Yourdkhani Mostafa, Leme-Kraus Ariene Arcas, Aydin Berdan, Bedran-Russo Ana Karina, White Scott R
Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, 405 North Mathews Avenue, Urbana, IL 61801, USA.
Department of Restorative Dentistry, College of Dentistry, University of Illinois at Chicago, 801 South Paulina Street, Chicago, IL 60612, USA.
Dent Mater. 2017 Jun;33(6):630-636. doi: 10.1016/j.dental.2017.03.009. Epub 2017 Apr 6.
To sustain the bioactivity of proanthocyanidins-rich plant-derived extracts via encapsulation within biodegradable polymer microcapsules.
Polylactide microcapsules containing grape seed extract (GSE) were manufactured using a combination of double emulsion and solvent evaporation techniques. Microcapsule morphology, size distribution, and cross-section were examined via scanning electron microscopy. UV-vis measurements were carried out to evaluate the core loading and encapsulation efficiency of microcapsules. The bioactivity of extracts was evaluated after extraction from capsules via solvent partitioning one week or one year post-encapsulation process. Fifteen human molars were cut into 7mm×1.7mm×0.5mm thick mid-coronal dentin beams, demineralized, and treated with either encapsulated GSE, pristine GSE, or left untreated. The elastic modulus of dentin specimens was measured based on three-point bending experiments as an indirect assessment of the bioactivity of grape seed extracts. The effects of the encapsulation process and storage time on the bioactivity of extracts were analyzed.
Polynuclear microcapsules with average diameter of 1.38μm and core loading of up to 38wt% were successfully manufactured. There were no statistically significant differences in the mean fold increase of elastic modulus values among the samples treated with encapsulated or pristine GSE (p=0.333), or the storage time (one week versus one year storage at room temperature, p=0.967).
Polynuclear microcapsules containing proanthocyanidins-rich plant-derived extracts were prepared. The bioactivity of extracts was preserved after microencapsulation.
通过将富含原花青素的植物提取物包封在可生物降解的聚合物微胶囊中来维持其生物活性。
采用复乳法和溶剂蒸发技术相结合的方法制备了含有葡萄籽提取物(GSE)的聚乳酸微胶囊。通过扫描电子显微镜检查微胶囊的形态、尺寸分布和横截面。进行紫外可见光谱测量以评估微胶囊的核心负载量和包封效率。在包封过程后一周或一年通过溶剂分配从胶囊中提取提取物后,评估提取物的生物活性。将15颗人类磨牙切成7mm×1.7mm×0.5mm厚的中冠牙本质梁,进行脱矿处理,并用包封的GSE、原始GSE处理或不进行处理。基于三点弯曲实验测量牙本质标本的弹性模量,作为葡萄籽提取物生物活性的间接评估。分析了包封过程和储存时间对提取物生物活性的影响。
成功制备了平均直径为1.38μm、核心负载量高达38wt%的多核微胶囊。在用包封的或原始的GSE处理的样品之间,弹性模量值的平均增加倍数没有统计学上的显著差异(p = 0.333),储存时间(室温下储存一周与一年,p = 0.967)之间也没有显著差异。
制备了含有富含原花青素的植物提取物的多核微胶囊。微胶囊化后提取物的生物活性得以保留。