Lifeboat Foundation

This is a link to the video. https://www.youtube.com/watch?v=hptgw_-59YY

Thanks to MassDevice, we learned of a new company that’s developed a small surgical robot for performing laparoscopic procedures that may lower the cost and offer robotic capability to clinics that don’t have millions of dollars in discretionary funds. Virtual Incision Corporation is a spin-off out of the University of Nebraska and the company just raised $11.2M in equity financing to sponsor a feasibility study of its robotic technology.

The system was designed to fit almost completely into the abdominal cavity via a single incision, with only the handle and cables staying on top. It’s intended for surgeries that are often performed in an open fashion that can benefit from robotic laparoscopy, such as colon resections.

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A device that reanimates organs taken from dead patients has shown promise in heart transplant surgeries, though it’s raising some ethical concerns, as well. As MIT Technology Review reports, the so-called “heart in a box” uses tubing and oxygen to pump blood and electrolytes into hearts from recently deceased patients, allowing the organs to continue functioning within a chamber. The system, developed by Massachusetts-based Transmedics, has been successfully deployed in at least 15 heart transplants in the UK and Australia, and is awaiting regulatory approval in the US.

Until now, hearts used for transplants have usually been extracted from brain-dead patients; those from dead patients have been considered too damaged. Once removed, the hearts are also stored and transported in cold temperatures to avoid rapid deterioration, though scientists have begun using devices like the heart in a box to keep the organs warm and functioning. That, doctors say, could increase the pool of donated hearts by between 15 and 30 percent.

Some say the $250,000 device is still too expensive to be deployed widely, and that it needs greater automation. For medical ethicists, the question is how long surgeons should wait before removing a heart that has stopped. “How can you say it’s irreversible, when the circulatory function is restored in a different body?” Robert Truog, an ethicist at Harvard University, tells MIT Technology Review. “We tend to overlook that because we want to transplant these organs.” Truog says he believes those patients can be considered dead, though it’s ultimately a decision for family members to make. “They are dying and it’s permissible to use their organs. The question is whether they are being harmed, and I would say they are not.”

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A key mystery of the DNA replication process has been unraveled by researchers from King Abdullah University of Science and Technology (KAUST).

Before a bacterium can divide, it must make a copy of its genetic material, the circular DNA molecules that resemble bunched rubber bands, through a process called DNA replication. In this process, the two strands of DNA making up the circular DNA molecule unwind and separate to become templates for generating new strands.

To ensure the process is well regulated, the bacterium has set a number of “roadblocks,” or termination sites on the DNA, to ensure the permanent stoppage of replication forks, Y-shaped structures formed between the strands as the DNA molecule splits.

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A UCSF-led team has developed a technique to build tiny models of human tissues, called organoids, more precisely than ever before using a process that turns human cells into a biological equivalent of LEGO bricks. These mini-tissues in a dish can be used to study how particular structural features of tissue affect normal growth or go awry in cancer. They could be used for therapeutic drug screening and to help teach researchers how to grow whole human organs.

The new technique — called DNA Programmed Assembly of Cells (DPAC) and reported in the journal Nature Methods on August 31, 2015 — allows researchers to create arrays of thousands of custom-designed organoids, such as models of human mammary glands containing several hundred cells each, which can be built in a matter of hours.

There are few limits to the tissues this technology can mimic, said Zev Gartner, PhD, the paper’s senior author and an associate professor of pharmaceutical chemistry at UCSF. “We can take any cell type we want and program just where it goes. We can precisely control who’s talking to whom and who’s touching whom at the earliest stages. The cells then follow these initially programmed spatial cues to interact, move around, and develop into tissues over time.”

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Engineers at the University of Toronto just made assembling functional heart tissue as easy as fastening your shoes. The team has created a biocompatible scaffold that allows sheets of beating heart cells to snap together just like Velcro™.

“One of the main advantages is the ease of use,” says biomedical engineer Professor Milica Radisic, who led the project. “We can build larger tissue structures immediately before they are needed, and disassemble them just as easily. I don’t know of any other technique that gives this ability.”

Growing heart muscle cells in the lab is nothing new. The problem is that too often, these cells don’t resemble those found in the body. Real heart cells grow in an environment replete with protein scaffolds and support cells that help shape them into long, lean beating machines. In contrast, lab-grown cells often lack these supports, and tend to be amorphous and weak. Radisic and her team focus on engineering artificial environments that more closely imitate what cells see in the body, resulting in tougher, more robust cells.

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Learning the secrets of brain plasticity means learning how to help those suffering from stroke or dementia.

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“Increasing automation limits the ability of authorities to profit off human error.”

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A Tesla Model S has reportedly been driven 452.8 miles (728.7 km) on a single charge in a feat that, according to driver Bjørn Nyland and the World Record Academy, sets a new world record for an electric production car.

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Ice creams and hot summer days seem to go together perfectly, until you realise the heat of the latter is turning the former into a melting mass of deliciousness oozing down the side of your cone.

Luckily for us, scientists have discovered a naturally occurring protein that can be used in ice cream to make it more resistant to melting than the ice creams we enjoy today. According to researchers at the Universities of Edinburgh and Dundee in Scotland, the protein, which is called BslA, will allow ice cream to stay frozen for longer by binding together the air, fat and water in the product.

Not only will this make ice cream more impervious to things like heat, but the researchers say it also results in a super-smooth consistency. The protein, which can be made inside friendly bacteria, adheres to fat droplets and air bubbles, making for a more stable ice cream mixture that prevents the development of ice crystals.

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