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Interrogating erosion-based drug liberation phenomena from hydrophilic matrices using near infrared (NIR) spectroscopy

机译:使用近红外(NIR)光谱从亲水性基质询问基于腐蚀的药物释放现象

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摘要

The present work explores the application of in situ near infrared (NIR) imaging to determine the drug release mechanisms from hydrophilic matrices containing a low solubility model drug (Compound A, with aqueous solubility at 37 ??C ??0.05 mg/mL). Correlation maps generated from the NIR data determined the extent drug and HPMC co-localisation. Judicious thresholding facilitated band separation of low drug/HPMC ratio and high drug/HPMC ratio. A pseudo-image time-series confirmed the dominant erosion release mechanisms. The gel layer region showed low drug concentration with progressive dissolution. However, large drug aggregates remained unchanged even when fully "immersed" within the gel layer. From the correlation maps, further discrimination was possible for the pure drug signal, generating a highly contrasted image that enabled individual particle tracking. These contrasted images also revealed the evolution of single or clusters of drug particles. Initially, an aggregative process involving the drug particles occurred, with a subsequent migration process of such particles. This second process dominated the subsequent 90 min before significant erosion. In summary, this study has provided tentative confirmation that NIR imaging has the potential to afford insights into drug liberation phenomena where erosion is the predominant release mechanism. ? 2012 Elsevier B.V. All rights reserved.
机译:本工作探索了应用原位近红外(NIR)成像技术确定包含低溶解度模型药物(化合物A,在37°C≤0.05 mg / mL的水溶性)的亲水性基质中释放药物的机制。从NIR数据生成的相关图确定了药物和HPMC的共定位程度。明智的阈值化促进了低药物/ HPMC比和高药物/ HPMC比的谱带分离。伪图像时间序列证实了主要的侵蚀释放机制。凝胶层区域显示出低的药物浓度并逐渐溶解。然而,即使完全“浸没”在凝胶层中,大的药物聚集体也保持不变。从相关图中,可以对纯药物信号进行进一步区分,从而生成高对比度的图像,从而可以进行单个粒子跟踪。这些对比的图像还揭示了单个或成簇的药物颗粒的演变。最初,发生了涉及药物颗粒的聚集过程,随后发生了这种颗粒的迁移过程。第二个过程在随后的90分钟内占主导地位,之后才出现明显的侵蚀。总而言之,这项研究提供了初步的证实,即近红外成像有可能提供深入了解以释放是主要释放机制的药物释放现象的潜能。 ? 2012 Elsevier B.V.保留所有权利。

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