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聚合物纳米胶囊的设计以提高其淋巴靶向能力。

Design of polymeric nanocapsules to improve their lympho-targeting capacity.

机构信息

Center for Research in Molecular Medicine & Chronic Diseases (CIMUS), Health Research Institute of Santiago de Compostela (IDIS), School of Pharmacy, Universidade de Santiago de Compostela, Campus Vida, 15706 Santiago de Compostela, Spain.

Institute for Research in Biomedicine, Università della Svizzera Italiana, via Vincenzo Vela 6, 6500 Bellinzona, Switzerland.

出版信息

Nanomedicine (Lond). 2019 Dec;14(23):3013-3033. doi: 10.2217/nnm-2019-0206. Epub 2019 Nov 7.

Abstract

To design lympho-targeted nanocarriers with the capacity to enhance the activity of associated drugs/antigens whose target is within the lymphatic system. : Inulin (INU)-based nanocapsules (NCs), negatively charged and positively charged chitosan NCs were prepared by the solvent displacement techniques. The NCs were produced in two sizes: small (70 nm) and medium (170-250 nm). results indicated that small NCs interacted more efficiently with dendritic cells than the larger ones. The study of the NCs biodistribution in mice, using 3D reconstruction of the popliteal lymph node, showed that small INU NCs have the greatest access and uniform accumulation in different subsets of resident immune cells. Small and negatively charged INU NCs have a potential as lympho-targeted antigen/drug nanocarriers.

摘要

设计具有增强药物/抗原活性的淋巴靶向纳米载体,这些药物/抗原的靶标位于淋巴系统内。:采用溶剂置换技术制备了基于菊粉(INU)的纳米胶囊(NC)、带负电荷和带正电荷的壳聚糖 NC。NC 制备成两种大小:小(70nm)和中(170-250nm)。结果表明,小 NC 与树突状细胞的相互作用比大 NC 更有效。通过对后肢淋巴结的 3D 重建研究 NC 的体内分布,表明小 INU NC 具有最大的进入和均匀地积累在不同的常驻免疫细胞亚群中的潜力。小的带负电荷的 INU NC 作为淋巴靶向抗原/药物纳米载体具有潜力。

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