首页> 外文会议>International conference on nanotechnology 2013 >BIODISTRIBUTION OF POLY (LACTIC- CO-GLYCOLIC) ACID (PLGA) AND PLGA/CHITOSAN NANOPARTICLES IN F344 RATS ORALLY EXPOSED TO NANOPARTICLES FOR SEVEN DAYS
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BIODISTRIBUTION OF POLY (LACTIC- CO-GLYCOLIC) ACID (PLGA) AND PLGA/CHITOSAN NANOPARTICLES IN F344 RATS ORALLY EXPOSED TO NANOPARTICLES FOR SEVEN DAYS

机译:暴露于纳米颗粒的F344大鼠中多聚(乳酸-乙醇酸)(PLGA)和PLGA /壳聚糖纳米颗粒的生物分布

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1. Following repeat-dose administration, PLGA NPs reached liver, spleen, kidney, tteart, lung, and brain, with highest concentrations (%dose/g) in the spleen, intestine, kidney, and lung 2. NP concentration in brain and heart measured the lowest concentrations 3. A maximum of 46.1% PLGA and 41.1 % PLGA/chi of daily dose or 6.6% PLGA and 5.9% PLGA/chi of total dose was recovered after 7 days of daily gavage with 3 mg NPs/dose. 4. For oral delivery, NP concentrations are much smaller than NP concentration rn the same tissue for IV treated animals 5. Biodistribution of PLGA and PLGA/Chi were not significantly different.
机译:1.重复给药后,PLGA NPs到达肝,脾,肾,tteart,肺和脑,在脾,肠,肾和肺中的浓度最高(%dose / g)。2。心脏测得的最低浓度为3。每日灌胃3毫克NPs /剂量后,每天总剂量的最高PLGA和4 mg / chi分别为46.1%和41.1%PLGA / chi和5.9%PLGA / chi。 4.对于口服给药,对于经IV处理的动物,NP浓度远小于同一组织中的NP浓度。5. PLGA和PLGA / Chi的生物分布无显着差异。

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