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首页> 外文期刊>Toxicology Research >Role of surface charge in bioavailability and biodistribution of tri-block copolymer nanoparticles in rats after oral exposure
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Role of surface charge in bioavailability and biodistribution of tri-block copolymer nanoparticles in rats after oral exposure

机译:口服后大鼠体内表面电荷在三嵌段共聚物纳米颗粒生物利用度和生物分布中的作用

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Tri-block copolymer nanoparticles (TCNP) are increasingly utilized, especially in drug delivery and diagnostics platforms. From in vitro studies, surface charge was observed to influence the transport of TCNP across the Caco-2 monolayers grown on transwell inserts. The objective of this study was to investigate the influence of surface charge on bioavailability and biodistribution of TCNP after oral exposure in vivo and to compare with the in vitro data. To attain the set objectives, monodisperse (45 +/- 5 nm), fluorescent and differently charged (positive and negative) TCNP were orally administered to inbred Fischer 344 rats. Blood samples were collected at t = 0, 1/2, 1, 2, 4 and 6 h followed by sacrifice of the animals and collection of the major organs (lungs, liver, kidney, spleen, brain, intestine, and tibia). Quantitative assessments of TCNP in blood and organs were performed by fluorescence measurements. TCNP of both surface charges got absorbed and appeared in the blood within 1/2 h of oral administration. No significant difference in bioavailability and biodistribution could be found between positive and negative TCNP. Both the TCNP, irrespective of charge, showed major accumulation in the liver, kidneys and spleen, were detected in the brain and did not cause any significant increase in the serum alkaline phosphatase levels. Contrary to the in vitro data, surface charge was not found to influence the in vivo bioavailability and biodistribution of TCNP after oral exposure. The obtained results encourage further development of such TCNP, especially for drug delivery purposes.
机译:三嵌段共聚物纳米颗粒(TCNP)越来越多地被利用,尤其是在药物输送和诊断平台中。从体外研究中,观察到表面电荷会影响TCNP跨过跨孔插入片段上生长的Caco-2单层的转运。这项研究的目的是调查体内口服暴露后表面电荷对TCNP的生物利用度和生物分布的影响,并与体外数据进行比较。为了达到设定的目标,对近交Fischer 344大鼠口服单分散(45 +/- 5 nm),荧光和带不同电荷(正负)的TCNP。在t = 0、1 / 2、1、2、4和6 h采集血样,然后处死动物并采集主要器官(肺,肝,肾,脾,脑,肠和胫骨)。通过荧光测量对血液和器官中TCNP进行定量评估。两种表面电荷的TCNP在口服后1/2小时内就被吸收并出现在血液中。阳性和阴性TCNP之间的生物利用度和生物分布均无显着差异。两种TCNP,不论是否带电,均显示在肝脏,肾脏和脾脏中大量积累,在大脑中被检测到,并没有引起血清碱性磷酸酶水平的任何显着增加。与体外数据相反,口服接触后未发现表面电荷影响TCNP的体内生物利用度和生物分布。获得的结果鼓励了这种TCNP的进一步开发,特别是用于药物递送目的。

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