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25 March 2026
Acknowledging the Contributions of Our Reviewers in 2025


As a pioneer in open access publishing, MDPI maintains rigorous publication standards. This mission relies on the dedication and expertise of our reviewers, who invest their time and knowledge to ensure the quality and integrity of the research we publish.

In 2025, over 209,000 reviewers contributed to the peer-review process at MDPI, providing more than 1.3 million review reports for our journals. To express our gratitude, MDPI’s Reviewer Recognition Program highlights reviewers across over 400 journals, featuring those who have assessed at least one manuscript and agreed to be acknowledged.

In addition, MDPI has identified its Top 1000 Reviewers of 2024 to recognize those whose expertise, dedication, and thoughtful evaluations were particularly outstanding.

Many journals have also established Outstanding Reviewer Awards to honor our reviewers’ commitment to publication excellence. Together with the Exceptional Reviewer List, we showcase the importance of reviewers’ work and their time and dedication.

These initiatives serve to express our deepest appreciation and gratitude towards the whole reviewer community. In recognition of their contributions, we also welcome new researchers to join this community. If you would like to contribute to open access publishing, learn more about the reviewers’ benefits and sign up to join us.

24 March 2026
Molecules | Interview with Prof. Dr. Qidong You, a Scientific Committee Member for the 5th Molecules Medicinal Chemistry Symposium (MMCS 2026)


Prof. Qidong You
is a National Model Teacher, National High-Level Talent, and National Distinguished Teacher. He is a Professor and Doctoral Supervisor at China Pharmaceutical University and Chief Scientist of the Jiangsu Key Laboratory of Drug Design and Optimization. He holds key positions in multiple national and provincial academic committees, including the China Committee for Terminology in Science and Technology, the State Pharmacopoeia Commission, the Chinese Pharmaceutical Association, and the Medicinal Chemistry Committee of the Jiangsu Pharmaceutical Association. He has been honored with numerous national and provincial awards for science and technology as well as teaching achievements. He has led over 20 major national research projects, published more than 500 SCI papers, filed over 100 patents internationally, with 70 granted, and edited over 20 monographs and textbooks.

1. Could you briefly introduce your team’s current research focus? What initially inspired this research direction?
Our team is a core group within the Jiangsu Provincial Key Laboratory of Drug Design and Druggability Optimization. It consists of five Professors: Prof. Qidong You (Professor and Doctoral Supervisor at China Pharmaceutical University, Scholar of the National Major Talent Program, and Chief Scientist of the Provincial Key Laboratory); Prof. Zhengyu Jiang (Professor and Doctoral Supervisor at China Pharmaceutical University, Young Scholar of the National Major Talent Program, and Director of the Provincial Key Laboratory); Prof. Lei Wang (Professor and Doctoral Supervisor at China Pharmaceutical University, Recipient of the National Natural Science Foundation of China Young Scientist Fund (Type B), and Secretary of the Provincial Key Laboratory); Prof. Xiaoke Guo (Professor and Doctoral Supervisor at China Pharmaceutical University, Young Scholar of the National Major Talent Program, and Principal Investigator (PI) of the Provincial Key Laboratory); and Prof. Xiaoli Xu (Professor and Doctoral Supervisor at China Pharmaceutical University, Young Scholar of the National Major Talent Program, and Principal Investigator (PI) of the Provincial Key Laboratory). In addition, the team is supported by two Associate Professors and five postdoctoral fellows.
The main research direction of our team focuses on the chemical regulation of functional protein molecules through interactions among biological macromolecules in vivo. Our goal is to transform targets that are difficult or even impossible to address with traditional small-molecule design into druggable targets through novel mechanisms of action and molecular design strategies, thereby conducting original research to discover innovative drugs. The specific research directions cover the following three aspects:

  • Medicinal Chemistry of Bifunctional Small Molecules: We conduct research on the medicinal chemistry of bifunctional small molecules and develop new protein degradation technologies to expand the scope and precision of targeted protein degradation;
  • Regulation of the Chaperone (e.g., HSP90)–Co-chaperone (e.g., CDC37, PP5)–Client Protein (e.g., CDK4/6, ASK1) System: We focus on regulatory research on the chaperone–co-chaperone–client protein system, and design innovative Homodimerization Inducing Molecules (HIMs) to selectively block the folding and maturation of protein kinases in vivo, thereby inducing their degradation;

  • Discovery and Development of Innovative Drugs Targeting Epigenetic Regulators: We carry out the discovery and development of innovative drugs targeting epigenetic regulatory proteins and combine this with research on nucleic acid immune recognition mechanisms. We design novel molecules for precise regulation targeting nucleic acid sensors (e.g., the dsDNA-sensing pathway cGAS-STING and Z-form nucleic acid-binding proteins) to explore potential new targets and pathways for the treatment of immune-related diseases.
    The interactions of biological macromolecules in vivo, including protein–protein and protein–nucleic acid interactions, form the foundation of life processes. These interaction networks not only carry the recognition and transmission of biological signals in vivo, but also directly determine the biological functions of functional protein molecules. Traditional medicinal chemistry research on small-molecule design focuses on designing molecules for a single cavity of a single target, making it difficult to address drug design for difficult-to-drug and undruggable targets with complex mechanisms and high selectivity requirements. The regulation of functional protein molecules by biological macromolecular interactions in vivo is based on understanding the regulatory network of biological macromolecules, combined with chemical biology research. It involves developing new protein degradation technologies, designing innovative target protein ligands, conducting HIM design for the HSP90-CDC37-PP5 chaperone system and HSP90 itself to precisely affect the folding, maturation, and release of protein kinases, designing small-molecule regulators for methylation-modified proteins and their associated reader proteins, and creating novel molecules that can achieve precise regulation targeting nucleic acid sensors.

2. In your opinion, what will the most noteworthy hotspots, breakthrough points, or development trends in the field of medicinal chemistry be in the coming years? Could you elaborate on them for us?

  1. Blurring Boundaries Between Traditional Small Molecules and Biologics, and Convergent Development: Drug modalities are breaking through the traditional boundaries between small molecules and biologics. Protein degradation technologies have transformed the drug intervention paradigm from “targeted binding” to “induced elimination”; conjugate drugs, represented by Antibody–Drug Conjugates (ADCs), have introduced new paradigms for targeted drugs; and new modification and optimization strategies have achieved dual breakthroughs in the stability and targeting of peptide and nucleic acid drugs. The emergence of these new molecular modalities has continuously blurred the boundaries between small molecules and biologics, driving medicinal chemistry toward greater convergence. PROTACs and molecular glues have moved from the conceptual stage to clinical application. In the future, more emphasis will be placed on their “regulatability” and “tissue specificity” to overcome current issues such as off-target toxicity and poor bioavailability.
  2. Artificial Intelligence as the Core Driver: Artificial intelligence (AI) has become the core driver of medicinal chemistry and drug molecular design. The in-depth involvement of AI is no longer merely an auxiliary tool; it has begun to dominate molecular design, greatly shortening the cycle from target discovery to preclinical candidate compounds. AI will play a more important role in compound screening, ADMET prediction, and de novo molecule generation, accelerating the process from target validation to lead compound discovery.
  3. Nucleic Acid Immunity and Epigenetic Regulation Mechanisms as New Frontiers for Innovative Drug R&D: Nucleic acid immunity and epigenetic regulation mechanisms have become newly developed frontiers for innovative drug research and development. The in-depth exploration of nucleic acid immune regulation mechanisms, the discovery of new targets, and the design and optimization of oligonucleotide drugs as messengers or tools will lead to the development of novel molecules with intelligent targeting capabilities, controlled-release behavior, and regulable immunogenicity. In-depth integration of chemical epigenetics: we will not only inhibit “writers” and “erasers”, but also precisely regulate “readers” and open new therapeutic windows by intervening in dynamic regulatory processes, such as RNA methylation.
  4. Further Development of New Drug Molecular Design Technologies: Through the design of covalent drugs, allosteric inhibitors, and protein–protein interaction inhibitors, an increasing number of targets previously considered “difficult-to-drug” and “undruggable” (such as transcription factors, phosphatases, and scaffold proteins) will be transformed into intervenable targets.
3. As a member of the Scientific Committee for this conference, what aspects of the agenda or discussion topics are most appealing to you? How would you assess the conference's role in advancing the discipline?
The most appealing aspect of this conference is that it comprehensively covers the most noteworthy hotspots in medicinal chemistry today, which also represent future development trends. The conference themes include not only classic areas such as chemical biology (Session Topic 1), natural products (Session Topics 4 and 5), and the classic target GPCR (Session Topic 6), but also cutting-edge technological fields such as AI-driven drug research and development (Session Topic 2) and DNA-encoded library technology (Session Topic 7). These kinds of “integration of classic and new” discussions often spark the most wonderful ideas. In addition, as mentioned earlier, bifunctional molecules, such as PROTACs, which target protein degradation, are current research hotspots. Session Topic 3, which focuses on emerging drug modalities based on proximity effects, will also be a topic of great concern to everyone. Finally, the sharing of cutting-edge medicinal chemistry case studies (Session Topic 8) will ground these technologies in reality, showing which molecules have entered the clinic and which strategies have been proven feasible.
The conference's role in promoting the development of the discipline lies in:
  • Cross-disciplinary Integration: It breaks down the barriers between medicinal chemistry, biology, and clinical medicine, and promotes in-depth communication among experts from multiple disciplines;
  • Focus on Translation: The agenda setting not only focuses on “discovery”, but also emphasizes “translation”, building a bridge between academia and industry, which helps accelerate the progress from basic research to preclinical candidate compounds.
    With the emergence of these comprehensive, novel, and important topics, this conference will play a key role in advancing the field of medicinal chemistry.

4. What advice would you give to young scholars in similar fields to advance their academic research?
First, cultivate interdisciplinary thinking and devote oneself to academic research with a calm mind. Young scholars should strive to become “versatile talents” with in-depth expertise in their field; a solid scientific research foundation is always the foundation for establishing themselves. At the same time, medicinal chemistry is an interdisciplinary subject. Therefore, scholars not only need to delve deeply into their subfields but also to develop horizontally and integrate knowledge. Young scholars should take the initiative to integrate into the trend of interdisciplinary development but not be led astray by it.
Second, consolidate the foundation and return to the problem's essence. When choosing research topics, let the “problem” lead, rather than being driven by “hotspots”. Current research hotspots are diverse and changing rapidly; it is crucial to maintain independent thinking and let the scientific problems you care about drive you forward, rather than blindly chasing current hotspots. This is the fundamental way for young people to quickly form their own research characteristics. As researchers in medicinal chemistry, we should never lose the “basic skills” of medicinal chemistry.
Third, remain open and cooperative, dare to challenge, and maintain resilience. Medicinal chemistry is inherently an interdisciplinary subject, and the era of working alone is over. Take the initiative to knock on the door of the neighboring laboratory and discuss your molecules with the biologists and pharmacologists there. Clearly, in the field of drug research, every inactive compound is valuable; it tells us which direction to take. Maintain the craftsmanship of meticulously refining molecular structures, because ultimately, what patients receive must be a high-quality drug, not just a research paper.

5. Based on your research experience, how do you think academia and industry can better collaborate to accelerate the translation of medicinal chemistry research into practical applications?
This is a core issue related to the efficiency of drug research and development. The mission of academia should still be to pursue original innovations that industry cannot, dare not, or lacks the patience to pursue. Academic research should address unmet clinical needs, genuine scientific problems, and bottleneck technologies. By adhering to these two points, academia and industry can achieve better long-term cooperation.
The cooperation between academia and industry can be optimized from three dimensions: “talent, platform, and mechanism”.
First, a two-way flow of talent. Academia needs to cultivate chemists who understand “druggability”, while industry also needs to maintain sensitivity to cutting-edge science. I encourage young people to experience the rhythm of research and development in enterprises, and I also welcome industrial scientists to return to campuses to share practical experience. Innovation occurs when ideas collide.
Second, co-construction and sharing of platforms. As discussed at our conference, technologies such as DNA-encoded libraries and AI-driven research and development require significant infrastructure investment. If academia and industry can jointly build joint laboratories, with academia providing “targets” and “ideas” and industry providing “libraries” and “computing power”, then “DNA-encoded libraries” can become a real discovery engine, rather than a luxury that each party pursues independently.
Third, flexible and innovative mechanisms. Academia should be good at “enriching” their discoveries; even providing an additional co-crystal structure or one more preliminary metabolic data point can help industry judge the value of a project. Industry also needs to dare to “invest early and invest in small projects”, get involved when the project is still in its infancy, and use industry experience to guide chemical modification, avoiding academia from going all the way down an unworkable path.
In general, ideal cooperation is not a simple “money-for-molecule” transaction but a deep, trusting partnership. Whether publishing papers in top journals or promoting drugs to the market, our common goal is to conquer diseases and benefit humanity.

Introduction of MMCS 2026:
Conference date:
14–17 May 2026 (Beijing Time);
Location: Beiyuan Grand Hotel, Beijing, China;
Abstract Acceptance Notification: 27 March 2026;
Early Bird Registration Deadline: 3 April 2026.

Conference Chairs:

  • Prof. Dr. Xiaoguang Lei, (Peking University, China);
  • Prof. Dr. Diego Muñoz-Torrero, (University of Barcelona, Spain).

For more details: https://sciforum.net/event/MMCS2026.

For any enquiries regarding the event, please contact mmcs2026@mdpi.com.

20 March 2026
Meet Us at the EUROPT(R)ODE XVII Conference, 29 March 2026–1 April 2026, Jena, Germany


MDPI will be attending the EUROPT(R)ODE XVII conference, which will be held from 29 March to 1 April 2026, in Jena, Germany.

EUROPT(R)ODE XVII will be hosted in Jena, Germany, the historic “City of Light”, and chaired by Professor Jürgen Popp, Scientific Director of the Leibniz Institute of Photonic Technology. This conference is a flagship international event dedicated to the advancement of chemical and biochemical optical sensing. It will gather leading scientists, engineers, and industry professionals to explore the latest innovations, foster interdisciplinary collaboration, and discuss the future direction of the field.

The four-day conference will feature six plenary lectures by world-renowned researchers such as Alexey Gorshkov (USA), Laura Na Liu (Germany), and Ralf Jungmann (Germany). These will be complemented by parallel sessions covering a wide spectrum of topics, from fundamental research in plasmonic, quantum-enhanced sensing and single-molecule detection to applied technologies in wearables, microfluidics and AI-driven data analytics. With over one hundred oral presentations and a dedicated poster session, the conference will showcase cutting-edge work from leading research groups across the globe.

The following MDPI journals will be represented:

If you plan to attend this conference, please feel free to stop by our booth and have a conversation with us. Our delegates look forward to meeting you in person and answering any questions that you may have. For more information about the conference, please visit the following link: https://europtrode2026.org/.

9 March 2026
Meet Us at the Second International Conference on Nano Energy and Technology (ICNEAT-2026), 27–30 March 2026, Shantou, China


Conference:
The Second International Conference on Nano Energy and Technology
Date: 27–30 March 2026
Location:
Shantou, China

MDPI will be attending the second International Conference on Nano Energy and Technology as an exhibitor, and we are welcoming researchers from different backgrounds to visit and share their latest ideas with us.

ICNEAT-2026 will bring together these disciplines, focusing on nanostructures, energy storage and conversion, and advanced materials and devices, as well as artificial intelligence for materials. The conference will offer a global forum for leading researchers to share cutting-edge findings, for industry to engage directly with academia, and for students and early-career scientists to explore the latest advances.

The following MDPI journals will be represented:

If you are planning on attending this conference, please do not hesitate to contact us. Our delegates look forward to meeting you in person and answering any questions that you may have. For more information about the conference, please visit the following website: https://sites.gtiit.edu.cn/matec/icneat2026/.

4 March 2026
Meet Us at the 35th CCS Congress, 11–14 April 2026, Chongqing, China


Conference:
The 35th CCS Congress
Organization: Chinese Chemical Society
Date: 11–14 April 2026
Place: Chongqing, China
Booth: #D65

The CCS Congress is the highest level, largest scale, and most influential comprehensive academic exchange platform in the field of chemistry in China. The 35th CCS Congress has set up 72 academic branches, and the academic forums are being expanded (the exact number is not yet clear, but it is known that there were 14 last year). During the annual conference, a series of diverse activities such as forums and continuing education programs will be held simultaneously. Additionally, the “New Technologies, Products, and Instruments Achievement Exhibition” will take place, featuring participation from relevant universities, research institutes, enterprises, book publishing, and academic journals. Conference topics will include organic chemistry, inorganic chemistry, chemistry of natural products, applied chemistry, material chemistry, physical chemistry, environmental chemistry, photochemistry, colloid and interface chemistry, green chemistry, spectrochemistry, nuclear chemistry, etc.

The following MDPI journals will be represented:

If you plan on attending this conference, feel free to stop at booth #D65. Our delegates look forward to meeting you in person to answer any questions you may have.

For more information about the conference, please visit the following link: https://www.chemsoc.org.cn/meeting/35th/.

4 March 2026
MDPI’s 2025 Best Paper Awards—Award-Winning Papers Announced


MDPI is honored to announce the recipients of the 2025 Best Paper Awards, celebrating exceptional research for its scientific merit and broad impact. After a rigorous evaluation process conducted by Academic Editors, this year’s awards showcase papers that stand out for their innovation, relevance, and high-quality presentation.

Out of a highly competitive pool, 396 winning papers have been recognized for their exceptional contributions. We congratulate these authors for pushing the boundaries of their respective disciplines.

At MDPI, we are dedicated to broadening the reach of innovative science. To learn more about the award-winning papers and explore research projects in your field of study, please visit the following links:

About MDPI Awards:

To reward the global research community and enhance academic dialogue, MDPI journals regularly host award programs across diverse scientific disciplines. These awards, serving as a source of inspiration and recognition, help raise the influence of talented individuals who have been credited with outstanding achievements and whose work drives the advancement of their fields.

Explore the Best Paper Awards open for participation, please click here.

 

28 February 2026
MDPI INSIGHTS: The CEO’s Letter #32 - MDPI China and Thailand, China Science Daily, 1,000 Partnerships, R2R

Welcome to the MDPI Insights: The CEO's Letter.

In these monthly letters, I will showcase two key aspects of our work at MDPI: our commitment to empowering researchers and our determination to facilitating open scientific exchange.


Opening Thoughts

Reflections from China: Year-End-Celebrations and Open Access Publishing

In February, I had the pleasure of joining over a thousand colleagues from our Tongzhou and Haidian offices at their end-of-year annual celebration in Beijing.

Spending time with our teams in China is also a powerful reminder of the scale and complexity of MDPI as a global organization. Our colleagues in Beijing, Wuhan, and across the country play a significant role in our day-to-day operations and long-term development. I’m grateful for the hospitality, collaboration, and commitment shown by our managers and teams in China, alongside colleagues worldwide, who have helped steadily build MDPI, brick by brick, over the years.

Below are some data on Open Access (OA) publishing in China and our collaboration in this important research market.

Open Access Publishing in China

China has been the world’s leading country in research and review article publication volume since 2019, exceeding one million publications in 2025. Over the past five years, the gap between China and the second-ranked country, the United States, has continued to widen.

In 2025:

  • 47% of China’s research output was published Open Access
  • Of those OA publications, 76% were Gold Open Access (approximately 382,930 articles)
  • The overall OA distribution remained stable compared with 2024, with Gold OA increasing by 1%

Over the past five years (2021–2025):

  • China published 4,398,050 research and review articles
  • Approximately 48% of this output was OA

According to Dimensions, when comparing the top 20 countries by publication volume (2021–2025):

  • China ranks 1st worldwide in publication volume
  • China ranks 9th in citation performance within this group (for comparison, the US ranks 2nd in publication volume and 10th in citation ranking)
  • Average citations per article: 12.51

Among the top 10 universities globally by publication volume, six are Chinese institutions, alongside Harvard University (USA), the University of São Paulo (Brazil), the University of Toronto (Canada), and the University of Oxford (UK).

MDPI and China

China is an important and long-standing part of MDPI’s global publishing ecosystem:

  • In 2025, MDPI was the largest fully Open Access publisher in China
  • MDPI published 22% of China’s Gold Open Access output (82,133 papers)
  • We received 290,999 submissions from China-affiliated authors and published 82,133 articles
  • There are 8,500+ active Editorial Board Members based in China
    • 64% (5,438) have an H-index above 26
  • MDPI works with:
    • 117 Editors-in-Chief
    • 103 Section Editors-in-Chief
  • 71 China-based institutions currently hold IOAP agreements with MDPI, seven of which rank among the top 10 Chinese institutions by publication volume

China's scale in research output means that the publishing platforms chosen by Chinese scholars will continue to influence the direction of scholarly publishing. At the same time, MDPI’s strength comes from its international collaboration, with colleagues, editors, reviewers, and authors working together across regions and disciplines.

Thank you to all our colleagues in China, and around the world, who support MDPI’s publishing activities across departments and help advance open access research every day.

Impactful Research

“Progress in open science is built through trust, dialogue, and relationships”

Behind the Scenes: A Conversation with China Science Daily

During my trip to Beijing, I also had the opportunity to visit China Science Daily and take part in an interview and broader exchange with their team in Beijing. Visits like this matter because progress in open science is built not only through platforms and infrastructure, but also through trust, dialogue, and relationships across research communities and regions.

China Science Daily: History Museum

As part of the visit, I was given a tour of their History Museum, which offers a thorough perspective on the evolution of China’s first science and technology newspaper, established in 1959. The exhibition highlights how the organization developed into a trusted institution connecting research with the public and policymakers. It was a helpful reminder that at the core of publishing is stewardship, credibility, and long-term public engagement with science.

An Open Exchange on Open Science

During the visit, I met with Dr. Zhao Yan, Editor-in-Chief of ScienceNet. We had an open and engaging conversation about MDPI’s role in Open Access, the evolution of open science globally, and the potential for more collaboration going forward. He especially appreciated the candid and personal nature of our exchange, noting that this kind of dialogue feels important in a landscape where trust and transparency matter.

Interview on Open Access

I also participated in an interview with Ms. Yan Jie, from the Online Media Center and Editor-in-Chief of ScienceNet, China Science Daily. Our discussion covered the growth of Open Access over the past 30 years, MDPI’s mission and values, academic integrity, collaboration with the Chinese research community, and MDPI’s own 30th anniversary milestone. It was a great opportunity to reflect on how open science has matured, and where shared responsibility across publishers, institutions, and researchers continues to matter most.

“Progress in open science is built by more than scale and infrastructure”

I’m sharing a few photos from the visit as a glimpse behind the scenes. The full interview will be published by China Science Daily in due course, and I look forward to sharing it when it is available.

More broadly, visits like this reinforce something I’ve always believed in: progress in open science is built not only through scale and infrastructure, but also through continued dialogue, mutual respect, collaboration, and a willingness to listen across regions and perspectives. That remains central to our work, especially as MDPI reflects on 30 years of publishing, built together.

Inside MDPI

Bangkok Visit: Growth, Partnership, and Local Impact

In February, I also had the opportunity to visit our Bangkok office for the second time in two years to support their local meetings and deliver a training session on how we present MDPI at a corporate level.

It’s easy to spend time with our colleagues in Thailand. From Editorial and Production to Conferences, Marketing, Design, and our Regional Journal Relations Specialist (RJRS), the team continues to grow in scale and professionalism. I’d also like to recognize our local management and admin teams, who have been steadily expanding our office and supporting more than 500 colleagues on the ground.

Academic Partnerships

During the visit, we met with the Engineering Department at King Mongkut’s Institute of Technology Ladkrabang (KMITL). Our discussion focused on the recent MDPI developments, Institutional Open Access Program (IOAP) opportunities, Author Publishing Workshops (APW), and the potential use of JAMS to support their institutional journal.

“MDPI is the third-largest OA publisher in Thailand”

We also shared insights into the growth of Open Access (OA) in Thailand and KMITL’s own publishing trends. These conversations matter because institutions are looking for sustainable ways to support their researchers. Our IOAP agreements are one simple example of how we can provide value in this area while maintaining accessibility for authors.

Thailand and MDPI: 2025 Snapshot

Our Bangkok office, officially launched in 2022, has been growing to support over 500 staff members while continuing to expand its engagement in scholar visits, workshops, and conference collaborations. As at 2025, Thailand submissions to MDPI have increased about 21% and publications by about 25%, maintaining a rejection rate close to the company average. MDPI is the third-largest OA publisher in Thailand, publishing 15% of all Gold OA output in 2025.

Representing MDPI Externally

During the visit, I delivered a training session on how we present MDPI at external events.

This session covered topics related to:

  • Our aim and guiding principles
  • High-level company milestones and Indexing facts and figures
  • Industry partnerships and collaborations
  • Market trends in OA and subscription publishing
  • Country-specific publishing data and collaborations with MDPI
  • Insights from our Voice of Community report

I find that while many colleagues are very familiar with the specific journal for which they have responsibility, fewer have visibility into the broader MDPI ecosystem and the company’s global positioning. These sessions help build alignment, confidence, and consistency in how we represent the company.

What stands out most is that MDPI’s growth is not abstract: it’s visible in the people, the partnerships, and the professionalism developing across our offices.

Coming Together for Science

1,000 Institutional Partners: A Milestone Built on Trust

This month, we reached an important milestone: more than 1,000 institutions worldwide are now part of MDPI’s Institutional Open Access Program (IOAP). On paper, that is a number. In practice, it represents trust.

This milestone symbolizes thousands of conversations with libraries and institutions. It stands for negotiations, renewals, consortium expansions, and, most importantly, relationships built over time. It reflects the work of colleagues across publishing, institutional partnerships, marketing, editorial, finance, and many other teams who contribute to making these agreements operational.

In 2025 alone, more than 61,300 research articles benefited from article processing charge (APC) discounts through IOAP agreements. Tens of thousands of authors were able to publish through a simplified and structured process. At the same time, institutional administrators gained clearer oversight and streamlined workflows.

Why IOAP Matters

When we launched IOAP, the objective was straightforward: to reduce barriers for researchers while supporting institutions in navigating the evolving OA landscape. Over the past decade, the research ecosystem has changed. Funder mandates, national policies, and Plan S–aligned requirements have accelerated the transition to OA.

Institutions need publishing partners who provide transparency, scalability, and operational efficiency. IOAP was designed to support that reality.

For colleagues who would like to better understand the program, this blog-post overview of MDPI’s IOAP provides additional context, including common questions around the transition to OA and how our institutional partnerships are structured.

“Institutions need publishing partners who provide transparency, scalability, and operational efficiency”

Recent Examples

Our agreements continue to evolve across regions:

These examples show that institutions seek structured, predictable models that support their researchers at scale.

Looking Ahead

Crossing the threshold of 1,000 partners tells us that institutions see MDPI not just as a publisher but as a reliable operational partner in advancing open science. This milestone is not a finish line. It is a reminder that the work continues.

Thank you to the entire IOAP team and to all colleagues who contributed to reaching this achievement.

P.S. You can read about this milestone across industry outlets, including STM Publishing News, ALPSP, Research Information, EurekAlert, Brightsurf, among others. You can also read about the coverage in Poland (e.g., media-room, bomega) Korea (newstap), and Romania (EduLike).

Closing Thoughts

Reflections from the Researcher to Reader Conference

During 24–25 February, I attended the 2026 Researcher to Reader Conference in London, UK. Leaders from across scholarly publishing, research infrastructure, libraries, and technology gathered to discuss AI and research integrity, peer review reform, metadata and infrastructure, community engagement, open research policy, and the evolving role of publishers in a rapidly shifting ecosystem.

The conversations were open and honest, and at times uncomfortable – exactly what we need at times. Below are a few reflections that stayed with me.

The Battle for Knowledge: What Becomes Accepted as ‘True’?

One recurring theme was not whether science evolves but whether our infrastructure is resilient enough to sustain trust at scale. Science does not promise certainty: it promises process. As publishing systems grow more complex and become more technologically mediated, the question is how intentionally we design, monitor, and strengthen that process.

Peer Review: Speed, Credentials, and Structural Loops

Researchers consistently call for faster peer review. At the same time, reviewer credentials are often tied to publication records. This creates a structural loop. Publishing history opens reviewing opportunities, reviewing strengthens credentials, and those without early access remain outside the cycle.

There is a need for us to reflect on how opportunity circulates within our systems: we should ask how we create more inclusive pathways for researchers globally to participate in peer review.

Community Engagement Workshop

One of the highlights of R2R was the workshop format, whereby small groups met repeatedly over two days and moved from ideas to tangible strategies.

I joined the Community Engagement workshop led by Lou Peck (CEO at The International Bunch) and Godwyns Onwuchekwa (Principal Consultant at Global Tapestry Consulting). We explored two deceptively simple questions: What is a community? and What does engagement truly mean?

“Engagement requires shared design and shared responsibility”

Too often, organizations equate communication with engagement. The framework discussed mapped a maturity spectrum – from enablement (broadcasting, informing and consulting) to true engagement (collaborating and co-creating).

It was a useful reminder of the fact that if we want trust and loyalty, engagement must go beyond announcements and surveys. It requires shared design and shared responsibility.

AI: Democratization or Digital Colonialism?

I especially enjoyed the thought-provoking presentation from Nikesh Gosalia (Chief Partnership Officer at Cactus Communications), which highlighted an uncomfortable reality:

  • 93% of AI-generated content is in English
  • Approximately 2% is in French
  • Approximately 2% is in German
  • More than 7,000 languages are represented in less than 5% of the content within large AI systems

The implications are profound. Is AI democratizing access to scholarly publishing (making it easier for researchers everywhere to participate in global knowledge production)? Or are we encoding colonialism at scale (entrenching linguistic and structural hierarchies, and making it harder for voices from the Global South to be heard)?

AI is already reshaping how research is created, reviewed, discovered, and shared. Its potential is enormous. But its impact depends not only on capability, but on governance, design, and intentionality. Publishers, funders, and researchers all share responsibility in shaping how these systems evolve.

Ethicality in practice (Lightening Talk)

It was also great to have our colleague Dr Miloš Čučulović (Head of Technology Innovation at MDPI) present MDPI’s Ethicality platform during a lightning talk.

“Technology alone is not the answer”

Ethicality embeds AI-driven checks directly into the submission workflow, supporting editors proactively rather than reacting after publication. As we scale, tools like this help balance trust, efficiency, and research integrity.

This goes back into the underlying theme of the conference that technology alone is not the answer. However, technology embedded thoughtfully within clear governance frameworks can strengthen confidence in the editorial process.

Final thought

The question is no longer whether technology will transform research infrastructure: it is already doing so. The real question is what role each of us will play in shaping that transformation deliberately, with structural maturity, inclusive governance, and engagement that moves from informing to co-creating.

Science needs to evolve, responsibly. And that responsibility extends not only to what we publish, but also to how the systems behind publication are designed. Some important topics to continue reflecting on both internally and within our broader community.

Stefan Tochev
Chief Executive Officer
MDPI AG

20 February 2026
MDPI Virtual Academic Publishing Workshop (New Harvest), 25 February 2026


This Academic Publishing Workshop will be led by MDPI Regional Journal Relations Specialist, Dr. Sally Wu, on “Author Training”. Participants will receive practical advice on essential aspects of writing academic articles. Participants will leave with a clearer understanding of the academic publishing landscape and how to successfully contribute to it.

Date: 25 February 2026
Time: 11:30 a.m.–1:30 p.m. EST

Schedule:

Speaker

Program

Time in EST

Dr. Sally Wu

Introduction

11:30–11:40 a.m.

Dr. Sally Wu

Tips for Writing Great Research Papers

  • Structuring a research paper
  • Tips for every section of a research paper
  • Q&A Session

11:40 a.m.–12:15 p.m.

Dr. Sally Wu

How to Respond to Peer Reviewers

  • Peer Review Reports
  • Examples of Response to Reviewers
  • Q&A Session

12:15–12:50 p.m.

Dr. Sally Wu

AI in Publishing: Challenges and Opportunities

  • AI in scientific publishing
  • How to use AI ethically
  • Q&A Session

12:50–13:30 p.m.

Speakers:

Dr. Sally Wu received a PhD in medical science from the University of Toronto in the fall of 2025. She joined MDPI in February 2025 as an Assistant Editor for Cells. She was recently promoted to Regional Journal Relations Specialist position in August. In this role, she works with many journals, liaising with authors, board members, and EiCs. She has attended several conferences across North America, hosted scholar visits, and taken part in other outreach events.

18 February 2026
MDPI’s Open Access Program Reaches 1,000 Institutions Worldwide

MDPI has surpassed the milestone of 1,000 partners within the Institutional Open Access Program (IOAP). The agreements span 59 countries, covering North and South America, Europe, Asia, Africa, and Oceania.

Last year alone, more than 150 new libraries and academic institutions joined MDPI’s IOAP. With the expansion of an existing consortium deal in Sweden we welcomed a further 75 partners to the program in January 2026, enabling us to surpass the 1,000-partners milestone.

The IOAP supports affiliated researchers by streamlining submission processes, reducing administrative burdens, and offering discounted Article Processing Charges (APCs). Through IOAP membership, more than 61,300 research articles received APC discounts in 2025, driving greater visibility and accessibility for partner institutions and global research communities alike.

"This milestone marks a significant step towards expanding MDPI’s global impact," said Stefan Tochev, MDPI's CEO. "Reaching 1,000 IOAP partnerships is a true testament to the growing trust and collaboration we’ve built with universities, libraries, and research organizations worldwide. We are proud to lead the way in Open Access publishing, ensuring researchers have the support they need to reach global audiences." "The success of our program is reflected in the growing global demand for Open Science and quality publishing services," said Becky Castellon, MDPI institutional partnerships manager. "Equally, institutions are increasingly seeking Open Access publishing options that support funder and national mandates. Joining the IOAP makes compliance simple."

11 February 2026
Meet Us Online at the 30th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-30), 5–19 November 2026


We are pleased to announce that the 30th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-30) organized by the MDPI journal Molecules (ISSN: 1420-3049, IF: 4.6, CiteScore: 8.6) will take place virtually from 5 to 19 November 2026 (Central European Time).

As the longest-running electronic conference in the world, the Electronic Conferences on Synthetic Organic Chemistry (ECSOC) is a series of conferences that have been held online since 1997. ECSOC-30 offers a dynamic global platform for chemists to present cutting-edge research, exchange innovative ideas, and foster collaboration. We welcome your insights and contributions to advance the future of synthetic organic chemistry.

Conference Chair:
Prof. Dr. Julio A. Seijas, Department of Organic Chemistry, University of Santiago de Compostela, Lugo, Spain.

Topics of Interest:
S1. General Organic Synthesis;
S2. Chemistry of Bioorganics, Medicinal and Natural Products;
S3. Design and Application of Organic/Supramolecular Assemblies;
S4. Physical Organic Chemistry.

Important Dates:
Abstract Submission Deadline: 1 July 2026;
Abstract Acceptance Notification: 10 August 2026;
Full File Submission Deadline: 15 September 2026;
Full File Acceptance Notification: 16 October 2026;
Registration Deadline: 2 November 2026.

Guide for Authors:
Please submit your abstract at the following link by 1 July 2026: https://sciforum.net/user/submission/create/1722.

Please use the following link to register for the event for free by 2 November 2026: https://sciforum.net/event/ecsoc-30?section=#registration.

For more information, you may refer to the “Instructions for Authors” section of the following website: https://sciforum.net/event/ecsoc-30?section=#instructions.

Best Paper Award and Best Presentation Award:
Six winners will be selected for this award. The winners will receive a certificate and CHF 200 each.

For any inquiries regarding the event, please contact: ecsoc@mdpi.com.

We look forward to receiving your contribution to ECSOC-30!

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