2011
DOI: 10.1016/j.biomaterials.2011.04.063
|View full text |Cite
|
Sign up to set email alerts
|

In vivo distribution, pharmacokinetics, and toxicity of aqueous synthesized cadmium-containing quantum dots

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

10
125
1

Year Published

2012
2012
2018
2018

Publication Types

Select...
6
2
1

Relationship

3
6

Authors

Journals

citations
Cited by 176 publications
(136 citation statements)
references
References 36 publications
10
125
1
Order By: Relevance
“…S4C). Hepato-renal toxicity is a well-known issue preventing the approval of QDs for biomedical applications, and the observed damage is likely attributed to the leakage of the QDs out of the LbL shell (34,35). To our knowledge, this is the first report of the head-to-head comparison of toxicities of NIR-II probes in an identical LbL platform.…”
Section: Resultsmentioning
confidence: 92%
“…S4C). Hepato-renal toxicity is a well-known issue preventing the approval of QDs for biomedical applications, and the observed damage is likely attributed to the leakage of the QDs out of the LbL shell (34,35). To our knowledge, this is the first report of the head-to-head comparison of toxicities of NIR-II probes in an identical LbL platform.…”
Section: Resultsmentioning
confidence: 92%
“…They found that the biodistribution was largely dependent on hydrodynamic diameters of the QDs, blood circulation time, and types of organs. Based on histological and biochemical quantitative analysis, and real-time body weight measurement, we further revealed that, the aqQDs produced no overt adverse effect to mice [28]. These studies are important for understanding the in vivo toxicity of QDs, and for designing QDs with acceptable biocompability for biomedical applications.…”
Section: Biosafety Assessment Of Ii-vi Qdsmentioning
confidence: 72%
“…Potential effects on the lungs include damage to membranes, cytotoxicity, genotoxicity, apoptosis (induced programmed cell death), necrosis (cell death due to toxic interference with vital cell functions), inflammation, fibrosis, and cancer [1-3, and references therein]. Inhaled nanoparticles may penetrate the alveolar-capillary barrier between the respiratory and circulatory system, and thus be translocated from the lungs [2,3,[30][31][32][33][34][35][36][37][38][39][40][41][42], and references therein]. When the nanoparticles translocate to the circulatory system, other organs may also be affected [1-3, 15, 16, 30-32, 39-42].…”
Section: Determinants Of Human Inhalation Hazards Of Persistent Enginmentioning
confidence: 99%
“…For instance, as pointed out before, Choi et al [39] found that noncationic nanoparticles \34 nm were rapidly translocated from the lungs, whereas cationic nanoparticles of a similar size were not. The generation of Ag ions by silver nanoparticles [82] and the release of ionic Cd and Se from CdSe quantumdots [16,36,84,85] are determinants of nanoparticle hazard. Metal solubility has been found a determinant in cytotoxicity of metal oxide and metal hydroxide nanoparticles [19,86].…”
Section: Determinants Of Human Inhalation Hazards Of Persistent Enginmentioning
confidence: 99%