scholarly journals Bioaccessibility Assessment of Cu, Fe, K, Mg, P, and Zn in Thermally Treated Lamb Meat

Author(s):  
Julymar de Higuera ◽  
Herick Santos ◽  
Aline de Oliveira ◽  
Ana Rita Nogueira

A bioaccessibility test with raw and cooked lamb meat samples was performed. The evaluated cooking devices were grill, microwave oven, air fryer, pressure cooker, and electric oven. Physicochemical parameters and the total mass fraction of Cu, Fe, K, Mg, P, and Zn were determined in raw and cooked samples by inductively coupled plasma optical emission spectrometry (ICP OES). The trueness was evaluated using certified reference materials, with recoveries from 87 to 101%. The pressure cooking presented the major changes, including the highest values of internal temperature, loss of inorganic elements after cooking, and the lowest values of moisture and analyte mass fractions. An in vitro gastrointestinal simulation was performed, and the method was validated by an addition and recovery test, in which the trueness varied from 87 to 115%. The bioaccessibility ranged between 28-56, 4-19, 68-76, 41-54, 48-57, and 1-21% for Cu, Fe, K, Mg, P, and Zn, respectively. The cooking methods promoted changes in the meat samples, thus affecting the bioaccessibility of the nutrients. Based on the recommended dietary intake (RDI) calculation, lamb meat can be considered a good Fe, P, and Zn source.

2020 ◽  
Vol 9 (3) ◽  
Author(s):  
Dhary Alewy Almashhadany ◽  
Hawraz Sami Khalid ◽  
Hoshyar Saadi Ali

Food contamination with heavy metals may pose a serious threat to human health. Fishes are the most common seafood globally. This study aimed to evaluate the levels of heavy metals in different fishes sold in Erbil city markets. The targeted heavy metal elements were cadmium (Cd), chromium (Cr), cobalt (Co), copper (Cu), lead (Pb), mercury (Hg), manganese (Mn), nickel (Ni), selenium (Se), and zinc (Zn). Seventeen dorsal meat samples were digested and subjected to metal analysis by Inductively Coupled Plasma Optical Emission Spectrometry. Co, Mn, Cu and Se were detected in all samples, while cadmium was below the detectable level in all samples. The average concentrations of targeted trace elements were 0.03±0.016, 0.02±0.03, 0.07±0.08, 0.10±0.08, 0.03±0.03, and 2.90±3.33 mg/kg for cobalt, chromium, copper, manganese, nickel, and zinc, respectively. Lead was only found in one sample (5.88%). On the contrary, mercury was detected in all samples but in low concentration (0.14±0.07). All detected heavy metals with specified permissible limits by FAO/WHO were significantly lower than the permissible limits. Based on detected levels of targeted heavy metals, consumption of such fish has no potential risks to human.


2013 ◽  
Vol 32 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Adriane Medeiros Nunes ◽  
Rafael Arromba de Sousa ◽  
Caroline Santos da Silva ◽  
Rafaella Regina Alves Peixoto ◽  
Mariana Antunes Vieira ◽  
...  

2021 ◽  
Vol 5 (1) ◽  
pp. 19-25
Author(s):  
Mariele Samuel Nascimento ◽  
Gabriel Toneto Druzian ◽  
Rochele Sogari Picoloto ◽  
Paola Azevedo Mello ◽  
Erico M. M. Flores

A method based on microwave-induced combustion (MIC) was applied for medicinal plants digestion allowing further chlorine determination by potentiometry using ion-selective electrode (ISE). Sample masses ranging from 500 to 1000 mg were evaluated for MIC digestion. Water and 10, 25, 50, and 100 mmol/L NH4OH were investigated as absorbing solutions. The accuracy of the proposed method was evaluated by using certified reference materials (CRMs), by recovery tests (500 µg/g), and also by comparison with the results obtained by inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave-assisted alkaline extraction (MAE). Using water or NH4OH solutions (10 to 100 mmol/L), recoveries close to 100% and relative standard deviation lower than 5% were obtained. Results were in agreement with CRMs values (better than 95%) and also with those values obtained by using the MAE method. The main advantage of the proposed method was the complete combustion of high sample mass (1000 mg) resulting in low quantification limit (12.5 µg/g) and chlorine determination at low concentration by ISE. Another advantage of the proposed method was the high chlorine stability in digests (up to 30 days of storage) even using water as absorbing solution, which is in agreement with green analytical chemistry recommendations. Finally, the proposed MIC method was applied for commercial medicinal plants and the chlorine concentration was in the range of 59.4 ± 1.4 to 2038 ± 70 µg/g. The proposed MIC method was considered suitable for quality control for chlorine determination in medicinal plants.


2004 ◽  
Vol 87 (1) ◽  
pp. 151-156 ◽  
Author(s):  
Carmen S Kira ◽  
Franca D Maio ◽  
Vera A Maihara

Abstract A fast procedure was developed for determination of Ca, Cr, Cu, Fe, K, Mg, Mn, Na, P, and Zn in milk samples. This procedure consisted of a partial digestion with hydrochloric acid on a hot plate. The results obtained were compared with 3 other digestion procedures (dry ashing and 2 microwave digestions). All the procedures showed similar precision levels, with coefficients of variation <10% for most analyzed elements. Accuracy was evaluated by using certified reference materials, and the values obtained were within the confidence intervals for these products. The results obtained were not considered statistically different. The partial digestion on a hot plate with HCl can be very practical for laboratories with relatively large numbers of sample analyses.


2017 ◽  
Vol 100 (6) ◽  
pp. 1879-1884 ◽  
Author(s):  
Manuela Ruiz-de-Cenzano ◽  
Arancha Rochina-Marco ◽  
Óscar López-Salazar ◽  
Maria Luisa Cervera ◽  
Miguel de la Guardia

Abstract Children’s fast food menus, including hamburgers served with french fries, dessert, and a soft drink, were analyzed to obtain the mineral profile of trace elements. The developed analytical methodology involved sample digestion under pressure inside a microwave oven with a mixture of HNO3 and H2O2 and inductively coupled plasma-optical emission spectrometry. The method was validated by carrying out the analysis of certified reference materials (NIST 1570a spinach leaves, NCS ZC73016 chicken, and NIST 1568a rice flour) and using recovery experiments. Repeatability was verified by analyzing replicate samples. Twenty-six elements were studied, 12 of which—aluminum, barium, calcium, copper, iron, potassium, lithium, magnesium, manganese, sodium, strontium, and zinc—were quantitatively determined. Results were compared with other studies of fast food and children’s menus published in the literature, and the nutritional value of samples was assessed with dietary intake guidelines.


Molecules ◽  
2020 ◽  
Vol 25 (5) ◽  
pp. 1256
Author(s):  
Maja Welna ◽  
Anna Szymczycha-Madeja ◽  
Pawel Pohl

Commercially bottled birch saps (BSs) were analyzed for several nutrient (Ca, Cu, Fe, Mg, and Zn) and toxic (As, Cd, Ni, and Pb) elements using inductively coupled plasma optical emission spectrometry (ICP OES). The method was validated under the conditions of several sample preparation procedures, including a traditional digestion as well as alternative non-digestion schemes. It was found that the direct analysis of untreated BSs gives the best results, i.e., limits of detection at 0.02–5.8 ng mL−1, precision better than 5%, accuracy from 98.0% to 104.5% and determination of 12 elements in a short time (~1 min per sample). The multi-element analysis of nine commercially available bottled BSs showed that they contained mainly Mg and Ca, small quantities of Mn, Zn, Cu, and Fe, but are free from toxic elements such as As, Cd, Ni, and Pb. Additionally, the nutritional value of BSs was examined using in vitro gastro-intestinal digestion (GID) to determine the bioaccessible fraction of elements. Accordingly, bioaccessibility of nutritious ones (Ca, Cu, Fe, Mg, Zn) was <40%. Drinking daily 1 L of BSs covered <2.5% of recommended dietary intakes (RDIs) of the aforementioned elements. Only the bioaccessibility of Mn highly contributes to its RDI.


2009 ◽  
Vol 102 (6) ◽  
pp. 825-834 ◽  
Author(s):  
Supannee Sripanyakorn ◽  
Ravin Jugdaohsingh ◽  
Wacharee Dissayabutr ◽  
Simon H. C. Anderson ◽  
Richard P. H. Thompson ◽  
...  

Dietary Si (orthosilicic acid; OSA) appears important in connective tissue health, and although the sources and intakes of Si are well established, its absorption is not. Si absorption was measured from eight high-Si-containing sources: alcohol-free beer; OSA solution (positive control); bananas; green beans; supplemental choline-stabilised OSA (ChOSA); supplemental monomethyl silanetriol (MMST); supplemental colloidal silica (CS); magnesium trisilicate British Pharmacopoeia antacid (MTBP). Two of the supplements and the antacid were pre-selected following an in vitro dissolution assay. Fasting, healthy subjects (CS, n 3; others, n ≥ 5) each ingested two of the sources separated by a 1-week wash-out period. Blood and urine were collected and measured for total Si concentrations by inductively coupled plasma optical emission spectrometry. Absorption, based on urinary Si excretion, was highest for MMST and alcohol-free beer (64 % of dose), followed by green beans (44 %), OSA (43 %), ChOSA (17 %), bananas and MTBP (4 %) and CS (1 %). Peak serum concentrations occurred by 0.5 h for MMST and green beans, 1.5 h for OSA and alcohol-free beer, 2 h for ChOSA and CS, and 4 h for MTBP. Area under the serum curves correlated positively with urinary Si output (r 0·82; P < 0·0001). Absorption of Si from supplements and antacids was consistent with their known chemical speciation and kinetics of dissolution under simulated gastrointestinal conditions. Monomeric silicates were readily absorbed, while particulate silicates were decreasingly well absorbed with increasing polymerisation. The present results highlight the need to allow for relative absorption of Si from different foods or supplements in subsequent epidemiological and intervention studies.


2011 ◽  
Vol 1355 ◽  
Author(s):  
Sofia Dembski ◽  
Moritz Milde ◽  
Emeline Dassonneville ◽  
Carsten Gellermann ◽  
Torsten Klockenbring ◽  
...  

ABSTRACTLuminescent lanthanide doped SiO2/Hydroxylapatite (HAp) core/shell nanoparticles (NPs) were synthesized by sol-gel technology. The resulting NPs exhibited an amorphous SiO2 core and a crystalline luminescent shell. The formation of the HAp layer was possible at pH 8.5. The characterization of the resulting NPs was done by transmission electron microscopy, X-ray diffraction analysis, inductively-coupled plasma combined with optical emission spectrometry, and photoluminescence spectroscopy. Additionally, the newly developed SiO2/HAp:Ln3+ core/shell NPs were tested for their biocompatibility, e. g. by an in vitro cell culture based assay.


Sign in / Sign up

Export Citation Format

Share Document