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超声增强刺激响应性和生物相容性苯丙氨酸衍生水凝胶的凝胶化

Ultrasound-Enhanced Gelation of Stimuli-Responsive and Biocompatible Phenylalanine-Derived Hydrogels.

作者信息

Buxaderas Eduardo, Moglie Yanina, Figueroa Aarón Baz, Alegre-Requena Juan V, Grijalvo Santiago, Saldías César, Herrera Raquel P, Marqués-López Eugenia, Díaz Díaz David

机构信息

Instituto de Química del Sur (CONICET-UNS), Departamento de Química, Universidad Nacional del Sur, Av. Alem 1253, Bahía Blanca 8000, Argentina.

Instituto Universitario de Bio-Orgánica Antonio González, Universidad de La Laguna, Avda. Astrofísico Francisco Sánchez 2, 38206 La Laguna, Spain.

出版信息

Gels. 2025 Feb 23;11(3):160. doi: 10.3390/gels11030160.

Abstract

Stimuli-responsive materials, particularly supramolecular hydrogels, exhibit a dynamic adaptability to external factors such as pH and ultrasound. Among these, phenylalanine (Phe)-derived hydrogels are promising due to their biocompatibility, biodegradability, and tunable properties, making them ideal for biomedical applications. This study explores the effects of pH and ultrasound on the gelation properties of -substituted Phe derivatives, with a primary focus on the role of ultrasound in optimizing the gelation process. A series of -substituted Phe derivatives were synthesized via reductive amination and hydrolysis. Hydrogel formation was possible with two of these compounds, namely and , using the following two methods: heating-cooling (H-C) and heating-ultrasound-cooling (H-US-C). The critical gelation concentration (CGC), gelation kinetics, thermal stability (), and viscoelastic properties were assessed. Morphological and cytotoxicity analyses were performed to confirm the suitability of these gels for biomedical applications. Both and derivatives demonstrated enhanced gelation under the H-US-C protocol compared to H-C, with notable reductions in CGC (up to 47%) and gelation time (by over 90%). Ultrasound-induced gels led to an improved network density and stability, while maintaining thermal reversibility and mechanical properties comparable to those of hydrogels formed without ultrasound. Cytotoxicity studies confirmed a high biocompatibility, with cell viability rates above 95% across the tested concentrations. Given the similar rheological and morphological properties of the hydrogels regardless of the preparation method, drug release experiments were performed with representative gel samples and demonstrated the efficient encapsulation and controlled release of 5-fluorouracil and methotrexate from the hydrogels, supporting their potential as pH-responsive drug delivery platforms. This study highlights the role of ultrasound as a powerful tool for accelerating and optimizing the gelation process of supramolecular hydrogels, which is particularly relevant for applications requiring rapid gel formation. The developed Phe-based hydrogels also demonstrate promising characteristics as drug delivery systems.

摘要

刺激响应性材料,特别是超分子水凝胶,对外部因素如pH值和超声波表现出动态适应性。其中,苯丙氨酸(Phe)衍生的水凝胶因其生物相容性、生物降解性和可调性而具有广阔前景,使其成为生物医学应用的理想选择。本研究探讨了pH值和超声波对β-取代Phe衍生物凝胶化性质的影响,主要关注超声波在优化凝胶化过程中的作用。通过还原胺化和水解合成了一系列β-取代Phe衍生物。其中两种化合物,即[具体化合物1]和[具体化合物2],可通过以下两种方法形成水凝胶:加热-冷却(H-C)和加热-超声-冷却(H-US-C)。评估了临界凝胶化浓度(CGC)、凝胶化动力学、热稳定性([具体热稳定性指标])和粘弹性性质。进行了形态学和细胞毒性分析,以确认这些凝胶在生物医学应用中的适用性。与H-C方法相比,[具体化合物1]和[具体化合物2]衍生物在H-US-C方案下均表现出增强的凝胶化,CGC显著降低(高达47%),凝胶化时间缩短(超过90%)。超声诱导的凝胶导致网络密度和稳定性提高,同时保持与无超声形成的水凝胶相当的热可逆性和机械性能。细胞毒性研究证实了高生物相容性,在测试浓度范围内细胞存活率高于95%。鉴于无论制备方法如何,水凝胶的流变学和形态学性质相似,对代表性凝胶样品进行了药物释放实验,结果表明水凝胶能够有效包封和控制释放5-氟尿嘧啶和甲氨蝶呤,支持其作为pH响应性药物递送平台的潜力。本研究强调了超声波作为加速和优化超分子水凝胶凝胶化过程的有力工具的作用,这对于需要快速凝胶形成的应用尤为重要。所开发的基于Phe的水凝胶作为药物递送系统也表现出有前景的特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb9/11942152/44f7bbaad46d/gels-11-00160-g001.jpg

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