期刊文献+

褐藻胶寡糖食用安全性毒理学评价 被引量:1

Toxicological Evaluation for the Edible Safety of alginate oligosaccharide
原文传递
导出
摘要 目的:对褐藻胶寡糖的食用安全性进行毒理学评价。方法:采用小鼠急性经口毒性试验、遗传毒性试验(Ames试验、小鼠骨髓细胞微核试验、小鼠精母细胞染色体畸变试验)和大鼠28天经口毒性试验。结果:小鼠急性经口半数致死剂量(LD50)大于15000 mg/kg BW;Ames试验、小鼠骨髓细胞微核试验、小鼠精母细胞染色体畸变试验结果均为阴性;在28天经口毒性试验中,大鼠的生长发育、血液学、血生化、尿常规及病理组织学检查未见与受试物相关的异常变化。结论:在试验剂量范围内,褐藻胶寡糖为实际无毒,无遗传毒性,28天经口毒性试验未发现明显毒性反应。 Objective:To assess the edible safety of alginate oligosaccharide.Methods:The toxicity of alginate oligosaccharide was investigated by acute oral test,genetic toxicity test including Ames test,mice marrow cell micronucleus test and mice spermatocyte chromosome aberration test,and 28-day oral toxicity test in rats.Results:The acute oral LD50(50%lethal dose)in mice was over 15000 mg/kg BW.No evidences of genotoxic activity to mice were foud.BY 28-day oral toxicity test,no significant changes in organ weight,hematologic,serum biochemical and urinalysis were noted,and no test substance-related pathological changes were found.Conclusion:No acute oral toxicity or genotoxicity of alginate oligosaccharide was found in this test dose range,and the toxicity of alginate oligosaccharide was not observed at the end of 28-day oral toxicity test.
作者 刘泳廷 郑冲 刘玲 叶建方 LIU Yong-ting;ZHENG Chong;LIU Ling;YE Jian-fang(Center for Disease Control and Prevention of Guizhou Province,Guiyang550004,China)
出处 《微量元素与健康研究》 CAS 2019年第3期5-8,共4页 Studies of Trace Elements and Health
关键词 褐藻胶寡糖 急性毒性 遗传毒性 28天经口毒性 安全性评价 alginate oligosaccharide acute toxicity Genotoxicity 28-day oral toxicity Safety evaluation
  • 相关文献

参考文献1

二级参考文献34

  • 1Natsume M, Kamo Y, Hirayama M, et al. lsolaand characterization of alginate-derived oligosaccharides with root growth-promoting activities[J]. Carbohydr Res.1994, 258, 187.
  • 2Tomoda Y, Umemura K, Adachi T. Promotion of Barely Root Elongation under Hypoxic Conditions by alginate lyase-lysate [J]. Biosci Biotech Biochem, 1994, 58:202.
  • 3Quoc HN, Naotsugu N, Xuan TL, et al. GrowthPromotion of plants with depolymerized alginate by irradiation [J]. Radiation Phys Chem, 2000, 59(1) : 97.
  • 4Iwasaki K, Matsubara Y. Purification of alginate oligosaccharides with root growth- promoting activity toward lettuce [J]. Biosci Biotech Biochem. 2000, 64 (5):1067
  • 5Lee KY, Mooney DJ. Hydrogels in tissue engineer-ing [J]. ChemRev, 2001, 101(7): 1869.
  • 6Murata Y, Sasaki N, Miyamoto E, et al. Use of fioating alginate gel beads for stomach- specific drug delivery [J]. Eur J Pharma Biopharma , 2000, 50(2):221.
  • 7Constantinidis I, Rask I, Long RC, et al. Effects of alginate composition on the metabolic, secretory, and growth characteristics of entrapped bTC3 mouse insulinoma cells [J]. Biomaterials, 1999, 20(21); 2019.
  • 8KIck G, Pfeffermann A, Ryser C, et al. Biocompatibility of mannuronic acid-rich alginates [J]. Biomaterials, 1997, 18(10):707.
  • 9Orive G Ponce S,Hern RM,et al Biocompatibility of microcapsules for cell immobilization elaborated with different type of alginates [J]. Biomaterials, 2002, 23(18):3825.
  • 10Vacanti CA, Bonassar LJ, An overview of tissueengineered bone [J], Clin Orthop, 1999, 367: 375.

共引文献40

同被引文献13

引证文献1

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部