首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Characterisation of transmission Raman spectroscopy for rapid quantitative analysis of intact multi-component pharmaceutical capsules.
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Characterisation of transmission Raman spectroscopy for rapid quantitative analysis of intact multi-component pharmaceutical capsules.

机译:透射拉曼光谱的表征,用于完整多组分药物胶囊的快速定量分析。

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A detailed characterisation of the performance of transmission Raman spectroscopy was performed from the standpoint of rapid quantitative analysis of pharmaceutical capsules using production relevant formulations comprising of active pharmaceutical ingredient (API) and 3 common pharmaceutical excipients. This research builds on our earlier studies that identified the unique benefits of transmission Raman spectroscopy compared to conventional Raman spectroscopy. These include the ability to provide bulk information of the content of capsules, thus avoiding the sub-sampling problem, and the suppression of interference from the capsule shell. This study demonstrates, for the first time, the technique's insensitivity to the amount of material held within the capsules. Different capsules sizes with different overall fill weights (100-400 mg) and capsule shell colours were assayed with a single calibration model developed using only one weight and size sample set (100 mg) to a relative error of typically <3%. The relative root mean square error of prediction of the concentration of API for the main sample set (nominal content 75%, w/w) was 1.5% with a 5s acquisition time. Models built using the same calibration set also predicted the 3 low level excipients with relative errors of 5-15%. The quantity of API was also predicted (with a relative error within approximately 3%) using the same model for capsules prepared with different generations of API (i.e. API manufactured via different processes). The study provides further foundation blocks for the establishment of this emerging technique as a routine pharmaceutical analysis tool, capitalising on the inherently high chemical specificity of Raman spectroscopy and the non-invasive nature of the measurement. Ultimately, this technique has significant promise as a Process Analytical Technology (PAT) tool for online production application.
机译:从快速定量分析胶囊的角度出发,使用包含活性药物成分(API)和3种常见药物赋形剂的生产相关配方,对透射拉曼光谱的性能进行了详细的表征。这项研究建立在我们较早的研究的基础上,这些研究确定了透射拉曼光谱与传统拉曼光谱相比的独特优势。这些功能包括提供胶囊内容的大量信息的能力,从而避免了二次采样问题,并抑制了胶囊壳的干扰。这项研究首次证明了该技术对胶囊中容纳的物质不敏感。使用仅使用一个重量和大小的样品组(100 mg)开发的单个校准模型,分析具有不同总填充重量(100-400 mg)和不同颜色的胶囊壳颜色的胶囊,相对误差通常<3%。采集时间为5s时,主样品组(标称含量为75%,w / w)的API浓度预测的相对均方根误差为1.5%。使用相同校准集建立的模型还预测了3种低水平赋形剂,相对误差为5-15%。对于使用不同世代的API(即通过不同工艺制造的API)制备的胶囊,使用相同的模型也可以预测API的数量(相对误差在3%以内)。该研究利用拉曼光谱固有的高化学特异性和测量的非侵入性特性,为建立这种新兴技术作为常规药物分析工具提供了进一步的基础。最终,该技术作为在线生产应用程序的过程分析技术(PAT)工具具有巨大的前景。

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