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小鼠对量子点的透皮吸收和代谢
引用本文:唐蕾,张春玲,宋光明,徐忠伟,金迅.小鼠对量子点的透皮吸收和代谢[J].生物化学与生物物理进展,2012,39(2):188-193.
作者姓名:唐蕾  张春玲  宋光明  徐忠伟  金迅
作者单位:中国人民武装警察部队医学院;南开大学物理科学学院;中国人民武装警察部队医学院;中国人民武装警察部队医学院;中国人民武装警察部队医学院
基金项目:中国人民武装警察部队医学院重点项目(WYZ201003)
摘    要:皮肤是身体的最大器官,能够直接与含纳米材料的防晒霜、化妆品等接触,但是人们对纳米材料的皮肤渗透性却了解不多.本文研究了水溶性硫硒化镉(CdSeS)量子点纳米颗粒的皮肤渗透性和在体内的代谢情况.将雄性ICR鼠背部脱毛,在脱毛部位涂抹直径约为5 nm、发光波长为620 nm的量子点0.32 nmol,然后检测皮肤和心、肝、脾、肺、肾中量子点沉积量随时间的变化情况.荧光显微像显示,量子点能够堆积在皮肤的表皮层中和真皮层的毛囊和腺体中,电感耦合等离子体质谱(inductively coupled plasma-mass spectrometry,ICP-MS)结果表明,透皮吸收的量子点能够沉积在器官中,并且肝和肾中沉积的量子点代谢缓慢,涂抹量子点5天之后,肾脏中残存的镉离子浓度仍超过14 ng/g.这些结果表明,量子点能够被小鼠透皮吸收,而且对肝和肾产生严重影响.

关 键 词:量子点,纳米颗粒,透皮吸收,代谢路径,ICP-MS
收稿时间:2011/7/12 0:00:00
修稿时间:2011/9/25 0:00:00

Transdermal Delivery Through in vivo Mouse Skin and Metabolic Path of Quantum Dots
TANG Lei,ZHANG Chun-Ling,SONG Guang-Ming,XU Zhong-Wei and JIN Xun.Transdermal Delivery Through in vivo Mouse Skin and Metabolic Path of Quantum Dots[J].Progress In Biochemistry and Biophysics,2012,39(2):188-193.
Authors:TANG Lei  ZHANG Chun-Ling  SONG Guang-Ming  XU Zhong-Wei and JIN Xun
Institution:1)(1) Medical College of Chinese People′s Armed Police Force,Tianjin 300162,China;2) College of Physics Science,Nankai University,Tianjin 300071,China)
Abstract:Skin is the largest organ of the body and is a potential route of exposure to sunscreens and cosmetics containing nanoparticles, but the permeability of the skin to these nanoparticles is unknown. In this paper, we studied the transdermal delivery capacity through mouse skin of water-soluble CdSeS quantum dots (QDs) and the deposition of these QDs in the body. QD solution was coated on the dorsal hairless skin of male ICR mice. Fluorescence microscope was used to observe the deposition of QDs in mouse skin and heart, liver, spleen, lung and kidney. Inductively coupled plasma-mass spectrometry (ICP-MS) was used to measure the 111Cd concentration to indicate the concentration of QDs in plasma and organs. The fluorescence images show that QDs can penetrate into the dermal layer and deposit in the organs through blood circulation. ICP-MS result indicates that QDs deposit seriously in liver and kidney, and they are difficult to clear. 111Cd concentration is still more than 14 ng/g in kidney after 5 days. These results suggest that QDs has in vivo transdermal delivery capacity through mouse skin and is harmful to the liver and kidney.
Keywords:quantum dots  nanoparticles  transdermal delivery  metabolism  ICP-MS
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