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源自酿酒酵母的水溶性葡聚糖硫酸酯的开发、理化特性及临床前疗效评估

Development, physicochemical characterization and preclinical efficacy evaluation of a water soluble glucan sulfate derived from Saccharomyces cerevisiae.

作者信息

Williams D L, Pretus H A, McNamee R B, Jones E L, Ensley H E, Browder I W, Di Luzio N R

机构信息

Department of Physiology, Tulane University School of Medicine, New Orleans, Louisiana 70112-2699.

出版信息

Immunopharmacology. 1991 Nov-Dec;22(3):139-55. doi: 10.1016/0162-3109(91)90039-2.

Abstract

This report describes the development, characterization and preclinical efficacy evaluation of water soluble glucan sulfate. Glucan sulfate was derived from insoluble beta-1,3-D-glucan isolated from Saccharomyces cerevisiae. The proposed repeating unit empirical formula of glucan sulfate is [(C6H10O5)5.3H2SO4]n. Two polymer peaks were resolved by aqueous high-performance size exclusion chromatography (HPSEC) with on-line multi-angle laser light scattering (MALLS) photometry and differential viscometry. Peak 1 (MW = 1219697 Da) represents approximately 1% of the total polymers, while peak 2 (MW = 8884 Da) accounts for approximately 99% of polymers. 13C-NMR spectroscopy suggests that glucan sulfate polymer strands may be partially cross-linked. Glucan sulfate (250 mg/kg, i.v.) increased (P less than 0.01) macrophage vascular clearance of 131I-reticuloendothelial emulsion by 42% (P less than 0.01) and in vitro bone marrow proliferation by 46% (P less than 0.05). Glucan sulfate (250 mg/kg, i.v.) increased (P less than 0.05) median survival time of C57B1/6J mice with syngeneic melanoma B16 or sarcoma M5076. In addition, glucan sulfate immunoprophylaxis increased resistance of mice to challenge with Escherichia coli, Candida albicans or Mouse Hepatitis Virus strain A-59. We concluded that: (1) insoluble beta-1,3-D-glucan can be converted to a water soluble sulfated form; (2) glucan sulfate activates macrophages and stimulates bone marrow; (3) glucan sulfate exerts antitumor therapeutic activity, and (4) glucan sulfate immunoprophylaxis will modify the course of experimental infectious disease.

摘要

本报告描述了水溶性葡聚糖硫酸酯的研发、特性及临床前疗效评估。葡聚糖硫酸酯源自从酿酒酵母中分离出的不溶性β-1,3-D-葡聚糖。葡聚糖硫酸酯的提议重复单元经验式为[(C6H10O5)5.3H2SO4]n。通过配备在线多角度激光光散射(MALLS)光度法和示差粘度法的水性高效尺寸排阻色谱(HPSEC)解析出两个聚合物峰。峰1(分子量 = 1219697道尔顿)约占聚合物总量的1%,而峰2(分子量 = 8884道尔顿)约占聚合物总量的99%。13C-核磁共振光谱表明葡聚糖硫酸酯聚合物链可能部分交联。葡聚糖硫酸酯(250毫克/千克,静脉注射)使131I-网状内皮乳液的巨噬细胞血管清除率提高了42%(P < 0.01),体外骨髓增殖提高了46%(P < 0.05)。葡聚糖硫酸酯(250毫克/千克,静脉注射)使患有同基因黑色素瘤B16或肉瘤M5076的C57B1/6J小鼠的中位生存时间延长(P < 0.05)。此外,葡聚糖硫酸酯免疫预防增强了小鼠对大肠杆菌、白色念珠菌或小鼠肝炎病毒A-59株攻击的抵抗力。我们得出以下结论:(1)不溶性β-1,3-D-葡聚糖可转化为水溶性硫酸化形式;(2)葡聚糖硫酸酯激活巨噬细胞并刺激骨髓;(3)葡聚糖硫酸酯具有抗肿瘤治疗活性;(4)葡聚糖硫酸酯免疫预防将改变实验性传染病的病程。

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