Acute oral toxicity evaluation of biodegradable and pH-sensitive hydrogel based on polycaprolactone, poly(ethylene glycol) and methylacrylic acid (MAA)

被引:33
作者
Chen, Xian [1 ,2 ]
Qian, ZhiYong [1 ]
Gou, MaLing [3 ]
Chao, GuoTao [3 ]
Zhang, YangDe [4 ]
Gu, YingChun [5 ]
Huang, MeiJuan [1 ]
Wang, JiWei [4 ]
Pan, YiFeng [4 ]
Wei, YuQuan [1 ]
Chen, JianPing [2 ]
Tu, MingJing [3 ]
机构
[1] Sichuan Univ, W China Hosp, W China Med Sch, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, W China Sch Preclin & Forens Med, Dept Parasitol, Chengdu 610041, Peoples R China
[3] Sichuan Univ, Coll Mat Sci & Engn, Chengdu 610065, Peoples R China
[4] Cent S Univ, Natl Key Lab Nanobiol Technol, Changsha 410008, Peoples R China
[5] Sichuan Univ, Dept Text & Clothing, Chengdu 610065, Peoples R China
关键词
biodegradable; pH-sensitive hydrogel; biocompatible; acute oral toxicity evaluation; histopathologic examination;
D O I
10.1002/jbm.a.31350
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
In this article, a novel biodegradable and pH-sensitive hydrogel based on polycaprolactone, poly(ethylene glycol) and methylacrylic acid (MAA), was prepared by UV-initiated free radical polymerization. The obtained hydrogel was characterized by H-1 NMR and FTIR. The acute toxicity tests and histopathological study were performed in BALB/c mice. In acute oral toxicity test, mice were orally administered with a total 15 g/kg body weight (b.w.) of P(CL-MAA-EG) hydrogels, and were observed continuously for 14 days. For histopathologic study, samples including heart, liver, lung, kidneys, spleen, stomach, and intestine, were histochemically prepared and stained with hematoxylin-eosin for histopathologic examination. No mortality or significant signs of acute toxicity was observed during the whole observation period, and no macroscopic alteration was found in the organs. Histopathological analysis of various organs also did not show any significant pathological changes. Thus, the maximal tolerance dose of P(CL-MAA-EG) hydrogels was calculated to be higher than 15 g/kg b.w. in BALB/c mice. It was suggested that the studied P(CL-MAA-EG) hydrogel in this article were nontoxic after acute oral administration and it might be a promising candidate as a novel oral drug carrier. (C) 2007 Wiley Periodicals, Inc. J Biomed Mater Res.
引用
收藏
页码:589 / 597
页数:9
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