
You Don't Want to Know Where Scientists Just Found 27 Million Tons of Plastic
Researchers from the Royal Netherlands Institute for Sea Research (NIOZ) and Utrecht University claim to be the first to provide a real estimate of ocean-polluting nanoplastics. Their research indicates that the North Atlantic Ocean alone hosts 27 million tons of floating plastic particles less than 1 micrometer (μm) in size.
'Plastic pollution of the marine realm is widespread, with most scientific attention given to macroplastics and microplastics. By contrast, ocean nanoplastics (<1 μm) remain largely unquantified, leaving gaps in our understanding of the mass budget of this plastic size class,' they explained in a study published earlier this month in the journal Nature. 'Our findings suggest that nanoplastics comprise the dominant fraction of marine plastic pollution.'
To reach these conclusions, Utrecht graduate student and study co-author Sophie ten Hietbrink collected water samples from 12 locations while working aboard a research vessel traveling from the Azores to the continental shelf of Europe. She filtered the samples of anything larger than one micrometer and conducted a molecular analysis on what was left behind. The team then extrapolated its results to the entire North Atlantic Ocean.
27 million tons is 'a shocking amount,' Ten Hietbrink said in a NIOZ statement. 'But with this we do have an important answer to the paradox of the missing plastic.' Namely, that a large part of it is floating in our oceans, invisible to the naked eye.
Unfortunately, there are a number of ways nanoparticles can end up in the oceans. While some likely arrive via rivers, others fall out of the sky with rain or on their own as 'dry deposition.' (Yes, we've even found plastic pollution in the sky). Nanoparticles can also form when large pieces of plastic already in the ocean are broken down by waves and/or sunlight, according to the researchers. The question now is how this pollution is impacting the world and its creatures—including us.
'It is already known that nanoplastics can penetrate deep into our bodies. They are even found in brain tissue. Now that we know they are so ubiquitous in the oceans, it's also obvious that they penetrate the entire ecosystem; from bacteria and other microorganisms to fish and top predators like humans,' said Helge Niemann, a geochemist at NIOZ and another co-author of the study. 'How that pollution affects the ecosystem needs further investigation.'
The missing plastic paradox, however, is not completely solved, because not all plastics were represented in the samples. The team didn't find polyethylene or polypropylene, for example.
'It may well be that those were masked by other molecules in the study. We also want to know if nanoplastics are as abundant in the other oceans. It is to be feared that they do, but that remains to be proven,' Niemann added. 'The nanoplastics that are there, can never be cleaned up. So an important message from this research is that we should at least prevent the further pollution of our environment with plastics.'
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Associated Press
an hour ago
- Associated Press
Aicuris Presents Pharmacokinetic Data from the First-in-Human Clinical Trial of AIC468, a Novel Antisense Oligonucleotide Targeting BK Virus, at World Transplant Congress
Wuppertal, Germany, August 5, 2025 - Aicuris Anti-infective Cures AG today announced initial clinical data from its ongoing first-in-human Phase 1 trial with AIC468. The novel antiviral antisense oligonucleotide is in development for the treatment of BK virus (BKV) infections in kidney transplant recipients. The interim results, presented at the World Transplant Congress in San Francisco on August 4, 2025, provide an overview of PK characteristics of AIC468 from the Phase 1 clinical trial in healthy volunteers. 'BK virus infections represent a serious and persistent threat for immunocompromised patients with a high risk of renal damage or kidney loss after transplantation. The PK results and safety data to date are very encouraging and provide us with valuable insights for the continued development of this differentiated program,' said Cynthia Wat, MD, CMO of Aicuris. 'Our goal is to achieve tangible therapeutic solutions for immunocompromised patients with kidney transplants, and these strong PK and safety data are an important step for us in achieving this goal.' FIH trial data from 72 healthy volunteer subjects, six single ascending dose (SAD) subcutaneous cohorts, one intravenous dose level and two multiple ascending dose (MAD) subcutaneous cohorts were presented at World Transplant Congress. AIC468 was safe and well tolerated across all cohorts investigated to date. The product candidate achieved excellent bioavailability (82%), rapid absorption, and distribution to peripheral tissues. A favorable half-life together with pre-clinical data, suggests that efficacious kidney concentrations can be attained by weekly or less frequent dosing regimens within the investigated dose range. Additionally, renal clearance for AIC468 accounted for less than 2% of the total clearance, representing a negligible route of elimination. Tissue uptake and subsequent metabolism appear to be the primary route of clearance, supporting the observed benign safety profile. The trial is progressing as planned in the third MAD cohort. 'Aicuris continues to build momentum by executing on our clinical trial strategy and achieving the first positive data set for our third clinical program for immunocompromised patients,' added Larry Edwards, CEO of Aicuris. 'In the second half of 2025 we expect data from the Phase 1 program to allow us to rapidly advance AIC468 into a Phase 2a proof-of-mechanism trial in H1 2026 to demonstrate its value for patients.' The randomized, double-blind, placebo-controlled first-in-human trial ( 2023-510074-13-00 ) is designed to evaluate the safety, tolerability and pharmacokinetics of AIC468 in healthy volunteers. SAD cohorts tested AIC468 or a placebo control in a total of 56 healthy volunteers across six subcutaneous (25 mg to 600 mg) and one intravenous dose level (200 mg). In the MAD cohorts an additional 24 subjects receive five repeated doses of AIC468 (130 mg, 230mg and 330 mg). Dosing in all SAD and the first two MAD cohorts have been successfully completed. The trial is progressing as planned in the third MAD cohort with data expected later this year. About BKV BKV is a ubiquitous polyomavirus that infects most people in early childhood, typically without symptoms. In immunocompromised individuals, such as organ transplant recipients, BKV can reactivate, leading to serious health issues. In kidney transplant patients, BKV reactivation can cause BK virus-associated nephropathy (BKVAN), affecting up to 10% of recipients and potentially resulting in graft loss. Current management involves reducing immunosuppressive therapy, which increases the risk of graft rejection. Despite its prevalence, there is no approved antiviral treatment specifically for BKV. About AIC468 AIC468 is an antisense oligonucleotide therapy designed to treat BK virus reactivation in kidney transplant patients which can pose a significant health risk for these patients. The candidate blocks viral replication within infected cells by inhibiting splicing of the pre-mRNA that encodes for the virus' large T-antigen. This innovative approach has already demonstrated potent antiviral activity along with a favorable pharmacokinetic and safety profile in preclinical studies and is currently being evaluated in a Phase 1 clinical trial. About Aicuris Aicuris is meeting the needs of the growing population of immunocompromised people who require precise therapies to effectively treat infection. Our flagship product, PREVYMIS®, marketed by our partner MSD, prevents CMV in a defined group of transplant recipients. Our pivotal Phase 3 candidate, pritelivir, aims to address refractory HSV infections in a broad population of patients with weakened immune systems. For immunocompromised people, an otherwise manageable infection can mean life or death. Aicuris, with its expertise and growing pipeline, is committed to providing therapeutic solutions for them now and in the future. Contact: Aicuris Anti-infective Cures AG [email protected] Trophic Communications Dr. Stephanie May and Dr. Charlotte Spitz Phone: +49 171 3512733 Email: [email protected]


WIRED
an hour ago
- WIRED
How Supercomputing Will Evolve, According to Jack Dongarra
Aug 5, 2025 5:00 AM WIRED talked with one of the most influential voices in computer science about the potential for AI and quantum to supercharge supercomputers. Jack Dongarra in Lindau in July 2025. Photograph: Patrick Kunkel/Lindau Nobel Laureate Meetings High-performance supercomputing—once the exclusive domain of scientific research—is now a strategic resource for training increasingly complex artificial intelligence models. This convergence of AI and HPC is redefining not only these technologies, but also the ways in which knowledge is produced, and takes a strategic position in the global landscape. To discuss how HPC is evolving, in July WIRED caught up with Jack Dongarra, a US computer scientist who has been a key contributor to the development of HPC software over the past four decades—so much so that in 2021 he earned the prestigious Turing Award. The meeting took place at the 74th Nobel Laureate Meeting in Lindau, Germany, which brought together dozens of Nobel laureates as well as more than 600 emerging scientists from around the world. This interview has been edited for length and clarity. Jack Dongarra on stage at the 74th Lindau Nobel Laureate Meetings. Photograph: Patrick Kunkel/Lindau Nobel Laureate Meetings WIRED: What will be the role of artificial intelligence and quantum computing in scientific and technological development in the coming years? Jack Dongarra: I would say AI is already playing an important role in how science is done: We're using AI in many ways to help with scientific discovery. It's being used in terms of computing and helping us to approximate how things behave. So I think of AI as a way to get an approximation, and then maybe refine the approximation with the traditional techniques. Today we have traditional techniques for modeling and simulation, and those are run on computers. If you have a very demanding problem, then you would turn to a supercomputer to understand how to compute the solution. AI is going to make that faster, better, more efficient. AI is also going to have an impact beyond science—it's going to be more important than the internet was when it arrived. It's going to be so pervasive in what we do. It's going to be used in so many ways that we haven't really discovered today. It's going to serve more of a purpose than the internet has played in the past 15, 20 years. Quantum computing is interesting. It's really a wonderful area for research, but my feeling is we have a long way to go. Today we have examples of quantum computers—hardware always arrives before software—but those examples are very primitive. With a digital computer, we think of doing a computation and getting an answer. The quantum computer is instead going to give us a probability distribution of where the answer is, and you're going to make a number of, we'll call it runs on the quantum computer, and it'll give you a number of potential solutions to the problem, but it's not going to give you the answer. So it's going to be different. With quantum computing, are we caught in a moment of hype? I think unfortunately it's been oversold—there's too much hype associated with quantum. The result of that typically is that people will get all excited about it, and then it doesn't live up to any of the promises that were made, and then the excitement will collapse. We've seen this before: AI has gone through that cycle and has recovered. And now today AI is a real thing. People use it, it's productive, and it's going to serve a purpose for all of us in a very substantial way. I think quantum has to go through that winter, where people will be discouraged by it, they'll ignore it, and then there'll be some bright people who figure out how to use it and how to make it so that it is more competitive with traditional things. There are many issues that have to be worked out. Quantum computers are very easy to disturb. They're going to have a lot of 'faults'—they will break down because of the nature of how fragile the computation is. Until we can make things more resistant to those failures, it's not going to do quite the job that we hope that it can do. I don't think we'll ever have a laptop that's a quantum laptop. I may be wrong, but certainly I don't think it'll happen in my lifetime. Quantum computers also need quantum algorithms, and today we have very few algorithms that can effectively be run on a quantum computer. So quantum computing is at its infancy, and along with that the infrastructure that will use the quantum computer. So quantum algorithms, quantum software, the techniques that we have, all of those are very primitive. When can we expect—if ever—the transition from traditional to quantum systems? So today we have many supercomputing centers around the world, and they have very powerful computers. Those are digital computers. Sometimes the digital computer gets augmented with something to enhance performance—an accelerator. Today those accelerators are GPUs, graphics processing units. The GPU does something very well, and it just does that thing well, it's been architected to do that. In the old days, that was important for graphics; today we're refactoring that so that we can use a GPU to satisfy some of the computational needs that we have. In the future, I think that we will augment the CPU and the GPU with other devices. Perhaps quantum would be another device that we would add to that. Maybe it would be neuromorphic—computing that sort of imitates how our brain works. And then we have optical computers. So think of shining light and having that light interfere, and the interference basically is the computation you want it to do. Think of an optical computer that takes two beams of light, and in the light is encoded numbers, and when they interact in this computing device, it produces an output, which is the multiplication of those numbers. And that happens at the speed of light. So that's incredibly fast. So that's a device that perhaps could fit into this CPU, GPU, quantum, neuromorphic computer device. Those are all things that perhaps could combine. How is the current geopolitical competition—between China, the United States, and beyond—affecting the development and sharing of technology? The US is restricting computing at a certain level from going to China. Certain parts from Nvidia are no longer allowed to be sold there, for example. But they're sold to areas around China, and when I go visit Chinese colleagues and look at what they have in their their computers, they have a lot of Nvidia stuff. So there's an unofficial pathway. At the same time, China has pivoted from buying Western technology to investing in its own technology, putting more funding into the research necessary to advance it. Perhaps this restriction that's been imposed has backfired by causing China to accelerate the development of parts that they can control very much more than they could otherwise. The Chinese have also decided that information about their supercomputers should not be advertised. We do know about them—what they look like, and what their potential is, and what they've done—but there's no metric that allows us to benchmark and compare in a very controlled way how those computers compare against the machines that we have. They have very powerful machines that are probably equal to the power of the most significant machines that we have in the US. They're built on technology that was invented or designed in China. They've designed their own chips. They compete with the chips that we have in the computers that are in the West. And the question that people ask is: Where were the chips fabricated? Most chips used in the West are fabricated by the Taiwan Semiconductor Manufacturing Company. China has technology, which is a generation or two behind the technology that TSMC has, but they're going to catch up. My guess is that some of the Chinese chips are also fabricated in Taiwan. When I ask my Chinese friends 'Where were your chips manufactured?' they say China. And if I push them and say 'Well, were they manufactured in Taiwan?' the answer to that comes back eventually is Taiwan is part of China. Jack Dongarra on the shores of Lake Constance at the 74th Nobel Laureate Meeting. Photograph: Gianluca Dotti/Wired How will the role of programmers and developers change as AI evolves? Will we get to write software using only natural language? AI has a very important role I think in helping to take away some of the time-consuming parts of developing programs. It's gotten all the information about everybody else's programs that's available and then it synthesizes that and then can push that forward. I've been very impressed when I have asked some of these systems to write a piece of software to do a certain task; the AI does a pretty good job. And then I can refine that with another prompt, saying 'Optimize this for this kind of computer,' and it does a pretty good job of that. In the future, I think more and more we will be using language to describe a story to AI, and then have it write a program to carry out that function. Now of course, there are limits—and we have to be careful about hallucinations or something giving us the wrong results. But maybe we can build in some checks to verify the solutions that AI produces and we can use that as a way of measuring the potential accuracy of that solution. We should be aware of the potential problems, but I think we have to move ahead in this front. This story originally appeared on WIRED Italia and has been translated from Italian.
Yahoo
2 hours ago
- Yahoo
New Scientific Data with TrkA-NAM ACD137 Against Knee Osteoarthritis to be Presented at Pain Conference
STOCKHOLM, SE / / August 5, 2025 / AlzeCure Pharma AB (publ) (FN STO:ALZCUR), a pharmaceutical company that develops candidate drugs for diseases affecting the nervous system, focusing on Alzheimer's disease and pain, today announced that an abstract about the preclinical project TrkA-NAM ACD137 against osteoarthritis and other severe pain conditions has been accepted for presentation at the international pain conference NeuPSIG 2025, to be held in Berlin, Germany, September 4-6. The abstract, titled Analgesic and anti-inflammatory effects of ACD137, a potent and selective negative allosteric modulator of TrkA , will be presented at NeuPSIG 2025 by Märta Segerdal, Head of Development and Chief Medical Officer at AlzeCure Pharma. Co-authors are Pontus Forsell, Maria Backlund, Veronica Lidell, Azita Rasti, Cristina Parrado-Fernandez, Johan Sandin and Gunnar Nordvall. The results show that the lead drug candidate in the project, ACD137, has potent analgesic effects in several different preclinical pain models. The analgesic effect of ACD137 in the study was as potent as the effect of the anti-NGF antibody Tanezumab, which has demonstrated significant and robust pain relief in several clinical trials. ACD137 achieves its effect by blocking NGF-mediated signaling via TrkA receptors, a biological mechanism with strong genetic, preclinical and clinical validation for its role in pain. These positive preclinical data in models of osteoarthritis, neuropathic pain and nociceptive pain further strengthen previous positive analgesic results obtained with ACD137 and further underline its broad applicability in various severe pain conditions, including osteoarthritis. "These data demonstrate that our drug candidate ACD137 is a highly potent and selective TrkA-NAM that exhibits significant analgesic effects in relevant preclinical animal models. Furthermore, this small molecule TrkA-NAM has the potential to avoid some of the side effects observed with anti-NGF antibodies due to a more selective mechanism of action, while maintaining analgesic efficacy," said Pontus Forsell, project leader and Head of Discovery and Research at AlzeCure Pharma. "The project is based on a mechanism with strong validation, both preclinically and clinically. The results we have for TrkA-NAM in pain are promising, and the fact that we also have anti-inflammatory effects with our substance opens up for broader application. The fact that this is also a mechanism that is not linked to the side effects and addiction problems observed with opioids and antibodies is of course also important for a potential future approval," said Martin Jönsson, CEO of AlzeCure Pharma AB. The abstract and the poster will be available on AlzeCure's website after the presentation ( For more information, please contact Martin Jönsson, CEOTel: +46 707 86 94 About AlzeCure Pharma AB (publ) AlzeCure ® is a Swedish pharmaceutical company that develops new innovative drug therapies for the treatment of severe diseases and conditions that affect the central nervous system, such as Alzheimer's disease and pain - indications for which currently available treatment is very limited. The company is listed on Nasdaq First North Premier Growth Market and is developing several parallel drug candidates based on three research platforms: NeuroRestore ® , Alzstatin ® and Painless. NeuroRestore consists of two symptomatic drug candidates where the unique mechanism of action allows for multiple indications, including Alzheimer's disease, as well as cognitive disorders associated with traumatic brain injury, sleep apnea and Parkinson's disease and is being prepared for phase 2. The Alzstatin platform focuses on developing disease-modifying and preventive drug candidates for early treatment of Alzheimer's disease. Painless is the company's research platform in the field of pain and contains two projects: ACD440, which is a drug candidate in the clinical development phase for the treatment of neuropathic pain with positive phase 2 results, and TrkA-NAM, which targets severe pain in conditions such as osteoarthritis. AlzeCure aims to pursue its own projects through preclinical research and development through an early clinical phase, and is continually working on business development to find suitable outlicensing solutions with other pharmaceutical companies. FNCA Sweden AB is the company's Certified Adviser. For more information, please visit About TrkA-NAMThe TrkA-NAM project, which is in research phase, is focused on the treatment of pain. The target mechanism, NGF / TrkA signaling, is well-validated both preclinically and clinically and provides a promising alternative to new analgesics without the side effects and addiction problems observed with opioids. Substances developed in the project have recently been shown to also have anti-inflammatory properties. For the TrkA-NAM drug project, we have leveraged our knowledge concerning the underlying biology for the NeuroRestore platform in order to develop new compounds that focus on providing pain relief in conditions associated with severe pain. The goal of the project is to develop a small-molecule TrkA-negative allosteric modulator for the treatment of osteoarthritis pain and other severe pain disorders. The global osteoarthritis market is expected to reach USD 11.0 billion by 2025, from USD 7.3 billion in 2020. Growth in this market is driven by factors such as the increasing occurrence of osteoarthritis, the growing aging population, and an increase in the number of sports injuries. Over 400 million people worldwide suffer from painful and activity-limiting osteoarthritis of the hip or knee. Many patients experience insufficient pain relief or side effects with current treatment, which today usually consist of NSAIDs or opiates and there is a great need for more effective and better tolerated drugs in this field. Read more about TrkA-NAM on our homepage. Image Attachments Martin Jönsson CEO And Pontus Forsell Head Of D&R AlzeCure Pharma Attachments New scientific data with TrkA-NAM ACD137 against knee osteoarthritis to be presented at pain conference SOURCE: AlzeCure Pharma View the original press release on ACCESS Newswire Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data