates with Reza Shahbazian-Yassar, the Richard and Elizabeth Henes Associate Professor in the Department of Mechanical Engineering-Engineering Mechanics at Michigan Tech. Shahbazian-Yassar’s highly interdisciplinary background on cellulose nanocrystals as biomaterials, funded by the National Science Foundation’s (NSF) Biomaterials Program, helped inspire the lab’s new 3D printing research. “Cellulose nanocrystals with extremely good mechanical properties are highly desirable for bioprinting of scaffolds that can be used for live tissues,” says Shahbazian-Yassar.
“We wanted to target a big issue,” Shokuhfar says, explaining that nerve regeneration is a particularly difficult biomedical engineering conundrum. “We are born with all the nerve cells we’ll ever have, and damaged nerves don’t heal very well.”
Other facilities are trying to address this issue as well. Many feature large, room-sized machines that have built-in cell culture hoods, incubators and refrigeration. The precision of this equipment allows them to print full organs. But innovation is more nimble at smaller scales.
“We can pursue nerve regeneration research with a simpler printer set-up,” says Shayan Shafiee, a PhD student working with Shokuhfar. He gestures to the small gray box across the lab bench.
He opens the red box under the top side of the printer’s box. Inside the plastic casing, a large syringe holds a red jelly-like fluid. Shafiee replenishes the needle-tipped printer, pulls up his laptop and, with a hydraulic whoosh, he starts to print a tissue scaffold.
3D Bioprinting Nerve Cells
This May, Marvel released its latest Avengers epic, complete with a 3D printed superhero called The Vision. The android system is printed in a massive 3D printer called The Cradle and is a tribute to both current science and past fiction.
Sci-fi has long dreamed of constructing flesh—think of Luke Skywalker’s hand or LeeLoo in The Fifth Element—but while 3D bioprinting is happening, reality has not quite caught up to that vision. Right now, bioprinting focuses on building up one tissue at a time.
At his lab bench in the nanotechnology lab at Michigan Tech, Shafiee holds up a petri dish. Inside is what looks like a red gummy candy, about the size of a half-dollar.
“This is based on fractal geometry,” Shafiee explains, pointing out the small crenulations and holes pockmarking the jelly. “These are similar to our vertebrae—the idea is to let a nerve pass through the holes.”
Making the tissue compatible with nerve cells begins long before the printer starts up. Shafiee says the first step is to synthesize a biocompatible polymer that is syrupy—but not too thick—that can be printed. That means Shafiee and Shokuhfar have to create their own materials to print with; there is no Amazon.com or even a specialty shop for bioprinting nerves.
Nerves don’t just need a biocompatible tissue to act as a carrier for the cells. Nerve function is all about electric pulses. This is where Shokuhfar’s nanotechnology research comes in: Last year, she was awarded a CAREER grant from NSF for her work using graphene in biomaterials research. “Graphene is a wonder material,” she says. “And it has very good electrical conductivity properties.”
The team is extending the application of this material for nerve cell printing. “Our work always comes back to the question, is it printable or not?” Shafiee says, adding that a successful material—a biocompatible, graphene-bound polymer—may just melt, mush or flat out fail under the pressure of printing. After all, imagine building up a substance more delicate than a soufflé using only the point of a needle. And in the nanotechnology world, a needlepoint is big, even clumsy.
Shafiee and Shokuhfar see these issues as mechanical obstacles that can be overcome.
“It’s like other 3D printers, you need a design to work from,” Shafiee says, adding that he will tweak and hone the methodology for printing nerve cells throughout his dissertation work. He is also hopeful that the material will have use beyond nerve regeneration.
Although widespread medical use of bioprinting is probably a decade or two away, in this lab, the future sits on a tabletop in a little gray box. 

Tuesday, March 17, 2015

Research on injectable oriented hydrogels for spinal cord repair - Maybe stroke?

And with a great stroke association following up on promising research this would be looked at to repurpose it for stroke repair. We need to repair 12 km (7.5 miles) of connections for each minute of infarct. But nothing will occur.

Research on injectable oriented hydrogels for spinal cord repair - Maybe stroke?


The research objective of Dr.-Ing. Laura De Laporte, junior group leader at DWI – Leibniz Institute for Interactive Materials in Aachen, is to develop a minimally invasive therapy for spinal cord injury. Her goal and her scientific approach to develop an injectable material with the ability to provide biochemical and physical guidance for regenerating nerves across the injury site, was selected by the European Research Council (ERC). Laura De Laporte now receives a 1.5 Million Euro ERC Starting Grant for her project ANISOGEL.
Spinal cord injury affects approximately two million people worldwide and is devastating as it leads to a loss of motor and sensory function below the point of injury. Regenerative therapies therefore try to restore nerve tracts and their function. Human neural stem cells or oligodendrocytes, which form the myelin sheet around the nerve cells, have been successfully transplanted into the damaged area and have created a spark of hope. To support these transplanted and other native cells at the injury site, and to guide neuron growth across this area, scientists are also investigating nerve bridges that are made of biomaterials, provide functional domains, and release growths factors. Unfortunately, such implants still face the challenge to stimulate the growing nerves to cross the point of injury and reenter the healthy spinal cord to rebuild functional connections.
In her project ANISOGEL, Laura De Laporte will engineer an injectable biomaterial that can be used as a matrix for a minimally invasive therapy to support oriented regeneration of damaged nerves. The material is based on a soft, water-rich polymeric network (hydrogel), which gels in situ and can be designed to mimic the conditions of the natural cell environment. The physical, chemical, and biological properties of these gels can be tailored bottom-up to resemble the body’s own extracellular matrix that provides mechanical and biological support to the cells.
“A hydrogel-based approach is not new. The innovative aspect about ANISOGEL is that we want to synthesize a material that can be hierarchically structured and form an anisotropic architecture in situ,” explains De Laporte. “This will improve the cells’ spatial orientation, which is crucial for nerve repair. The hydrogel will be further modified with biological signaling molecules to create an environment that stimulates cellular processes necessary for spinal cord regeneration and to regain functionality.”
Laura De Laporte received her Masters in Chemical Engineering at the University of Ghent and obtained her PhD in the laboratory of Prof. Lonnie Shea at Northwestern University in the United States. There, she focused on the development of multiple channel bridges with the ability for DNA and protein delivery for spinal cord repair. As a post-doctoral researcher at EPFL (Switzerland) in the laboratory of Prof. Jeffrey Hubbell, she engineered extracellular matrix-like hydrogels for tissue and nerve repair. She started her junior research group at DWI in October 2013. With the ERC Starting Grant, the European Research Council supports her work for the next five years.