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动物暴露染毒系统
产品介绍
动物暴露染毒系统为染毒舱和监控系统分体式设计,用于大小鼠、兔子、猴子等全身暴露染毒,暴露染毒舱尺寸可定制。
产品特点
染毒舱采用铝合金框架, 四周为透明PMMA材质, 方便观察;
可选配不锈钢材质;
具有通风换气功能, 保证动物的氧供应, 防止C02及异昧积累:
内置风扇混匀器, 保证舱内气溶胶浓度一致:
集成化传感器舱模块, 全方位监控。
染毒舱(型号:WBC-M)
容积180L,
外尺寸:700×580×620mm;
可容纳大号大鼠笼2个或中号大鼠笼4个:
其他尺寸可定制。
配置比例
动物暴露染毒系统(型号:WBE-B)
• 染毒舱
• 气溶胶发生器 (种类自选-干粉、液体气溶胶发生器、香烟烟雾发生器、柴油尾气发生器......)
• 染毒监控系统z监测温度、 湿度、 氧气、 二氧化碳气源及流量调节系统
• 废气处理系统
• (选配)气溶胶浓度监测、 粒径分布检测等
型号选择
名称 | 型号 | 说明 | 单位 |
全身暴露染毒系统 | WBE-B-WDF-M | 用于干粉型、 PM2. 5颗粒物暴露 | 套 |
全身暴露染毒系统 | WBE-B-NSF-M | 用于液体气溶胶暴露 | 套 |
全身暴露染毒系统 | WBE-B-CSM-M | 用于香烟烟气暴露 | 套 |
全身暴露染毒系统 | WBE-B-CY-M | 用于柴油尾气暴露 | 套 |
参考文献
[1]Jushan Zhang,Mo Xue,Rong Pan, Yujie Zhu,Zhongyang Zhang, Haoxiang Cheng, Johan L M Björkegren, Jia Chen, Zhiqiang Shi,Ke Hao"An e-cigarette aerosol generation, animal exposure and toxicants quantification system to characterize in vivo nicotine kinetics in arterial and venous blood"[J].bioRxiv preprint doi.
[2]Wenchuan Qi,Lu Liu,Qian Zeng, Ziyang Zhou,Daohong Chen,Bin He,Siyao Gong,Lei Gao,Xiao Wang,Jian Xiong,Dingjun Cai,Shuguang Yu,Ling Zhao,Contribution of cuproptosis and Cu metabolism-associated genes to chronic obstructive pulmonary disease,[J].J Cell Mol Med. 2023;00:1–11.
[3]Guolin Zhao,William Ho,Jinxian Chu, Xiaojian Xiong, Bin Hu,Kofi Oti Boakye-Yiadom,Xiaoyang Xu,Xue-Qing Zhang,Inhalable siRNA Nanoparticles for Enhanced Tumor-Targeting Treatment of KRAS-Mutant Non-Small-Cell Lung Cancer,[J]ACS Applied Materials&Interfaces,2023-06-24,DOI:10.1021/acsami.3c05007.
[4]Liu X, Zhao L, Wang R, et al. TRPM2 exacerbates airway inflammation by regulating oxidized-CaMKⅡ in allergic asthma[J]. Heliyon, 2024, 10(1): e23634.
[5]Tian X, Gao Y, Ma W, et al. Establishment of an Inhalation Administration Non-invasive Murine Model for Rapidly Testing Drug Activity against Mycobacterium tuberculosis[J]. bioRxiv, 2024: 2024.02. 27.582260.
[6]Liu L, Tang Z, Zeng Q, et al. Transcriptomic Insights into Different Stimulation Intensity of Electroacupuncture in Treating COPD in Rat Models[J]. Journal of Inflammation Research, 2024: 2873-2887.
[7]Dong Y, Dong Y, Zhu C, et al. Targeting CCL2-CCR2 signaling pathway alleviates macrophage dysfunction in COPD via PI3K-AKT axis[J]. Cell Communication and Signaling, 2024, 22(1): 364.
[8]Shen S, Huang Q, Liu L, et al. GATA2 downregulation contributes to pro-inflammatory phenotype and defective phagocytosis of pulmonary macrophages in chronic obstructive pulmonary disease[J]. Aging (Albany NY), 2024, 16(19): 12928.
[9]Zou X, Huang Q, Kang T, et al. An integrated investigation of mitochondrial genes in COPD reveals the causal effect of NDUFS2 by regulating pulmonary macrophages[J]. Biology Direct, 2025, 20(1): 4.
[10]Tian X, Gao Y, Li C, et al. A novel non-invasive murine model for rapidly testing drug activity via inhalation administration against Mycobacterium tuberculosis[J]. Frontiers in Pharmacology, 2025, 15: 1400436.
[11]Liu K, Liu R, Zhang C, et al. Suzi Daotan Decoction alleviates asthmatic airway remodeling through the AMPK/SIRT1/PGC-1α signaling pathway and PI3K/AKT signaling pathway[J]. Scientific Reports, 2025, 15(1): 6690.
[12]Huang Q, Kang T, Shen S, et al. Extracellular vesicular delivery of ceramides from pulmonary macrophages to endothelial cells facilitates chronic obstructive pulmonary disease[J]. Cell Communication and Signaling, 2025, 23(1): 124.
[13]Zeng H, Liu X, Liu P, et al. Exercise's protective role in chronic obstructive pulmonary disease via modulation of M1 macrophage phenotype through the miR-124-3p/ERN1 axis[J]. Science Progress, 2025, 108(3): 00368504251360892.
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*此介绍及参数为产品基础信息,可能滞后于产品更新,具体参数请与我司联系。