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拉曼光谱法作为一种制药混合过程的 PAT 工具:优缺点。

Raman spectroscopy as a PAT for pharmaceutical blending: Advantages and disadvantages.

机构信息

Chiesi Farmaceutici S.p.A., R&D, Chemistry Manufacturing and Control, Via Palermo 26 A, 43122 Parma, Italy.

SAIMP srl, Via Mangini28/D/1, 16031 Sori, Genova, Italy.

出版信息

J Pharm Biomed Anal. 2018 Feb 5;149:329-334. doi: 10.1016/j.jpba.2017.11.030. Epub 2017 Nov 8.

Abstract

Raman spectroscopy has been positively evaluated as a tool for the in-line and real-time monitoring of powder blending processes and it has been proved to be effective in the determination of the endpoint of the mixing, showing its potential role as process analytical technology (PAT). The aim of this study is to show advantages and disadvantages of Raman spectroscopy with respect to the most traditional HPLC analysis. The spectroscopic results, obtained directly on raw powders, sampled from a two-axis blender in real case conditions, were compared with the chromatographic data obtained on the same samples. The formulation blend used for the experiment consists of active pharmaceutical ingredient (API, concentrations 6.0% and 0.5%), lactose and magnesium stearate (as excipients). The first step of the monitoring process was selecting the appropriate wavenumber region where the Raman signal of API is maximal and interference from the spectral features of excipients is minimal. Blend profiles were created by plotting the area ratios of the Raman peak of API (A) at 1598cm and the Raman bands of excipients (A), in the spectral range between 1560 and 1630cm, as a function of mixing time: the API content can be considered homogeneous when the time-dependent dispersion of the area ratio is minimized. In order to achieve a representative sampling with Raman spectroscopy, each sample was mapped in a motorized XY stage by a defocused laser beam of a micro-Raman apparatus. Good correlation between the two techniques has been found only for the composition at 6.0% (w/w). However, standard deviation analysis, applied to both HPLC and Raman data, showed that Raman results are more substantial than HPLC ones, since Raman spectroscopy enables generating data rich blend profiles. In addition, the relative standard deviation calculated from a single map (30 points) turned out to be representative of the degree of homogeneity for that blend time.

摘要

拉曼光谱已被积极评估为一种用于粉末混合过程的在线实时监测工具,并且已被证明在确定混合终点方面是有效的,显示了其作为过程分析技术(PAT)的潜在作用。本研究的目的是展示拉曼光谱相对于最传统的 HPLC 分析的优缺点。直接在原始粉末上获得的光谱结果,在实际情况下从两轴混合器中采样,与从相同样品获得的色谱数据进行了比较。用于实验的配方混合物由活性药物成分(API,浓度为 6.0%和 0.5%)、乳糖和硬脂酸镁(作为赋形剂)组成。监测过程的第一步是选择合适的波数区域,在该区域中 API 的拉曼信号最大,并且赋形剂的光谱特征干扰最小。通过绘制 API 的拉曼峰(A)在 1598cm 处的面积比与在 1560 和 1630cm 之间的光谱范围内的赋形剂的拉曼带(A)的面积比作为混合时间的函数来创建混合比曲线:当面积比的时间依赖性分散最小化时,可以认为 API 含量是均匀的。为了实现拉曼光谱的代表性采样,每个样品都通过微拉曼仪的聚焦激光束在电动 XY 台上进行了映射。仅对于 6.0%(w/w)的浓度,发现两种技术之间存在良好的相关性。然而,应用于 HPLC 和拉曼数据的标准偏差分析表明,拉曼结果比 HPLC 结果更可靠,因为拉曼光谱能够生成丰富的数据混合比曲线。此外,从单个图谱(30 个点)计算出的相对标准偏差被证明代表了该混合时间的均匀度程度。

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