Storage stability of sterilized liquid extracts from pomegranate peel

Pomegranate marc, a byproduct of commercial juice production, has shown promise as a starting material for the recovery of health promoting phenolic compounds. The stability of aqueous extracts prepared from pomegranate marc was evaluated in preparation to directly using these extracts as nutraceuticals or food additives. The liquid extracts were produced under extraction conditions of 25 °C, water to peel ratio of 50 : 1 (w/w) for 2 min, and then sterilized at 121 °C for 10 s. Storage conditions tested included 3 different pH values (3.5, 5.0, and 7.0) and 2 packaging methods (no light and exposure to light). The extracts were evaluated for industrial (pH, total soluble solid content, and clarity), color, spectral, and antioxidant characteristics over a period of 180 d. The results showed that both pH value and packaging method significantly influenced the industrial and color characteristics of the extracts. The high pH had a negative effect on spectral and antioxidant characteristics. Therefore, the recommended storage conditions are low pH and with dark packaging to maintain the high storage stability. After 180 d of storage, extracts stored at low pH (3.5) in dark packaging still retained 67% and 58% of their total soluble phenolic concentration and antioxidant activity, compared with 61% and 43% for high pH (7.0) samples, and were composed of high concentrations of punicalagins A and B, gallic, and ellagic acids. PRACTICAL APPLICATION: The present research developed an effective recovery of phenolic compounds from pomegranate marc to be used as nutraceuticals or food additives. The aqueous extract product has good quality characteristics with high industrial and color stability, and total phenolic content and antioxidant activity, when stored at pH 3.5 in dark packaging for up to 180 d. The evaluation results of storage stability reported here are important for commercialization.     

Metal levels in blood, muscle and liver of water snakes (Nerodia spp.) from New Jersey, Tennessee and South Carolina

Reptiles, particularly snakes, could serve as bioindicators of contamination because some are comparatively long-lived, exhibit different trophic levels, and are at the top of their food chains. We test the null hypothesis that there are no differences in the concentrations of heavy metals in the blood, muscle and liver of water snakes (Nerodia spp.) from rivers in New Jersey, Tennessee and South Carolina. While the former site is in an urban/suburban area, the latter two sites are relatively rural and are located on Department of Energy sites. For the snakes from New Jersey, there were significant differences in metal concentrations among tissues for all metals, the highest levels for arsenic and selenium were in liver and kidney, for cadmium were in the liver, for chromium and lead were in skin, and for mercury and manganese were in the muscle. Body length was not correlated with metal levels, and there were more significant correlations for skin with internal tissues than for blood with other tissues. There were more significant correlations for mercury than for other metals. In comparing metal levels among states, levels were generally higher for snakes collected from South Carolina. These data indicate that, since water snakes accumulate contaminants differentially as a function of location, they can be useful bioindicators of environmental exposure to contaminants. Moreover, because of their wide geographical distribution and use of varying trophic compartments, this genus can be useful for cross-site comparisons.     

On-tissue chemical derivatization in mass spectrometry imaging

Mass spectrometry imaging (MSI) combines molecular and spatial information in a valuable tool for a wide range of applications. Matrix-assisted laser desorption/ionization (MALDI) is at the forefront of MSI ionization due to its wide availability and increasing improvement in spatial resolution and analysis speed. However, ionization suppression, low concentrations, and endogenous and methodological interferences cause visualization problems for certain molecules. Chemical derivatization (CD) has proven a viable solution to these issues when applied in mass spectrometry platforms. Chemical tagging of target analytes with larger, precharged moieties aids ionization efficiency and removes analytes from areas of potential isobaric interferences. Here, we address the application of CD on tissue samples for MSI analysis, termed on-tissue chemical derivatization (OTCD). MALDI MSI will remain the focus platform due to its popularity, however, alternative ionization techniques such as liquid extraction surface analysis and desorption electrospray ionization will also be recognized. OTCD reagent selection, application, and optimization methods will be discussed in detail. MSI with OTCD is a powerful tool to study the spatial distribution of poorly ionizable molecules within tissues. Most importantly, the use of OTCD−MSI facilitates the analysis of previously inaccessible biologically relevant molecules through the adaptation of existing CD methods. Though further experimental optimization steps are necessary, the benefits of this technique are extensive.