Huang Ronghua, Mendis Eresha, Kim Se-Kwon
Department of Chemistry, Pukyong National University, Busan 608-737, South Korea.
Int J Biol Macromol. 2005 Jul;36(1-2):120-7. doi: 10.1016/j.ijbiomac.2005.05.001.
Scavenging activity of hydroxyethyl chitosan sulfate (HCS) against 2,2-diphenyl-1-picrylhydrazyl (DPPH), hydroxyl and carbon-centered radical species were studied using electron spin resonance (ESR) spectroscopy. In addition, its antioxidant activity to retard lipid peroxidation was also evaluated in a linoleic acid model system. HCS could scavenge DPPH (33.78%, 2.5 mg/mL) and carbon-centered radicals (67.74%, 0.25 mg/mL) effectively. However, chitosan sulfate did not exhibit any scavenging activity against hydroxyl radicals, but increased its generation. This was different from the published literature and was presumed due to the loss of chelating ability on Fe2+. This assumption could further confirm from the results obtained for Fe2+-ferrozine method that upon sulfation chitooligosaccharides lost its chelation properties. Therefore, HCS can be identified as antioxidant that effectively scavenges carbon centered radicals to retard lipid peroxidation.
使用电子自旋共振(ESR)光谱研究了硫酸羟乙基壳聚糖(HCS)对2,2-二苯基-1-苦基肼自由基(DPPH)、羟基自由基和碳中心自由基的清除活性。此外,还在亚油酸模型体系中评估了其抑制脂质过氧化的抗氧化活性。HCS能有效清除DPPH(33.78%,2.5mg/mL)和碳中心自由基(67.74%,0.25mg/mL)。然而,硫酸壳聚糖对羟基自由基没有任何清除活性,反而增加了其生成。这与已发表的文献不同,推测是由于对Fe2+的螯合能力丧失。这一假设可以从Fe2+-菲罗嗪法得到的结果进一步证实,即硫酸化的壳寡糖失去了其螯合性能。因此,HCS可被鉴定为一种抗氧化剂,能有效清除碳中心自由基以抑制脂质过氧化。