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揭示基于刺激响应性丝素蛋白的离子凝胶配方的合理开发。

Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations.

作者信息

Shmool Talia A, Martin Laura K, Jirkas Andreas, Matthews Richard P, Constantinou Anna P, Vadukul Devkee M, Georgiou Theoni K, Aprile Francesco A, Hallett Jason P

机构信息

Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.

Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, U.K.

出版信息

Chem Mater. 2023 Jul 20;35(15):5798-5808. doi: 10.1021/acs.chemmater.3c00303. eCollection 2023 Aug 8.

Abstract

We present an approach for the rational development of stimuli-responsive ionogels which can be formulated for precise control of multiple unique ionogel features and fill niche pharmaceutical applications. Ionogels are captivating materials, exhibiting self-healing characteristics, tunable mechanical and structural properties, high thermal stability, and electroconductivity. However, the majority of ionogels developed require complex chemistry, exhibit high viscosity, poor biocompatibility, and low biodegradability. In our work, we overcome these limitations. We employ a facile production process and strategically integrate silk fibroin, the biocompatible ionic liquids (ILs) choline acetate ([Cho][OAc]), choline dihydrogen phosphate ([Cho][DHP]), and choline chloride ([Cho][Cl]), traditional pharmaceutical excipients, and the model antiepileptic drug phenobarbital. In the absence of ILs, we failed to observe gel formation; yet in the presence of ILs, thermoresponsive ionogels formed. Systems were assessed via visual tests, transmission electron microscopy, confocal reflection microscopy, dynamic light scattering, zeta potential and rheology measurements. We formed diverse ionogels of strengths ranging between 18 and 642 Pa. Under 25 °C storage, formulations containing polyvinylpyrrolidone (PVP) showed an ionogel formation period ranging over 14 days, increasing in the order of [Cho][DHP], [Cho][OAc], and [Cho][Cl]. Formulations lacking PVP showed an ionogel formation period ranging over 32 days, increasing in the order of [Cho][OAc], [Cho][DHP] and [Cho][Cl]. By heating from 25 to 60 °C, immediately following preparation, thermoresponsive ionogels formed below 41 °C in the absence of PVP. Based on our experimental results and density functional theory calculations, we attribute ionogel formation to macromolecular crowding and confinement effects, further enhanced upon PVP inclusion. Holistically, applying our rational development strategy enables the production of ionogels of tunable physicochemical and rheological properties, enhanced drug solubility, and structural and energetic stability. We believe our rational development approach will advance the design of biomaterials and smart platforms for diverse drug delivery applications.

摘要

我们提出了一种用于合理开发刺激响应性离子凝胶的方法,该方法可用于精确控制多种独特的离子凝胶特性,并满足特定的药物应用需求。离子凝胶是引人注目的材料,具有自愈特性、可调的机械和结构性能、高热稳定性和导电性。然而,大多数已开发的离子凝胶需要复杂的化学过程,表现出高粘度、生物相容性差和低生物降解性。在我们的工作中,我们克服了这些限制。我们采用简便的生产工艺,并策略性地整合了丝素蛋白、生物相容性离子液体(ILs)醋酸胆碱([Cho][OAc])、磷酸二氢胆碱([Cho][DHP])和氯化胆碱([Cho][Cl])、传统药物赋形剂以及抗癫痫模型药物苯巴比妥。在没有离子液体的情况下,我们未观察到凝胶形成;然而,在有离子液体的情况下,形成了热响应性离子凝胶。通过视觉测试、透射电子显微镜、共聚焦反射显微镜、动态光散射、zeta电位和流变学测量对体系进行了评估。我们形成了强度范围在18至642 Pa之间的多种离子凝胶。在25℃储存条件下,含有聚乙烯吡咯烷酮(PVP)的制剂显示离子凝胶形成期超过14天,按[Cho][DHP]、[Cho][OAc]和[Cho][Cl]的顺序增加。缺乏PVP的制剂显示离子凝胶形成期超过32天,按[Cho][OAc]、[Cho][DHP]和[Cho][Cl]的顺序增加。在制备后立即从25℃加热到60℃时,在没有PVP的情况下,热响应性离子凝胶在41℃以下形成。基于我们的实验结果和密度泛函理论计算,我们将离子凝胶的形成归因于大分子拥挤和限制效应,在加入PVP后进一步增强。总体而言,应用我们的合理开发策略能够生产出具有可调物理化学和流变学性质、增强药物溶解度以及结构和能量稳定性的离子凝胶。我们相信我们的合理开发方法将推动用于多种药物递送应用的生物材料和智能平台的设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62b9/10413859/05163ba9d963/cm3c00303_0002.jpg

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