Synthesis and pH-responsive properties of bacteria mimicking hydrogel capsules

Veronika Kozlovskaya and Eugenia Kharlampieva
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Abstract

The evolution of a non-spherical shape of microorganisms helped them survive by evading capture and digestion, which is crucial for their biological functioning. Synthetic imitation of the non-spherical shapes of various microorganisms and cells can enhance the ability of synthetic particulates to deliver therapeutics inside the body. Herein, we synthesized non-spherical polymer hydrogel microcapsules with bacteria-mimicking shapes, including prolate ellipsoid, peanut, and hourglass shapes similar to some pathogen microorganisms like Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Corynebacterium diphtheriae. The hydrogel shells were synthesized through a multilayer assembly of hydrogen-bonded poly(methacrylic acid) (PMAA) and non-ionic poly(N-vinylpyrrolidone) (PVPON) homopolymers on the surfaces of non-porous iron oxide microparticles of 2 μm in length. After covalent cross-linking of PMAA layers, followed by the release of PVPON at pH = 8 and the dissolution of the particle templates, curved rod-shaped (PMAA) multilayer hydrogel microcapsules with a pH-responsive shell were obtained. Attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) analysis confirmed the covalent cross-linking of the shell and the release of PVPON from the capsule shell networks. The (PMAA) hydrogel capsules demonstrated excellent retention of their ellipsoid, peanut, and hourglass shapes after core dissolution in acidic solutions despite a nanothin (∼40 nm) hydrogel membrane. Remarkably, all systems retained bacteria-like shapes in solutions at pH = 8, increasing in size by 20–30%, as confirmed by confocal fluorescence microscopy. All bacteria-like shaped microcapsules demonstrated homogeneous swelling in all directions regardless of the coating location at the initial particle perimeter, indicating similar cross-linking for all shapes and no effect of the iron oxide particle surfaces on the formation of the hydrogel shell. This work can help develop polymeric non-spherical particulates that are adaptable and on-demand for biomedical applications, including advanced targeting of pathological tissues and developing artificial cells with intelligent responses to environmental cues. Synthetic imitation of bacteria-like shapes and morphological flexibility demonstrated in this work using a multilayer assembly of polymer hydrogel capsules can bring new insights into the understanding and synthetic reproduction of properties essential for the synthetic particulates to evade the immune system and increase tissue targeting. These properties can be critical for developing unconventional particulates for controlled delivery and advanced imaging.

Abstract Image

模拟水凝胶胶囊细菌的合成及其ph响应特性
非球形微生物的进化帮助它们通过逃避捕获和消化而存活下来,这对它们的生物功能至关重要。合成模仿各种微生物和细胞的非球形形状可以增强合成颗粒在体内输送治疗药物的能力。在此,我们合成了具有细菌模拟形状的非球形聚合物水凝胶微胶囊,包括长形椭球状,花生状和沙漏状,类似于一些病原体微生物,如金黄色葡萄球菌,枯草芽孢杆菌,大肠杆菌和白喉棒状杆菌。将氢键聚甲基丙烯酸(PMAA)和非离子型聚n-乙烯基吡咯烷酮(PVPON)均聚物在长度为2 μm的无孔氧化铁微粒表面进行多层组装,合成了水凝胶壳。将PMAA层共价交联,在pH = 8时释放PVPON,溶解颗粒模板,得到具有pH响应壳的弯曲棒状(PMAA)多层水凝胶微胶囊。衰减全反射-傅里叶变换红外光谱(ATR-FTIR)分析证实了壳的共价交联和PVPON从胶囊壳网络释放。(PMAA)水凝胶胶囊在酸性溶液中溶解后,尽管有纳米薄(~ 40 nm)的水凝胶膜,但仍能很好地保持椭球、花生和沙漏形状。值得注意的是,共聚焦荧光显微镜证实,在pH = 8的溶液中,所有系统都保持了细菌样形状,尺寸增加了20-30%。所有类细菌形状的微胶囊在各个方向上都表现出均匀的膨胀,而与初始颗粒周长的涂层位置无关,这表明所有形状的微胶囊都具有相似的交联,并且氧化铁颗粒表面对水凝胶壳的形成没有影响。这项工作可以帮助开发适应性强且按需的非球形聚合物颗粒,用于生物医学应用,包括病理组织的高级靶向和开发对环境线索有智能反应的人工细胞。利用聚合物水凝胶胶囊的多层组装,合成模仿细菌样形状和形态灵活性,可以为合成颗粒逃避免疫系统和增加组织靶向性所必需的特性的理解和合成复制带来新的见解。这些特性对于开发非常规颗粒进行控制输送和高级成像至关重要。
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