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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >Construction of hollow DNA/PLL microcapsule as a dual carrier for controlled delivery of DNA and drug
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Construction of hollow DNA/PLL microcapsule as a dual carrier for controlled delivery of DNA and drug

机译:构建中空DNA / PLL微胶囊作为双重载体以控制DNA和药物的递送

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摘要

DNA/poly-L-lysine (PLL) capsules were constructed through a layer-by-layer (LbL) self-assembly of DNA and PLL on CaCO3 microparticles, and then used as dual carriers for DNA and drug after dissolution of carbonate cores. The permeability of DNA/PLL microcapsules was investigated with fluorescence probes with different molecular weights by confocal microscopy. The result revealed that the fluorescence probes were able to penetrate the capsule walls even its molecular weight up to 150 kDa. The resultant capsules were used to load drug model molecules-fluorescein isothiocyanate (FITC)-dextran (4 kDa) via spontaneous deposition mechanism. DNA/PLL capsules were used as dual drug carriers for concurrent delivery DNA and FITC-dextran molecules by salt-triggered capsule decomposition. The amount of released DNA and drug can be controlled by adjusting ionic strength. The larger salt concentration, the more DNA and drug were released. Two remedial agents could be simultaneously introduced to the diseased region by using this carrier system. which may really improve curative effect due to the synergetic effect of DNA and drug.
机译:通过在CaCO3微粒上对DNA和PLL进行逐层(LbL)自组装来构建DNA /聚L-赖氨酸(PLL)胶囊,然后在碳酸盐核心溶解后用作DNA和药物的双重载体。通过共聚焦显微镜用不同分子量的荧光探针研究了DNA / PLL微胶囊的通透性。结果表明,即使分子量高达150 kDa,荧光探针也能够穿透胶囊壁。所得胶囊用于通过自发沉积机理加载药物模型分子-异硫氰酸荧光素(FITC)-右旋糖酐(4 kDa)。 DNA / PLL胶囊被用作双重药物载体,用于通过盐触发的胶囊分解同时递送DNA和FITC-葡聚糖分子。可以通过调节离子强度来控制释放的DNA和药物的量。盐浓度越大,释放的DNA和药物越多。通过使用该载体系统,可以将两种治疗剂同时引入患病区域。由于DNA和药物的协同作用,可能真正提高疗效。

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