Abstract |
The aim of this study was to look for a new medicine in diagnosing and treating of glioblastoma. Radioiodine-labeled anti- epidermal growth factor receptor (EGFR) binding nanoparticles were constructed. In vitro cell-binding assays were confirmed by confocal microscopy and flow cytometry. Cell cytotoxicity assays were evaluated by MTT assay; radionuclide uptake assays were performed by γ-counter. Radioiodine-imaging studies were conducted using a xenograft nude mouse model in vivo. The results showed that EGFR significantly enhanced the uptake and accumulation of BSA-PCL in the experimental model of xenografts in nude mice, suggesting improved specific nanoparticle-based delivery. In conclusion, the data showed 131I-EGFR-BSA-PCL leading radioiodine therapy for U251 and U87 cells had a good effect in vitro and in vivo. Thus, 131I-EGFR-BSA-PCL may provide a new method for glioblastoma treatment.
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Authors | Chengxia Li, Jian Tan, Jin Chang, Wei Li, Zhongyun Liu, Ning Li, Yanhui Ji |
Journal | Oncology reports
(Oncol Rep)
Vol. 38
Issue 5
Pg. 2919-2926
(Nov 2017)
ISSN: 1791-2431 [Electronic] Greece |
PMID | 28901480
(Publication Type: Journal Article)
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Chemical References |
- Iodine Radioisotopes
- Polyesters
- Radiopharmaceuticals
- polycaprolactone
- Serum Albumin, Bovine
- EGFR protein, human
- ErbB Receptors
- Cetuximab
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Topics |
- Animals
- Brain Neoplasms
(diagnostic imaging, drug therapy, metabolism)
- Cattle
- Cell Line, Tumor
- Cell Survival
(drug effects)
- Cetuximab
(administration & dosage, chemistry, pharmacology)
- ErbB Receptors
(metabolism)
- Glioblastoma
(diagnostic imaging, drug therapy, metabolism)
- Humans
- Iodine Radioisotopes
(administration & dosage, chemistry)
- Mice
- Nanoparticles
(administration & dosage, chemistry)
- Neoplasm Transplantation
- Polyesters
(administration & dosage, chemistry)
- Radiopharmaceuticals
(administration & dosage, chemistry)
- Serum Albumin, Bovine
(administration & dosage, chemistry)
- Tomography, Emission-Computed, Single-Photon
(methods)
- Xenograft Model Antitumor Assays
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