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用于亲脂性化合物递送的皮克林油微滴在微流控条件下封装到海藻酸盐微凝胶中

Microfluidic Encapsulation of Pickering Oil Microdroplets into Alginate Microgels for Lipophilic Compound Delivery.

作者信息

Marquis Mélanie, Alix Valentin, Capron Isabelle, Cuenot Stéphane, Zykwinska Agata

机构信息

UR1268 Biopolymères Interactions Assemblages, INRA, rue de la Géraudière F-44316 Nantes, France.

Institut des Matériaux Jean Rouxel (IMN), Université de Nantes-CNRS, Rue de la Houssinière 44322 Nantes, France.

出版信息

ACS Biomater Sci Eng. 2016 Apr 11;2(4):535-543. doi: 10.1021/acsbiomaterials.5b00522. Epub 2016 Mar 29.

Abstract

Alginate microgels are widely used as delivery systems in food, cosmetics, and pharmaceutical industries for encapsulation and sustained release of hydrophilic compounds and cells. However, the encapsulation of lipophilic molecules inside these microgels remains a great challenge because of the complex oil-core matrix required. The present study describes an original two-step approach allowing the easy encapsulation of several oil microdroplets within alginate microgels. In the first step, stable oil microdroplets were formed by preparing an oil-in-water (O/W) Pickering emulsion. To stabilize this emulsion, we used two solid particles, namely the cotton cellulose nanocrystals (CNC) and calcium carbonate (CaCO). It was observed that the surface of the oil microdroplets formed was totally covered by a CNC layer, whereas CaCO particles were adsorbed onto the cellulose layer. This solid CNC shell efficiently stabilized the oil microdroplets, preventing them from undesired coalescence. In the second step, oil microdroplets resulting from the Pickering emulsion were encapsulated within alginate microgels using microfluidics. Precisely, the outermost layer of oil microdroplets composed of CaCO particles was used to initiate alginate gelation inside the microfluidic device, following the internal gelation mode. The released Ca ions induced the gel formation through physical cross-linking with alginate molecules. This innovative and easy to carry out two-step approach was successfully developed to fabricate monodisperse alginate microgels of 85 μm in diameter containing around 12 oil microdroplets of 15 μm in diameter. These new oil-core alginate microgels represent an attractive system for encapsulation of lipophilic compounds such as vitamins, aroma compounds or anticancer drugs that could be applied in various domains including food, cosmetics, and medical applications.

摘要

海藻酸盐微凝胶作为一种递送系统,在食品、化妆品和制药行业中被广泛用于亲水性化合物和细胞的包封与缓释。然而,由于所需的油核基质复杂,将亲脂性分子包封在这些微凝胶中仍然是一个巨大的挑战。本研究描述了一种新颖的两步法,可轻松地将多个油微滴包封在海藻酸盐微凝胶中。第一步,通过制备水包油(O/W)皮克林乳液形成稳定的油微滴。为了稳定该乳液,我们使用了两种固体颗粒,即棉纤维素纳米晶体(CNC)和碳酸钙(CaCO)。观察到形成的油微滴表面完全被一层CNC覆盖,而CaCO颗粒吸附在纤维素层上。这种固体CNC壳有效地稳定了油微滴,防止它们发生不期望的聚结。第二步,使用微流控技术将皮克林乳液产生的油微滴包封在海藻酸盐微凝胶中。具体而言,由CaCO颗粒组成的油微滴最外层用于按照内部凝胶化模式在微流控装置内引发海藻酸盐凝胶化。释放出的Ca离子通过与海藻酸盐分子的物理交联诱导凝胶形成。这种创新且易于实施的两步法成功开发出来,用于制备直径为85μm的单分散海藻酸盐微凝胶,其中包含约12个直径为15μm的油微滴。这些新型的油核海藻酸盐微凝胶是一种有吸引力的系统,可用于包封亲脂性化合物,如维生素、香料化合物或抗癌药物,可应用于包括食品、化妆品和医疗应用在内的各个领域。

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