Separation of water-soluble vitamins by reversed-phase high performance liquid chromatography with ultra-violet detection: Application to polyvitaminated premixes

2005 ◽  
Vol 1070 (1-2) ◽  
pp. 49-56 ◽  
Author(s):  
Olivier Heudi ◽  
Tamara Kilinç ◽  
Patric Fontannaz
Separations ◽  
2021 ◽  
Vol 8 (9) ◽  
pp. 152
Author(s):  
Rayudika Aprilia Patindra Purba ◽  
Siwaporn Paengkoum ◽  
Pramote Paengkoum

There is a growing demand to enhance pharmaceutical and food safety using synergistic compounds from Piper sarmentosum Roxb., such as polyphenols and water-soluble vitamins. However, information on standardized analytical methods to identify and quantify these compounds of interest is limited. A reversed-phase high-performance liquid chromatography with diode-array detection (HPLC-DAD)-based method was developed to simultaneously detect and quantify the amounts of tannin, flavonoid, cinnamic acid, essential oil, and vitamins extracted from P. sarmentosum leaves using methanol, chloroform, and hexane. Commercially and non-commercially-cultivated P. sarmentosum leaves were subjected to seven different drying treatments (shade; sun; air oven at 40 °C, 60 °C, 80 °C, and 100 °C; and freeze-drying) for three consecutive months. Most compounds were detected most efficiently at a detection wavelength of 272 nm. The developed method displayed good detection limits (LOD, 0.026–0.789 µg/mL; LOQ, 0.078–2.392 µg/mL), linearity (R2 > 0.999), precision (%RSD, <1.00), and excellent accuracy (96–102%). All P. sarmentosum leaf extracts were simultaneously tested and analytically compared without time-consuming fractionation. Methanolic plant extracts showed better peak area and retention time splits compared to chloroformic and hexanoic extracts. Differences in synergistic compound composition were dependent on the type of drying treatment but not on cultivation site and time of sampling. Flavonoid was identified as the dominant phytochemical component in P. sarmentosum leaves, followed by the essential oil, cinnamic acid, ascorbic acid, and tannin. Overall, we present a simple and reproducible chromatographic method that can be applied to identify different plant compounds.


1981 ◽  
Author(s):  
P B B Jones ◽  
J D Wark ◽  
R G G Russell

Prostacyclin production has been proposed as a fundamental mechanism by which intact vascular endothelium maintains a non-thrombogenic surface. Interest in a reliable assay for its stable breakdown product 6-keto prostaglandin F1α (6-KPGF1α) is, therefore, considerable. Previous studies have emphasised the need to reduce sample complexity prior to the quantification of PG’s by radioimmunoassay (RIA). This has been achieved by extraction of PG’s into organic solvents or onto resin columns followed by separation of PG metabolites by reversed-phase high-performance liquid chromatography (HPLC), but retention times are long if adequate resolution is to be obtained. By using an 8-min gradient elution programme with acetonitrile/water/acetic acid and a 6 ml/min flow rate through Waters reversed-phase (Radial Pak A) column under radial compression good separation of 6-KPGF1α from its closely-related metabolites 13,14-dihydro 6-KPGF1α 6, 15-diketo PGF1α as well as from other PG species was achieved as detected by ultra-violet absorbance spectrometry. In applying the method to the measurement of 6-KPGF1α in urine, PG’s were extracted onto a resin column, eluted in methanol and the extract subjected to HPLC as described. Good resolution of immunoassayable PG metabolites and known cross-reacting species was achieved. This method provides a significant improvement on existing PG assays by reducing sample-processing time dramatically, and is suitable for routine and repetitive clinical use.


2016 ◽  
Vol 13 (2) ◽  
pp. 1
Author(s):  
Hannis Fadzillah Mohsin ◽  
Ratni Suriyani Jalal ◽  
Ibtisam Abdul Wahab ◽  
Abdul Rasyid Zulkifli ◽  
Muhammad Faxrurrazy Sadiran

The Pandanus species (Pandanaceae family) was investigated, in order to set up a library of their chromatographic profiles. From a literature review, the most common Pandanus plant that was greatly examined was P. amaryllifolius (the fragrant screw pine), followed by P. sanderi. Here, the chromatographic data from an extract of a relatively unfamiliar Pandanus is also presented. The leaves of P. monotheca were extracted by using methanol. Later, the extract was filtered, prior to a Reversed-Phase High Performance Liquid Chromatography (RP-HPLC) experiments. The automated system was set to run by gradient elution (acetonitrile:water). The flow rate was maintained at 1 ml/min, otherwise stated in a number of attempts. The ultra-violet absorbance of the Pandanus’ constituents was measured via Multiple Wavelength Detector. From the chromatogram, the major peaks for Pandanus’ compounds were eluted (λ = 220, 260 and 360 nm) and the retention times were recorded. The lower absorbance readings of other minor peaks could be due to various minor secondary metabolites, such as the furolignan. The different elution time depends on the polarity of the composition. In short, Pandanus’ phytochemicals could be obtained via alcoholic extraction. The utilisation of modern chromatographic applications enables the scientists to discover and subsequently, purify single component of the complex natural mixtures. This finding can be beneficial to the research areas in botanical study, pharmacognostical assessment and biotechnology industry. It is aimed that more Pandanus species could be learnt for the future.


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