Source abstract
Abstract
In the chemical world, evolution is mirrored in the origin of nanoscale supramolecular structures from molecular subunits. The complexity of function acquired in a supramolecular system over a molecular subunit can be harnessed in the treatment of cancer. However, the design of supramolecular nanostructures is hindered by a limited atomistic level understanding of interactions between building blocks. Here, we report the development of a computational algorithm, which we term Volvox after the first multicellular organism, that sequentially integrates quantum mechanical energy-state- and force-field-based models with large-scale all-atomistic explicit water molecular dynamics simulations to design stable nanoscale lipidic supramolecular structures. In one example, we demonstrate that Volvox enables the design of a nanoscale taxane supramolecular therapeutic. In another example, we demonstrate that Volvox can be extended to optimizing the ratio of excipients to form a stable nanoscale supramolecular therapeutic. The nanoscale taxane supramolecular therapeutic exerts greater antitumor efficacy than a clinically used taxane in vivo. Volvox can emerge as a powerful tool in the design of nanoscale supramolecular therapeutics for effective treatment of cancer.
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Affiliations
Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115, United States
Harvard−MIT Division of Health Sciences and Technology, Cambridge, Massachusetts 02139, United States
India Innovation Research Center, Invictus Oncology, New Delhi 110092, India
Harvard Digestive Diseases Center, Boston, Massachusetts 02115, United States
Dana Farber Cancer Institute, Boston, Massachusetts 02115, United States
Funding
National Cancer Institute · Indo-US Science and Technology Forum · American Lung Association · U.S. Department of Defense · American Cancer Society