Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/104219
Title: Perylene-derived single-component organic nanoparticles with tunable emission : efficient anticancer drug carriers with real-time Monitoring of drug release
Authors: Li, Xin
Zhu, Pengcheng
Tan, Nguan Soon
Ågren, Hans
Zhao, Yanli
Jana, Avijit
Nguyen, Kim Truc
Keywords: DRNTU::Science::Biological sciences
DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2014
Source: Jana, A., Nguyen, K. T., Li, X., Zhu, P., Tan, N. S., Ågren, H., et al. (2014). Perylene-Derived Single-Component Organic Nanoparticles with Tunable Emission: Efficient Anticancer Drug Carriers with Real-Time Monitoring of Drug Release. ACS Nano, in press.
Series/Report no.: ACS Nano
Abstract: An organic nanoparticle-based drug delivery system with high drug loading efficacy (79 wt %) was developed using a perylene-derived photoremovable protecting group, namely, perylene-3,4,9,10-tetrayltetramethanol (Pe(OH)4). The anticancer drug chlorambucil was protected by coupling with Pe(OH)4 to form photocaged nanoparticles (Pe(Cbl)4). The photorelease mechanism of chlorambucil from the Pe(Cbl)4 conjugate was investigated experimentally by high-resolution mass spectrometry and theoretically by density functional theory calculations. The Pe(Cbl)4 nanoparticles perform four important roles: (i) a nanocarrier for drug delivery, (ii) a phototrigger for drug release, (iii) a fluorescent chromophore for cell imaging, and (iv) a photoswitchable fluorophore for real-time monitoring of drug release. Tunable emission of the perylene-derived nanoparticles was demonstrated by comparing the emission properties of the Pe(OH)4 and Pe(Cbl)4 nanoparticles with perylene-3-ylmethanol. These nanoparticles were subsequently employed in cell imaging for investigating their intracellular localization. Furthermore, the in vivo toxicity of the Pe(OH)4 nanoparticles was investigated using the mouse model. Histological tissue analysis of five major organs, i.e., heart, kidney, spleen, liver, and lung, indicates that the nanoparticles did not show any obvious damage to these major organs under the experimental conditions. The current research presents a successful example of integrating multiple functions into single-component organic nanoparticles for drug delivery.
URI: https://hdl.handle.net/10356/104219
http://hdl.handle.net/10220/19427
ISSN: 1936-0851
DOI: 10.1021/nn501073x
Rights: © 2014 American Chemical Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
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