纤维蛋白封闭剂对SD大鼠连续腹腔注射给药14天的毒性研究

戴小宇; 朱海; 张晓冬; 张晓芳; 宗英; 戴益民; 张淑英; 袁伯俊; 陆国才

doi:10.3969/j.issn.1006-0111.2015.03.010

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纤维蛋白封闭剂对SD大鼠连续腹腔注射给药14天的毒性研究

戴小宇, 朱海, 张晓冬, 张晓芳, 宗英, 戴益民, 张淑英, 袁伯俊, 陆国才

文章导航 > 药学实践与服务 > 2015 > 33(3): 231-234

戴小宇, 朱海, 张晓冬, 张晓芳, 宗英, 戴益民, 张淑英, 袁伯俊, 陆国才. 纤维蛋白封闭剂对SD大鼠连续腹腔注射给药14天的毒性研究[J]. 药学实践与服务, 2015, 33(3): 231-234. doi: 10.3969/j.issn.1006-0111.2015.03.010

引用本文:

DAI Xiaoyu, ZHU Hai, ZHANG Xiaodong, ZHANG Xiaofang, ZONG Ying, DAI Yimin, ZHANG Shuying, YUAN Bojun, LU Guocai. Repeat-dose toxicity study of fibrin sealant in SD rats[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(3): 231-234. doi: 10.3969/j.issn.1006-0111.2015.03.010

Citation:

DAI Xiaoyu, ZHU Hai, ZHANG Xiaodong, ZHANG Xiaofang, ZONG Ying, DAI Yimin, ZHANG Shuying, YUAN Bojun, LU Guocai. Repeat-dose toxicity study of fibrin sealant in SD rats[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(3): 231-234. doi: 10.3969/j.issn.1006-0111.2015.03.010

纤维蛋白封闭剂对SD大鼠连续腹腔注射给药14天的毒性研究

doi: 10.3969/j.issn.1006-0111.2015.03.010

第二军医大学药物安全性评价中心, 上海 200433

基金项目: "重大新药创制"科技重大专项(2014ZX09J14106);上海市公共卫生重点实验室建设计划(12GWZX0501);上海市自然科学基金(13ZR1449400)

Repeat-dose toxicity study of fibrin sealant in SD rats

Center for New Drug Evaluation, Second Military Medical University, Shanghai 200433, China

摘要: 目的评价SD大鼠连续腹腔注射纤维蛋白封闭剂的安全性。方法 SD大鼠雌雄分别按体质量随机分4组, 即空白对照组、纤维蛋白封闭剂低剂量组、中剂量组和高剂量组, 每组20只, 雌雄各半。3个给药组的给药剂量分别为85.5、171.0和342.0 mg/kg, 每天腹腔注射给药, 连续14 d, 恢复期28 d, 进行一般症状、血液学、血液生化和病理组织学等指标检测。结果与空白对照组相比, 纤维蛋白封闭剂中、高剂量组大鼠第14天的白细胞计数显著升高, 纤维蛋白原显著降低, 中、高剂量组大鼠脾脏的脏器重量有增加趋势。组织病理学检查发现部分高剂量动物腹腔出现残留药物引起的纤维肉芽组织包裹。上述变化指标在恢复期结束时基本可恢复。结论大鼠腹腔注射纤维蛋白封闭剂85.5~342.0 mg/kg, 安全剂量为85.5 mg/kg, 毒性剂量为171.0 mg/kg。毒性靶系统或靶部位为血液系统、免疫系统和给药局部, 毒性作用可逆。
- 纤维蛋白封闭剂 /
- SD大鼠 /
- 重复给药毒性 /
- 临床前安全性
Abstract: Objective To evaluate the safety of fibrin sealant (FS) intraperitoneal injection in SD rats. Methods 80 male and female SD rats were randomly divided into four groups (0, 85.5, 171.0, 342.0 mg/kg) by body weight. All rats were intraperitoneally injected with vehicle or FS daily for 14 days followed by a 28-day recovery period. The clinical signs, hematological and biochemical indices were measured. The pathology were observed. Results Increase of white blood cell count (WBC) and decrease of fibrinogen (FIB) in d 14 were found in 171.0 mg/kg and 342.0 mg/kg dosage groups. Furthermore, the tendency of weight increase of spleen were found in 171.0 mg/kg and 342.0 mg/kg dosage groups. Pathological exams of peritoneal cavity found that there were granulation tissues containing FS in some of the rats in 342.0 mg/kg group. All of these changes got reversed after the recovery period. Conclusion The safety dose in this study is considered to be 85.5 mg/kg, and the toxicity dose is 171.0 mg/kg. The target toxicity systems or site of FS in SD rats are hematological system, immune system and injection site. The toxic effects of FS are reversible.
- fibrin sealant /
- SD rats /
- repeat-dose toxicity /
- preclinical safety

[1]	Spotnitz WD.Hemostats,sealants,and adhesives:a practical guide for the surgeon[J].Am Surg,2012,78(12):1305-1321.
[2]	王平瑜,白雪峰,王保卫,等.人纤维蛋白胶对人肝损伤的止血护创作用[J].中国医学创新,2011,8(6):9-11.
[3]	谢钧韬,叶建宇,尹耀新,等.纤维蛋白封闭剂在腹腔镜胆囊切除术右副肝管处理中的应用[J].中华腔镜外科杂志(电子版),2010,3(2):205-207.
[4]	Mao Y, Xia ZN, Zhang XF,et al.Evaluation of subchronic toxicity of SIM010603,a potent inhibitor of receptor tyrosine kinase,after 28-day repeated oral administration in SD rats and beagle dogs[J].Food Chem Toxicol,2012,50(5):1256-1270.
[5]	Gong XL, Gao TT, Zhao LJ,et al.Subchronic safety evaluation of CMS-1 (a botanical antihypertensive product derived from Semen Cnidium monnieri)in Sprague-Dawley rats and beagle dogs[J].Regul Toxicol Pharmacol,2014,69(3):558-571.
[6]	王春仁,王召旭,宋谊萍,等.医用纤维蛋白胶亚急性毒性实验研究[J].中国药事杂志,2007,21(7):472-477.
[7]	Bjorenson JE,Grove HF,List MG Sr,et al.Effects of hemostatic agents on the pH of body fluids[J].J Endod,1986,12:289.
[8]	Ibrahim MF,Aps C,Young CP.A foreign body reaction to Surgicel mimicking an abscess following cardiac surgery[J].Eur J Cardiothorac Surg,2002,22(3):489-490.
[9]	Chapman WC,Wren SM,Lebovic GS,et al.Effective management of bleeding tumor resection with a collagen-based hemostatic agent[J].Am Surg,2002,68(9):802-807.
[10]	Tomizawa Y.Clinical benefits and risk analysis of topical hemostats: a review [J].J Artif Organs,2005,8(3):137-142.

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纤维蛋白封闭剂对SD大鼠连续腹腔注射给药14天的毒性研究

doi: 10.3969/j.issn.1006-0111.2015.03.010

第二军医大学药物安全性评价中心, 上海 200433

基金项目: "重大新药创制"科技重大专项(2014ZX09J14106);上海市公共卫生重点实验室建设计划(12GWZX0501);上海市自然科学基金(13ZR1449400)

收稿日期: 2014-08-27
修回日期: 2014-12-30

关键词:

纤维蛋白封闭剂 /

SD大鼠 /

重复给药毒性 /

临床前安全性

摘要: 目的评价SD大鼠连续腹腔注射纤维蛋白封闭剂的安全性。方法 SD大鼠雌雄分别按体质量随机分4组, 即空白对照组、纤维蛋白封闭剂低剂量组、中剂量组和高剂量组, 每组20只, 雌雄各半。3个给药组的给药剂量分别为85.5、171.0和342.0 mg/kg, 每天腹腔注射给药, 连续14 d, 恢复期28 d, 进行一般症状、血液学、血液生化和病理组织学等指标检测。结果与空白对照组相比, 纤维蛋白封闭剂中、高剂量组大鼠第14天的白细胞计数显著升高, 纤维蛋白原显著降低, 中、高剂量组大鼠脾脏的脏器重量有增加趋势。组织病理学检查发现部分高剂量动物腹腔出现残留药物引起的纤维肉芽组织包裹。上述变化指标在恢复期结束时基本可恢复。结论大鼠腹腔注射纤维蛋白封闭剂85.5~342.0 mg/kg, 安全剂量为85.5 mg/kg, 毒性剂量为171.0 mg/kg。毒性靶系统或靶部位为血液系统、免疫系统和给药局部, 毒性作用可逆。

English Abstract

Repeat-dose toxicity study of fibrin sealant in SD rats

Center for New Drug Evaluation, Second Military Medical University, Shanghai 200433, China

Received Date: 2014-08-27
Rev Recd Date: 2014-12-30

Keywords:

Abstract: Objective To evaluate the safety of fibrin sealant (FS) intraperitoneal injection in SD rats. Methods 80 male and female SD rats were randomly divided into four groups (0, 85.5, 171.0, 342.0 mg/kg) by body weight. All rats were intraperitoneally injected with vehicle or FS daily for 14 days followed by a 28-day recovery period. The clinical signs, hematological and biochemical indices were measured. The pathology were observed. Results Increase of white blood cell count (WBC) and decrease of fibrinogen (FIB) in d 14 were found in 171.0 mg/kg and 342.0 mg/kg dosage groups. Furthermore, the tendency of weight increase of spleen were found in 171.0 mg/kg and 342.0 mg/kg dosage groups. Pathological exams of peritoneal cavity found that there were granulation tissues containing FS in some of the rats in 342.0 mg/kg group. All of these changes got reversed after the recovery period. Conclusion The safety dose in this study is considered to be 85.5 mg/kg, and the toxicity dose is 171.0 mg/kg. The target toxicity systems or site of FS in SD rats are hematological system, immune system and injection site. The toxic effects of FS are reversible.

引用本文: