研究目的
Comparing semiconductor nanocrystal toxicity in pregnant mice and non-human primates to assess the potential risks of engineered nanomaterials during pregnancy.
研究成果
Semiconductor nanocrystals can cross the placental barrier in both mice and macaques, but cause significant miscarriage in primates without observable pathological changes in fetuses. This indicates a need for precautions against gestational exposure to engineered nanomaterials, as primate responses may better predict human risks.
研究不足
The study is limited to specific animal models (mice and macaques) and may not fully translate to humans. The sample size for macaques is small (n=5 treated), and long-term effects beyond 3 years were not fully explored. The mechanisms underlying the differential toxicity between species are not fully elucidated.
1:Experimental Design and Method Selection:
The study used intravenous injection of phospholipid micelle-encapsulated CdSe/CdS/ZnS semiconductor nanocrystals in pregnant mice and cynomolgus macaques to evaluate toxicity. Methods included ICP-MS for cadmium concentration analysis, haematological and biochemical marker assessments, and histopathological examinations.
2:Sample Selection and Data Sources:
Pregnant BALB/c mice and cynomolgus macaques were used. Mice were grouped and treated at different embryonic days and dosages. Macaques were treated at 14 weeks post-conception with a dosage of 25 mg kg-
3:Control groups received saline or no treatment. Data were collected from blood, urine, and tissue samples. List of Experimental Equipment and Materials:
Equipment included ICP-MS system (Elan DRC-II, PerkinElmer SCIEX Instruments), ultrasound scanner (Esaote Aquila Pro, Pie Medical), blood analyzers (Sysmex XS-800i, Roche STA-R Evolution, Cobas 6000-C501), urinalysis units (Roche URISYS 2400, Sysmex UF-100i), microscope (Olympus BX60), and rotary evaporator (Labconco). Materials included CdSe/CdS/ZnS nanocrystals, DSPE-mPEG phospholipids, and standard laboratory chemicals.
4:Experimental Procedures and Operational Workflow:
Nanocrystals were synthesized and encapsulated. Animals were injected intravenously, and samples were collected at specified time points. Blood and urine tests, ultrasound scans, and tissue harvesting were performed. Histological sections were prepared and analyzed.
5:Data Analysis Methods:
Statistical analysis used ANOVA and Student's unpaired two-tailed t-test with a P value < 0.05 considered significant. Data are presented as mean ± SD.
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Microscope
BX60
Olympus
Used for observing histological sections of tissues.
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ICP-MS system
Elan DRC-II
PerkinElmer SCIEX Instruments
Used for trace elemental analysis of cadmium concentrations in blood and tissues.
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Ultrasound scanner
Aquila Pro
Esaote (Pie Medical)
Used for monitoring fetal development and uterus in pregnant macaques.
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Blood analyzer
XS-800i
Sysmex
Used for hematology analysis of blood samples.
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Blood analyzer
STA-R Evolution
Roche
Used for coagulation analysis of blood samples.
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Blood analyzer
Cobas 6000-C501
Roche
Used for chemistry analysis of blood samples.
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Urinalysis unit
URISYS 2400
Roche
Used for urinalysis of urine samples.
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Urinalysis unit
UF-100i
Sysmex
Used for urinalysis of urine samples.
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Rotary evaporator
Labconco
Used for evaporating chloroform during nanocrystal encapsulation.
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