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壳寡糖的分子量和脱乙酰度对抗肿瘤活性的影响。

Effects of the molecular weight and the degree of deacetylation of chitosan oligosaccharides on antitumor activity.

作者信息

Park Jae Kweon, Chung Mi Ja, Choi Ha Na, Park Yong Il

机构信息

Department of Biotechnology, The Catholic University of Korea, Bucheon, Gyeonggi-do 420-743, Korea; E-Mails:

出版信息

Int J Mol Sci. 2011 Jan 6;12(1):266-77. doi: 10.3390/ijms12010266.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b78/3039952/84746086bddb/ijms-12-00266f1.jpg

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