## Abstract Parkinson's disease (PD) is a very serious neurological disorder, and current methods of treatment fail to achieve long‐term control. SCH 420814 is a potent, selective and orally active adenosine A~2A~ receptor antagonist discovered by Schering‐Plough. Stability testing provides evidenc
Analysis of Aloe-based phytotherapeutic products by using nano-LC-MS
✍ Scribed by Salvatore Fanali; Zeineb Aturki; Giovanni D'Orazio; Anna Rocco; Anna Ferranti; Laura Mercolini; Maria Augusta Raggi
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 234 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1615-9306
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✦ Synopsis
Abstract
This article proposes a chromatographic method for the analysis of extracts of Aloe plants. The method was developed with a laboratory assembled nano‐LC system coupled with a UV detector, followed by an IT‐mass spectrometer. With a step gradient mode of ACN/H~2~O mixtures and employing a capillary column packed with C~18~ (100 μm id), a complete separation of the following anthrones was achieved: aloin (in its two isomeric forms A and B), 5‐hydroxyaloin and 7‐hydroxyaloin (in its two isomeric forms A and B). The optimized nano‐LC‐MS method was validated for the quantification of aloin, the main component of Aloe with known pharmacological activities. RSD values obtained for retention time and peak areas were 1.3 and 12.1%, respectively. LOD and LOQ values of 0.4 and 1.5 μg/mL were obtained for each aloin isomer. The method was applied to the analysis of Aloe vera and A. ferox extracts in order to acquire a fingerprint, characteristic for each plant. Several phenolic compounds were detected by UV and identified by MS. A. vera and A. ferox showed different profiles and it was possible to discriminate them. Several commercial formulations, declared to contain Aloe extracts, were analyzed. Comparing their chromatograms with those obtained from A. vera and A. ferox, it was possible to recognize the Aloe species and to determine aloin.
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