دورية أكاديمية

Reversed HILIC Gradient: A Powerful Strategy for On-Line Comprehensive 2D-LC

التفاصيل البيبلوغرافية
العنوان: Reversed HILIC Gradient: A Powerful Strategy for On-Line Comprehensive 2D-LC
المؤلفون: Soraya Chapel, Florent Rouvière, Davy Guillarme, Sabine Heinisch
المصدر: Molecules, Vol 28, Iss 9, p 3907 (2023)
بيانات النشر: MDPI AG, 2023.
سنة النشر: 2023
المجموعة: LCC:Organic chemistry
مصطلحات موضوعية: comprehensive 2D-LC, on-line LC × LC, reversed HILIC, orthogonality, pharmaceuticals, peptides, Organic chemistry, QD241-441
الوصف: The aim of the present work is to evaluate the possibilities and limitations of reversed hydrophilic interaction chromatography (revHILIC) mode in liquid chromatography (LC). This chromatographic mode consists of combining a highly polar stationary phase (bare silica) with a gradient varying from very low (1–5%) to high (40%) acetonitrile content (reversed gradient compared to HILIC). The retention behavior of revHILIC was first compared with that of reversed-phase LC (RPLC) and HILIC using representative mixtures of peptides and pharmaceutical compounds. It appears that the achievable selectivity can be ranked in the order RPLC > revHILIC > HILIC with the two different samples. Next, two-dimensional liquid chromatography (2D-LC) conditions were evaluated by combining RPLC, revHILIC, or HILIC with RPLC in an on-line comprehensive (LC × LC) mode. evHILIC × RPLC not only showed impressive performance in terms of peak capacity and sensitivity, but also provided complementary selectivity compared to RPLC × RPLC and HILIC × RPLC. Indeed, both the elution order and the retention time range differ significantly between the three techniques. In conclusion, there is no doubt that revHILIC should be considered as a viable option for 2D-LC analysis of small molecules and also peptides.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1420-3049
Relation: https://www.mdpi.com/1420-3049/28/9/3907; https://doaj.org/toc/1420-3049
DOI: 10.3390/molecules28093907
URL الوصول: https://doaj.org/article/177a46a640054c9c8dd76214ada16f10
رقم الأكسشن: edsdoj.177a46a640054c9c8dd76214ada16f10
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14203049
DOI:10.3390/molecules28093907