Category Archives: Health

What is new in the field of Health. Trending topics, and cutting edge research in the are of Health. Press Releases that give us updates on Health.

Gilad&Gilad enters Taiwan with AgmaVet®, a Veterinary Product for Nerve Health


“There are over 1,000 active animal clinics in Taiwan and our professional sales team already covers 80% of them. Together with Gilad&Gilad expertise and reputation we are making AgmaVet® readily available to them.”

Gilad&Gilad a health science company based in Henderson, Nevada, with core competency in Neuroscience and the exclusive supplier of AgmaVet®, a unique veterinary dietary product for nerve health, has initiated a collaboration with Pet Enjoy Bio-Science Co., Ltd. for distribution in Taiwan.

According to Dr. Gad M. Gilad, CEO of Gilad&Gilad, “The Ministry of Health of Taiwan has issued a permit allowing our collaborating distributor, Pet Enjoy Bio-Science, to import and distribute AgmaVet in Taiwan. Pet Enjoy was founded by a team highly experienced in the veterinary market, very proficient in marketing and sales of superior pet healthcare products in Taiwan and East Asia.” Dr. Gilad adds that “this collaboration is part of Gilad&Gilad’s ongoing efforts to expand worldwide distribution and sales and allows us to establish presence in this thriving region.”

AgmaVet is a novel first-of-its-kind nutraceutical product affording what is surely the best available solution for maintaining healthy, pain-free nerve functions. “Using AgmaVet® to fortify the daily intake of the nutraceutical G-Agmatine® (Gilad&Gilad’s proprietary brand of agmatine) provides a safe and most effective solution for nerve resilience, normal sensory functions and nerve-dependent muscle strength, which are cardinal for good quality of life,” says Dr. Gilad.

“We are pleased to collaborate with Gilad&Gilad and to be the distributor of AgmaVet in Taiwan,” says Mr. PeterTu, General Manager of Pet Enjoy Bio-Science. “There is a growing demand in Taiwan’s veterinary pet market for good quality healthcare products and the companion animal health market is expected to grow considerably in the coming years,” he adds. “There are over 1,000 active animal clinics in Taiwan and our professional sales team already covers 80% of them. Together with Gilad&Gilad expertise and reputation we are making AgmaVet® readily available to them.”

According to export.gov (11/8/2019), the online portal of the International Trade Administration, US Department of Commerce, Taiwan’s pet food (dog and cat food) market rallied on import demand, growing by 11 percent to nearly $180 million, more than doubling over the past decade.

About Gilad&Gilad LLC

Gilad&Gilad is a health science company with core competency in Neuroscience. The company has developed the exclusive Agmaceuticals(TM) line of products based on the breakthrough discovery of the neuroprotective properties agmatine. AgmaVet® is the first-of-its-kind nutraceutical for animals containing G-Agmatine® (the best brand of agmatine), with superior effectiveness for healthy nerve functions. – For further information, visit https://ForNerveHealth.com.

About Pet Enjoy Bio-Science

Pet Enjoy Bio-Science is a company based in Taiwan with expertise in marketing, distribution and sales of best solutions to unmet needs of the veterinary clinical practice and of animal healthcare by pet owners. Its mission is to become the best animal healthcare distribution partner in the ASIAN market. – For further information, visit http://www.petenjoy-bio.com.

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New study identifies trigger that turns dormant cancer stem cells into active ones


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A new study released today in STEM CELLS identifies, for the first time, two morphologically and functionally different types of cancer stem cells found in cervical cancer. Of the two types, one exhibits an overexpression of cPLA2α, a key enzyme that triggers the transformation of dormant cancer stem cells into active ones, resulting in cervical cancer metastasis and recurrence. The information in this study could lead to new targets for treatments to halt tumor recurrence and metastatic spread. Also, it might accelerate the development of combination therapies.

The current standard of treatments for cervical cancer – the second leading cause of cancer death in young women worldwide — is radiotherapy and chemotherapy. However, the cancer’s resistance to chemotherapy and radiation, combined with a tendency to metastasis in the lymph nodes or recur in the pelvis, leaves doctors searching for more effective treatments.

Cervical cancer stem cells (CCSCs) are considered the major culprit behind the cancer’s ability to overcome these treatments. At the same time, a majority of cancer stem-like cells or tumor-initiating cells remain dormant. It takes a change in their microenvironment to spur them to metastasize.

“The mechanisms responsible for this must be identified to design more suitable therapies for the different subpopulations of cancer stem cells (CSCs) in various tissue-specific cancers,” said Hua Guo, Ph.D., who headed up the investigation along with Yuchao He, Ph.D. The two are colleagues at Tianjin Medical University Cancer Institute and Hospital. Researchers at Tianjin University of Traditional Chinese Medicine and at the Center for Translational Cancer Research, Peking University First Hospital, also participated in the study.

Although several cell surface antigens have been identified in CCSCs, these markers vary among tumors because of CSC heterogeneity. However, whether these markers specifically distinguish CCSCs with different functions is unclear. The study published in STEM CELLS sought to resolve this question. And in fact, its findings demonstrate that CCSCs exist in two biologically distinct phenotypes, characterized by different levels of cPLA2α expression.

“Our study showed for the first time that overexpression of cPLA2α results in a phenotype associated with mesenchymal traits, including increased invasive and migration abilities. On the other hand, CCSCs with cPLA2α downregulation show dormant epithelial characteristics,” said Dr. Guo. “In addition, cPLA2α regulates the reversible transition between mesenchymal and epithelial CCSC states through PKCζ, an atypical protein that governs cancer cell state changes.”

Dr. He added, “Now that we know cPLA2α triggers this transformation, we believe that cPLA2α might be an attractive therapeutic target for eradicating different states of CCSCs to eliminate tumors more effectively.”

“The novel study by Dr. Guo and team is of very high importance in understanding the transition between dormant cancer stem cells, which evade chemotherapy and radiation treatments, and actively dividing cells which can be better targeted, said Dr. Jan Nolta, Editor-in-Chief of STEM CELLS. “I applaud the group for this important discovery which will help researchers develop better treatments for cervical cancer.”

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The full article, “cPLA2α reversibly regulate different subsets of cancer stem cells transformation in cervical cancer,” can be accessed at https://stemcellsjournals.onlinelibrary.wiley.com/doi/abs/10.1002/stem.3157.

Figure Caption: This study revealed that there are two morphologically and functionally distinct cancer stem cell populations regulated by cPLA2α in cervical cancer. cPLA2α might be a unique marker to identify different cancer stem cell populations and trigger quiescent epithelial cancer stem cells transform to invasive mesenchymal states. Overexpression of cPLA2α resulted in a CD44+CD24- phenotype with mesenchymal traits, whereas cervical cancer stem cells (CCSCs) with cPLA2α downregulation expressed CD133 and showed epithelial characteristics. cPLA2α, as a key role to reversely regulate CCSCs states and EMT, might provide innovative therapeutic strategies intended to halt tumor recurrence and metastasis.

About the Journal: STEM CELLS, a peer reviewed journal published monthly, provides a forum for prompt publication of original investigative papers and concise reviews. The journal covers all aspects of stem cells: embryonic stem cells/induced pluripotent stem cells; tissue-specific stem cells; cancer stem cells; the stem cell niche; stem cell epigenetics, genomics and proteomics; and translational and clinical research. STEM CELLS is co-published by AlphaMed Press and Wiley.

About AlphaMed Press: Established in 1983, AlphaMed Press with offices in Durham, NC, San Francisco, CA, and Belfast, Northern Ireland, publishes three internationally renowned peer-reviewed journals with globally recognized editorial boards dedicated to advancing knowledge and education in their focused disciplines. STEM CELLS® (http://www.StemCells.com) is the world’s first journal devoted to this fast paced field of research. THE ONCOLOGIST® (http://www.TheOncologist.com) is devoted to community and hospital-based oncologists and physicians entrusted with cancer patient care. STEM CELLS TRANSLATIONAL MEDICINE® (http://www.StemCellsTM.com) is dedicated to significantly advancing the clinical utilization of stem cell molecular and cellular biology. By bridging stem cell research and clinical trials, SCTM will help move applications of these critical investigations closer to accepted best practices.

About Wiley: Wiley, a global company, helps people and organizations develop the skills and knowledge they need to succeed. Our online scientific, technical, medical and scholarly journals, combined with our digital learning, assessment and certification solutions, help universities, learned societies, businesses, governments and individuals increase the academic and professional impact of their work. For more than 200 years, we have delivered consistent performance to our stakeholders. The company’s website can be accessed at http://www.wiley.com.

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Grain Foods Foundation Welcomes Siddhartha Angadi, PhD, FACSM, to Scientific Advisory Board


Siddhartha Angadi, PhD, FACSM

This is the perfect time to add Dr. Angadi’s expertise to the Foundation. We look forward to raising the visibility of the evidence-based dietary recommendations that result from his research among the nutrition community and the public.

The Grain Foods Foundation is excited to announce the addition of Siddhartha Angadi, PhD, FACSM, to its Scientific Advisory Board, effective February 1, 2020. A fellow of the American College of Sports Medicine, Dr. Angadi is currently an Assistant Professor at the College of Health Solutions at Arizona State University.

A cardiovascular exercise physiologist by training, Dr. Angadi’s research focuses on the complex interactions between exercise and physical activity, diet, and drugs in both healthy individuals and those with serious illnesses such as congestive heart failure, breast cancer, and end-stage renal disease.

“Given the rising prevalence of and deaths resulting from the illnesses that Dr. Angadi studies, this is the perfect time to add his expertise to the Foundation,” said Christine Cochran, executive director for the Grain Foods Foundation. “His research is impressive in both volume and breadth, and we look forward to raising the visibility of the evidence-based dietary recommendations that result from it among the nutrition community and the public.”

Dr. Angadi cites his most recent research – one Nutrients study that investigates the effects of glycemic index and dietary fiber on cardiovascular disease risk in adults, and another that examines the role of dietary fiber consumption on cardiovascular health in pediatric populations – as evidence that he clearly shares this ambition.

“I’m elated to join the Scientific Advisory Board,” Angadi said. “There’s a tremendous amount of misinformation out there when it comes to the role of diet in human health and disease, from one fad diet claiming that dietary fiber isn’t essential to another claiming that we’d all be better off without gluten. So I’m thrilled to partner with the Grain Foods Foundation and have the opportunity to help separate fact from fiction.”

Dr. Angadi joins the current members of the Scientific Advisory Board:

  • Glenn Gaesser, PhD (Chairman), Professor of Exercise Science and Health Promotion and Director of the Healthy Lifestyles Research Center at Arizona State University;
  • Dyan Hes, MD, owner and medical director of Gramercy Pediatrics in New York City;
  • Sylvia Melendez-Klinger, DBA, MS, RD, LDN, founder of Hispanic Food Communications;
  • Richard D. Mattes, MPH, PhD, RD, Distinguished Professor of Nutrition Science at Purdue University;
  • Julie Miller Jones, PhD, LN, CNS, Professor Emeritus at St. Catherine University;
  • Bruce Young, MD, Silverman Professor of Obstetrics and Gynecology at New York University School of Medicine;
  • Angela Ginn-Meadow, RD, LDN, CDE, Senior Education Coordinator at the University of Maryland’s Center for Diabetes and Endocrinology;
  • Pamela Cureton, RD, LDN, Division of Pediatric Gastroenterology and Nutrition at the University of Maryland School of Medicine;
  • Hannah Holscher, PhD, RD, Assistant Professor of Nutrition in the Department of Food Science and Human Nutrition at the University of Illinois.


About Grain Foods Foundation

Formed in 2004, Grain Foods Foundation (GFF) is a group of thought leaders and advocates for ALL grain foods and believes everybody needs grain food to enjoy a happy and healthy life. Committed to nutrition education programming that is firmly rooted in science, GFF is a strong advocate for our members, and a resource for consumers and the media who want to learn more about the role of grains in a well-balanced eating pattern. GFF offers research-based information and resources to members, partners, influencers, policymakers and consumers through a comprehensive communications campaign, conferences, webinars, research tools, social media and more. GFF is committed to bringing fact-based information and common sense to the consumer. For more information, visit grainfoodsfoundation.org.

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Regen Suppliers is Now Offering FDA Cleared PDO Max Thread Lift Products


pdo max thread distributor

Now Offering PDO Max Threads (888) 568-6909

Regen Suppliers recognized that PDO Max products are not only first rate quality, but also available in fifteen different styles. The feedback we have received from providers is that they are better than any others on the market!

Regen Suppliers is now offering the top FDA Cleared threads available on the market, PDO Max. The first rate PDO thread lift products are not only one of the only FDA Cleared options available, there are fifteen different types in the portfolio.

Non invasive thread lift procedures are increasing exponentially in popularity, as they represent an excellent nonoperative method of reducing wrinkles and helping individuals look younger without the risks of an invasive surgery.

According to company VP Kathleen Francesca, “Regen Suppliers recognized that PDO Max products are not only first rate quality, but also available in fifteen different styles. The feedback we have received from providers is that they are better than any others on the market!”

PDO Max threads are available in several styles including Smuth (Smooth), Levo (Barbed) Threads, and Ciclone (Twisted) as well. The thread lift procedures are not only extremely popular for facial rejuvenation, but also being used for neck, knee, arm, abdomen and buttock lift procedures as well. The combination of smooth and barbed threads allow for sufficient new collagen and elastin formation for long lasting results.

In addition to offering all the styles of PDO Max threads, Regen Suppliers has teamed up with R3 Medical Training for its PDO Thread Lift Training Course. The Courses offer PDO Thread Lift Certification Training, as there is a steep learning curve to gain expertise. Many providers are now offering thread lift procedures in conjunction with regenerative biologics such as PRP, stem cells and exosomes. Regen Suppliers offers all of these biologics as well.

Those interested in PDO Thread Lift products should contact Regen Suppliers at (888) 568-6909.

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Strategic Radiology Adds First Oregon Practice, Diagnostic Imaging Northwest


Diagnostic Imaging Northwest

Phillip Baker, MD, PhD, President, Diagnostic Imaging Northwest

Our philosophy of practice is to be an active and valued participant in our communities and the institutions where we provide care. We think that membership in Strategic Radiology and the SR–Patient Safety Organization will help us continue to put the patient and referring physician first.

Diagnostic Imaging Northwest (DINW) has aligned with Strategic Radiology’s coalition of independent private radiology practices, bringing the current number of members to 27 and bolstering the organization’s presence in the Northwest. The group includes 12 subspecialty-trained radiologists.

“We are pleased to be welcoming Diagnostic Imaging Northwest into the Strategic Radiology coalition of independent practices,” said Arl Van Moore Jr, MD, FACR, CEO and chair, Strategic Radiology. “The practice brings a combination of excellent, quality-minded radiologists, a demonstrated willingness to collaborate, and a commitment to Strategic Radiology’s core values.”

DINW was founded nearly 100 years ago and during the past century has built a strong relationship with Legacy Health’s Good Samaritan Hospital, a leading subspecialty hospital In Portland with an oncology center operated in partnership with Oregon Health & Science University. It also provides subspecialty coverage for Skyline Hospital, in White Salmon, Washington.

The practice’s radiologists serve as department medical directors at both hospital sites and provide diagnostic mammography and breast biopsy for a new breast center operated by Women’s Health Associates, a 100-physician group of primarily OB-GYN physicians.

“Our philosophy of practice is to be an active and valued participant in our communities and the institutions where we provide care,” said Phillip D. Baker, MD, PhD, president, DINW. “We think that membership in Strategic Radiology and the SR–Patient Safety Organization will help us continue to put the patient and referring physician first.”

DINW is a partner in Legacy Health Partners, an accountable care organization with more than 2,500 physician members. The practice has been an integral member of the Portland health care provider community since the 1920s, introducing Oregon’s first CT scanner and first dedicated breast imaging center, both at Legacy Good Samaritan.

About Strategic Radiology

Strategic Radiology is a coalition of independent, private radiology practices, representing more than 1,100 radiologists. The coalition’s goal is to achieve higher quality patient care and more cost-efficient delivery of medical imaging through an integrated approach of shared data and best practices, interchanging clinical expertise, and consolidating certain practice expenses. It operates the nation’s only radiology-focused Patient Safety Organization listed by the Agency for Healthcare Research and Quality. http://www.StrategicRadiology.org.

SR Members:


  • Asheville Radiology Associates; Asheville, NC
  • Casper Medical Imaging and Outpatient Radiology; Casper, WY
  • Central Illinois Radiological Associates; Peoria, IL
  • Diagnostic Imaging Northwest; Portland, OR
  • Gaston Radiology; Gastonia, NC
  • The Hill Medical Corporation; Pasadena, CA
  • Huron Valley Radiology; Ann Arbor, MI
  • Inland Imaging; Spokane, WA
  • Mecklenburg Radiology Associates; Charlotte, NC
  • Medical Center Radiology Group; Orlando, FL
  • Minneapolis Radiology Associates; Minneapolis, MN
  • Modesto Radiological Medical Group (MRMG); Modesto, CA
  • Mountain Medical Physician Specialists; Salt Lake City, UT
  • Naugatuck Valley Radiological Associates; Waterbury, CT
  • Northwest Radiology; Indianapolis, IN
  • Quantum Radiology; Atlanta, GA
  • Radiologic Medical Services; Iowa City, IA
  • Radiology Associates; Jeffersonville, IN
  • Radiology Associates of Macon; Macon, GA
  • Radiology Associates of North Texas; Dallas/Fort Worth, TX
  • Radiology Associates of Tallahassee; Tallahassee, FL
  • Rome Radiology Group; Rome, GA
  • Southeast Radiology, Ltd.; Glen Mills, PA
  • Tower Imaging Medical Group; Santa Monica, CA
  • United Imaging Consultants; Mission, KS
  • University Radiology; East Brunswick, NJ
  • X-Ray Consultants; South Bend, IN

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Catalent Announces Supplying Blueprint Medicines’ Precision Therapy AYVAKIT™ (avapritinib)


We thank the entire Catalent Nottingham team for their continued support these past four years in helping us rapidly develop this important advancement in precision therapy and make a significant difference for patients with high medical needs.

Catalent, the leading global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene and cell therapies, and consumer health products, welcomes the announcement by Blueprint Medicines Corporation that the U.S. Food and Drug Administration (FDA) has approved AYVAKIT™ (avapritinib) for the treatment of adults with unresectable or metastatic gastrointestinal stromal tumor (GIST) harboring a platelet-derived growth factor receptor alpha (PDGFRA) exon 18 mutation, including PDGFRA D842V mutations.

Catalent’s Nottingham U.K. facility has supported Blueprint Medicines’ development program since 2015, from formulation development, clinical product supply and now commercial supply of AYVAKIT.

“We are delighted to help support Blueprint Medicines with commercial supply for this important medicine, recently approved by the FDA, which provides a new treatment option for patients with this disease,” commented Jonathan Arnold, President of Oral and Specialty Delivery at Catalent. “We have built a global network of development and clinical and commercial supply centers with the specific skills and expertise to help innovators like Blueprint Medicines meet challenging milestones for important novel therapies such as this.”

Jeff Albers, Chief Executive Officer of Blueprint Medicines, added, “We thank the entire Catalent Nottingham team for their continued support these past four years in helping us rapidly develop this important advancement in precision therapy and make a significant difference for patients with high medical needs.”

AYVAKIT and Blueprint Medicines are trademarks of Blueprint Medicines Corporation.

Please click here to see the full Prescribing Information for AYVAKIT.

About Catalent

Catalent is the leading global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, cell and gene therapies, and consumer health products. With over 85 years serving the industry, Catalent has proven expertise in bringing more customer products to market faster, enhancing product performance and ensuring reliable global clinical and commercial product supply. Catalent employs over 13,000 people, including over 2,400 scientists and technicians, at more than 35 facilities, and in fiscal year 2019 generated over $2.5 billion in annual revenue. Catalent is headquartered in Somerset, New Jersey. For more information, visit http://www.catalent.com

More products. Better treatments. Reliably supplied.™

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EnduRx Pharmaceuticals Awarded $1.4MM of a $1.75MM Grant to Collaborate with MD Anderson Cancer Center to Develop a Novel Therapeutic for Triple-negative Breast Cancer


EnduRx Pharmaceuticals, advancing a drug delivery system intended to improve outcomes for patients with hard-to-treat solid tumors, has been awarded $1.4 million dollar Department of Defense grant. The 36-month project is a collaboration with MD Anderson Cancer Center in Houston and will advance a novel therapeutic for triple-negative breast cancer to the point of pre-IND meeting with the FDA. Total project grant award is $1.75 million dollars.

“With triple-negative breast cancer, so-called because it lacks the receptors that enable the use of treatments employed for other forms of breast cancer, only about 30% of patients at best respond to standard-of-care treatment.” said Stephan Morris, MD, EnduRx Principal Investigator. “There are currently few approved drugs available specifically for the treatment of this fast growing and poor-outcome type of breast cancer. Untreated, the cancer is likely to metastasize to the brain and parts of the body, and the five-year survival rate is then only a little over 10%, so there is an urgent need for an effective therapy,” Morris said. “This form of breast cancer is diagnosed in about 10-20% of breast cancer patients, with an even higher proportion occurring in African-American women. We are pleased to have this opportunity to work with Dr. Naoto Ueno’s breast cancer group at MD Anderson, whose access to patient-derived xenograft models should provide a high level of confidence that the EnduRx Pharmaceuticals therapeutic candidate will translate well into human subjects with triple-negative breast cancer.”

About EnduRx Pharmaceuticals

EnduRx Pharmaceuticals Inc., a Tucson firm, is part of OBDURO Biotechnologies, a San-Diego company formed in 2019, to improve delivery of drugs selectively to the site of disease and not elsewhere in the body. In 2020 OBDURO plans a funding round and will use the proceeds to further leverage the grant-sponsored activities and generate persuasive data aimed at securing pharma partnerships. EnduRx previously received a $1.75 million SBIR grant to develop a prototype of the drug delivery system. “Earlier work showed tumor-volume reductions of over 90% in mouse models, with some cures. The DoD grant will allow EnduRx to complete pharmacokinetic and toxicology analyses as well as additional anti-cancer efficacy studies, data which are required before clinical trials can be initiated.” said David Loynd, Chief Executive Officer of OBDURO and EnduRx.

About the Congressionally Directed Medical Research Programs:

CDMRP was established in 1992 when Congress first appropriated funds targeted specifically for breast cancer research. Since that time, additional research programs and topics have been added by Congress, and CDMRP has evolved into a global funding organization that fosters novel approaches to biomedical research in response to the expressed needs of its stakeholders — the American public, the military, and Congress. For more information about CDMRP go to https://cdmrp.army.mil/. The views expressed in this article are those of the author and may not reflect the official policy or position of the Department of the Army, Department of Defense, or the U.S. Government.

For further information:

David Loynd, President & CEO

EnduRx Pharmaceuticals, Inc.

dloynd@endurxpharm.com

(855) 368-2878

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Clean Air Gear’s New Product Eradicates Virus Particles


ViraKill-60 can inactivate airborne or surface virus particles

Clean Air Gear division of MicroSweep Corp. has introduced a novel new product that eradicates virus particles shed by a contagious person, whether they have symptoms or not. Virus particles are copies of the original virus that has been reproduced many-fold by an exhausted host-cell infection in a contagious person.

ViraKill-60 is a special type of portable air purifier that destroys virus particles using clean ozone, then neutralizes any remaining oxidant. Ozone will inactivate viruses on contact, even at very low residual concentrations. Ozone destroys viruses by diffusing through the protein coat into the nucleic acid core, resulting in damage to the viral RNA. Only 0.012 ppm of ozone removes all polio viral cells in less than 10 seconds.

The new ViraKill-60 (available at http://www.cleanairgear.com) creates temporary clean ozone that oxidizes viral particles on contact. Placed in a closed room and powered on, the unit cycles unattended for one hour. (The cleaning technology attacks organic molecules, including living cells, so the treatment area must be unoccupied while it cleans.) Treated premises can be reoccupied soon afterward because during the last ten minutes it neutralizes any ozone remaining in the treatment area. This is reliable because only clean ozone is produced, even in moist air, so there are no toxic byproducts to remove.

“ViraKill-60 can inactivate airborne or surface virus particles” said John Edwards, President of Clean Air Gear.

See ViraKill-60 at (http://www.cleanairgear.com) or email to info@virakill.com.

Clean Air Gear sells portable equipment to purify room air in the home and workplace.

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Memorial Neuroscience Institute Performs Its First Robotic Brain Surgery to Help Ease Epileptic Seizures


“We are committed in adopting technology that is at the forefront of surgical treatments for epilepsy. The use of the robot will help the Memorial Neuroscience Institute to provide the cutting edge care to our patients.”

The epilepsy team at Memorial Neuroscience Institute successfully completed its first use of a minimally-invasive, robotic device that helps pinpoint the origin of epileptic seizures on a patient.

The device, now in full use at Memorial Regional Hospital, is called a Robotized Surgical Assistant, or ROSA. With assistance from the robot, neurosurgeons only need to make small, precise incisions in the scalp and skull to place electrodes deep in the brain and investigate where seizures are triggered.

The robot also improves accuracy, safety and can significantly reduce total surgery time, said Tarek Zakaria, MD, Medical Director for the Adult Neurology Program and Epilepsy Program.

By using the new technology, more data will be available to the epilepsy team to offer patients more advanced treatment options and help them to achieve their dreams to be seizure free, Zakaria said.

“We are committed in adopting technology that is at the forefront of surgical treatments for epilepsy,” Zakaria said. “The use of the robot will help the Memorial Neuroscience Institute to provide the cutting edge care to our patients.”

When medication is not enough to control seizures, neurosurgeons like Christopher DeMassi, MD and Daxa Patel, MD may take a surgical approach. That includes altering or removing brain tissue at the location where a patient’s seizures begin. However, they can only do so if they can first zero in exactly where that origin is. This is where Rosa can assist.

Recently, they performed the two-part procedure on a 24-year-old female patient, who began having epileptic seizures at age eight and had exhausted all available medications.

The procedure, called robot-assisted stereoelectroencephalography (SEEG), was performed as part of the services offered by the Memorial Neuroscience Institute Comprehensive Epilepsy Center.

“Our goal is to always bring in the latest innovative technologies to achieve the best possible outcome for our patients,” DeMassi said. “This is just the latest advancement available to the South Florida community and keeps us at the front of epilepsy care.”

Surgeons used ROSA and a 3-D reconstruction of the patient’s brain to guide them where to surgically implant electrodes without having to remove sections of her skull. DeMassi and Patel then used the robot’s arm to make two- or three-millimeter holes in the scalp through which the electrode wires were passed.

With the electrodes in place, Zakaria and his team were later able to see part of the patient’s brain “light up” on a computer monitor as a seizure began, essentially flagging the point of origin.

“Memorial Neuroscience Institute is proud to offer the most technologically advanced and comprehensive services for our patients and the community,” said Haroula Protopapadakis Nordem, FACHE, Associate Administrator at Memorial Regional Hospital.

“The addition of the ROSA to our program will allow our surgeons to deliver more precise results in a less invasive manner and allow our physicians to treat patients who otherwise might not have had a feasible treatment option,” she said.

Memorial’s epilepsy center is accredited by the National Association of Epilepsy Centers (NAEC) as a Level 4 program, a designation for programs offering the highest level of comprehensive and specialized care.

Memorial Regional Hospital in Hollywood, Fla., is one of the largest hospitals in Florida and is a facility of Memorial Healthcare System, one of the largest healthcare systems in Florida. Its wide scope of medical services and programs includes Memorial Cancer Institute, Breast Cancer Center, Cardiac and Vascular Institute, Neuroscience Center, Comprehensive Weight-Loss Surgery Program, Family Birthplace, Center for Behavioral Health, Sickle Cell Day Hospital, Women’s Services, Fitness and Rehabilitation Center, and a level I Trauma Center. For more information, visit memorialregional.com.

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Next-generation Targeted Cytokine Therapy to be Explored on Advancements Series


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“Deka’s platform has the potential to enable discoveries of next generation therapies,” said Richard Lubin.

An upcoming episode of Advancements with Ted Danson, scheduled to broadcast 2Q/2020, will explore innovative treatment solutions for maladies, such as Inflammatory Bowel Disease (IBD), specifically Crohn’s Disease (Crohn’s), and Oncology. Check local listings for more info.

This segment will focus on a novel platform developed by Deka Biosciences, Inc. (Deka Biosciences), that will enable the delivery of next generation cytokine or combination of cytokines to a specific tissue of interest. Viewers will learn how this cutting-edge technology, termed Diakines™, has led to the development of two potential therapeutic molecules involving an affinity modified Interleukin 10 cytokine.

The show will also explore how Deka Biosciences is using Diakines™ to harness the spectrum of therapeutically useful and clinically validated IL10 and other cytokine specific biologies. Spectators will see how these Diakines™ can maximize patient benefits through improved PK/PD function combined with a MOA directed patient selection strategy.

“The biopharma industry has known for a while that cytokines play an integral role in immunology and disease management, and that delivery of cytokine therapeutics into diseased tissues will dramatically enhance therapeutic benefit,” said Dr. John Mumm, co-founder & CEO of Deka Biosciences. He continued to say, “Deka Biosciences has harnessed the wealth of clinical knowledge around cytokines and IL-10 in particular, to develop a novel delivery platform to enrich cytokine variants in effected tissues, coupled with methods to determine how to select the patients with the greatest likelihood of response to ensure that the right patients get the right medicines.”

In addition, the show will also inform about Deka Biosciences’ Precision Medicine strategy, which enables Deka to identify the right patients to treat with these new medicines.

“Deka’s platform has the potential to enable discoveries of next generation therapies,” said Richard Lubin, senior producer for DMG Productions and the Advancements series. “We are eager to explore how Deka is set to influence future treatment options for IBD, Crohn’s.”

About Deka Biosciences:

Deka BioSciences, Inc., is an early-stage biotech focused on creating the next generation targeted cytokine therapies to treat chronic illnesses such as Crohn’s Disease and Oncology. Deka’s focus is on the development of optimized disease specific IL-10 variants coupled with the DiakinesTM T1/2 life extension tissue targeting technology. In parallel, Deka has developed a Precision Medicine strategy by identifying the genetic signature that drives responses to treatment to enable the selection of the patients most likely to benefit from our therapies.

About Advancements and DMG Productions:

The Advancements series is an information-based educational show targeting recent advances across a number of industries and economies. Featuring state-of-the-art solutions and important issues facing today’s consumers and business professionals, Advancements focuses on cutting-edge developments, and brings this information to the public with the vision to enlighten about how technology and innovation continue to transform our world.

Backed by experts in various fields, DMG Productions is dedicated to education and advancement, and to consistently producing commercial-free, educational programming on which both viewers and networks depend.

For more information, please visit http://www.AdvancementsTV.com or call Richard Lubin at 866-496-4065.

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