Park Jae Kweon, Chung Mi Ja, Choi Ha Na, Park Yong Il
Department of Biotechnology, The Catholic University of Korea, Bucheon, Gyeonggi-do 420-743, Korea; E-Mails:
Int J Mol Sci. 2011 Jan 6;12(1):266-77. doi: 10.3390/ijms12010266.
Effects of the degree of deacetylation (DDA) and the molecular mass of chitosan oligosaccharides (CTS-OS), obtained from the enzymatic hydrolysis of high molecular weight chitosan (HMWC), on antitumor activity was explored. The DDA and molecular weights of CTS-OS were determined by matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-TOF MS) analysis. The CTS-OS were found to be a mixture of mainly dimers (18.8%), trimers (24.8%), tetramers (24.9%), pentamers (17.7%), hexamers (7.1%), heptamers (3.3%), and octamers (3.4%). The CTS-OS were further fractionated by gel-filtration chromatography into two major fractions: (1) COS, consisting of glucosamine (GlcN)(n), n = 3-5 with DDA 100%; and (2) HOS, consisting of (GlcN)(5) as the minimum residues and varying number of N-acetylglucosamine (GlcNAc)(n), n = 1-2 with DDA about 87.5% in random order. The cytotoxicities, expressed as the concentration needed for 50% cell death (CC(50)), of CTS-OS, COS, and HOS against PC3 (prostate cancer cell), A549 (lung cancer cell), and HepG2 (hepatoma cell), were determined to be 25 μg·mL(-1), 25 μg·mL(-1), and 50 μg·mL(-1), respectively. The HMWC was approximately 50% less effective than both CTS-OS and COS. These results demonstrate that the molecular weight and DDA of chitosan oligosaccharides are important factors for suppressing cancer cell growth.
研究了由高分子量壳聚糖(HMWC)酶解得到的壳寡糖(CTS-OS)的脱乙酰度(DDA)和分子量对其抗肿瘤活性的影响。通过基质辅助激光解吸/电离质谱(MALDI-TOF MS)分析确定了CTS-OS的DDA和分子量。发现CTS-OS主要是二聚体(18.8%)、三聚体(24.8%)、四聚体(24.9%)、五聚体(17.7%)、六聚体(7.1%)、七聚体(3.3%)和八聚体(3.4%)的混合物。CTS-OS通过凝胶过滤色谱进一步分离为两个主要部分:(1)COS,由葡萄糖胺(GlcN)(n)组成,n = 3 - 5,DDA为100%;(2)HOS,以(GlcN)(5)为最小残基,含有不同数量的N-乙酰葡萄糖胺(GlcNAc)(n),n = 1 - 2,DDA约为87.5%,排列随机。测定了CTS-OS、COS和HOS对PC3(前列腺癌细胞)、A549(肺癌细胞)和HepG2(肝癌细胞)的细胞毒性,以50%细胞死亡所需浓度(CC(50))表示,分别为25 μg·mL(-1)、25 μg·mL(-1)和50 μg·mL(-1)。HMWC的效果比CTS-OS和COS都低约50%。这些结果表明壳寡糖的分子量和DDA是抑制癌细胞生长的重要因素。