Quantification of Total Phenols and Antioxidants in Coffee Samples of Different Origins and Evaluation of the Effect of Degree of Roasting on Their Levels.

Phenolic and antioxidant compounds have received considerable attention due to their beneficial effects on human health. The aim of this study is to determine the content of total phenols and antioxidants in fifty-two coffee samples of different origins, purchased from the Jordanian local market, and investigate the effect of the degree of roasting on the levels of these compounds. The coffee samples were extracted using the hot water extraction method, while Folin−Ciocalteu (FC) and 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay methods were used to analyze these compounds. The results showed that the highest content of total phenol (16.55 mg/g equivalent to GAE) was found in the medium roasted coffee, and the highest content of antioxidants (1.07 mg/g equivalent to TEAC) content was found in the green coffee. Only light and medium roasted coffee showed a significant correlation (p < 0.05, R2 > 0.95) between the average of total phenolic and antioxidant content. A negative correlation between the antioxidant content and the degree of roasting (p < 0.05, R2 > 0.95) were shown, while it did not correlate with phenolic contents. Previously, a positive correlation between antioxidant and chlorogenic acids content was observed, with no correlation between the origin of coffee samples nor heavy metal content, which was previously determined for the same coffee samples. These findings suggest that the antioxidant content for coffee extracts is largely determined by its chlorogenic acid content, rather than the coffee origin or total phenolic and heavy metals content.

LC-MS/MS Screening, Total Phenolic, Flavonoid and Antioxidant Contents of Crude Extracts from Three Asclepiadaceae Species Growing in Jordan.

This study aimed to evaluate the antioxidant activity and total phenolic content (TPC) and total flavonoid content (TFC) of crude extracts obtained from three Asclepiadaceae species, namely, Calotropis procera L., Peruglaria tomentosa L., and Pentatropis spiralis (Forsk.) Decne. Both butanol and aq. methanol extracts of the three species showed the highest amount of phenol and flavonoid contents, which exhibited the greatest antioxidant activity in the scavenging of 2,2-diphenyl-2-picrylhydrazyl free radical (DPPH), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt radical cation (ABTS), ferrous chelating effect (FIC), and hydroxyl radical (HDR) assays. Phytochemical screening of the extracts revealed the presence of alkaloids, tannins, sponins, flavonoids, terpenoids, and glycosides. LC-MS analysis was carried out to identify the major compounds from each crude extract. A total of 12 phenolic compounds in the extracts of the 3 species were identified and quantified, including 9 flavonoids, 2 hydroxybenzoic acids, and 3 hydroxycinnamic acids. The current study also revealed a good correlation between total phenolic contents and the observed antioxidant activity of the crude extracts.

Quantification of Caffeine and Chlorogenic Acid in Green and Roasted Coffee Samples Using HPLC-DAD and Evaluation of the Effect of Degree of Roasting on Their Levels.

Chlorogenic acid and caffeine are among the important components in coffee beans, determining the taste and aroma. In addition, phenols and antioxidants content possess vital health values. The main aim of this study is to determine the levels of caffeine and chlorogenic acid in several coffee samples of different origins and degrees of roasting. The coffee samples were extracted using hot water. The levels of caffeine and chlorogenic acid were quantified using high-performance liquid chromatography (HPLC) equipped with a diode array detector, a reverse phase system, and an ODS column (C18). Total phenol and antioxidant contents were previously determined for the same samples. The results showed that the highest content of caffeine was found in the medium roasted coffee (203.63 mg/L), and the highest content of chlorogenic acid content was found in the green coffee (543.23 mg/L). The results demonstrated a negative correlation between the chlorogenic acid levels with the degree of roasting, while it showed a positive correlation between the caffeine levels with the degree of roasting till a certain point where the levels dropped in the dark roasted coffee. The origin of coffee samples did not show any effect on any of the measured variables. Antioxidant effects of coffee samples were largely determined by chlorogenic acid content.

Loading of Silver (I) Ion in L-Cysteine-Functionalized Silica Gel Material for Aquatic Purification.

The L-cysteine-functionalized silica (SG-Cys-Na+) matrix was effectively loaded with silver (I) ions using the batch sorption technique. Optimal Ag(I) loading into SG-Cys-Na+ reached 98% at pHi = 6, 80 rpm, 1 mg L-1, and a temperature of 55 °C. The Langmuir isotherm was found to be suitable for Ag(I) binding onto SG-Cys-Na+ active sites, forming a homogeneous monolayer (R2 = 0.999), as confirmed by FTIR spectroscopy. XRD analysis indicated matrix stability and the absence of Ag2O and Ag(0) phases, observed from diffraction peaks. The pseudo-second-order model (R2 > 0.999) suggested chemisorption-controlled adsorption, involving chemical bonding between silver ions and SG-Cys-Na+ surface. Thermodynamic parameters were calculated, indicating higher initial concentrations leading to increased equilibrium constants, negative ΔG values, positive ΔS values, and negative ΔH. This study aimed to explore silver ion saturation on silica surfaces and the underlying association mechanisms. The capability to capture and load silver (I) ions onto functionalized silica gel materials holds promise for environmental and water purification applications.

Multi-element determination of essential and toxic metals in green and roasted coffee beans: A comparative study among different origins using ICP-MS.

The aim of this study is to compare the elemental composition among different coffee varieties consumed in Jordan. Levels of different metallic elements in coffee samples; green and roasted coffee beans from five origins; Brazil, Ethiopia, Kenya, Columbia, and India, collected from the Jordanian market were investigated. Twenty-two elements, including essential and toxic elements such as potassium (K), magnesium (Mg), calcium (Ca), iron (Fe), aluminum (Al), manganese (Mn), copper (Cu), barium (Ba), strontium (Sr), zinc (Zn), chromium (Cr), lead (Pb), nickel (Ni), vanadium (V), cobalt (Co), gallium (Ga), uranium (U), cadmium (Cd), silver (Ag), lithium (Li), indium (In), bismuth (Bi), thorium (Th), and thallium (Ti), were determined using inductively coupled plasma-mass spectrometry (ICP-MS). The detected heavy metals and their intake per 1 cup of coffee did not largely contribute to the recommended daily intake (RDI) and tolerable upper limit of daily intake (TULD) in an adult with an average body weight of 80 kg. The ICP-MS versus flame atomic absorption spectrometry (FAAS) results were linearly fitted, and the correlation coefficients (R2 > 0.95) were better than 0.95 for the three checked elements. No significant difference between the results of the two techniques was observed (p > 0.05). The ANOVA results indicated the presence of a significant difference between the levels of Cr, Co, and Zn in green and roasted coffee beans. The results of this study indicated that the coffee consumed in Jordan did not contain toxic levels of heavy elements and is safe for consumption according to health organizations.

Wet and dry deposition fluxes of inorganic chemical species at a rural site in northern Jordan.

Wet and dry deposition samples were collected in a rural region in northern Jordan during the period of December 1998 to April 2000. Concentrations of 20 chemical species (Na, K, Ca, H(+), Mg, NH(4)(+), Cl(-), NO(3)(-), SO(4)(2-), Pb, Cd, Zn, Cu, Al, Fe, Mn, Mo, Ni, Sb, and V) were determined in collected samples. Most of the Al, Fe, Mn, Mo, Sb, and V were not soluble, whereas major ions (Na, K, Ca, H(+), Mg, NH(4)(+), Cl(-), NO(3)(-), and SO(4)(2-) ) and some trace elements (Cd, Cu, and Zn) were wet deposited mostly in the soluble form. Concentration of the soil-related elements and/or highly soluble species were washed out at the early stages of a precipitation event, and their concentrations were mostly controlled by dilution, whereas concentrations of anthropogenic species were controlled by other factors. Annual fluxes of the soil-related elements and ions were significantly higher than the primarily anthropogenic elements. This was attributed to the arid nature of the region and to the frequent input of the Saharan dust pulses.

Atmospheric deposition of major and trace elements in Amman, Jordan.

Wet and dry deposition samples were collected in the capital of Jordan, Amman. Concentrations of Al, Ba, Bi, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Sb, V, Zn, Fe, Sr, Mg2+, Ca2+, Na+, K+, Cl-, NO3- and SO(4)(2-), along with pH were determined in collected samples. Mean trace metal concentrations were similar or less than those reported for other urban regions worldwide, while concentrations of Ca2+ and SO(4)(2-) were among the highest. High Ca2+ concentrations were attributed to the calcareous nature of the local soil and to the influence of the Saharan dust. However, high SO(4)(2-) concentrations were attributed to the influence of both anthropogenic and natural sources. Except for Cl-, NO3-, SO(4)(2-) and Cu, monthly dry deposition fluxes of all measured species were higher than wet deposition fluxes. The annual wet deposition fluxes of trace metals were much lower than those reported for other urban areas worldwide.

Indirect flow-injection spectrophotometric determination of meloxicam, tenoxicam and piroxicam in pharmaceutical formulations.

A simple and sensitive indirect spectrophotometric method for the assay of meloxicam (MX), tenoxicam (TX) and piroxicam (PX) in pure and in pharmaceutical formulations by flow injection analysis (FIA) has been proposed. The method is based on the oxidation of these drugs by a known excess of N-bromosuccinimide (NBS) in an acidic medium, followed by a reaction of excess oxidant with chloranilic acid (CAA) to bleach its purple color. The absorbance values increased linearly with increasing concentrations of the drugs. Variables, such as the acidity, reagent concentrations, flow rate of reagents and other FI parameters were optimized to produce the most sensitive and reproducible results. The system obeyed Beer's low over concentration ranges of 10 - 160, 20 - 200 and 10 - 160 microg/ml for MX, TX and PX, respectively. The common excipients and additives did not interfere with their determinations. The method was successfully applied to the determinations of MX, TX and PX in various pharmaceutical preparations. The results obtained by the proposed method were found to be in good agreement with those found by the official HPLC methods.

Simultaneous determination of Cd, Pb, Cu, Zn, and Se in human blood of jordanian smokers by ICP-OES.

A total of 73 blood samples (56 from smokers and 17 from nonsmokers) were collected to determine the concentrations of selected heavy metal in the whole blood of smokers and nonsmokers living in and around the city of Amman, Jordan. Analysis of heavy metals in the whole blood samples of various groups took in consideration the number of cigarettes smoked per day. The analysis of blood samples was carried out using inductively coupled plasma optical emission spectrometry. This study aimed to evaluate the blood metal levels in smokers and nonsmokers and to assess the influence of smoking cigarettes on blood metal levels. The results were compared with those from a control group. The results indicated that the average concentrations of cadmium (Cd), lead (Pb), copper (Cu), zinc (Zn), and selenium (Se) were 0.0313, 0.344, 2.328, 3.214, and 0.332 mg/L, respectively. Statistical analysis of results indicated that these average concentrations were significantly higher compared with the average concentrations in nonsmokers (P < 0.05). Moreover, the correlations between blood metal and other blood metal levels in smokers, the correlations between blood metal and other blood metal levels in nonsmokers, and the correlations between blood metal concentration in smokers and its concentration in nonsmokers were calculated. The standard reference material (blood serum National Institute of Standards and Technology 1598) and the quality control were used to validate the reliability of the method used for the estimation of heavy metals in blood samples. Results revealed that there was an agreement between the certified values and the measured values.

Atmospheric deposition of major ions and trace metals near an industrial area, Jordan.

Al, Cd, Cr, Cu, Fe, Mn, Pb, Zn, NH4+, Mg2+, Ca2+, Na+, K+, Cl-, NO3- and SO4(2-), along with pH were determined in wet and dry deposition samples collected at Al-Hashimya, Jordan. Mean trace metal concentrations were similar or less than those reported for other urban regions worldwide, while concentrations of Ca2+ and SO4(2-) were the highest. The high Ca2+ concentrations were attributed to the calcareous nature of the local soil and to the influence of the Saharan dust, while the high concentrations of SO4(2-) were attributed to the influence of anthropogenic sources and Saharan dust soil. Except for SO4(2-), NO3-, and Ca2+, dry deposition fluxes of measured metals and ions were higher than their corresponding wet deposition fluxes. The high annual average pH values recorded for wet and dry deposition samples were attributed to the neutralization of acidity by alkaline species. Cd, Cr, Cu, Pb, Zn, NO3- and SO4(2-) were enriched in wet and dry deposition samples relative to crustal material, and a significant anthropogenic contribution to these elements and ions is tentatively suggested. Finally, the possible sources and the main factors affecting the concentrations of the measured species are discussed.

Water-soluble species and heavy metal contamination of the petroleum refinary area, Jordan.

The levels of lead, cadmium, copper, zinc, aluminum, chromium, and iron in street dust, soil, and plants in the Jordanian petroleum refinery were determined using flame and graphite-furnace atomic absorption spectrophotometry. Major cations (Li+, Na+, NH4+, K+, Mg2+, and Ca2+) and anions (F-, Cl-, NO3-, SO4(2-), and Br-) were also determined using suppression mode ion chromatography. Generally, higher levels of the heavy metals studied were found in street dust samples than in soil samples. On the other hand, except Cl-, and Li+ ions, other anions and cations showed higher concentrations in soil than in street dust samples. For plant samples, unwashed samples showed higher levels of heavy metals than their washed counterparts, indicating that dust fall is a source of heavy metal contamination.