Multifunctional quantum dot-polypeptide hybrid nanogel for targeted imaging and drug delivery

• Published in: Nanoscale Vol. 6; no. 19; pp. 11282 - 11292
• Main Authors: Yang, Jie, Yao, Ming-Hao, Wen, Lang, Song, Ji-Tao, Zhang, Ming-Zhen, Zhao, Yuan-Di, Liu, Bo
• Format: Journal Article
• Language: English
• Published: England 07.10.2014
• Subjects: Antineoplastic Agents - administration & dosage; Cancer; Drug delivery systems; Electrophoresis; Flow cytometry; HeLa Cells; Humans; Imaging; Light scattering; Microscopy, Fluorescence - methods; Nanocapsules - administration & dosage; Nanocapsules - chemistry; Nanocapsules - ultrastructure; Nanostructure; Neoplasms, Experimental - drug therapy; Neoplasms, Experimental - metabolism; Neoplasms, Experimental - pathology; Oligopeptides - chemistry; Oligopeptides - pharmacokinetics; Particle Size; Polyethylene Glycols - chemistry; Polyethylene Glycols - therapeutic use; Polyethyleneimine - chemistry; Polyethyleneimine - therapeutic use; Quantum Dots; Self assembly; Treatment Outcome
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/c4nr03058c

A new type of multifunctional quantum dot (QD)-polypeptide hybrid nanogel with targeted imaging and drug delivery properties has been developed by metal-affinity driven self-assembly between artificial polypeptides and CdSe-ZnS core-shell QDs. On the surface of QDs, a tunable sandwich-like microstructure consisting of two hydrophobic layers and one hydrophilic layer between them was verified by capillary electrophoresis, transmission electron microscopy, and dynamic light scattering measurements. Hydrophobic and hydrophilic drugs can be simultaneously loaded in a QD-polypeptide nanogel. In vitro drug release of drug-loaded QD-polypeptide nanogels varies strongly with temperature, pH, and competitors. A drug-loaded QD-polypeptide nanogel with an arginine-glycine-aspartic acid (RGD) motif exhibited efficient receptor-mediated endocytosis in αvβ3 overexpressing HeLa cells but not in the control MCF-7 cells as analyzed by confocal microscopy and flow cytometry. In contrast, non-targeted QD-polypeptide nanogels revealed minimal binding and uptake in HeLa cells. Compared with the original QDs, the QD-polypeptide nanogels showed lower in vitro cytotoxicity for both HeLa cells and NIH 3T3 cells. Furthermore, the cytotoxicity of the targeted QD-polypeptide nanogel was lower for normal NIH 3T3 cells than that for HeLa cancer cells. These results demonstrate that the integration of imaging and drug delivery functions in a single QD-polypeptide nanogel has the potential for application in cancer diagnosis, imaging, and therapy.