摘要:
由于独特的抗菌特性,纳米银(AgNP)在诸多领域得到广泛应用,但是其生物有效性、动物组织分布及排出尚不清楚。将聚乙烯吡咯烷酮包被的AgNP溶液按照10 mg·kg-1给雌性SD大鼠灌胃,采用ICP-MS检测SD大鼠组织、粪便及尿液中总银浓度。结果表明,AgNP通过小肠吸收后,可以通过血液循环快速分布在肝、肾、脾、肺、脑等靶器官。灌胃后1 h,大鼠各组织中总银浓度达到最大值(肝、肾、脾、肺、脑中银浓度分别为(0.29 ±0.13) mg·kg-1、(0.23 ±0.04) mg·kg-1、(0.17 ±0.05) mg·kg-1、(0.11 ±0.01) mg·kg-1、(0.06 ±0.02) mg·kg-1),之后银浓度随时间而降低,直至和对照组无显著性差异。在灌胃途径下,AgNP对SD大鼠的有效性为8.5%,且73%的AgNP是通过粪便的途径排出体外。
Abstract:
Due to the unique antimicrobial properties, nanosilver (AgNP) are widely applied in many fields. However, its bioavailability, tissue distribution and excretion in rats are less known. Female Sprague-Dawley rats were treated by a single intragastic administration of 10 mg·kg-1 polyvinylpyrrolidone-AgNPs, and rat tissues, feces and urine were collected periodically to analyze total Ag concentrations by ICP-MS. The results showed that after uptake by gastrointestine, AgNP was transported via the blood circulation and distributed to tissues such as liver, kidney, spleen, lung, and brain. At 1 h after AgNP exposure, total silver accumulation in those tissues peaked (i.e. 0.29 ±0.13 mg·kg-1, 0.23 ±0.04 mg·kg-1, 0.17 ±0.05 mg·kg-1, 0.11 ±0.01 mg·kg-1 and 0.06 ±0.02 mg·kg-1 for liver, kidney, spleen, lung and brain, respectively), and declined to background levels over time. Our calculation showed that the bioavailability of AgNP to Sprague-Dawley rats via intragastric administration was 8.5%. Especially, 73% of the dosed AgNP was excreted via feces.