4.8 Article

Mesoporous Silica Nanoparticle-Supported Lipid Bilayers (Protocells) for Active Targeting and Delivery to Individual Leukemia Cells

Journal

ACS NANO
Volume 10, Issue 9, Pages 8325-8345

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.6b02819

Keywords

mesoporous silica nanoparticle; supported lipid bilayer; colloidal stability; chorioallantoic membrane; leukemia cell targeting

Funding

  1. NIH National Cancer Institute (NCI) [UO1 CA151792-01]
  2. Leukemia and Lymphoma Society (LLS) Specialized Center of Research (SCOR) [7010-14]
  3. Sandia National Laboratories Laboratory Directed Research and Development (LDRD) program
  4. New Mexico Cancer Nanoscience and Microsystems Training Center (CNTC)
  5. George D. Montoya Research Scholarship
  6. Edmund J. and Thelma W. Evans Charitable Trust Scholarship
  7. Charlotte and William Kraft Graduate Fellowship
  8. Gabrielle's Angel Foundation
  9. UNM Science, Technology, Engineering, and Mathematics (STEM) Talent Expansion Program
  10. National Institute of General Medical Sciences [T34GM008751]
  11. UNM NSMS Research Experience for Undergraduates Program
  12. U.S. Department of Energy (DOE), Office of Basic Energy Sciences (BES), Division of Materials Sciences and Engineering
  13. Air Force Office of Scientific Research [FA 9550-1-14-066]
  14. National Science Foundation [1344298]
  15. University of California's Center for Environmental Implications of Nanotechnology (CEIN) grant [DBI-1266377]
  16. NCI [P30 CA118110]
  17. Div Of Chem, Bioeng, Env, & Transp Sys
  18. Directorate For Engineering [1344298] Funding Source: National Science Foundation

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Many nanocarrier cancer therapeutics currently under development, as well as those used in the clinical setting, rely upon the enhanced permeability and retention (EPR) effect to passively accumulate in the tumor micro environment and kill cancer cells. In leukemia, where leukemogenic stem cells and their progeny circulate within the peripheral blood or bone marrow, the EPR effect may not be operative. Thus, for leukemia therapeutics, it is essential to target and bind individual circulating cells. Here, we investigate mesoporous silica nanoparticle (MSN)-supported lipid bilayers (protocells), an emerging class of nanocarriers, and establish the synthesis conditions and lipid bilayer composition needed to achieve highly monodisperse protocells that remain stable in complex media as assessed in vitro by dynamic light scattering and cryo-electron microscopy and ex ovo by direct imaging within a chick chorioallantoic membrane (CAM) model. We show that for vesicle fusion conditions where the lipid surface area exceeds the external surface area of the MSN and the ionic strength exceeds 20 mM, we form monosized protocells (polydispersity index <0.1) on MSN cores with varying size, shape, and pore size, whose conformal zwitterionic supported lipid bilayer confers excellent stability as judged by circulation in the CAM and minimal opsonization in vivo in a mouse model. Having established protocell formulations that are stable colloids, we further modified them with anti-EGFR antibodies as targeting agents and reverified their monodispersity and stability. Then, using intravital imaging in the CAM, we directly observed in real time the progression of selective targeting of individual leukemia cells (using the established REH leukemia cell line transduced with EGER) and delivery of a model cargo. Overall, we have established the effectiveness of the protocell platform for individual cell targeting and delivery needed for leukemia and other disseminated disease.

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