-

Science

The most amazing health innovations of 2018

Posted on

 

Countless new products and medications hit stores’ shelves and doctors’ prescription pads every year. Many are a result of small tweaks to already available treatments. A select few, though, totally change the game: A preventative migraine drug slashes monthly headaches in half, an injectable gene restores sight to those with a degenerative eye condition, and a better-designed sunscreen helps more people keep damaging rays at bay. These 10 medical advances represent how science, technology, and creative thinking can help us live longer, better lives.

Aimovig by Amgen & Novartis

Aimovig by Amgen & Novartis

The first migraine-prevention drug
Twelve percent of people worldwide live with the pounding head pain and other debilitating effects of migraine. What’s worse? The drugs commonly used to prevent the attacks are meant for other ailments—high blood pressure, seizures, depression. These medicines don’t always work and often cause intolerable side effects. The newly-approved drug Aimovig is the first to prevent migraines by targeting a specific molecular interaction involved in the disorder. The medicine blocks a neurotransmitter called the calcitonin gene related peptide (CGRP), which stimulates brain cells active in migraines. The monthly injection reduces the number of monthly migraine attacks by an average of 50 percent, with far fewer side effects.

Amgen

Black Girl Sunscreen SPF 30 Moisturizing Lotion by Black Girl Sunscreen

 

Black Girl Sunscreen SPF 30 Moisturizing Lotion by Black Girl Sunscreen

 

Finally, sunscreen designed for dark skin
Everyone who soaks up the sun needs skin protection. Yet, most sunscreens leave an undesirable white cast on darker skin that won’t fade until washed off with soap. Black Girl Sunscreen, though, is specifically designed for people of color. The FDA-approved product includes a blend of UVA- and UVB-fighting chemicals selected because their chemistry avoids that white residue. The lotion also contains multiple moisturizers to help prevent dry skin.

Black Girl Sunscreen

Abilify MyCite by Otsuka America Pharmaceutical & Proteus Digital Health

Abilify MyCite by Otsuka America Pharmaceutical & Proteus Digital Health

 

A pill that tells when it’s popped
As many as half of people who need daily medications don’t take their drugs on the prescribed schedule, which can reduce effectiveness. Technology incorporated in the antipsychotic medicine Abilify now lets physicians and patients track when meds go down. Once swallowed, embedded sensors in the high-tech drug—dubbed Abilify MyCite—generate an electrical signal that a band-aid-sized skin patch picks up and transmits to a nearby mobile device. Abilify MyCite is the first digital drug to gain FDA approval, but the sensor’s maker, Proteus Digital Health, plans to incorporate its device into other medicines, as well.

Proteus Digital Health

 

Luxturna by Spark Therapeutics

Luxturna by Spark Therapeutics

 

Replacing bad genes with good ones
In a group of inherited eye disorders collectively known as retinal dystrophy, faulty genes lead photoreceptors (retinal cells critical to vision) to slowly die over time, degrading sight. Luxturna is the first treatment for the condition, and also the first gene therapy to perform its cell modification within the body. It’s for people who have a mutation in a gene called RPE65 and consists of a benign virus that contains a healthy version of the gene. Treatment involves just one injection in each eye. After infusion, the virus ferries the gene into retinal cells. Then, a protein encoded by the gene restores the function of any remaining photoreceptors, thus slowing or stopping further vision loss. Researchers say Luxturna could pave the way for future treatments that deliver healthy genes into cells that lack them.

Spark Therapeutics

Confirm Rx insertable cardiac monitor by Abbott

Confirm Rx insertable cardiac monitor by Abbott

 

Heart monitor the size of a paper clip
Abnormal heart rhythms known as arrhythmias, in which the ticker beats too fast or too slow, come with a risk for strokes and heart attacks. If a patient has suspicious symptoms, such as palpitations or fainting, a doctor will often test for an arrhythmia by having them wear an unwieldy device for a couple days to record the electrical signals that control heart contraction. Abbott’s Confirm Rx, a paper-clip-sized device inserted under the skin, makes the same measurements, but is much less onerous to patients. It continuously monitors the heart’s electrical activity by performing a single-lead electrocardiogram, and it transmits the data via Bluetooth to the doctor for review.

Abbott

 

Eversense Continuous Glucose Monitoring System by Senseonics Holding

Eversense Continuous Glucose Monitoring System by Senseonics Holding

 

The three-month blood-sugar monitor
Many people with diabetes prick a finger several times a day to measure their blood-sugar (glucose) levels. They need the information to determine how much insulin to take to prevent levels from rising too high. Aside from being painful and annoying, finger sticks don’t track sugar between tests—a concern because chronically high levels can lead to heart disease, blindness, and kidney failure. Some existing devices avoid the bloodletting and measure glucose continuously for a week. But the Eversense Continuous Glucose Monitoring System does it for far longer: a full 90 days. The sensing component, which is about the size of a grain of rice, sits directly under the skin. It measures glucose every five minutes and sends the readings to a nearby mobile device for reference and storage.

Senseonics Holding

Apple Watch Series 4 by Apple

Apple Watch Series 4 by Apple

 

Arrhythmia-spotting smartwatch
Smartwatches can track your steps, count your pulse, and even guide you through a deep, relaxing breathe. Now, the Apple Watch has taken a giant leap forward in the medical sphere: The Series 4 can do an electrocardiogram (ECG) to measure the electrical activity of the heart—a test usually performed in a doctor’s office. When you hold a finger firmly on the digital crown, conductors in the back of the watch and the circlet measure your heart’s electrical pulses and display the rhythm on-screen. Apple’s ECG is greenlit to detect a type of arrhythmia called atrial fibrillation (a condition in which the upper chambers of the heart tremble instead of beat, affecting blood flow). It’s not as powerful a test as those in doctors’ offices, and how well it stacks up against other arrhythmia detectors isn’t clear yet. However, its potential benefit to public health can’t be understated: In the future, if users can opt-in to sharing their data with research studies, it could help doctors identify early warning signs of the disease.

Apple

Butterfly iQ by Butterfly

Butterfly iQ by Butterfly

 

Ultrasounds for everyone
Ultrasounds are incredibly useful: They allow physicians to visualize our internal organs, muscles, tendons, and even the blood vessels in our hearts. But the machines are also cumbersome and expensive. Costly piezoelectric crystals must be carefully incorporated into each probe, and different areas of the body require their own probes; a high-frequency ultrasound reaches shallow tissue just under the skin, while a low-frequency one visualizes tissue deep under the skin, like the heart muscle. The Butterfly iQ is different. Instead of a piezo crystal, the device uses a far cheaper silicon chip that can generate frequencies needed for any depth. This reduces the cost of an ultrasound machine from $40,000 or more to just $2,000, putting the purchase within reach of more physicians.

Butterfly

Shingrix by GlaxoSmithKline Biologicals

Shingrix by GlaxoSmithKline Biologicals

 

Surefire shingles vaccine
At some point in life, one in three Americans will suffer from shingles, a painful, itchy, and blistery rash that develops on one side of the body. Caused by the same virus as chickenpox in children, the rash usually resolves over a few weeks. Other times, though, it can cause pain in the affected area that persists for months or years. And, in rare cases, it can also lead to hearing and vision loss and strokes. The sole vaccine that was available until recently prevented the condition only about half the time. Late last year, though, the FDA approved Shingrix, a vaccine that prevents the rash in 90 percent of recipients in the first year and still works in 85 percent of patients four years later. Shingrix consists of a protein found on the virus’s surface and a substance that enhances immune responses; when the immune system “sees” the protein, it seeks out and attacks the virus itself, preventing trouble.

GlaxoSmithKline Biologicals

 

 


Biktarvy by Gilead Sciences

Biktarvy by Gilead Sciences

 

The most-potent HIV drug yet
People infected with HIV, a type of retrovirus, must adhere strictly to treatment with antiretrovirals to avoid AIDS, the stage of infection that severely hampers the immune system’s ability to fight other attackers. This year, the FDA approved the most-potent therapy yet. Brand-named Biktarvy, the once-daily pill contains three drugs that tamp the virus in different ways, and together are more effective than they would be as solo treatments. One ingredient in particular, Bictegravir, is entirely new, and recent studies show it to be at least as effective as other anti-HIV retro virals on the market, with fewer side effects. It blocks one of the HIV proteins that plays a key role in spreading the virus throughout the body, and Bictegravir’s distinctive structure also minimizes unwanted interactions with other drugs.

Gilead Sciences

source: https://www.popsci.com/best-health-innovations-2018?fbclid=IwAR0NqnCDrFcaqK-bs4VFDCkaDFRKnN6lIZXRrkQ_Sh1-XdWBNGr-gP7Wsb8#page-3

This Biodegradable Pill Could Replace Painful Injections

Posted on

d3cb0a444115f0e713796b36bcb256c0web

Image: MIT

Many drugs cannot be taken orally as they get broken down in the gastrointestinal (GI) tract by enzymes before they’re absorbed. Until now, these drugs have had to be delivered via injection, which can be painful, and previous attempts to ‘encapsulate’ them have been expensive, impractical and ultimately unsuccessful.

But there may be a better solution. Published in the Journal of Pharmaceutical Sciences, researchers at Massachusetts Institute of Technology (MIT) in the US have collaborated with the Massachusetts General Hospital to design an acrylic capsule that’s covered with tiny stainless steel needles.

The capsule can be swallowed, and once it reaches the GI tract, the pH-sensitive coating dissolves, uncovering the small micro-needles. The drug is then released into these needles, which slowly inject it directly into the stomach lining. Thankfully, as there are no pain receptors in the GI tract, this process is painless.

The prototype has been tested on pigs, where a needle-coated capsule containing insulin – the hormone required by diabetics that regulates blood sugar levels – was administered orally. The results showed that this insulin was successfully injected into the stomach lining, small intestine, and colon, and that there were no signs of tissue damage as the capsule moved through the digestive tract.

Of particular interest was the fact the pigs’ blood glucose levels decreased more rapidly after they were given insulin via the needle-coated capsule than when the drug was administered via subcutaneous injection, suggesting this new method may actually be more effective.

“The kinetics are much better, and much faster-onset, than those seen with traditional under-the-skin administration,” said Giovanni Traverso, one of the lead researchers of the study, in a press release.

The team predict that this revolutionary form of drug delivery will be beneficial for vaccines, as well as antibodies required in cancer treatments and other autoimmune disorders such as Crohn’s disease.

“For molecules that are particularly difficult to absorb, this would be a way of actually administering them at much higher efficiency,” said Traverso.

The next step is to refine the capsule so that it is made of a degradable polymer that can naturally release its drug alongside the contractions of the digestive tract.

This new method of drug delivery can potentially redefine the face of immunisation and other needle-administered practises. The real question is, will people feel more comfortable with many small needles inside of them, as opposed to one large one outside of them?

This Biodegradable Pill Could Replace Painful Injections

This Biodegradable Pill Could Replace Painful Injections.

Posted by Hashem Al-Ghaili on Sunday, November 11, 2018

 

 

Watch more about the new drug-delivery method:

[youtube https://www.youtube.com/watch?v=PBCa5bM3zjg?enablejsapi=1]
source MIT
This article was originally published at www.sciencealert.com

World of Atoms

Posted on

 

 

https://www.facebook.com/clubphysicsnp/videos/222766195065530/

Stress Depression and their effect to Brain

Posted on

 

 

How Stress Affects Your Brain

Stress Changes Your Brain and Affects its Functions.

Posted by Hashem Al-Ghaili on Wednesday, November 7, 2018

 

https://www.youtube.com/watch?v=uQd_i0jm1NE

Stress symptoms: Effects on your body and behavior

Stress symptoms may be affecting your health, even though you might not realize it. You may think illness is to blame for that nagging headache, your frequent insomnia or your decreased productivity at work. But stress may actually be the culprit.

Common effects of stress

Indeed, stress symptoms can affect your body, your thoughts and feelings, and your behavior. Being able to recognize common stress symptoms can give you a jump on managing them. Stress that’s left unchecked can contribute to many health problems, such as high blood pressure, heart disease, obesity and diabetes.

Common effects of stress on your body

  • Headache
  • Muscle tension or pain
  • Chest pain
  • Fatigue
  • Change in sex drive
  • Stomach upset
  • Sleep problems

Common effects of stress on your mood

  • Anxiety
  • Restlessness
  • Lack of motivation or focus
  • Feeling overwhelmed
  • Irritability or anger
  • Sadness or depression

Common effects of stress on your behavior

  • Overeating or undereating
  • Angry outbursts
  • Drug or alcohol abuse
  • Tobacco use
  • Social withdrawal
  • Exercising less often

Act to manage stress

If you have stress symptoms, taking steps to manage your stress can have numerous health benefits. Explore stress management strategies, such as:

  • Regular physical activity
  • Relaxation techniques, such as deep breathing, meditation, yoga, tai chi or getting a massage
  • Keeping a sense of humor
  • Socializing with family and friends
  • Setting aside time for hobbies, such as reading a book or listening to music

Aim to find active ways to manage your stress. Inactive ways you may use to manage stress — such as watching television, surfing the Internet or playing video games — may seem relaxing, but they may increase your stress over the long term.

And be sure to get plenty of sleep and eat a healthy, balanced diet. Avoid tobacco use, excess caffeine and alcohol intake, and the use of illicit substances.

When to seek help

If you’re not sure if stress is the cause or if you’ve taken steps to control your stress but your symptoms continue, see your doctor. Your doctor may want to check for other potential causes. Or, consider seeing a professional counselor or therapist, who can help you identify sources of your stress and learn new coping tools.

Also, if you have chest pain, especially if it occurs during physical activity or is accompanied by shortness of breath, sweating, dizziness, nausea, or pain radiating into your shoulder and arm, get emergency help immediately. These may be warning signs of a heart attack and not simply stress symptoms.

How Hearing Works

Posted on

How Hearing Works

 

How Hearing Works

How Hearing Works.

Posted by Hashem Al-Ghaili on Friday, July 13, 2018

 

how hearing works

 

Hearing is an essential part of how we communicate with others and become aware of sounds that happen in our immediate environment. Our hearing abilities start in our ears with the channeling of sound along the hearing pathway which are turned into electrical signs that travel to the brain (shown in the diagram above).

The hearing pathway is divided into four distinct sections that play important and unique parts in our overall hearing abilities.

These sections are shown below show in more detail how hearing works:

  • Outer Ear
  • Middle Ear
  • Inner Ear
  • Vestibule.

Hearing Loss occurs when one or more parts of the ear and/or the parts of the brain that make up the hearing pathway do not function normally.

For a quick and visual overview of how hearing works, hearing loss and hearing technologies try using our Interactive Ear.

Outer Ear

outerear

The Outer Ear captures and concentrates the sounds we hear and channels them into the Middle Ear. The Outer Ear is made up of two parts called the Pinna and the Ear Canal. The Pinna is a soft and flexible tissue that makes up the most of the visible ear. It plays an important role in shaping the sound to help the brain work out the direction from which sounds are coming.

The Ear Canal is the physical pathway that directs sound, which has arrived at the Outer Ear, also known as the Pinna into the Middle Ear.

Middle Ear

middle

The Middle Ear starts with the Tympanic Membrane, better known as the Eardrum, which vibrates due to differences in pressure caused by soundwaves.

The Eardrum is connected to three small interconnected bones called the Ossicles that vibrate with the Eardrum.

The last of these bones, called the Stapes, the passes on these vibrations into the Inner Ear.

 

Inner Ear

InnerEar

The Inner Ear contains the organs that create our sense of hearing and balance. The Cochlea is the organ in that converts mechanical sound vibrations into nerve signals. using hair-like nerve filaments, called hair cells. These hair cells are arranged so that different cells respond to different pitches.

The electrical currents produced in the Cochlea are then transmitted to the auditory nerve, which passs through several ‘relay stations’ in the Brainstem before reaching a more complex part of the brain, the Auditory Cortex, where the information contained sound can interpret and understood.

The Vestibule

vestibule

The Vestibule, with its Semicircular Canals, is the organ that provides us with our sense of balance, direction and spatial orientation. Vestibule problems can be linked to hearing problems such as Hyperacusis,Meniere’s Disease, Tinnitus and Vertigo, which can also affect a person’s balance.

 

 

https://youtu.be/0NJ_EAQjR3c

 

 

 

 

 

New Self-Healing Concrete Uses Fungus To Fix Cracks

Posted on

USING FUNGI TO FIX BRIDGES

Assistant professor Congrui Jin (center) with two Binghamton University graduate students from the Mechanical Engineering Department. Image Credit: Jonathan Cohen.

Binghamton University researchers have been working on a self-healing concrete that uses a specific type of fungi as a healing agent.

[youtube https://www.youtube.com/watch?v=IC88GhAiXgk?showinfo=1&controls=1&modestbranding=1&portrait=0&rel=0&enablejsapi=1&origin=https:%2F%2Fwww.binghamton.edu]

America’s crumbling infrastructure has been a topic of ongoing discussion in political debates and campaign rallies. The problem of aging bridges and increasingly dangerous roads is one that has been well documented and there seems to be a consensus from both democrats and republicans that something must be done.

However, spending on infrastructure improvement has continually gone down. The New York Times reported in 2016, based on a report for the Bureau of Economic Analysis, that “in the 1950s and ’60s, federal, state and local governments were spending twice as much on the nation’s public infrastructure, relative to the size of the economy, as they are today.”

The hesitancy to invest in America’s infrastructure may come from a number of sources, but the fact remains that most want something to be done before the consequences are too severe.

Binghamton University assistant professor Congrui Jin has been working on this problem since 2013, and recently published her paper “Interactions of fungi with concrete: significant importance for bio-based self-healing concrete” in the academic journal Construction & Building Materials.

This research is the first application of fungi for self-healing concrete, a low-cost, pollution-free and sustainable approach.

New Self-Healing Concrete Uses Fungus To Fix Cracks

New self-healing concrete uses fungus to fix cracks.

Posted by Hashem Al-Ghaili on Thursday, July 5, 2018

Why is infrastructure crumbling?

Jin’s studies have looked specifically at concrete and found that the problem stems from the smallest of cracks in the concrete.

“Without proper treatment, cracks tend to progress further and eventually require costly repair,” said Jin. “If micro-cracks expand and reach the steel reinforcement, not only the concrete will be attacked, but also the reinforcement will be corroded, as it is exposed to water, oxygen, possibly CO2 and chlorides, leading to structural failure.”

These cracks can cause huge and sometimes unseen problems for infrastructure. One potentially critical example is the case of nuclear power plants that may use concrete for radiation shielding.

What can be done?

While remaking a structure would replace the aging concrete, this would only be a short-term fix until more cracks again spring up. Jin wanted to see if there was a way to fix the concrete permanently.

“This idea was originally inspired by the miraculous ability of the human body to heal itself of cuts, bruises and broken bones,” said Jin. “For the damaged skins and tissues, the host will take in nutrients that can produce new substitutes to heal the damaged parts.”

Jin worked with associate professor Ning Zhang from Rutgers University, and professor Guangwen Zhou and associate professor David Davies from Binghamton University with support from the Research Foundation for the State University of New York’s Sustainable Community Transdisciplinary Area of Excellence Program. Together, the team set out to find a way to heal concrete.

The team found an unusual answer, a fungus called Trichoderma reesei.

When this fungus is mixed with concrete, it originally lies dormant — until the first crack appears.

“The fungal spores, together with nutrients, will be placed into the concrete matrix during the mixing process. When cracking occurs, water and oxygen will find their way in. With enough water and oxygen, the dormant fungal spores will germinate, grow and precipitate calcium carbonate to heal the cracks,” explained Jin.

“When the cracks are completely filled and ultimately no more water or oxygen can enter inside, the fungi will again form spores. As the environmental conditions become favorable in later stages, the spores could be wakened again.”

The research is still in fairly early stages with the biggest issue being the survivability of the fungus within the harsh environment of concrete. However, Jin is hopeful that with further adjustments the Trichoderma reesei will be able to effectively fill the cracks.

“There are still significant challenges to bring an efficient self-healing product to the concrete market. In my opinion, further investigation in alternative microorganisms such as fungi and yeasts for the application of self-healing concrete becomes of great potential importance,” said Jin

 

 

Can bacteria-slaying viruses defeat antibiotic-resistant infections?

Posted on

Phages like these studding an Escherichia coli bacterium target specific bacteria, complicating their use in medicine.
 
EYE OF SCIENCE/SCIENCE SOURCE

Can bacteria-slaying viruses defeat antibiotic-resistant infections? A new U.S. clinical center aims to find out

One piece of good news can make all the difference. In the fight against antibiotic-resistant infections, a decades-old approach based on bacteria-slaying viruses called phages has been sidelined by technical hurdles, dogged by regulatory confusion, and largely ignored by drug developers in the West. But 2 years ago, researchers at the University of California, San Diego (UCSD), used phages to knock out an infection that nearly killed a colleague. Propelled by that success and a handful of others since, UCSD is now launching a clinical center to refine phage treatments and help companies bring them to market.

A first in North America, the center will initially consist of 16 UCSD researchers and physicians. It aims to be a proving ground for a treatment that has long been available in parts of Eastern Europe, but that still lacks the support of rigorous clinical trials. “There have been just a ton of failures and false starts,” says Paul Bollyky, a microbiologist and physician at Stanford University Medical Center in Palo Alto, California, who studies phages. “The fact that a major American medical center is going to set up an ongoing enterprise around phage therapy … that’s kind of a game changer for the field, at least in the United States.”

Turning phages—found in soil, water, and sewage—into treatments isn’t straightforward. Because each of the millions of phage strains in nature targets a specific bacterium, putting them to use means finding the specific phages that attack the menace at hand. Still, clinical centers overseas, in Georgia and Poland, have reported encouraging results with phages over the years. And the rise of antibiotic-resistant infections has prompted a handful of U.S. companies and research centers to reconsider the approach.

The case that mobilized the UCSD team hit close to home. In 2015, UCSD psychologist Tom Patterson was airlifted home after a vacation in Egypt when a drug-resistant strain of the bacterium Acinetobacter baumannii invaded his pancreas. As available antibiotics failed and Patterson fell into a coma, his wife, UCSD epidemiologist Steffanie Strathdee, launched an international effort to find strains of phage that might save him. After treatment with a variety of phages donated by San Diego–based biotech AmpliPhi Biosciences, Texas A&M University, and the U.S. Navy, Patterson made a dramatic recovery.

“Everybody’s been talking about this case,” Bollyky says. “Not only did he survive the treatment, which can’t be taken for granted, but he also got better, and miraculously so.” Patterson received some of the phages intravenously—an approach considered risky because toxins from bacteria used to grow the phages could linger in the mixture. His recovery helped allay safety fears, and it turned Strathdee into a self-described “phage wrangler,” who helped match other patients with the right mixture of experimental phages. Since her husband’s recovery, the UCSD team has successfully cleared infections in five more people with phage cocktails, under a U.S. Food and Drug Administration (FDA) process designed for emergencies where no approved treatments are available.

But a string of anecdotes does little to answer key scientific questions: What is the safest and most effective way to administer phages? How well do phages target the site of infection? How quickly are bacteria likely to develop resistance? “Those are the kinds of things you have to ask in structured clinical trials,” says Robert Schooley, a UCSD physician and infectious disease researcher who treated Patterson and oversaw the other recent cases.

So he and Strathdee proposed the new clinical center, which will launch with a 3-year, $1.2 million grant from UCSD. The Center for Innovative Phage Applications and Therapeutics (IPATH) won’t manufacture any phage treatments itself, but it will collaborate with companies and academic groups outside UCSD on multicenter clinical trials. IPATH will initially focus on treating patients with chronic, drug-resistant infections related to organ transplants, implanted devices such as pacemakers or joint replacements, and cystic fibrosis. Schooley is discussing possible trials with a team at the National Institute of Allergy and Infectious Diseases, and with two companies that have provided phages to patients at UCSD: AmpliPhi and Adaptive Phage Therapeutics (APT), based in Gaithersburg, Maryland, which has licensed the Navy’s phage collection.

Running phages through modern clinical testing has proved difficult in the past. A European Union–sponsored trial known as PhagoBurn was all but derailed by a series of setbacks. “It was not an ideal trial, let me say it like that,” says Jean-Paul Pirnay, a bioengineer at Queen Astrid Military Hospital in Brussels, one of the partners in PhagoBurn. A key obstacle was the fact that the trial targeted burn wounds, which often harbor multiple bacterial infections. That made it hard to test the effects of a phage therapy aimed at just one species. Designed to include 220 patients, the trial ultimately recruited only 27, and it has not yet published its results.

The anticipated trials at UCSD, on the other hand, will focus on patients with a single, known bacterial infection, Schooley says. But he admits it will still be tricky to design trials that isolate the effect of phages without withholding other potentially beneficial treatments, including antibiotics. (Ultimately, Schooley and many others expect phages to work in tandem with antibiotics—not to replace them.)

IPATH collaborators will also have to navigate a drug approval system suited to more conventional treatments. Because a phage cocktail will often have to be custom-designed for an individual, regulatory agencies may not have a single product to evaluate for safety and efficacy. But after initial talks with FDA, Greg Merril, APT’s CEO, is confident the agency will be flexible. He plans to seek approval for an entire library of phages—about 100 for each bacterial species—from which doctors could create a cocktail of one to five phages for a patient.

In the meantime, Strathdee says the UCSD team plans to keep securing phages for individual cases under FDA’s emergency pathway. She and Schooley already get several inquiries a week from patients and families fighting drug-resistant infections. “We hope to not send people with superbugs away, but to welcome them with open arms,” she says. “Right now, they don’t have anywhere to go.”

Pirnay, whose team finds and formulates phages to treat infections related to battlefield injuries, has a piece of advice for the UCSD group: “Be careful not to create too high an expectancy with the public,” he says. “Even when you do not say that you will be able to treat everything, you create a demand with desperate patients.”

Voyage into the world of atoms

Posted on

This animation shows the structure of matter at smaller and smaller scales. Zooming into a human hair, we pass through hair cells, fibril structures, keratin molecules, carbon atoms, nuclei, neutrons, protons, and finally quarks.

The Standard Model explains how the basic building blocks of matter interact, governed by four fundamental forces. Find out more: http://home.cern/…/physi…/standard-model

Voyage into the world of atoms

This animation shows the structure of matter at smaller and smaller scales. Zooming into a human hair, we pass through hair cells, fibril structures, keratin molecules, carbon atoms, nuclei, neutrons, protons, and finally quarks.The Standard Model explains how the basic building blocks of matter interact, governed by four fundamental forces. Find out more: http://home.cern/about/physics/standard-modelVideo: Daniel Dominguez/CERN

Posted by CERN on Sunday, April 15, 2018

Physicists confirm the discovery of fifth force of nature

Posted on

UCI physicists confirm possible discovery of fifth force of nature

Light particle could be key to understanding dark matter in universe

UCI physicists confirm possible discovery of fifth force of nature
“If confirmed by further experiments, this discovery of a possible fifth force would completely change our understanding of the universe,” says UCI professor of physics & astronomy Jonathan Feng, including what holds together galaxies such as this spiral one, called NGC 6814. ESA/Hubble & NASA; Acknowledgement: Judy Schmidt
Irvine, Calif., August 15, 2016 – Recent findings indicating the possible discovery of a previously unknown subatomic particle may be evidence of a fifth fundamental force of nature, according to a paper published in the journal Physical Review Letters by theoretical physicists at the University of California, Irvine.

 

“If true, it’s revolutionary,” said Jonathan Feng, professor of physics & astronomy. “For decades, we’ve known of four fundamental forces: gravitation, electromagnetism, and the strong and weak nuclear forces. If confirmed by further experiments, this discovery of a possible fifth force would completely change our understanding of the universe, with consequences for the unification of forces and dark matter.”

The UCI researchers came upon a mid-2015 study by experimental nuclear physicists at the Hungarian Academy of Sciences who were searching for “dark photons,” particles that would signify unseen dark matter, which physicists say makes up about 85 percent of the universe’s mass. The Hungarians’ work uncovered a radioactive decay anomaly that points to the existence of a light particle just 30 times heavier than an electron.

“The experimentalists weren’t able to claim that it was a new force,” Feng said. “They simply saw an excess of events that indicated a new particle, but it was not clear to them whether it was a matter particle or a force-carrying particle.”

The UCI group studied the Hungarian researchers’ data as well as all other previous experiments in this area and showed that the evidence strongly disfavors both matter particles and dark photons. They proposed a new theory, however, that synthesizes all existing data and determined that the discovery could indicate a fifth fundamental force. Their initial analysis was published in late April on the public arXiv online server, and a follow-up paper amplifying the conclusions of the first work was released Friday on the same website.

The UCI work demonstrates that instead of being a dark photon, the particle may be a “protophobic X boson.” While the normal electric force acts on electrons and protons, this newfound boson interacts only with electrons and neutrons – and at an extremely limited range. Analysis co-author Timothy Tait, professor of physics & astronomy, said, “There’s no other boson that we’ve observed that has this same characteristic. Sometimes we also just call it the ‘X boson,’ where ‘X’ means unknown.”

Feng noted that further experiments are crucial. “The particle is not very heavy, and laboratories have had the energies required to make it since the ’50s and ’60s,” he said. “But the reason it’s been hard to find is that its interactions are very feeble. That said, because the new particle is so light, there are many experimental groups working in small labs around the world that can follow up the initial claims, now that they know where to look.”

Like many scientific breakthroughs, this one opens entirely new fields of inquiry.

One direction that intrigues Feng is the possibility that this potential fifth force might be joined to the electromagnetic and strong and weak nuclear forces as “manifestations of one grander, more fundamental force.”

Citing physicists’ understanding of the standard model, Feng speculated that there may also be a separate dark sector with its own matter and forces. “It’s possible that these two sectors talk to each other and interact with one another through somewhat veiled but fundamental interactions,” he said. “This dark sector force may manifest itself as this protophobic force we’re seeing as a result of the Hungarian experiment. In a broader sense, it fits in with our original research to understand the nature of dark matter.”

About the University of California, Irvine: Founded in 1965, UCI is the youngest member of the prestigious Association of American Universities. The campus has produced three Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UCI has more than 30,000 students and offers 192 degree programs. It’s located in one of the world’s safest and most economically vibrant communities and is Orange County’s second-largest employer, contributing $5 billion annually to the local economy. For more on UCI, visit www.uci.edu.

Media access: Radio programs/stations may, for a fee, use an on-campus ISDN line to interview UCI faculty and experts, subject to availability and university approval. For more UCI news, visit news.uci.edu. Additional resources for journalists may be found at communications.uci.edu/for-journalists.

 

Physicists confirm the discovery of fifth force of nature

Physicists confirm the discovery of fifth force of nature.

Posted by Hashem Al-Ghaili on Wednesday, June 13, 2018

Compound made inside human body stops viruses from replicating

Posted on

Date: June 20, 2018
Source: Penn State
Summary:
A team of researchers has identified the mode of action of viperin, a naturally occurring enzyme in humans and other mammals that is known to have antiviral effects on viruses such as West Nile, hepatitis C, rabies, and HIV. This discovery could allow researchers to develop a drug that could act as a broad-spectrum therapy for a range of viruses, including Zika.
 FULL STORY

A structural model of viperin a naturally occurring enzyme in humans that is known to have antiviral effects on viruses such as West Nile, hepatitis C, rabies, and HIV. A new study led by researchers from Penn State and the Albert Einstein College of Medicine reveals the mode of action of viperin, which facilitates an important reaction that results in the production of ddhCTP, a molecule that prevents viruses from copying their genetic material.
Credit: David W. Gohara, Ph.D

The newest antiviral drugs could take advantage of a compound made not by humans, but inside them. A team of researchers has identified the mode of action of viperin, a naturally occurring enzyme in humans and other mammals that is known to have antiviral effects on a wide variety of viruses, including West Nile, hepatitis C, rabies, and HIV.

The enzyme facilitates a reaction that produces the molecule ddhCTP, which prevents viruses from copying their genetic material and thus from multiplying. This discovery could allow researchers to develop a drug that induces the human body to produce this molecule and could act as a broad-spectrum therapy for a range of viruses. A paper describing the study appears online on June 20th in the journal Nature.

“We knew viperin had broad antiviral effects through some sort of enzymatic activity, but other antivirals use a different method to stop viruses,” said Craig Cameron, professor and holder of the Eberly Chair in Biochemistry and Molecular Biology at Penn State and an author of the study. “Our collaborators at the Albert Einstein College of Medicine, led by senior authors Tyler Grove and Steven Almo, revealed that viperin catalyzes an important reaction that results in the creation of a molecule called ddhCTP. Our team at Penn State then showed the effects of ddhCTP on a virus’s ability to replicate its genetic material. Surprisingly, the molecule acts in a similar manner to drugs that were developed to treat viruses like HIV and hepatitis C. With a better understanding of how viperin prevents viruses from replicating, we hope to be able to design better antivirals.”

A virus typically co-opts the host’s genetic building blocks to copy its own genetic material, incorporating molecules called nucleotides into new strands of RNA. The molecule ddhCTP mimics these nucleotide building blocks and becomes incorporated into the virus’s genome. Once incorporated into a new strand of the virus’s RNA, these “nucleotide analogs” prevent an enzyme called RNA polymerase from adding more nucleotides to the strand, thus preventing the virus from making new copies of its genetic material.

“Long ago, the paradigm was that in order to kill a virus, you had to kill the infected cell,” said Cameron. “Such a paradigm is of no use when the virus infects an essential cell type with limited capacity for replenishment. The development of nucleotide analogs that function without actually killing the infected cell changed everything.”

Most nucleotide analogs on the market are humanmade, but there are often complications with using these synthetic drugs. Because nucleotides are used by many proteins and enzymes of the cell, numerous opportunities exist for analogs to interfere with normal cellular function.

“The major obstacle to developing therapeutically useful antiviral nucleotides is unintended targets,” said Jamie Arnold, associate research professor of biochemistry and molecular biology at Penn State and an author of the paper. “For example, a few years ago we discovered that a nucleotide analog under development for treatment of hepatitis C could interfere with the production of RNA in mitochondria, subcellular organelles important for energy production in the patient’s own cells. That meant people with mitochondrial dysfunction are predisposed to any negative effects of this unintended interference.”

The molecule ddhCTP, however, does not appear to have any unintended targets. The research team suspects that the natural origin of the compound within the human body necessitates that it be nontoxic.

“Unlike many of our current drugs, ddhCTP is encoded by the cells of humans and other mammals,” said Cameron. “We have been synthesizing nucleotide analogs for years, but here we see that nature beat us to the punch and created a nucleotide analog that can deal with a virus in living cells and does not exhibit any toxicity to date. If there’s something out there that’s going to work, nature has probably thought of it first. We just have to find it.”

To verify the effectiveness of ddhCTP, the research team showed that the molecule inhibited the RNA polymerases of dengue virus, West Nile virus and Zika virus, which are all in a group of viruses called flaviviruses. Then they investigated whether the molecule halted replication of Zika virus in living cells.

“The molecule directly inhibited replication of three different strains of Zika virus,” said Joyce Jose, assistant professor of biochemistry and molecular biology at Penn State and an author of the paper. “It was equally effective against the original strain from 1947 as it was against two strains from the recent 2016 outbreak. This is particularly exciting because there are no known treatments for Zika. This study highlights a new avenue of research into natural compounds like ddhCTP that could be used in future treatments.”

Together, these results demonstrate promising antiviral effects of ddhCTP on a variety of flaviviruses. However, the RNA polymerases of human rhinovirus and poliovirus, which are in a group called picornaviruses, were not sensitive to the molecule. The researchers plan to investigate the polymerase structures of these viruses to better understand why flaviviruses are sensitive to ddhCTP while the picornaviruses tested in this study are not. This investigation may also offer insights into how flaviviruses might develop resistance to the molecule.

“Development of resistance to an antiviral agent is always an issue,” said Cameron, “Having some idea of how resistance happens, or being able to prevent it from happening, will be critical if this is to be used as a broad-spectrum therapy.”


Story Source:

Materials provided by Penn State. Note: Content may be edited for style and length.


Journal Reference:

  1. Anthony S. Gizzi, Tyler L. Grove, Jamie J. Arnold, Joyce Jose, Rohit K. Jangra, Scott J. Garforth, Quan Du, Sean M. Cahill, Natalya G. Dulyaninova, James D. Love, Kartik Chandran, Anne R. Bresnick, Craig E. Cameron, Steven C. Almo. A naturally occurring antiviral ribonucleotide encoded by the human genome. Nature, 2018; DOI: 10.1038/s41586-018-0238-4