Symposium Sessions | ||
Monday May 15 | ||
10:30 | Cancer Nanotechnology | |
1:30 | Diagnostics & Bioimaging | |
Tuesday May 16 | ||
Cancer Nanotechnology: Posters | ||
Symposium Program | ||
Monday May 15 | ||
10:30 | Cancer Nanotechnology | National Harbor 4 |
Session chair: Mansoor M. Amiji, Northeastern University; Anil Patri, U.S. Food and Drug Administration | ||
10:30 | Targeting Approaches to Address the Spectrum of Hot and Cold Tumors (invited presentation) P. Sapra, Pfizer, US | |
10:55 | Innovations in Cancer Treatment (invited presentation) L. Levy, Nanobiotix SA, FR | |
11:20 | Integrated Nanoplatform for Cancer imaging and Treatment (invited presentation) S. Achilefu, Washington University School of Medicine, US | |
11:45 | Achieving Effective Vascular and Extravascular Targeted Drug Delivery with Lipid Nanoparticles and Micelles (invited presentation) G. Lanza, Washington University School of Medicine, US | |
12:10 | Cancer Nanomedicines: Challenges and Opportunities, vol. 3: pp. 126-129 L. Tamarkin, CytImmune Sciences, Inc., US | |
1:30 | Diagnostics & Bioimaging | National Harbor 8 |
Session chair: Ryan Roeder, University of Notre Dame, US | ||
1:30 | Translating Nanotechnology and Microfluidics for Epigenetic Detection of Cancer (invited presentation) J. Wang, Johns Hopkins University, US | |
1:55 | Carcinoma cellular uptake, imaging, and targeting by RGDS- and TAT-conjugated upconversion and/or magnetic nanoparticles, vol. 3: pp. 114-117 D. Horák, U. Kostiv, V. Proks, D. Jirák, Institute of Macromolecular Chemistry AS CR, CZ | |
2:15 | Point-of-Care (POC) Micro Biochip for Cancer Diagnostics, vol. 3: pp. 110-113 B.B. Nunna, E.S. Lee, New Jersey Institute of Technology, US | |
2:35 | Tumor Detection Using Novel Texture Analysis Methods C. Zhou, Lehigh Univeristy, US | |
2:55 | Hybrid Vesicular Assemblies for Cancer Imaging and Therapy (invited presentation) Z. Nie, University of Maryland, US | |
Tuesday May 16 | ||
Cancer Nanotechnology: Posters | Expo Hall D & E | |
Gold Nanoparticles Reduce Inflammation in Cerebral Microvessels of Septic Mice, But Do Not Alter Tumor Progression in Glioblastoma-Induced Mice S. Rodrigues, R. Silva, L. Fernandes, D. Di Bella, L. Colli, E. Akamine, M. Carvalho, University of Sao Paulo, BR | ||
Modular Nanoparticle Probes for Personalized in Vitro and in Vivo Imaging of Cancer Cell Populations, vol. 3: pp. 122-125 P.D. Nallathamby, K. Cowden-Dahl, R.K. Roeder, University of Notre Dame, US | ||
Enhancement of anticancer action of traditional (doxorubicin and cisplatin) and experimental (landomycin A) drugs by their delivery in vivo with novel C60-fullerene-based nanocarriers possessing innate ROS-modulating activity, vol. 3: pp. 130-133 R. Panchuk, S. Prylutska, N. Skorokhyd, L. Lehka, L. Skivka, V. Hurmach, M. Evstigneev, J. Piosik, W. Berger, Yu. Prylutskyy, P. Scharff, R. Stoika, S. Vari, Institute of Cell Biology NAS of Ukraine, UA | ||
Stimuli-sensitive Theranostic for Targeted Imaging-Guided Drug Delivery Y. Haik, Hamad bin Khalifa University, QA | ||
Microfluidics Manufacture of Verteporfin Loaded Liposomes Composed of Natural and Synthetic Lipids Using a Scalable Microfludic Platform A. Thomas, A. Brown, S.M. Garg, K. Ou, J. Singh, S. Chang, M. Ma, S. Sidhu, B. Versteeg, M. Assadian, A. Armstead, G. Heuck, S. Ip, T.J. Leaver, A.W. Wild, R. Lockard, R.J. Taylor, E.C. Ramsay, Precision NanoSystems Inc., CA | ||
Nanotechnology has the potential to have a revolutionary impact on cancer diagnosis and therapy. It is universally accepted that early detection of cancer is essential even before anatomic anomalies are visible. A major challenge in cancer diagnosis in the 21st century is to be able to determine the exact relationship between cancer biomarkers and the clinical pathology, as well as, to be able to non-invasively detect tumors at an early stage for maximum therapeutic benefit. For breast cancer, for instance, the goal of molecular imaging is to be able to accurately diagnose when the tumor mass has approximately 100-1000 cells, as opposed to the current techniques like mammography, which require more than a million cells for accurate clinical diagnosis.
In cancer therapy, targeting and localized delivery are the key challenges. To wage an effective war against cancer, we have to have the ability to selectively attack the cancer cells, while saving the normal tissue from excessive burdens of drug toxicity. However, because many anticancer drugs are designed to simply kill cancer cells, often in a semi-specific fashion, the distribution of anticancer drugs in healthy organs or tissues is especially undesirable due to the potential for severe side effects. Consequently, systemic application of these drugs often causes severe side effects in other tissues (e.g. bone marrow suppression, cardiomyopathy, neurotoxicity), which greatly limits the maximal allowable dose of the drug. In addition, rapid elimination and widespread distribution into non-targeted organs and tissues requires the administration of a drug in large quantities, which is often not economical and sometimes complicated due to non-specific toxicity. This vicious cycle of large doses and the concurrent toxicity is a major limitation of current cancer therapy. In many instances, it has been observed that the patient succumbs to the ill effects of the drug toxicity far earlier than the tumor burden.
This symposium will address the potential ways in which nanotechnology can address these challenges. Distinguished speakers will summarize the current state of the art and future barriers. Contributions are also solicited in the following topics.
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