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

纳米载体 生物物理学 介孔二氧化硅 脂质双层 癌细胞 原细胞 纳米技术 双层 材料科学 化学 纳米颗粒 生物 生物化学 介孔材料 癌症 遗传学 催化作用
作者
Paul N. Durfee,Yu‐Shen Lin,Darren R. Dunphy,Ayşe J. Muñiz,Kimberly S. Butler,Kevin R. Humphrey,Amanda J. Lokke,Jacob O. Agola,Stanley S. Chou,I‐Ming Chen,Walker Wharton,Jason L. Townson,Cheryl L. Willman,C. Jeffrey Brinker
出处
期刊:ACS Nano [American Chemical Society]
卷期号:10 (9): 8325-8345 被引量:188
标识
DOI:10.1021/acsnano.6b02819
摘要

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 microenvironment 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 EGFR) 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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