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 >Headspace-SPME-GC/MS as a simple cleanup tool for sensitive 2,6-diisopropylphenol analysis from lipid emulsions and adaptable to other matrices.
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Headspace-SPME-GC/MS as a simple cleanup tool for sensitive 2,6-diisopropylphenol analysis from lipid emulsions and adaptable to other matrices.

机译:Headspace-SPME-GC / MS是一种简单的净化工具,可用于从脂质乳剂中进行灵敏的2,6-二异丙基苯酚分析,并适用于其他基质。

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摘要

Due to increased regulatory requirements, the interaction of active pharmaceutical ingredients with various surfaces and solutions during production and storage is gaining interest in the pharmaceutical research field, in particular with respect to development of new formulations, new packaging material and the evaluation of cleaning processes. Experimental adsorption/absorption studies as well as the study of cleaning processes require sophisticated analytical methods with high sensitivity for the drug of interest. In the case of 2,6-diisopropylphenol - a small lipophilic drug which is typically formulated as lipid emulsion for intravenous injection - a highly sensitive method in the concentration range of mug/l suitable to be applied to a variety of different sample matrices including lipid emulsions is needed. We hereby present a headspace-solid phase microextraction (HS-SPME) approach as a simple cleanup procedure for sensitive 2,6-diisopropylphenol quantification from diverse matrices choosing a lipid emulsion as the most challenging matrix with regard to complexity. By combining the simple and straight forward HS-SPME sample pretreatment with an optimized GC-MS quantification method a robust and sensitive method for 2,6-diisopropylphenol was developed. This method shows excellent sensitivity in the low mug/l concentration range (5-200mug/l), good accuracy (94.8-98.8%) and precision (intraday-precision 0.1-9.2%, inter-day precision 2.0-7.7%). The method can be easily adapted to other, less complex, matrices such as water or swab extracts. Hence, the presented method holds the potential to serve as a single and simple analytical procedure for 2,6-diisopropylphenol analysis in various types of samples such as required in, e.g. adsorption/absorption studies which typically deal with a variety of different surfaces (steel, plastic, glass, etc.) and solutions/matrices including lipid emulsions.
机译:由于法规要求的提高,活性药物成分在生产和储存过程中与各种表面和溶液的相互作用在药物研究领域引起了人们的兴趣,特别是在开发新配方,新包装材料和评估清洁工艺方面。实验性吸附/吸收研究以及清洁过程的研究需要对目标药物具有高灵敏度的复杂分析方法。对于2,6-二异丙基苯酚-一种通常被配制成用于静脉内注射的脂质乳剂的小型亲脂性药物-一种马克杯/升浓度范围内的高灵敏度方法,适用于包括脂质在内的多种不同样品基质需要乳液。我们在此提出一种顶空-固相微萃取(HS-SPME)方法,作为一种简单的纯化程序,用于从各种基质中选择灵敏的脂类作为最具挑战性的基质,用于从各种基质中进行灵敏的2,6-二异丙基苯酚定量。通过将简单,直接的HS-SPME样品预处理与优化的GC-MS定量方法相结合,开发了一种鲁棒且灵敏的2,6-二异丙基苯酚方法。此方法在低杯子/升浓度范围(5-20​​0mug / l)中显示出极好的灵敏度,良好的准确性(94.8-98.8%)和精度(日内精度0.1-9.2%,日间精度2.0-7.7%)。该方法可轻松适用于其他较简单的基质,例如水或药签提取物。因此,所提出的方法有潜力用作在各种类型的样品中进行2,6-二异丙基苯酚分析的单一且简单的分析程序,例如,例如,美国专利No.5,886,650。吸附/吸收研究通常涉及各种不同的表面(钢,塑料,玻璃等)以及溶液/基质(包括脂质乳剂)。

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