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基于含有阿魏酸/羟丙基-β-环糊精包合物的混合静电纺丝麦醇溶蛋白纳米纤维的活性食品包装涂层

Active Food Packaging Coatings Based on Hybrid Electrospun Gliadin Nanofibers Containing Ferulic Acid/Hydroxypropyl-Beta-Cyclodextrin Inclusion Complexes.

作者信息

Sharif Niloufar, Golmakani Mohammad-Taghi, Niakousari Mehrdad, Hosseini Seyed Mohammad Hashem, Ghorani Behrouz, Lopez-Rubio Amparo

机构信息

Department of Food Science and Technology, School of Agriculture, Shiraz University, km 12 Shiraz-Esfahan Highway, 71441-65186 Shiraz, Iran.

Department of Food Nanotechnology, Research Institute of Food Science and Technology (RIFST), km 12 Mashhad-Quchan Highway, 91895/157/356 Mashhad, Iran.

出版信息

Nanomaterials (Basel). 2018 Nov 7;8(11):919. doi: 10.3390/nano8110919.

DOI:10.3390/nano8110919
PMID:30405064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6266051/
Abstract

In this work, hybrid gliadin electrospun fibers containing inclusion complexes of ferulic acid (FA) with hydroxypropyl-beta-cyclodextrins (FA/HP-β-CD-IC) were prepared as a strategy to increase the stability and solubility of the antioxidant FA. Inclusion complex formation between FA and HP-β-CD was confirmed by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimeter (DSC), and X-ray diffraction (XRD). After adjusting the electrospinning conditions, beaded-free fibers of gliadin incorporating FA/HP-β-CD-IC with average fiber diameters ranging from 269.91 ± 73.53 to 271.68 ± 72.76 nm were obtained. Control gliadin fibers containing free FA were also produced for comparison purposes. The incorporation of FA within the cyclodextrin molecules resulted in increased thermal stability of the antioxidant compound. Moreover, formation of the inclusion complexes also enhanced the FA photostability, as after exposing the electrospun fibers to UV light during 60 min, photodegradation of the compound was reduced in more than 30%. Moreover, a slower degradation rate was also observed when compared to the fibers containing the free FA. Results from the release into two food simulants (ethanol 10% and acetic acid 3%) and PBS also demonstrated that the formation of the inclusion complexes successfully resulted in improved solubility, as reflected from the faster and greater release of the compounds in the three assayed media. Moreover, in both types of hybrid fibers, the antioxidant capacity of FA was kept, thus confirming the suitability of electrospinning for the encapsulation of sensitive compounds, giving raise to nanostructures with potential as active packaging structures or delivery systems of use in pharmaceutical or biomedical applications.

摘要

在本研究中,制备了含有阿魏酸(FA)与羟丙基-β-环糊精(FA/HP-β-CD-IC)包合物的混合麦醇溶蛋白电纺纤维,作为提高抗氧化剂FA稳定性和溶解性的一种策略。通过傅里叶变换红外光谱(FTIR)、差示扫描量热仪(DSC)和X射线衍射(XRD)证实了FA与HP-β-CD之间形成了包合物。调整电纺条件后,获得了平均纤维直径在269.91±73.53至271.68±72.76nm之间、不含珠粒的含有FA/HP-β-CD-IC的麦醇溶蛋白纤维。还制备了含有游离FA的对照麦醇溶蛋白纤维用于比较。FA纳入环糊精分子导致抗氧化化合物的热稳定性增加。此外,包合物的形成还增强了FA的光稳定性,因为在将电纺纤维暴露于紫外光60分钟后,该化合物的光降解减少了30%以上。而且,与含有游离FA的纤维相比,降解速率也较慢。在两种食品模拟物(10%乙醇和3%乙酸)和磷酸盐缓冲盐溶液(PBS)中的释放结果也表明,包合物的形成成功地提高了溶解性,这从三种测定介质中化合物更快、更多的释放中得到体现。此外,在两种类型的混合纤维中,FA的抗氧化能力得以保持,从而证实了电纺用于封装敏感化合物的适用性,产生了具有作为活性包装结构或用于制药或生物医学应用的递送系统潜力的纳米结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/ad87780db3ef/nanomaterials-08-00919-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/c8a324d975ae/nanomaterials-08-00919-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/f3bb0d1dc551/nanomaterials-08-00919-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/b77d27a434ab/nanomaterials-08-00919-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/7109d857eb2a/nanomaterials-08-00919-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/0425bd59afac/nanomaterials-08-00919-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/ad87780db3ef/nanomaterials-08-00919-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/c8a324d975ae/nanomaterials-08-00919-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/f3bb0d1dc551/nanomaterials-08-00919-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/b77d27a434ab/nanomaterials-08-00919-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/7109d857eb2a/nanomaterials-08-00919-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/0425bd59afac/nanomaterials-08-00919-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c210/6266051/ad87780db3ef/nanomaterials-08-00919-g006.jpg

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