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淀粉膜的无序化作为影响生物活性物质释放速率的一个因素。

Disordering of Starch Films as a Factor Influencing the Release Rate of Biologically Active Substances.

作者信息

Podgorbunskikh Ekaterina, Kuskov Timofei, Matveeva Anna, Ulihin Artem, Bychkov Aleksey, Lomovskiy Igor, Polienko Yuliya

机构信息

Institute of Solid State Chemistry and Mechanochemistry SB RAS, 18 Kutateladze Str., 630090 Novosibirsk, Russia.

Department of Natural Sciences, Novosibirsk State University, 2 Pirogova Str., 630090 Novosibirsk, Russia.

出版信息

Polymers (Basel). 2023 May 13;15(10):2303. doi: 10.3390/polym15102303.

Abstract

The release of a spin probe (nitroxide radical) from polymer films was studied by electron paramagnetic resonance (EPR). The films were fabricated from starch having different crystal structures (A-, B-, and C-types) and disordering degrees. Film morphology (analysis of the scanning electron microscopy (SEM)) depended on the presence of dopant (nitroxide radical) to a larger extent rather than on crystal structure ordering or polymorphic modification. The presence of nitroxide radical led to additional crystal structure disordering and reduced the crystallinity index from the X-ray diffraction (XRD) data. Polymeric films made of amorphized starch powder were able to undergo recrystallization (crystal structure rearrangement), which manifested itself as an increase in crystallinity index and phase transition of the A- and C-type crystal structures to the B-type one. It was demonstrated that nitroxide radical does not form an individual phase during film preparation. According to the EPR data, local permittivity of starch-based films varied from 52.5 to 60.1 F/m, while bulk permittivity did not exceed 17 F/m, which demonstrates that local concentration of water is increased in the regions near the nitroxide radical. The mobility of the spin probe corresponds to small stochastic librations and is indicative of the strongly a mobilized state. The application of kinetic models made it possible to find out that substance release from biodegradable films consists of two stages: matrix swelling and spin probe diffusion through the matrix. Investigation of the release kinetics for nitroxide radical demonstrated that the course of this process depends on the type of crystal structure of native starch.

摘要

通过电子顺磁共振(EPR)研究了自旋探针(氮氧自由基)从聚合物薄膜中的释放。这些薄膜由具有不同晶体结构(A 型、B 型和 C 型)和无序度的淀粉制成。薄膜形态(扫描电子显微镜(SEM)分析)在很大程度上取决于掺杂剂(氮氧自由基)的存在,而不是晶体结构的有序性或多晶型改性。氮氧自由基的存在导致额外的晶体结构无序,并根据 X 射线衍射(XRD)数据降低了结晶度指数。由非晶态淀粉粉末制成的聚合物薄膜能够发生重结晶(晶体结构重排),表现为结晶度指数增加以及 A 型和 C 型晶体结构向 B 型晶体结构的相变。结果表明,在薄膜制备过程中氮氧自由基不会形成单独的相。根据 EPR 数据,淀粉基薄膜的局部介电常数在 52.5 至 60.1 F/m 之间变化,而体介电常数不超过 17 F/m,这表明在氮氧自由基附近区域水的局部浓度增加。自旋探针的迁移率对应于小的随机摆动,表明处于强烈的非移动状态。应用动力学模型可以发现,生物可降解薄膜中物质的释放包括两个阶段:基质溶胀和自旋探针通过基质的扩散。对氮氧自由基释放动力学的研究表明,该过程的进程取决于天然淀粉的晶体结构类型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa64/10222158/4b0b11d62c0e/polymers-15-02303-g001.jpg

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