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通过反射干涉光谱法在动态流动条件下实时原位监测纳米多孔植入物中的药物释放。

Real-time and in situ drug release monitoring from nanoporous implants under dynamic flow conditions by reflectometric interference spectroscopy.

机构信息

School of Chemical Engineering, The University of Adelaide, Adelaide, SA 5005, Australia.

出版信息

ACS Appl Mater Interfaces. 2013 Jun 26;5(12):5436-42. doi: 10.1021/am4013984. Epub 2013 Jun 14.

Abstract

Herein, we present an innovative approach to monitoring in situ drug release under dynamic flow conditions from aluminum implants featuring nanoporous anodic alumina (NAA) covers used as a model of drug-releasing implants. In this method, reflectometric interference spectroscopy (RIfS) is used to monitor in real-time the diffusion of drug from these nanoporous implants. The release process is carried out in a microfluidic device, which makes it possible to analyze drug release under dynamic flow conditions with constant refreshing of eluting medium. This setup mimics the physiological conditions of biological milieu at the implant site inside the host body. The release of a model drug, indomethacin, is established by measuring the optical thickness change with time under four different flow rates (i.e. 0, 10, 30, and 50 μL min(-1)). The obtained data are fitted by a modified Higuchi model, confirming the diffusion-controlled release mechanism. The obtained release rate constants demonstrate that the drug release depends on the flow rate and the faster the flow rate the higher the drug release from the nanoporous covers. In particular, the rate constants increase from 2.23 ± 0.02 to 12.47 ± 0.04 μg min(-1/2) when the flow rate is increased from 10 to 50 μL min(-1), respectively. Therefore, this method provides more reliable and relevant information than conventional in vitro drug release methods performed under static conditions.

摘要

在此,我们提出了一种创新的方法,用于监测在动态流动条件下从带有纳米多孔阳极氧化铝 (NAA) 覆盖层的铝植入物中原位释放药物,纳米多孔阳极氧化铝覆盖层被用作释放药物植入物的模型。在这种方法中,反射干涉光谱学 (RIfS) 用于实时监测药物从这些纳米多孔植入物中的扩散。释放过程在微流控装置中进行,这使得可以在不断更新洗脱介质的情况下分析动态流动条件下的药物释放。该装置模拟了宿主体内植入部位生物环境的生理条件。通过在四种不同流速(即 0、10、30 和 50 μL min(-1))下测量随时间的光学厚度变化来建立模型药物吲哚美辛的释放。通过修正的 Higuchi 模型拟合获得的数据,证实了扩散控制的释放机制。获得的释放速率常数表明,药物释放取决于流速,流速越快,纳米多孔覆盖物的药物释放速度越快。特别是,当流速从 10 增加到 50 μL min(-1)时,药物释放的速率常数从 2.23 ± 0.02 增加到 12.47 ± 0.04 μg min(-1/2)。因此,与在静态条件下进行的传统体外药物释放方法相比,该方法提供了更可靠和相关的信息。

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