Hillery A M, Jani P U, Florence A T
Centre for Drug Delivery Research, School of Pharmacy, University of London, UK.
J Drug Target. 1994;2(2):151-6. doi: 10.3109/10611869409015904.
Uptake by gut epithelial tissue of 60 nm polystyrene particles was studied in female Sprague-Dawley rats (180 g, 9 weeks old) after 5 days oral dosing by gavage (14 mg/kg). The gut was divided into lymphoid and non-lymphoid tissue of the small and large intestine, prior to analysis for polystyrene by gel permeation chromatography (GPC). Approximately 10% of the administered dose was recovered from the entire gastrointestinal tract. The total percentage of the administered dose taken up through lymphoid tissue was statistically much greater than through non-lymphoid tissue. It was estimated that 60% of the uptake in the small intestine occurred through the Peyer's patches, even though the patches comprised a small percentage of the total surface area of the small intestinal tissue. A significant amount of the total uptake was shown to occur in the large intestine, particularly in the lymphoid sections of this tissue. These results were confirmed by fluorescence microscopy.
在雌性斯普拉格-道利大鼠(180克,9周龄)中,通过灌胃(14毫克/千克)进行5天口服给药后,研究了60纳米聚苯乙烯颗粒在肠道上皮组织中的摄取情况。在通过凝胶渗透色谱法(GPC)分析聚苯乙烯之前,将肠道分为小肠和大肠的淋巴组织和非淋巴组织。从整个胃肠道中回收了约10%的给药剂量。通过淋巴组织摄取的给药剂量的总百分比在统计学上远高于通过非淋巴组织摄取的百分比。据估计,小肠中60%的摄取是通过派尔集合淋巴结发生的,尽管这些集合淋巴结在小肠组织的总表面积中所占比例很小。结果表明,总摄取量的很大一部分发生在大肠,特别是在该组织的淋巴部分。这些结果通过荧光显微镜得到了证实。