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构建一种微流控平台,该平台带有核壳结构的CdSSe@ZnS量子点编码超顺磁性氧化铁微球,用于从[具体水果名称]果实中筛选和定位基质金属蛋白酶-2抑制剂

Construction of a Microfluidic Platform With Core-Shell CdSSe@ZnS Quantum Dot-Encoded Superparamagnetic Iron Oxide Microspheres for Screening and Locating Matrix Metalloproteinase-2 Inhibitors From Fruits of .

作者信息

Tao Yi, Pan Meiling, Zhu Fei, Liu Qing, Wang Ping

机构信息

College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, China.

出版信息

Front Nutr. 2022 Apr 14;9:869528. doi: 10.3389/fnut.2022.869528. eCollection 2022.

Abstract

The microfluidic platform is a versatile tool for screening and locating bioactive molecules from functional foods. Here, a layer-by-layer assembly approach was used to fabricate core-shell CdSSe@ZnS quantum dot encoded superparamagnetic iron oxide microspheres, which served as a carrier for matrix metalloproteinase-2. The matrix metalloproteinase-2 camouflaged magnetic microspheres was further incorporated into a homemade microfluidic platform and incubated with extracts of fruits of . The flow rate of the microfluidic platform was tuned. The major influencing parameters on ligand binding, such as dissociate solvents, incubation pH, ion strength, temperature, and incubation time were also optimized by using ellagic acid as a model compound. The specific binding ligands were sent for structure elucidation by mass spectrometry. The absolute recovery of ellagic acid ranged from 101.14 to 102.40% in the extract of under the optimal extraction conditions. The linearity was pretty well in the range of 0.009-1.00 mg·ml ( = 0.9995). The limit of detection was 0.003 mg·ml. The relative SDs of within-day and between-day precision were <1.91%. A total of thirteen ligands were screened out from fruits of , which were validated for their inhibitory effect by enzyme assay. Of note, eleven new matrix metalloproteinase-2 inhibitors were identified, which may account for the antitumor effect of fruits of .

摘要

微流控平台是一种用于从功能性食品中筛选和定位生物活性分子的多功能工具。在此,采用层层组装方法制备了核壳型硫化镉硒@硫化锌量子点编码的超顺磁性氧化铁微球,其作为基质金属蛋白酶-2的载体。将伪装的基质金属蛋白酶-2磁性微球进一步整合到自制的微流控平台中,并与[具体水果名称]果实提取物孵育。对微流控平台的流速进行了调整。还以鞣花酸为模型化合物,对配体结合的主要影响参数,如解离溶剂、孵育pH值、离子强度、温度和孵育时间进行了优化。将特异性结合配体送去进行质谱结构解析。在最佳提取条件下,鞣花酸在[具体水果名称]提取物中的绝对回收率为101.14%至102.40%。在0.009 - 1.00 mg·ml范围内线性良好(r² = 0.9995)。检测限为0.003 mg·ml。日内和日间精密度的相对标准差均<1.91%。从[具体水果名称]果实中总共筛选出13种配体,通过酶测定法验证了它们的抑制作用。值得注意的是,鉴定出了11种新的基质金属蛋白酶-2抑制剂,这可能解释了[具体水果名称]果实的抗肿瘤作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17ae/9046974/7e807629fcbe/fnut-09-869528-g0001.jpg

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