Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/22912
Title: Cytotoxicity assessment of functionalized CdSe, CdTe and InP quantum dots in two human cancer cell models
Authors: Liu, J
Hu, R
Liu, J
Zhang, B
Wang, Y
Liu, X
Law, WC 
Liu, L
Ye, L
Yong, KT
Keywords: Cancer cell
Cytotoxicity
Quantum dots
Issue Date: 2015
Publisher: Elsevier
Source: Materials science and engineering. C, materials for biological applications, 2015, v. 57, 5616, p. 222-231 How to cite?
Journal: Materials science and engineering. C, materials for biological applications 
Abstract: Abstract The toxicity of quantum dots (QDs) has been extensively studied over the past decade. Some common factors that originate the QD toxicity include releasing of heavy metal ions from degraded QDs and the generation of reactive oxygen species on the QD surface. In addition to these factors, we should also carefully examine other potential QD toxicity causes that will play crucial roles in impacting the overall biological system. In this contribution, we have performed cytotoxicity assessment of four types of QD formulations in two different human cancer cell models. The four types of QD formulations, namely, mercaptopropionic acid modified CdSe/CdS/ZnS QDs (CdSe-MPA), PEGylated phospholipid encapsulated CdSe/CdS/ZnS QDs (CdSe-Phos), PEGylated phospholipid encapsulated InP/ZnS QDs (InP-Phos) and Pluronic F127 encapsulated CdTe/ZnS QDs (CdTe-F127), are representatives for the commonly used QD formulations in biomedical applications. Both the core materials and the surface modifications have been taken into consideration as the key factors for the cytotoxicity assessment. Through side-by-side comparison and careful evaluations, we have found that the toxicity of QDs does not solely depend on a single factor in initiating the toxicity in biological system but rather it depends on a combination of elements from the particle formulations. More importantly, our toxicity assessment shows different cytotoxicity trend for all the prepared formulations tested on gastric adenocarcinoma (BGC-823) and neuroblastoma (SH-SY5Y) cell lines. We have further proposed that the cellular uptake of these nanocrystals plays an important role in determining the final faith of the toxicity impact of the formulation. The result here suggests that the toxicity of QDs is rather complex and it cannot be generalized under a few assumptions reported previously. We suggest that one have to evaluate the QD toxicity on a case to case basis and this indicates that standard procedures and comprehensive protocols are urgently needed to be developed and employed for fully assessing and understanding the origins of the toxicity arising from different QD formulations. ? 2015 Published by Elsevier B.V.
URI: http://hdl.handle.net/10397/22912
ISSN: 0928-4931
DOI: 10.1016/j.msec.2015.07.044
Appears in Collections:Journal/Magazine Article

Access
View full-text via PolyU eLinks SFX Query
Show full item record

SCOPUSTM   
Citations

28
Last Week
1
Last month
0
Citations as of Sep 7, 2017

WEB OF SCIENCETM
Citations

17
Last Week
0
Last month
0
Citations as of Sep 20, 2017

Page view(s)

71
Last Week
1
Last month
Checked on Sep 18, 2017

Google ScholarTM

Check

Altmetric



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.