Assist Prof Dr Matthias Bartneck | Cancer Therapy | Best Researcher Award

Assist Prof Dr Matthias Bartneck | Cancer Therapy | Best Researcher Award 

RWTH Aachen University | Germany

AUTHOR PROFILE

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EARLY ACADEMIC PURSUITS

Priv.-Doz. Dr. rer. nat. Matthias Bartneck embarked on his academic journey with a diploma in Biology from the University of Bielefeld (2001-2006). His diploma thesis focused on gene expression and metabolite profiling of human primary mamma carcinomas, under the supervision of Dr. Anke Becker. He continued his academic pursuits with a Doctor of Natural Sciences degree from RWTH Aachen (2007-2010), where his research centered on the interactions of human primary immune cells with various nanomaterials. This work was supervised by Prof. Gabriele Zwadlo-Klarwasser.

PROFESSIONAL ENDEAVORS

Dr. Bartneck’s professional career has been marked by a series of significant positions and collaborations. He has been employed at the Medical Faculty 10, Gastroenterology, and Faculty 1 Leibniz Institute for Interactive Materials DWI/RWTH Institute for Technical and Macromolecular Chemistry (ITMC) since 2023. He has also served as a guest lecturer at the Max Planck Research Training School Matter to Life. From 2018 to 2022, he was a lecturer at the Center for Functional Magnetic Materials, Immanuel Kant Baltic Federal University in Kaliningrad, Russia. Additionally, Dr. Bartneck has been a group leader at the Medical Faculty, Medical Clinic III, RWTH Aachen since 2014, focusing on immunomodulatory nanomedicine for inflammatory diseases and cancer.

CONTRIBUTIONS AND RESEARCH FOCUS ON CANCER THERAPY

Dr. Bartneck’s research has significantly advanced the fields of gastroenterology, hepatology, and nanomedicine. His work has delved into the development of novel nanocarriers for treating liver diseases and cancer, as well as the modulation of immune cell migration and activation in inflammatory diseases. His research has been supported by substantial funding, including grants from the German Research Foundation (DFG) and the Wilhelm Sander Foundation. His contributions include over 61 publications, 18 as the first author and 4 as the last author, along with 7 book chapters and 9 reviews.

CITATIONS

  • Zitate           4439
  • h-index        35
  • i10-index     49

IMPACT AND INFLUENCE

Dr. Bartneck’s research has had a profound impact on the scientific community, evidenced by a total of 3764 citations and an H-index of 32. His expertise in immunomodulatory nanomedicine has led to collaborations with prestigious institutions and industry partners, including Bayer Healthcare, Novartis, and Precision Nanosystems. His work has been recognized with several fellowships and awards, such as the Young Investigator Award from the European Association for the Study of the Liver (EASL).

ACADEMIC CITES

Dr. Bartneck has held numerous academic positions and provided significant contributions to teaching and mentoring. He has supervised a wide range of students, from bachelor to doctoral levels, across multiple disciplines including medicine, chemistry, and biology. His teaching roles have included lectures and practical courses in materials science, blood and defense, and inflammation at RWTH Aachen.

LEGACY AND FUTURE CONTRIBUTIONS

Dr. Bartneck’s legacy is marked by his interdisciplinary approach and dedication to advancing nanomedicine and immunology. He has secured research funds exceeding €1,500,000 in 2022 alone for the development of novel lipid-based nucleic acid therapeutics. His future contributions are expected to further enhance the understanding and treatment of inflammation-associated diseases and cancer. His continued collaborations with international academic and industry partners underscore his commitment to advancing scientific knowledge and innovation.

NOTABLE PUBLICATION:

 

Excellence in Translational Medicine in Oncology Award

Introduction: Welcome to the pinnacle of innovation in healthcare! The Excellence in Translational Medicine in Oncology Award is a beacon for those pushing the boundaries of research and clinical application in the fight against cancer. Join us in recognizing and celebrating the visionaries shaping the future of translational medicine.

Award Eligibility: Open to global medical professionals and researchers, this award has no age limits. To qualify, candidates must hold a doctoral degree, showcase significant contributions to translational medicine in oncology, and have a noteworthy publication record in reputable journals.

Evaluation Criteria: Candidates will be evaluated on the transformative impact of their translational research, the quality and relevance of publications, and their contributions to bridging the gap between laboratory discoveries and clinical applications in oncology.

Submission Guidelines: Entrants must submit a comprehensive package including a detailed biography, an abstract of their translational research, and supporting files. Adherence to specified format guidelines is crucial for a fair evaluation process.

Recognition and Community Impact: The award not only honors individual excellence but also acknowledges the broader impact of the recipient's work on the oncology community and patient care. Awardees will be recognized at prominent events, amplifying the reach and influence of their translational endeavors.

Drug Design and Clinical Trials

Drug Design and Clinical Trials

 

Introduction: Drug Design and Clinical Trials

The field of drug design and clinical trials represents a crucial bridge between scientific innovation and the improvement of human health. It encompasses the intricate processes involved in developing new pharmaceutical agents, assessing their safety and efficacy, and ultimately bringing them to the patients who need them. This dynamic and collaborative field plays a pivotal role in advancing medical treatments and therapeutics for a wide range of diseases and conditions.

Subtopics:

Rational Drug Design
: Rational drug design involves the targeted creation of new drugs based on a deep understanding of the biological mechanisms underlying diseases. This subtopic explores the principles and techniques used in designing drugs with enhanced specificity and effectiveness.

Preclinical Testing: Before advancing to human trials, potential drug candidates undergo rigorous preclinical testing. This subtopic discusses the various stages of preclinical testing, including in vitro and animal studies, to evaluate safety and efficacy.

Clinical Trial Phases: Clinical trials are divided into phases, each serving a distinct purpose. This subtopic outlines the different phases (Phase I, II, III, and IV) of clinical trials, highlighting their objectives and the types of participants involved.

Patient Recruitment and Informed Consent: The recruitment of participants and obtaining informed consent are critical ethical aspects of clinical trials. This subtopic explores the importance of ethical considerations, participant rights, and the informed consent process in clinical research.

Data Analysis and Regulatory Approval: After the completion of clinical trials, data analysis and regulatory approval processes determine the fate of a drug candidate. This subtopic delves into the statistical methodologies used to analyze trial data and the regulatory agencies responsible for approving new drugs for market release.