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动物雾化给药仪

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  • 询价
  • YSKD
  • 动物雾化给药仪
  • 北京
  • 2026年03月31日
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  • 企业认证

    • 详细信息
    • 文献和实验
    • 技术资料
    • 保修期

      12个月

    • 现货状态

      现货

    产品用途:
    通过高效双流体雾化发生器,结合无间断的涡流混匀技术,将液体供试品雾化成均匀稳定的气溶胶,对暴露腔内的大小鼠(或豚鼠)进行全身式雾化吸入给药实验。
    性能特点:
    采用高效双流体雾化器,克服了传统超声或超声振片的雾化弊端
    适用于发生各种液体、溶液、细微颗粒混悬液
    可实时添加供试品,单次雾化给药量更大
    产生的气溶胶粒径为肺部可沉积范围
    可选配微量发生模块,用于雾化珍贵微量液体供试品
    暴露腔采用透明材质,方便观察
    配有流量控制模块,加药更快速,清洗更方便
    具有废气处理模块,达到实验室安全排放要求
    应用范围:
    可用于小动物呼吸系统疾病造模(诱咳、引喘),纳米材料吸入毒性,哮喘和气道高反应性、(COPD)慢阻肺、肺纤维化、急性/新生呼吸窘迫综合症、急性肺损伤、表型研究、环境污染物机制研究、药物研发和药效评价等科研领域。产品细节图片1
     

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    图标文献和实验
    该产品被引用文献
    1. Introduction
    The antidegradant N-(1,3-Dimethylbutyl)-N′-phenyl-p-phenylenedi-
    amine (6PPD) is a phenylenediamine compound widely used as tire and
    rubber antioxidant to protect from oxygen and ozone (O3)[1,2]. Over
    the last half century, the usage of tires has dramatically risen as the
    number of automobiles worldwide has increased year by year. The mass
    percentage of 6PPD in tires is about 0.4 %-2 %, and 6PPD persistently
    enters the environment due to large amount emissions of tire wear
    particles[3]. Currently, the global environmental emissions of tire wear
    particles reached up to 5.9 million tons per year, and those tire wear
    particles account for 3–7 % of the particulate matter (PM2.5) in the air,
    increasing the risk of inhalation of 6PPD[4]. More seriously, environ-
    mental factors such as ground-level O3, ultraviolet A (UVA), high tem-
    perature, and high humidity can promote the aging processes of 6PPD[2,
    5,6], which may produce toxic derivatives and further aggravate envi-
    ronmental pollution and health burden.
    6PPD and its oxidized products were first detected in water, with
    environmental concentrations ranging from ng/L to μg/L levels, and
    have attracted attention due to the ecological risk[7]. An increasing
    number of studies have shown that environmental 6PPD and its aging
    products can attach to dust particles, which can diffuse into the air to
    form PM2.5 for long-distance transport[8,9]. The median total 6PPD
    concentrations in road dust, parking lot dust, and vehicle dust collected
    in southern Chinese cities were 226 ng/g, 232 ng/g, and 156 ng/g,
    respectively, which were much higher than those in indoor dust
    (14.0 ng/g)[10]. 6PPD-quinone (6PPDQ) is an important derivative of
    6PPD after ozonation, and the total detection rate of the 6PPDQ in PM2.5
    was 81 % in the urban environments of Taiyuan, Zhengzhou, and
    Guangzhou, China[9]. 6PPD and 6PPDQ have also been detected in
    PM2.5 in Hong Kong, China, and the daily intake of 6PPDQ for local
    general population is predicted to be 1.08 ng/kg/day[11]. Moreover,
    the detection rate of 6PPD and 6PPDQ in human urine in the South
    China was as high as 60–100 %, and the concentrations of 6PPD and
    6PPDQ in the urine of pregnant women (0.068–2.91 ng/mL) were
    significantly higher than those in adults (0.018–0.40 ng/mL) and chil-
    dren (0.015–0.076 ng/mL)[12,13]. In particular, workers in the rubber
    industry and those in traffic-relevant occupations are at risk of exposure
    to 6PPD and their quinone derivatives[14]. Considering the widespread
    detection of 6PPD and its aging products in airborne particles and bio-
    logical samples, long-term inhalation of those particles may pose a po-
    tential health risk to human, and further investigations on the inhalation
    toxicological effects on mammals are necessary.
    The currently thoroughly studied aging product, 6PPDQ, has a me-
    dian lethal concentration (LC50) of less than 1 μg/L for coho salmon[7],
    and may be neurotoxic and cardiotoxic to zebrafish at the concentra-
    tions of 10 µg/L[15,16]. In previous toxicity experiments, it has been
    found that 6PPDQ can cause multiple organ injury in mice by gavage
    (100 μg/kg) or intraperitoneal injection (0.4 mg/kg) for 28 days
    [17–19]. Nevertheless, it should be notable that the main exposure route
    for humans is inhalation of airborne dust containing 6PPD and its aging
    products[9,20,21], while whose respiratory toxicity largely remains to
    be investigated. The aging of 6PPD in environment is much more com-
    plex, which generate products including phenol, 4-[(1,3-dimethylbutyl)
    amino]-(4-DBAP), and 4-hydroxydiphenylamine(4-HDPA) more than
    just 6PPDQ[22]. In addition to O3, ultraviolet light has also been re-
    ported to accelerate the aging process of environmental contaminants
    through photoaging and even affect their toxicity[5,6]. Currently, few
    studies have examined the effects of O3 and UVA on the aging and
    toxicity of 6PPD, further study is urgently needed to support the health
    risk assessment and environmental management.
    In this study, we constructed an artificial accelerated aging system to
    investigate the effect of O3 and UVA on the aging process of 6PPD, and
    C57BL/6 male mice were exposed to 6PPD and differently aging 6PPDs
    to investigate the repeated inhalation toxicity heterogeneity at human-
    comparable levels, including respiratory system, neurobehavior alter-
    ation, and genetic damage. The study may contribute to the toxicolog-
    ical knowledge of 6PPD and its aging products, and provides a novel
    perspectives for the interference of environmental factors on the toxicity
    of pollutants.
    2. Methods and materials
    2.1. Chemicals
    6PPD (purity > 97.5 %) was purchased from Macklin (Shanghai,
    China). 6PPDQ (purity = 97.8 %) was purchased from Dr. Ehrenstorfer
    GmbH (German). 13C6-6PPDQ (purity > 98 %) was purchased from
    Cambridge Isotope Laboratories (Massachusetts, USA). HPLC-grade
    ammonium acetate, formic acid, and methanol were purchased from
    Sigma-Aldrich (USA).
    2.2. 6PPD aging reaction
    Oxidative aging of 6PPD by O3 was conducted in accordance to
    previous study[6,23]. Briefly, a total of 500 mg of 6PPD particles matter
    were ground into dark gray fine powder. The 6PPD powder was then
    spread on the bottom of a 1 L glass suction bottle and connected to the
    O3 reaction chamber. A combination of oxygen generator and O3
    generator (Guangzhou Chuavg Ozone Electric Equipment Co., China)
    were used to generate O3. According to our previous methodology
    (Table S1), the O3 flow rate was set at 0.5 L/min, in the oxidation aging
    reaction of 6PPD, O3 concentration of 20 ppm was used to react with
    500 mg 6PPD for 30 min for ozonation, and O3 concentration of
    200 ppm was used to react with 500 mg 6PPD for 120 min for perozo-
    nation. In UVA photoaging, the 6PPD powder was firstly spread on an
    8 * 8 cm2 flat plate and placed in a chamber with UVA irradiation (in-
    tensity of 300 μW/cm2) for 30 min, with a total irradiation dose of
    34.56 J. After UVA photoaging, the 6PPD powder was further to be
    oxidized by O3 aforesaid. After aging reaction, differently aging 6PPDs
    was dissolved in 50 mL of ethanol and stored at −20 ℃.
    2.3. 6PPDQ measurement and full wavelength scanning
    6PPDQ concentration is determined to evaluate the ozonation degree
    of 6PPD. According to previous studies[5,23], the concentrations of
    6PPDQ in the ethanol stock resolutions were determined by using a
    triple-quadrupole UPLC-MS/MS system (Acquity UPLC-Xero TQS,
    X. Li et al.
    Journal of Hazardous Materials 486 (2025) 137000
    2
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