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玛咖提取物包封多功能基质的设计,以支持细胞功能,刺激胶原蛋白合成,减少伤口感染。

Design of multiple-function matrix encapsulated with Marjoram extract to support cellular functions, stimulate collagen synthesis and decrease infection in wound.

机构信息

Department of Chemical Engineering, Ayatollah Amoli Branch, Islamic Azad University, Amol, Iran.

出版信息

Sci Rep. 2024 Sep 10;14(1):21109. doi: 10.1038/s41598-024-71525-w.

Abstract

This study aimed to assess the role of the combination of design techniques of the engineered substrates, and the effect of encapsulating Marjoram (Origanum Majorana L.) into the matrix network was studied. To this end, PVA-PEG matrices were designed through 3 techniques of freeze-thaw (FT), the combination of both methods of freeze-drying and freeze-thawing(FT-FD), and ternary technique(freeze-drying,freeze-thawing,cross-linking(FT-FD/CL)), by combining equal volume ratios of both polymers. The results indicated the ternary technique can provide better physicochemical properties(porosity: 96%, lower degradation rate, higher modulus) compared to FT and FT-FD methods. Afterward, encapsulation of Marjoram-extracted bio-actives in the matrix network designed with the ternary technique demonstrated that the increase in the extract concentration up to 3% can increase encapsulation efficiency. The encapsulation also caused a more cohesive network by better bonding between functional groups in herbal biomolecules and polymer chains of the matrix. Mass transport mechanisms and release kinetics of matrix-encapsulated bio-actives indicated a deviation from Fickian diffusion and the release by diffusion and swelling process. Biologically, matrix-loaded herbal carbohydrate(Epi-alpha-Cadinol) improved fibroblast adhesion and distribution on the substrate surface, and led to the better synthesis of collagen fibers, especially in 3% herbal extract, and antibacterial activities owing to the controlled release of sesquiterpenoids and N-Acetyl-L-proline.

摘要

本研究旨在评估工程化基底设计技术的组合,以及将马郁兰(Origanum Majorana L.)包封到基质网络中的效果。为此,通过 3 种冷冻-解冻技术(FT)、冷冻干燥和冷冻-解冻组合方法(FT-FD)以及冷冻干燥、冷冻-解冻、交联(FT-FD/CL)的三元技术,设计了 PVA-PEG 基质,通过结合两种聚合物的等体积比。结果表明,与 FT 和 FT-FD 方法相比,三元技术可以提供更好的物理化学性质(孔隙率:96%,降解率更低,模量更高)。随后,在采用三元技术设计的基质网络中包封马郁兰提取的生物活性物质表明,提取浓度增加到 3%可以提高包封效率。包封还通过草药生物分子的功能基团与基质聚合物链之间更好的键合,导致更具内聚性的网络。基质包封生物活性物质的质量传递机制和释放动力学表明,偏离了菲克扩散,通过扩散和溶胀过程释放。从生物学角度来看,基质负载的草药碳水化合物(表-α-衣兰醇)改善了成纤维细胞在基质表面的黏附和分布,并导致胶原蛋白纤维的更好合成,特别是在 3%的草药提取物中,由于倍半萜烯和 N-乙酰-L-脯氨酸的控制释放,还具有抗菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0efe/11387659/0e10133a4396/41598_2024_71525_Fig1_HTML.jpg

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