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Self-stabilising wheelchair from Israeli technology start-up lets you cruise through town while standing. Matthew Stock reports.

Nearly 20 years ago Amit Goffer suffered an accident that confined him to a wheelchair. Increasingly dissatisfied with what was on offer, the electrical engineer built this — the UPnRIDE. It’s a robotic exoskeleton that helps people paralysed from the waist down to stand tall in the outside world. (SOUNDBITE) (English) CHIEF TECHNICAL OFFICER AND FOUNDER OF UPNRIDE, DOCTOR AMIT GOFFER SAYING: “The UPnRIDE device, the whole idea is that you can use it outdoors as well as indoors and in a safe manner because they, it automatically balances you and stablizes you… The concept is new because you don’t see any disabled person rolling outside in a standing position so this is a breakthrough in the industry of wheelchair manufacturing, I’m sure that others will follow.” It goes from seated to standing at the push of a button. A gyroscope — similar to that in a two-wheeled Segway — along with self-stabilising software helps manoeuvre upright over uneven urban terrain.

Amazing — fighting cancer with a new drug that self-assembles from individual cells that interact with each other into a complex structure through weak supramolecular interactions.

The first multicellular organism, Volvox, evolved from self-assembly of individual cells. Inspired by this organism, researchers from Brigham and Women’s Hospital have developed a novel approach for treating cancer. Drawing from the lessons of evolution, they designed anti-cancer molecules that can self-assemble with each other into a complex structure through weak supramolecular interactions. The complex, supramolecular therapeutics home into the tumor, increasing anticancer efficacy and reducing side effects.

To engineer the supramolecular therapeutics, the researchers developed a first-of-its-kind computational algorithm that simulates how anticancer molecules interact with each other at the molecular and atomic level. This understanding led to the design of the most optimal building blocks that can click with each other like LEGO blocks to form the supramolecular therapeutic. The researchers have named this computational algorithm Volvox after the biological organism.

Ashish Kulkarni, PhD, an instructor in the Division of Engineering in the Department of Medicine at the Brigham and Women’s Hospital, and the lead author of the paper published in September issue of ACS Nano, said, “The algorithm saves a lot of time during the development of next generation cancer therapy. Before we even go into experimental analysis, we are able to see whether or not there is a high enough concentration of the drug for the treatment to be effective. We hope that our method can eventually be used to treat many different types of cancer.”

Doctors have long dreamed of delivering drugs to specific parts of your body, and they may soon have a clever way to do it: fish. UC San Diego researchers have developed nanoscale metallic fish (they’re just 800 nanometers long) that could carry medicine into the deeper reaches of your bloodstream. Each critter has a gold head and tailfin, as well as a nickel body joined by silver hinges. You only have to subject them to an oscillating magnetic field to make them swim — there’s no need for propellers or a passive (read: slow) delivery system. That, in turn, could make the drug carriers smaller even as they move quickly.

The technology definitely has its flaws. It’s not currently biodegradable, so you may be stuck with this school of fish unless there’s a way to flush them out. Gold and silver aren’t the cheapest metals, either. Scientists are working on biodegradability, however, and they’re hopeful that it will be useful for more than just guiding drugs. You could use to control individual cells, for example, or conduct certain forms of non-invasive surgery. It may just be a matter of refining the technique before you can get medicine exactly where you need it.

Continue reading “Nano-sized metal fish deliver targeted drugs to your body” »

A team of researchers at Jadavpur University here has developed a biodegradable energy harvester from raw fish scales that could in future replace pacemaker devices for the heart.

The energy harvester thus could be tapped as a sustainable green power source for next generation self-powered implantable medical devices.

It also has the potential for personal portable electronics with reduced e-waste elements said the researchers.

Continue reading “Indian Scientists Recycle FIsh Bio-Waste Into Green Energy” »

Finally, your pet can go to work for you.

The brain-computer interface is already being tested in humans with Lou Gehrig’s disease.

Continue reading “Monkey Types 12 Words per Minute With Brain-to-Keyboard Communication” »

This is actually pretty significant to see from DARPA; however, not a total shock given the importance of Synthetic Biology and various parties in the military understanding how CRISPR can be used as a weapon.

A new DARPA program could help unlock the potential of advanced gene editing technologies by developing a set of tools to address potential risks of this rapidly advancing field. The Safe Genes program envisions addressing key safety gaps by using those tools to restrict or reverse the propagation of engineered genetic constructs.

“Gene editing holds incredible promise to advance the biological sciences, but right now responsible actors are constrained by the number of unknowns and a lack of controls,” said Renee Wegrzyn, DARPA program manager. “DARPA wants to develop controls for gene editing and derivative technologies to support responsible research and defend against irresponsible actors who might intentionally or accidentally release modified organisms.”

Continue reading “Setting a Safe Course for Gene Editing Research” »

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The unprecedented success of this firefighter’s face transplant surpassed even his doctors’ expectations.

DARPA’s Safe Genes program aims to build a biosafety and biosecurity toolkit to reduce potential risks and encourage innovation in the field of genome editing

The Safe Genes program could help unlock the potential of advanced gene editing technologies by developing a set of tools to address potential risks of this rapidly advancing field. The Safe Genes program envisions addressing key safety gaps by using those tools to restrict or reverse the propagation of engineered genetic constructs.

“Gene editing holds incredible promise to advance the biological sciences, but right now responsible actors are constrained by the number of unknowns and a lack of controls,” said Renee Wegrzyn, DARPA program manager. “DARPA wants to develop controls for gene editing and derivative technologies to support responsible research and defend against irresponsible actors who might intentionally or accidentally release modified organisms.”

Continue reading “DARPA working on safe Gene Editing Research” »