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Biocatalytic response of multi-layer assembled collagen/hyaluronic acid nanoengineered capsules

机译:多层组装的胶原蛋白/透明质酸纳米工程胶囊的生物催化响应

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摘要

Biodegradable hollow capsules filled with fluorescently labelled bovine serum albumin (BSA) as a model drug were prepared via layer-by-layer (LbL) self-assembly of type-I collagen (COL) and hyaluronic acid (HA) using calcium carbonate micro-particles and co-precipitation method. Capsules loaded with fluorescein isothiocyanate (FITC)-BSA, tetramethylrhodamin isothiocyanate (TRITC)-BSA or Alex-Fluor-488-BSA, respectively, were characterised before and after core removal using Confocal Laser Scanning Microscopy (CLSM), whilst the morphologies of individual hollow capsules were assessed using Atomic Force Microscopy (AFM). The sustained release of the encapsulated FITC-BSA protein was attained using enzymatic degradation of the capsule shells by collagenase. The released profile of the fluorescently-labelled BSA indicated that it could be successfully controlled by modulating the number of layers and/or by collagen crosslinking either before or after the capsule's assembly.
机译:使用碳酸钙微胶囊,通过I型胶原蛋白(COL)和透明质酸(HA)的逐层(LbL)自组装,制备了填充有荧光标记牛血清白蛋白(BSA)作为模型药物的可生物降解的空心胶囊。颗粒和共沉淀法。分别使用共聚焦激光扫描显微镜(CLSM)表征了分别在异硫氰酸荧光素(FITC)-BSA,异硫氰酸四甲基罗丹明(TRITC)-BSA或Alex-Fluor-488-BSA装载的胶囊的特征,而单个胶囊的形态使用原子力显微镜(AFM)评估空心胶囊。包囊的FITC-BSA蛋白的持续释放是通过胶原酶对胶囊壳进行酶促降解而实现的。荧光标记的BSA的释放曲线表明,在胶囊组装之前或之后,可以通过调节层数和/或通过胶原交联来成功控制它。

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