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. 2019 May 14;14(10):1343–1365. doi: 10.2217/nnm-2018-0347

Figure 2. . In situ encapsulating drug molecules into nanoscale metal-organic frameworks.

Figure 2. 

(A) Topological structure of the fluorescein-loaded ZIF-8 framework. (B) pH-responsive fluorescein release profiles in PBS solution. (C) Cell viability of MCF-7 cells incubated with free CPT and CPT loaded ZIF-8 nanoparticles. (D) pH-induced in situ synthesis of drug-loaded zeolitic imidazolate framework-8 (ZIF-8) nanoparticles. (E) Cross-section of the electron tomogram of mesoporous structure distribution in the doxorubicin-loaded ZIF-8 nanoparticles. (F) Scanning electron microscope image of catalase-loaded ZIF-90 nanoparticles. (G) SDS-PAGE gel image (M: protein marker, lane 1: free catalase, lane 2: washed ZIF-90 with catalase on the surface, lane 3: catalase-loaded ZIF-90). (H) Confocal microscopy images of fluorescently (FITC)-labeled catalase-loaded ZIF-90 sample (left) and ZIF-90 with fluorescein isothiocyanate-catalase on its surface (right).

CPT: Camptothecin; ZIF-8: Zeolitic imidazolate framework-8.

(A) Reproduced with permission from [42] © American Chemical Society (2014).

(B) Reproduced with permission from [42] © American Chemical Society (2014).

(C) Reproduced with permission from [42] © American Chemical Society (2014).

(D) Reproduced with permission from [47] © American Chemical Society (2016).

(E) Reproduced with permission from [47] © American Chemical Society (2016).

(F) Reproduced with permission from [44] © American Chemical Society (2015).

(G) Reproduced with permission from [44] © American Chemical Society (2015).

(H) Reproduced with permission from [44] © American Chemical Society (2015).