Optimized Metal-Organic-Framework Nanospheres for Drug Delivery: Evaluation of Small-Molecule Encapsulation

被引:762
作者
Zhuang, Jia [1 ]
Kuo, Chun-Hong [1 ]
Chou, Lien-Yang [1 ]
Liu, De-Yu [2 ]
Weerapana, Eranthie [1 ]
Tsung, Chia-Kuang [1 ]
机构
[1] Boston Coll, Merkert Chem Ctr, Dept Chem, Chestnut Hill, MA 02467 USA
[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
关键词
ZIF-8; drug delivery; nanoparticles; cellular uptake; CELLULAR UPTAKE; HYDROGEN STORAGE; NANOPARTICLES; SIZE; CYTOTOXICITY; FUNCTIONALIZATION; CAMPTOTHECIN; ENDOCYTOSIS; STRATEGIES; CARRIERS;
D O I
10.1021/nn406590q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed a general synthetic route to encapsulate small molecules in monodisperse zeolitic imid-azolate framework-8 (ZIF-8) nanospheres for drug delivery. Electron microscopy, powder X-ray diffraction, and elemental analysis show that the small-molecule-encapsulated ZIF-8 nanospheres are uniform 70 nm particles with single-crystalline structure. Several small molecules, including fluorescein and the anticancer drug camptothecin, were encapsulated inside of the ZIF-8 framework. Evaluation of fluorescein-encapsulated ZIF-8 nanospheres in the MCF-7 breast cancer cell line demonstrated cell internalization and minimal cytotoxicity. The 70 nm particle size facilitates cellular uptake, and the pH-responsive dissociation of the ZIF-8 framework likely results in endosomal release of the small-molecule cargo, thereby rendering the ZIF-8 scaffold an ideal drug delivery vehicle. To confirm this, we demonstrate that camptothecin encapsulated ZIF-8 particles show enhanced cell death, indicative of internalization and intracellular release of the drug. To demonstrate the versatility of this ZIF-8 system, iron oxide nanoparticles were also encapsulated into the ZIF-8 nanospheres, thereby endowing magnetic features to these nanospheres.
引用
收藏
页码:2812 / 2819
页数:8
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