Nanomedicine

Despite many advances in targeted therapeutics and diagnostics, there is still a need for specific, effective therapies without side effects and mechanisms for early detection that ensure therapies have the best opportunity to be timely and effective

Empowering The
Immune S
ystem

Combatting disease with novel nanoimmunotherapeutics
that target trained immunity

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Trained immunity, a de facto innate immune memory, describes the process by which innate immune system activation results in enhanced responsiveness to subsequent triggers. Trained immunity naturally occurs through mechanistic epigenetic and metabolic reprogramming of innate immune cells. Our research focuses on how this immunological phenomenon can be purposefully induced or downregulated using our novel nanoimmunotherapeutics, as an approach to treating maladies including cancer, bacterial/viral infection, cardiovascular diseases, autoimmune disorders, and allograft rejection in organ transplantation. Through widespread collaboration with other leading researchers in the cutting-edge field of trained immunity, we continue to explore therapy regimens in which our nanoimmunotherapeutics can lead to improved clinical outcomes.

Chemical Engineering Of Nanomaterials

Designing and producing libraries of
highly biocompatible nanomaterials

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Design, synthesis, and characterization of our nanomaterials is the cornerstone of our research, group, and mission. Our lab has its origin story deeply intertwined with the field of nanomedicine, and we’re proud of the contributions we’ve made towards pioneering its application for immunotherapy. Our designs include but are not limited to apoA-1-based nanobiologics, nanoemulsions, liposomes, drug-loaded block-copolymer micelles, and nanocrystal-core lipoproteins. We have established a nanobiologic library, which is used to develop tailored immunotherapeutics for cardiovascular diseases, cancer, and transplantation. Furthermore, with our in-house radiochemistry suite, we are able to perform radiolabeling of our nano-platforms, enabling non-invasive tracking and tracing of our nanomaterials.

Cardiovascular
Nanoimmunotherapy

Immunomodulation therapies to tackle the
most prominent range of clinical ailments

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Atherosclerosis, a chronic disease of the large arteries, is one key underlying cause of myocardial infarction and stroke. Driven by cholesterol accumulation and subsequent inflammation in the vessel wall, atherosclerosis has historically been clinically treated by lipid-lowering treatments but remains a major threat to human health worldwide. Over the past 20 years, insights into cardiovascular immunopathology have opened up a range of potential therapeutic targets to reduce the risk of cardiovascular disease, which has shifted the focus from lipids to inflammation. Our lab has pioneered nanotechnology approaches to facilitate the specific targeting of innate immune cells. With continued research efforts focusing on this crucial and promising field, we believe our approaches can generate more effective immunomodulatory treatments to induce disease regression and prevent the recurrence of cardiovascular events.

Bridging the translational gap

In addition to mouse models, we focus strongly on translational research in large animals

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While hundreds of nanomedicine studies are produced every year, very few formulations are clinically approved. This is partly due to an undue reliance on murine studies, which suffer from limited value in accurately predicting translational efficacy in humans. To combat this experimental hindrance, our lab established a translational nanomedicine program with large animal models, ranging from rabbits to swine to non-human primates. It involves scaling up production and testing while in the preclinical phase, which provides a unique framework in preparing for clinical studies. In combination with access to clinical scanners through the BioMedical Engineering and Imaging Institute, we have the unique privilege to study our therapies and probes in large animal models while performing imaging studies using some of the most advanced multimodality systems available.

Message From The Lab Director

Willem J Mulder, PhD

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I started working in the field of nanomedicine as a chemistry student in The Netherlands, roughly twenty years ago. Since then, I have been captivated by the application of nanotechnology in medicine, particularly in immunology. Since my recruitment to Sinai in 2006, we have established a multidisciplinary ecosystem in which young scientists from diverse backgrounds can flourish and mature into the engineers, scientists, and medical doctors of tomorrow by participating in and driving innovative science today. Through exploring the biological, chemical, and experimental knowledge that interconnects chemistry, imaging, and immunology, our lab is able to create nanomaterials to tackle prolific medical conditions such as cancer, atherosclerosis, stroke, and organ transplantation.

News

Warrior Watch Study at Mount Sinai

Led by Robert Hirten, MD and Zahi Fayad, PhD, the study draws upon the collaborative efforts of the Mount Sinai COVID Informatics Center (MSCIC) and is open to all employees in the health system. It uses a unique phone App to administer questions and collect data from...

Mount Sinai Establishes BioMedical Engineering and Imaging Institute

Center aims to create state-of-the-art medical technology to transform patient care The Mount Sinai Health System announced the creation of the Biomedical Engineering and Imaging Institute (BMEII), the first of its kind in New York City, and one of a few in the world....

Latest Publications

Relation between resting amygdalar activity and cardiovascular events: a longitudinal and cohort study

Tawakol A, Ishai A, Takx RA, Figueroa AL, Ali A, Kaiser Y, Truong QA, Solomon CJ, Calcagno C, Mani V, Tang CY, Mulder WJ, Murrough JW, Hoffmann U, Nahrendorf M, Shin LM, Fayad ZA, Pitman RK 2017 Jan 12 · Lancet

Quantification of hepatocellular carcinoma heterogeneity with multiparametric magnetic resonance imaging

Hectors SJ, Wagner M, Bane O, Besa C, Lewis S, Remark R, Chen N, Fiel MI, Zhu H, Gnjatic S, Merad M, Hoshida Y, Taouli B 2017 May 26 · Sci Rep

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