Bioaccumulation and in-vivo dissolution of CdSe/ZnS with three different surface coatings by Daphnia magna

被引:15
|
作者
Lee, Byung-Tae [1 ]
Kim, Hyun-A [1 ]
Williamson, Jacob L. [2 ]
Ranville, James F. [2 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Environm Sci & Engn, Gwangju 500712, South Korea
[2] Colorado Sch Mines, Dept Chem & Geochem, Golden, CO 80401 USA
基金
新加坡国家研究基金会;
关键词
Quantum dot; Surface charge; Electrostatic attraction; Repulsion; Depuration; Retention; GOLD NANOPARTICLES; ENGINEERED NANOPARTICLES; SILVER NANOPARTICLES; CARBON NANOTUBES; QUANTUM DOTS; STABILITY; TOXICITY; EXPOSURE; WATER; AGGREGATION;
D O I
10.1016/j.chemosphere.2015.06.049
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Daphnia magna were exposed to nano-sized CdSe/ZnS quantum dots (QDs) having three different surface coatings. QDs were investigated for their aqueous stability in the test media (hard reconstituted laboratory water) and for their uptake, elimination, and in-vivo dissolution. Positively charged QDs (QEI) and negatively charged QDs (QSH) were electrostatically stable, whereas neutrally charged QDs (QSA) showed aggregation and sedimentation over 48-h. After 24 h of exposure to QDs (100 mu g/L as total Cd), the D. magna whole body Cd concentration significantly increased with no mortality for all QDs. Uptake patterns differed among the three coatings and Cd concentration reached 1460 +/- 50, 1014 +/- 99, and 584 +/- 81 mu g Cd/g dry wt for QEI, QSH, and QSA, respectively. Significant amounts of QEI and QSA (40% and 43%, respectively) remained in the D. magna after 24 h of depuration, while 89% QSH were readily excreted within the initial 1 h of the depuration stage. Soluble Cd was released from QDs during both the uptake and depuration. Release of Cd was higher in QEI and QSA than QSH, possibly resulting from the longer retention of QEI and QSA in the D. magna than QSH. These results imply that the surface charge of QDs plays a significant role in both the exposure to organisms and the in-vivo dissolution of nanoparticles. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:115 / 122
页数:8
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