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含多价三维过渡金属阳离子的海藻酸钠纳米凝胶的合成:在脲酶固定化中的应用

Synthesis of Alginate Nanogels with Polyvalent 3D Transition Metal Cations: Applications in Urease Immobilization.

作者信息

Saxena Abhishek, Sharda Shivani, Kumar Sumit, Kumar Benu, Shirodkar Sheetal, Dahiya Praveen, Sahney Rachana

机构信息

Amity Institute of Biotechnology, Amity University Uttar Pradesh, Noida 201303, India.

Radioanalytical Chemistry Division, Radiological Laboratories, Bhabha Atomic Research Centre, Mumbai 40008, India.

出版信息

Polymers (Basel). 2022 Mar 22;14(7):1277. doi: 10.3390/polym14071277.

Abstract

Biocompatible nanogels are highly in demand and have the potential to be used in various applications, e.g., for the encapsulation of sensitive biomacromolecules. In the present study, we have developed water-in-oil microemulsions of sodium alginate sol/hexane/Span 20 as a template for controlled synthesis of alginate nanogels, cross-linked with 3d transition metal cations (Mn, Fe, and Co). The results suggest that the stable template of 110 nm dimensions can be obtained by microemulsion technique using Span 20 at concentrations of 10mM and above, showing a zeta potential of -57.3 mV. A comparison of the effects of the cross-links on the morphology, surface charge, protein (urease enzyme) encapsulation properties, and stability of the resulting nanogels were studied. Alginate nanogels, cross-linked with Mn, Fe, or Co did not show any gradation in the hydrodynamic diameter. The shape of alginate nanogels, cross-linked with Mn or Co, were spherical; whereas, nanogels cross-linked with Fe (Fe-alginate) were non-spherical and rice-shaped. The zeta potential, enzyme loading efficiency, and enzyme activity of Fe-alginate was the highest among all the nanogels studied. It was found that the morphology of particles influenced the percent immobilization, loading capacity, and loading efficiency of encapsulated enzymes. These particles are promising candidates for biosensing and efficient drug delivery due to their relatively high loading capacity, biocompatibility, easy fabrication, and easy handling.

摘要

生物相容性纳米凝胶的需求量很大,并且有潜力用于各种应用,例如用于封装敏感生物大分子。在本研究中,我们制备了海藻酸钠溶胶/己烷/司盘20的油包水微乳液作为模板,用于可控合成与3d过渡金属阳离子(锰、铁和钴)交联的海藻酸钠纳米凝胶。结果表明,使用浓度为10mM及以上的司盘20通过微乳液技术可获得尺寸为110nm的稳定模板,其zeta电位为-57.3mV。研究了交联对所得纳米凝胶的形态、表面电荷、蛋白质(脲酶)封装性能和稳定性的影响。与锰、铁或钴交联的海藻酸钠纳米凝胶在流体动力学直径上没有显示出任何梯度变化。与锰或钴交联的海藻酸钠纳米凝胶形状为球形;而与铁交联的纳米凝胶(铁-海藻酸钠)是非球形的,呈米粒状。在所有研究的纳米凝胶中,铁-海藻酸钠的zeta电位、酶负载效率和酶活性最高。发现颗粒的形态影响包封酶的固定化百分比、负载量和负载效率。由于其相对较高的负载能力、生物相容性、易于制造和易于处理,这些颗粒是生物传感和高效药物递送的有前途的候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38e2/9002911/6a89631e4ad0/polymers-14-01277-g001.jpg

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