کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1199303 1493565 2014 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Determination of trace level genotoxic impurities in small molecule drug substances using conventional headspace gas chromatography with contemporary ionic liquid diluents and electron capture detection
ترجمه فارسی عنوان
تعیین سطح ناخالصی های ژنوتوکسیک ردیابی مواد دارویی مولکول های کوچک با استفاده از کروماتوگرافی گاز کوره های مغناطیسی معمولی با رقیق کننده های مایع معدنی یونی و تشخیص جذب الکترون
کلمات کلیدی
ناخالصی ژنوتوکسیک، مایع یونی، آلکیل / آریل هالید، ترکیب نیترو-معطر کروماتوگرافی گاز فضای مجازی، آشکارساز ضبط الکترون
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• A novel methodology using ionic liquids as diluents for headspace GC.
• Greatly broadening the applicability of headspace GC for high boiling analytes.
• Significant improvement on limit of detection compared to traditional DMSO diluent.
• Simplifying method transfer from development labs to quality control environments.
• Using conventional validated chromatographic data systems and GC instruments.

Ionic liquids (ILs) were used as a new class of diluents for the analysis of two classes of genotoxic impurities (GTIs), namely, alkyl/aryl halides and nitro-aromatics, in small molecule drug substances by headspace gas chromatography (HS-GC) coupled with electron capture detection (ECD). This novel approach using ILs as contemporary diluents greatly broadens the applicability of HS-GC for the determination of high boiling (≥130 °C) analytes including GTIs with limits of detection (LOD) ranging from 5 to 500 parts-per-billion (ppb) of analytes in a drug substance. This represents up to tens of thousands-fold improvement compared to traditional HS-GC diluents such as dimethyl sulfoxide (DMSO) and dimethylacetamide (DMAC). Various ILs were screened to determine their suitability as diluents for the HS-GC/ECD analysis. Increasing the HS oven temperatures resulted in varying responses for alkyl/aryl halides and a significant increase in response for all nitroaromatic GTIs. Linear ranges of up to five orders of magnitude were found for a number of analytes. The technique was validated on two active pharmaceutical ingredients with excellent recovery. This simple and robust methodology offers a key advantage in the ease of method transfer from development laboratories to quality control environments since conventional validated chromatographic data systems and GC instruments can be used. For many analytes, it is a cost effective alternative to more complex trace analytical methodologies like LC/MS and GC/MS, and significantly reduces the training needed for operation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1361, 26 September 2014, Pages 217–228
نویسندگان
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