Search

Vitamin K is one of the many health-promoting substances whose impact on the human body has been underestimated until recently. However, recently published research results have changed this situation, prompting some researchers to consider it a new panacea for diseases of old age. The result is a significant increase in interest in the accurate analysis of vitamin K in various types of samples, ranging from food, through dietary supplements, to biological matrices and clinical trials, both observational and interventional. This review summarizes the current state of knowledge about the proven and speculated biological activity of vitamin K and its importance for the world's aging societies, including the methods used for its isolation and analysis in various matrices types. Of all the analytical methods, the currently preferred methods of choice for the direct analysis of vitamin K are chromatographic methods, in particular liquid chromatography-tandem mass spectrometry. This technique, despite its sensitivity and selectivity, requires an appropriate stage of sample preparation. As there is still room for improvement in the efficiency of these methods, especially at the sample preparation stage, this review shows the directions that need to be taken to make these methods faster, more efficient and more environmentally friendly. [ABSTRACT FROM AUTHOR]

Chlorogenic acid (CQA) is one of phenolics commonly found in higher plants, possessing numerous health-promoting effects on humans. Unfortunately, it is easily degraded/transformed into other substances during extraction. Therefore, its reliable analysis requires a special approach that does not involve high temperatures. This paper presents a very simple method of CQA isolation using the sea sand disruption method with subsequent purification of the extract using the ion-pair solid-phase extraction process, followed by HPLC–DAD detection. It was found that control of the ion pairing reagent concentration and sample pH is crucial to improve purification, and that the best results, with recovery exceeding 98%, were obtained for 0.05 M tetrabutylammonium bisulfate at pH 7 when the ion pairs were formed directly in the extract and eluted from the C18 sorbent using an acidified methanol–water mixture. The practical potential of the developed procedure was verified by using it for CQA isolation from different plants. The approach represents one of the contemporary analytical trends and current advances in the solid phase extraction, in which several sorption extraction techniques are combined to ensure high-quality analytical results. [ABSTRACT FROM AUTHOR]

The aim of this paper is to present in the most comprehensive way the facts about the application of PLE in the analysis of secondary metabolites in plants. It is true that due to its specific extraction conditions, PLE is one of the most effective and versatile techniques of plant constituents isolation. It is also true that it has popularized the use of aqueous organic mixtures, and even water alone, for the extraction of nonpolar compounds. Yet, the same specific extraction conditions can lead to erroneous results of plant constituent content analysis. Disclosure of new facts about the application of PLE in the analysis of secondary plant metabolites provides an insight into an often overlooked aspect of extraction of active compounds from plants. • This review updates knowledge about the applicability of PLE. • It discusses the effectiveness and usefulness of PLE in the context of its achievements. • It discloses the limitations of PLE in the plant constituents content analysis. • Knowing all these facts can lead to the creation of a perfect method with a good method. [ABSTRACT FROM AUTHOR]

Abstract The aim of this paper was to present the diversity of analytical challenges in which the MSPD technique is useful and the variety of sorbents that are currently applied to meet these challenges with particular emphasis on new research areas in which the MSPD process started to be applied. In addition, the paper presents new tools to improve both the MSPD yields using the MSPD processes supported by centrifugation, ultrasound, microwave and magnetism and its selectivity combining MSPD with other extraction techniques in particular, with microextraction ones, such as liquid-liquid microextraction dispersion or homogeneous liquid-liquid microextraction. Facing the problem of the increased urgency for further reduction of sample preparation costs and organic solvent usage, alternative MSPD approaches such as the solventless MSPD mode and MSPD with sand used as a dispersing material in the so-called sea sand dispersion method were discussed. Highlights • This review updates knowledge about the applicability of MSPD. • It discuss the versatility and flexibility of MSPD in the context of its achievements and limitations. • Indicates new research areas in which MSPD began to be applied. • In addition, indicates those that in the near future should use this simple process. [ABSTRACT FROM AUTHOR]

Reliable plant analysis is a challenging task due to the physical character and chemical complexity of plant matrices. First of all, it requires the application of a proper sample preparation procedure to fully isolate the analyzed substances from the plant matrix. The high-temperature liquid-solid extraction is commonly applied for this purpose. In the light of recently published results, however, the application of high-temperature extraction for polyphenolics analysis in plants is disputable as it causes their transformation leading to erroneous quantitative estimations of these compounds. Experiments performed on different plants show that the transformation/degradation of quercetin and its glycosides is not induced by sea sand disruption method (SSDM) and prove the method to be most appropriate for the estimation of quercetin and its derivatives in plants. What is more, the application of SSDM in plant analysis allows the researcher, to determine which quercetin derivatives are native plant components and what is their true concentration. In other word, the application of SSDM in plant analysis eliminates errors in the study of plant metabolism involving quercetin and its derivatives. [ABSTRACT FROM AUTHOR]

The analytical procedures for determining plant constituents involve the application of sample preparation methods to fully isolate and/or pre-concentrate the analyzed substances. High-temperature liquid extraction is still applied most frequently for this purpose. The present paper shows that high-temperature extraction cannot be applied for the analysis of chlorogenic acids (CQAs) and their derivatives in plants as it causes the CQAs transformation leading to erroneous quantitative estimations of these compounds. Experiments performed on different plants (black elder, hawthorn, nettle, yerba maté, St John’s wort and green coffee) demonstrate that the most appropriate method for the estimation of CQAs/CQAs derivatives is sea sand disruption method (SSDM) because it does not induce any transformation and/or degradation processes in the analyzed substances. Owing to the SSDM method application we found that the investigated plants, besides four main CQAs, contain sixteen CQAs derivatives, among them three quinic acids. The application of SSDM in plant analysis not only allows to establish a true concentration of individual CQAs in the examined plants but also to determine which chlorogenic acids derivatives are native plant components and what is their concentration level. What is even more important, the application of SSDM in plant analysis allows to eliminate errors that may arise or might have arisen in the study of chlorogenic acids and their derivatives in plant metabolism. [ABSTRACT FROM AUTHOR]

Biological properties of menaquinone-7, one of the vitamin K2 vitamers (K2MK-7), both those proven and those that remain to be investigated, arouse extensive interest that goes beyond the strictly scientific framework. The most important of them is the prevention of age-related diseases, considering that we live in the times identified as the era of aging societies and many people are exposed to the vitamin K2MK-7 deficiency. Therefore, an effective analytical protocol that can be adopted as a diagnostic and preventive analytics tool is needed. Herein, a simple sample preparation method followed by the liquid chromatography-tandem mass spectrometry-based method (LC-MS/MS), was used for the selective and sensitive determination of K2MK-7 in serum samples. Under the optimized conditions, using 500 µL of serum and the same amount of n-hexane, the reproducibility and the accuracy were obtained in the ranges of 89–97% and 86–110%, respectively, and the limit of detection value was 0.01 ng/mL. This method was used for the routine analysis. Statistical interpretation of the data from 518 samples obtained during 2 years of practice allowed for obtaining information on the content and distribution of K2MK-7 in the Polish population, broken down by the sex and age groups. [ABSTRACT FROM AUTHOR]