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一种对 pH 响应的羧酸化 β-1,3-葡聚糖多糖,用于与聚合物客体形成配合物。

A pH-responsive carboxylic β-1,3-glucan polysaccharide for complexation with polymeric guests.

机构信息

Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Nishi-ku, Moto-oka 744, Fukuoka, 819-0395, Japan.

出版信息

Org Biomol Chem. 2011 Jun 7;9(11):4266-75. doi: 10.1039/c1ob05114h. Epub 2011 Apr 11.

Abstract

The helix-forming nature of β-1,3-glucan polysaccharides is a characteristic that has potential for producing gene carriers, bio-nanomaterials and other chiral nanowires. Herein, carboxylic curdlan (CurCOOH) bearing the β-1,3-polyglucuronic acid structure was successfully prepared from β-1,3-glucan polysaccharide curdlan (Cur) by one-step oxidation using a 4-acetamido-TEMPO/NaClO/NaClO(2) system as the oxidant. The resulting high-molecular-weight CurCOOH was proved to bear the 6-COOH group in 100% purity. The optical rotatory dispersion (ORD) spectra indicated that the obtained CurCOOH behaves as a water-soluble single-strand in various pH aqueous media. This advantage has allowed us to use CurCOOH as a polymeric host to form various macromolecular complexes. For example, complexation of CurCOOH with single-walled carbon nanotubes (SWNTs) resulted in a water-soluble one-dimensional architecture, which formed a dispersion in aqueous solution that was stable for several months, and much more stable than SWNTs complexes of the similar negatively-charged polyacrylic acid (PAA) and polymethacrylic acid (PMAA). It was shown that in the complex, SWNTs are effectively wrapped by a small amount of CurCOOH, enabling them to avoid electrostatic repulsion. This pH-responsive CurCOOH formed a very stable complex with cationic water-soluble polythiophenes (PT-1), which was stabilized not only by the hydrophobic interaction but also by the electrostatic attraction between trimethylammonium cations in PT-1 and dissociated anionic COO(-) groups in CurCOOH. The included PT-1 became CD-active only in the neutral to basic pH region, and the positive Cotton effect suggested that the conjugated main chain is twisted in the right-handed direction. We also found that CurCOOH can interact with polycytidylic acid (poly(C)) only under high NaCl concentrations, the binding and release of which could be controlled by a change in the salt concentration. We believe, therefore, that CurCOOH bearing a dissociable COOH group can act as a new potential polymeric host to construct novel polymeric complexes applicable for gene carriers, biosensors, chiral polymer assemblies, etc.

摘要

β-1,3-葡聚糖多糖的螺旋形成性质是一种具有生产基因载体、生物纳米材料和其他手性纳米线的潜力的特性。在此,通过使用 4-乙酰氨基-TEMPO/NaClO/NaClO(2)系统作为氧化剂对β-1,3-葡聚糖多糖凝乳多糖(Cur)进行一步氧化,成功制备了具有β-1,3-多葡糖醛酸结构的羧酸凝乳多糖(CurCOOH)。结果表明,所得的高分子量 CurCOOH 具有 100%纯度的 6-COOH 基团。旋光色散(ORD)光谱表明,所得的 CurCOOH 在各种 pH 水性介质中表现为水溶性单链。这一优势使我们能够使用 CurCOOH 作为聚合物主体形成各种大分子配合物。例如,CurCOOH 与单壁碳纳米管(SWNTs)的络合导致形成了一种水溶性一维结构,在水溶液中形成了分散体,该分散体在几个月内稳定,比具有相似负电荷的聚丙烯酸(PAA)和聚甲基丙烯酸(PMAA)的 SWNTs 络合物稳定得多。结果表明,在复合物中,SWNTs 被少量的 CurCOOH 有效地包裹,从而使它们能够避免静电排斥。这种 pH 响应性的 CurCOOH 与阳离子水溶性聚噻吩(PT-1)形成了非常稳定的复合物,这种稳定性不仅由疏水相互作用稳定,而且由 PT-1 中的三甲基铵阳离子与 CurCOOH 中解离的阴离子 COO(-)基团之间的静电吸引稳定。包含的 PT-1 仅在中性至碱性 pH 区域具有 CD 活性,正 Cotton 效应表明共轭主链以右手方向扭曲。我们还发现,只有在高 NaCl 浓度下,CurCOOH 才能与聚胞嘧啶核苷酸(poly(C))相互作用,其结合和释放可以通过改变盐浓度来控制。因此,我们认为具有可解离 COOH 基团的 CurCOOH 可以作为一种新的潜在聚合物主体,用于构建适用于基因载体、生物传感器、手性聚合物组装等的新型聚合物配合物。

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