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基于多价镍与聚组氨酸封端的聚乙二醇和 IDA 修饰的低聚壳聚糖的 pH 响应自修复水凝胶。

A pH-responsive self-healing hydrogel based on multivalent coordination of Ni with polyhistidine-terminated PEG and IDA-modified oligochitosan.

机构信息

CAS Key Laboratory of Soft Matter Chemistry, School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, 230026, P. R. China.

出版信息

J Mater Chem B. 2019 Jan 7;7(1):30-42. doi: 10.1039/c8tb02360c. Epub 2018 Nov 2.

Abstract

Metal coordination hydrogels have drawn intensive attention in controlled drug release due to their facile incorporation of stimuli and dynamic self-healing properties. However, many metal coordination hydrogels which are responsive to mild physiologically relevant stimuli are restricted by their poor stability in non-triggering environments. Here, we reported a new strategy for enhancing the neutral stability of a pH-responsive self-healing hydrogel based on multivalent metal coordination without loss of its responsiveness. The hydrogel was formed by multivalent coordination of Ni with polyhistidine (PHis) and multiple iminodiacetic acid (IDA) ligands which were modified on the terminal groups of polyethylene glycol (PEG) and the side groups of oligochitosan (OChi), respectively. By incorporating multivalent coordination, the hydrogel maintains its self-healing character and weak acid responsiveness; it can also be used as an injectable hydrogel by injecting it into a neutral environment. Through varying the PHis : IDA ratio, the mechanical strength and dynamic relaxation of the hydrogel can be regulated conveniently. More importantly, the hydrogels with multivalent coordination can remain stable and integral in neutral buffer (pH 7.4); meanwhile, they dissolve quickly in a weak acid environment (pH 5.5), which is similar to some tissue disease conditions. In contrast, the control hydrogel without multivalent coordination disintegrated within 4 hours in the neutral non-triggering buffer. Because the hydrogel consists of large amounts of coordinative Ni ions, it naturally possesses relatively high affinity to molecules containing polyhistidine motifs. Thus, pH-tuned controlled release of a model molecule, rhodamine-modified polyhistidine, was accomplished, with limited neutral leakage and quick release in weak acid. These results indicate potential applications for this multivalent coordination hydrogel in the controlled release field.

摘要

金属配位水凝胶由于其易于掺入刺激物和动态自修复特性,在控制药物释放方面引起了广泛关注。然而,许多对温和的生理相关刺激有响应的金属配位水凝胶受到其在非触发环境中稳定性差的限制。在这里,我们报道了一种新的策略,即在不损失其响应性的情况下,通过多价金属配位增强 pH 响应自修复水凝胶的中性稳定性。该水凝胶由多价镍与聚组氨酸(PHis)和多个亚氨基二乙酸(IDA)配体形成,聚组氨酸和多个亚氨基二乙酸配体分别修饰在聚乙二醇(PEG)末端基团和低聚壳聚糖(OChi)侧基上。通过引入多价配位,水凝胶保持其自修复特性和弱酸响应性;它也可以作为一种可注射水凝胶,注入到中性环境中。通过改变 PHis:IDA 的比例,可以方便地调节水凝胶的机械强度和动态松弛。更重要的是,具有多价配位的水凝胶可以在中性缓冲液(pH 7.4)中保持稳定和完整;同时,它们在弱酸环境(pH 5.5)中迅速溶解,类似于一些组织疾病状况。相比之下,没有多价配位的对照水凝胶在中性非触发缓冲液中在 4 小时内就会解体。由于水凝胶中含有大量配位的 Ni 离子,它自然对含有聚组氨酸基序的分子具有相对较高的亲和力。因此,实现了模型分子(罗丹明修饰的聚组氨酸)的 pH 调控控制释放,在中性条件下泄漏有限,在弱酸条件下快速释放。这些结果表明,这种多价配位水凝胶在控制释放领域具有潜在的应用前景。

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