Abstract:
The present invention relates to a core-shell network structure formed using a biocompatible biopolymer and to a composition comprising same. Said structure can be used as an alternative to synthetic chemical materials, such as polyethylene glycol (PEG), to effectively disperse an insoluble effective substance within a composition, thus addressing safety issues, and formulations can be preserved stably for a long time through said network structure. Furthermore, said structure and the composition comprising same may provide useful benefits for the skin in terms of skin barrier enhancement, skin moisturization, skin regeneration, or the like.
Abstract:
The present disclosure relates to a drug delivery carrier containing a lipid structure or a polymer particle which is covalently bonded to a cell-penetrating AP-GRR peptide (SEQ ID NO 1) or is modified with the peptide chain containing the peptide. The present disclosure also relates to a composition containing the drug delivery carrier and a physiologically active ingredient encapsulated in the carrier. The drug delivery carrier of the present disclosure can effectively deliver macromolecules that are difficult to be delivered into cells, thereby improving the bioavailability of the macromolecules.
Abstract translation:本公开内容涉及含有脂质结构或聚合物颗粒的药物递送载体,其共价结合到细胞穿透性AP-GRR肽(SEQ ID NO 1)或用含有肽的肽链进行修饰。 本公开还涉及包含药物递送载体和包封在载体中的生理活性成分的组合物。 本公开的药物递送载体可以有效地递送难以递送到细胞中的大分子,从而提高大分子的生物利用度。