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经口给予BALB/c小鼠后,131I-牛血清白蛋白负载明胶微球的生物分布——粒径研究

Biodistribution of 131I-BSA loaded gelatin microspheres after peroral application to BALB/c mice--particle size study.

作者信息

Mladenovska Kristina, Janevik Emilija I, Glavas Marija D, Kumbaradzi Emilija F, Goracinova Katerina

机构信息

Institute of Pharmaceutical Technology, Department of Biopharmacy, Faculty of Pharmacy, University Ss Cyril and Methodious, Skopje, Macedonia.

出版信息

Acta Pharm. 2003 Sep;53(3):187-97.

Abstract

Biodistribution studies of radiolabelled 131I-BSA loaded gelatin microspheres were carried out on BALB/c mice after peroral administration. To two groups, radiolabelled 131I-BSA gelatin microspheres of different particle size, 1.2 +/- 1.1 microm and 7.0 +/- 1.2 microm, were administered orally. To the control group, a solution of 131I-BSA was administered orally as well. Biodistribution was followed periodically within 15 days as the percent of total radioactivity present in the stomach and small intestine with Peyer's patches and mesentery, in colon with Peyer's patches, appendix and mesentery, in liver, spleen, blood, kidney, lungs and heart. Preliminary in vitro biodegradation and drug release studies confirmed the potential of gelatin microspheres to protect the antigen of interest from enzymatic degradation in the gut, and to release it in a controlled manner. The biodistribution data confirmed that particle uptake into Peyer's patches and passage to the liver and spleen via the mesentery lymph supply and nodes increased with decreasing particle size.

摘要

对经口给予放射性标记的131I-BSA负载明胶微球进行了BALB/c小鼠体内生物分布研究。将不同粒径(1.2±1.1微米和7.0±1.2微米)的放射性标记131I-BSA明胶微球经口给予两组小鼠。对照组经口给予131I-BSA溶液。在15天内定期跟踪生物分布情况,包括胃、有派尔集合淋巴结和肠系膜的小肠、有派尔集合淋巴结、阑尾和肠系膜的结肠、肝脏、脾脏、血液、肾脏、肺和心脏中总放射性的百分比。初步的体外生物降解和药物释放研究证实了明胶微球有潜力保护目标抗原免受肠道内酶的降解,并以可控方式释放该抗原。生物分布数据证实,随着粒径减小,派尔集合淋巴结对颗粒的摄取以及通过肠系膜淋巴供应和淋巴结向肝脏和脾脏的转运增加。

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