The noninvasive visualization of nude mice with subcutaneous injection indicates that the Eu3+/Gd3+−CaP vesicle-like nanospheres are suitable for in vivo bio-imaging.
Furthermore, the noninvasive visualization of nude mice with subcutaneous injection indicates that the Eu3+/Gd3+-doped HAp nanorods with the photoluminescent function are suitable for in vivo imaging.
The tumor growth in mice with subcutaneous transplantation of colon 26 tumor cells was significantly inhibited after a single i.v. injection of HSA-DB-L at a dose of 15 mg/kg without any significant body weight loss.
As shown in Fig. 22a c, bright spot of Ag2S QDs fluorescence was observed in the mice with subcutaneous and celiac injection compared with the ordinary mice.
In a previous imaging study, we demonstrated the feasibility of pretargeted immuno-PET using 68Ga- or 18F-labeled di-HSG peptides in mice with subcutaneous tumors [32].
Biodistribution and tumour targeting of the 111In-labelled PP-F11 were studied in female athymic BALB/c mice with subcutaneous tumours induced by inoculation of A431 cells.
Figure 4 Biodistribution of 68 Ga-Ex4NOD12, 68 Ga-Ex4NOD27 and 68 Ga-Ex4NOD40 in CD1 nu/nu mice with subcutaneous CHL-GLP-1R-positive tumours.
A biodistribution study was performed in mice with subcutaneous MDA-MB-468 and 125I-B-B4 125I-B-B4 125I-B-B4nd 96 h atter injection and compared with an isotype-matched control.
Materials and methods: To determine the optimal dose, mice with subcutaneous HER2-overexpressing tumours were injected with 5, 50, 100 or 200 μg of 64Cu-NOTA-F ab' 2 (2.2±0.64Cu-NOTA-F ab' 2iced 64Cu-NOTA-F ab' 2biodistribution.
Two TLR4 agonists, LPS and Spirulina complex polysaccharide, have demonstrated efficacy in mice with subcutaneous implantation of DBT and RSV-M gliomas, respectively (Chicoine et al., 2007; Kawanishi et al., 2013).
