4.8 Article

Mechanism-Independent Optimization of Combinatorial Nanodiamond and Unmodified Drug Delivery Using a Phenotypically Driven Platform Technology

Journal

ACS NANO
Volume 9, Issue 3, Pages 3332-3344

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.5b00638

Keywords

nanomedicine; nanodiamond; optimization; drug delivery; breast cancer; biocompatibility

Funding

  1. National Science Foundation CAREER Award [CMMI-1350197]
  2. Center for Scalable and Integrated NanoManufacturing [DMI-0327077]
  3. V Foundation for Cancer Research Scholars Award
  4. Wallace H. Coulter Foundation Translational Research Award
  5. National Cancer Institute [U54CA151880]
  6. Society for Laboratory Automation and Screening Endowed Fellowship
  7. Beckman Coulter Life Sciences
  8. [CMMI-0856492]
  9. [DMR-1343991]
  10. Direct For Mathematical & Physical Scien
  11. Division Of Materials Research [1343991] Funding Source: National Science Foundation
  12. Div Of Civil, Mechanical, & Manufact Inn
  13. Directorate For Engineering [0856492] Funding Source: National Science Foundation

Ask authors/readers for more resources

Combination chemotherapy can mediate drug synergy to improve treatment efficacy against a broad spectrum of cancers. However, conventional multidrug regimens are often additively determined, which have long been believed to enable good cancer-killing efficiency but are insufficient to address the nonlinearity in dosing. Despite improved clinical outcomes by combination treatment, multi-objective combination optimization, which takes into account tumor heterogeneity and balance of efficacy and toxicity, remains challenging given the sheer magnitude of the combinatorial dosing space. To enhance the properties of the therapeutic agents, the field of nanomedicine has realized novel drug delivery platforms that can enhance therapeutic efficacy and safety. However, optimal combination design that incorporates nanomedicine agents still faces the same hurdles as unmodified drug administration. The work reported here applied a powerful phenotypically driven platform, termed feedback system control (FSC), that systematically and rapidly converges upon a combination consisting of three nanodiamond-modified drugs and one unmodified drug that is simultaneously optimized for efficacy against multiple breast cancer cell lines and safety against multiple control cell lines. Specifically, the therapeutic window achieved from an optimally efficacious and safe nanomedicine combination was markedly higher compared to that of an optimized unmodified drug combination and nanodiamond monotherapy or unmodified drug administration. The phenotypically driven foundation of FSC implementation does not require any cellular signaling pathway data and innately accounts for population heterogeneity and nonlinear biological processes. Therefore, FSC is a broadly applicable platform for both nanotechnology-modified and unmodified therapeutic optimizations that represent a promising path toward phenotypic personalized medicine.

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