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Beilstein J. Nanotechnol. 2017, 8, 1457–1468, doi:10.3762/bjnano.8.145
Figure 1: Schematic representation of amphiphilic 6OCaproβCD (a), amphiphilic PC βCDC6 (b), chitosan (c) and ...
Figure 2: Time-dependent variation of particle size (nm) of PCX-loaded amphiphilic CD nanoparticles stored in...
Figure 3: Time-dependent variation of the PDI value of PCX-loaded amphiphilic CD nanoparticles stored in aque...
Figure 4: Time-dependent variation of the zeta potential value of PCX-loaded amphiphilic CD nanoparticles sto...
Figure 5: Cumulative release profile of PCX from different amphiphilic CD nanoparticles at pH 7.4 phosphate b...
Figure 6: Cytotoxicity of unloaded amphiphilic CD nanoparticles on L929 mouse fibroblast cell line with MTT a...
Figure 7: IC50 value of PCX solution in DMSO on MCF-7 human breast cancer cell line (n = 3, ± SD).
Figure 8: Anticancer activity of PCX-loaded amphiphilic CD nanoparticle formulations and PCX solution in DMSO...
Beilstein J. Nanotechnol. 2017, 8, 1446–1456, doi:10.3762/bjnano.8.144
Figure 1: Particle size of blank and drug-loaded nanoparticles (n = 3, ± SD).
Figure 2: Zeta potential of blank and drug-loaded nanoparticles (n = 3, ± SD).
Figure 3: Mean particle diameter of nanoparticle formulations over the course of 30 days (n = 3, ± SD).
Figure 4: Docetaxel encapsulation efficiency of nanoparticle formulations (n = 3, ± SD).
Figure 5: Cumulative release profile of DOC from nanoparticles (a) and nanoparticulate DOC from HpC films (b)...
Figure 6: Cell viability of blank nanoparticles for 24 and 48 h (n = 3, ± SD).
Figure 7: RG2 cell viability with blank and DOC-loaded nanoparticles for 24 and 48 h (n = 3, ± SD).