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Controlled delivery achieved with bi-layer matrix devices produced by co-injection moulding

机译:通过共注射成型生产的双层基质设备实现了受控的输送

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摘要

The aim of this study was to design new soy protein-based bi-layered co-injection moulded matrix systems aimed to achieve controlled drug delivery. The devices consisted of a drug-free outer layer (skin) and a drug-containing core. The systems overcame the inherent disadvantage of non-linear release associated with diffusion-controlled single-layer matrix devices by providing additional releasing area with time to compensate for the decreasing release rate. As expected, the bi-layer devices presented a significant decrease in drug release rate when compared with a correspondent single layer matrix system. The skin thickness and the degree of crosslinking of the core appeared to be very important tools to tailor the release patterns. Furthermore, due to the amphoteric nature of the soy protein, the developed devices evidenced a pH-dependent behaviour. The mechanisms of drug release were also elucidated at two different pH values: i) pH 5.0, near the isoelectric point of soy (low matrix solubility); and ii) pH 7.4, physiological pH (high matrix solubility). Consequently, changing the release medium from pH 5.0 to pH 7.4 after two hours, led to an abrupt increase in drug release and the devices presented a typical controlled drug delivery profile: slow release/fast release. These evidences may provide for the development of individual systems with different release onsets that in combination may exhibit drug releases at predetermined times in a pre-programmed way. Another possibility is the production of three-layer devices presenting bimodal release profiles (fast release/slow release/fast release) by similar technologies.
机译:这项研究的目的是设计新的基于大豆蛋白的双层共注射成型基质系统,旨在实现受控的药物输送。该装置由无药的外层(皮肤)和含药的芯组成。该系统通过随时间提供额外的释放区域来补偿降低的释放速率,从而克服了与扩散控制的单层矩阵器件相关的非线性释放的固有缺点。如所预期的,与相应的单层基质系统相比,双层装置在药物释放速率方面呈现出显着降低。表皮厚度和核的交联度似乎是调节释放模式的非常重要的工具。此外,由于大豆蛋白的两性性质,已开发的装置证明其具有pH依赖性行为。还阐明了在两个不同的pH值下药物释放的机制:i)pH 5.0,接近大豆的等电点(低基质溶解度); ii)pH 7.4,生理pH(高基质溶解度)。因此,在两小时后将释放介质从pH 5.0更改为pH 7.4,导致药物释放突然增加,并且该设备呈现出典型的受控药物释放曲线:缓慢释放/快速释放。这些证据可以提供具有不同释放开始的个体系统的开发,其可以以预定程序的方式组合在预定时间展现药物释放。另一种可能性是通过类似技术生产具有双峰释放曲线(快速释放/缓慢释放/快速释放)的三层设备。

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