4.2 Article

PEG-Citrate dendrimer second generation: is this a good carrier for imaging agents In Vitro and In Vivo?

期刊

IET NANOBIOTECHNOLOGY
卷 13, 期 6, 页码 560-564

出版社

WILEY
DOI: 10.1049/iet-nbt.2018.5360

关键词

drug delivery systems; cellular biophysics; molecular biophysics; fluorescence; cancer; tumours; drugs; nanomedicine; biomedical materials; dyes; toxicology; imaging agent; cancer tumours; cancer diagnosis; PEG-citrate dendrimer-G; FITC dye; cancer cells; FITC loading; vitro imaging; dendrimer-FITC; CT imaging; targeting nature; promised dendrimer; fluorescent images; imaging ability; Iohexol; FITC

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While cancer is the leading cause of human's deaths worldwide, finding an imaging agent which can detect cancer tumours is needed for cancer diagnosis. In the present study, PEG-citrate dendrimer-G(2) was used as a nano-carrier of FITC dye and Iohexol to help passive targeting and uptake of both imaging agents in cancer cells/tumour in vitro and in vivo. Dendrimer was synthesisedand the product characterised using LC-MS, FT-IR, DLS, ELS, AFM, and (HNMR)-H-1. After FITC loading into dendrimer, MTT was performed to determine the cytotoxicity of formulation on HEK-293 and MCF-7 cells. In vitro imaging using dendrimer-FITC was done via fluorescent microscope thereafter. Moreover, CT imaging using Iohexol was employed to show the targeting nature and ability of the complex to use as imaging agent in vivo. Data yielded in this study corroborate the notion that the promised dendrimer was synthesised properly and had no toxicity along with FITC on normal cell. Furthermore, CT and fluorescent images showed the targeting nature and imaging ability of Iohexol/FITC loaded dendrimer in vitro and in vivo. Overall, results showed promising characteristics of the novel complexes using dendrimer-G(2) both in vitro and in vivo.

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