用辛烷-1-胺改性的海藻酸钠水凝胶薄膜:增强的孔隙形成和在药物输送系统中的潜在应用

A. V. Sikach, V. V. Konovalova, I. S. Kolesnyk
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引用次数: 0

摘要

伤口敷料的使用越来越普及,特别是在战术和军事医学领域。开发能够促进伤口治疗和缩短愈合时间的伤口敷料是现代科学面临的挑战之一。因此,海藻酸钠(Alg)因其生物相容性、血液相容性和生物降解性而成为开发伤口敷料的良好候选材料。然而,海藻酸钠也有其不足之处,可以通过改性来解决。这项工作的目的是研究 Alg 改性对与 Ca2+ 离子交联的样品中乙铵释放动力学的影响。为此,研究人员开发了一种不使用有机溶剂、以 1-乙基-3-(3-二甲基氨基丙基)碳二亚胺盐酸盐(EDCl)为引发剂的海藻酸盐改性方法。海藻酸盐改性过程的最佳参数为温度 60 °С 和持续时间 24 小时。理化方法证实了改性的成功。使用氯化钙溶液作为交联剂,获得了基于辛烷-1-胺(AlgM)改性的海藻酸盐薄膜。我们对溶胀动力学进行了研究,发现基于 AlgM 的样品在 10 分钟后的溶胀程度(α = 0.71)是 Alg(α = 0.37)的两倍,这表明药物的释放速度更快。研究发现,乙铵的释放动力学不仅取决于溶胀动力学,还取决于药物的化学性质。将乙铵固定在海藻酸盐薄膜中作为杀菌药物模型。研究了乙铵在不同 pH 值下的释放动力学,这些 pH 值分别与健康皮肤(5.5)、开放性伤口(7.2)和发炎伤口(8.2)的 pH 值相对应。研究发现,与基于 Alg 的样品相比,基于 AlgM 的样品对 pH 值更为敏感,乙铵的释放时间也更长。产生这种效果的原因是,由于薄膜中的疏水-疏水相互作用,AlgM 出现了另一种保留乙铵的机制。在载药样品中观察到的延长释放特性使它们成为开发靶向给药系统和伤口敷料的理想候选材料,这与慢性伤口和烧伤伤口的治疗尤其相关。未来的研究重点是优化交联方法,探索改性海藻酸盐基材料在生物医学领域的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrogel films based on sodium alginate modified with octane-1-amine: enhanced pore formation and potential applications in drug delivery systems
The use of wound dressings is gaining more and more popularity, especially in the field of tactical and military medicine. Developing wound dressings capable of facilitating wound treatment and reducing healing time is one of the challenges of modern science. So, sodium alginate (Alg) is a good candidate for the development of wound dressings due to its bio- and hemocompatibility and biodegradability. However, Alg has its shortcomings, which can be dispatched by modification. The purpose of this work was to investigate the effect of Alg modification on the kinetics of ethonium release from crosslinked with Ca2+ ions samples. For this purpose, a method of Alg modifying with octane-1-amine was developed without the use of organic solvents and with the use of 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide hydrochloride (EDCl) as an initiator. The optimal parameters of alginate modification process were defined as 60 °С temperature and 24 hours duration. Physicochemical methods confirmed the success of the modification. Films based on the alginate modified with octane-1-amine (AlgM) were obtained using a calcium chloride solution as a crosslinker. The kinetics of swelling was studied and we found that the degree of swelling of the sample based on AlgM after 10 minutes is twice as large (α = 0.71) as for Alg (α = 0.37), which indicates a faster release of drugs. It has been found that the kinetics of release of ethonium depends not only on the kinetics of swelling but also on the chemical nature of the drug. The ethonium was immobilised in alginate films as a model of bactericidal drug. The kinetics of ethonium release was studied at different pH values corresponding to the pH of healthy skin (5.5), open wounds (7.2) and inflamed wounds (8.2). It was found that the release of ethonium from the sample based on AlgM is more pH-sensitive and prolonged, compared to the sample based on Alg. This effect is explained by the appearance of an additional mechanism of retention of ethonium by AlgM due to hydrophobic-hydrophobic interactions in the films. The prolonged release properties observed in the drug-loaded samples make them promising candidates for the development of targeted drug delivery systems and wound dressings, which are particularly relevant for the treatment of chronic and burn wounds. Future research will focus on optimizing the crosslinking method and exploring potential applications of modified alginate-based materials in biomedical sciences.
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