Search Results (11)

Source-separated, nitrified, and decontaminated human urine constitutes a promising plant fertilizer that contains a large share of the nitrogen and phosphorus in household wastewater, and other plant nutrients. However, human urine contains high levels of sodium and chloride that can affect salt-sensitive greenhouse crops. Replacing mineral fertilizer with nitrified urine fertilizer could reduce the environmental impact of lettuce production in hydroponic systems, if marketable yield, appearance, and produce quality are not affected. In the present study, a treatment combination of a nitrified urine fertilizer and mineral fertilizers was used to grow lettuce through the nutrient film technique. This was compared to a conventionally fertilized control treatment. No significant differences were observed regarding yield, phenotype, and contents of nitrate, heavy metals, phenolic acids, and chlorophyll in leaf tissue. Calcium content was significantly reduced and sodium was elevated in nitrified urine treatment. For the elements nitrogen, phosphorous, and potassium, a saving of 48%, 13%, and 15% was calculated, respectively. The calculated carbon footprint from the total fertilizer production was reduced by 20.52%, caused by the nitrified urine treatment. Based on these results, a nutrient solution composed of nitrified urine fertilizer combined with mineral fertilizer may be a promising alternative for growers to produce lettuce with a reduced environmental impact without loss of plant quantity and quality. Full article

The majority of nutrients in municipal wastewater originate from urine. However, when flush water is used, the urine is diluted and mixed with other organic household waste, losing its high-value stream content. This study investigated the effect of source-separated human urine on the population dynamics, nutrient removal, growth, and biogas content of mixed microalgae grown in 250 L raceway ponds. Overall, a maximum biomass concentration of 1847 mg/L was reached, with up to 90% nitrogen and 80% phosphorus removal efficiencies, along with 254.96 L/kg vs. biogas production. The microbial community analysis identified Chlorella sorokiniana (Chlorophyta, Trebouxiophyceae) as the species with the highest abundance, after confirmation with four different markers (16S rRNA, 18S rRNA, 23S rRNA, and tufA). Moreover, principal component analysis was applied to capture the effect of environmental factors on culture diversity. The abundance of Chlorella sorokiniana increased almost sevenfold when the culture was exposed to open systems compared to the small-scale study carried out in 1 L Erlenmeyer bottles in laboratory conditions, both grown in urine and synthetic media (BBM). In conclusion, the present study contributes to the potential to valorize urine with microalgae by showing its high biogas content, and reveals that microalgae can adapt to adverse environmental conditions by fostering their diversity. Full article

With the development of world economies and the continuous improvement of living standards, pharmaceutical and personal care products (PPCPs) have attracted significant attention because of their widespread detection in wastewater and the natural environment. Their biological toxicity, environmental persistence, and other hazardous characteristics might pose a threat to the ecological environment and human health. How to treat source-separated urine as a valuable recyclable resource has become a novel challenge. In this review, we briefly described the sources of pharmaceuticals, explored the various metabolic pathways of pharmaceuticals, and concluded that urinary excretion is the primary metabolic pathway of pharmaceuticals. Next, the current status of pharmaceutical contamination in human urine, sewage plants, and surface water was summarized. It is shown that the concentration of pharmaceuticals in human urine is usually 2–3 orders of magnitude higher than that in sewage plants and surface water. Then, the research progress of various technologies to treat pharmaceutical contaminants in urine was analyzed and compared, indicating the promise of advanced oxidation technologies to treat such wastewater, among which electrochemical oxidation has received widespread attention due to its advantages of cleanness, flexibility, and controllability. Therefore, the research progress of electrode materials and electrochemical technology to treat urine was reviewed, and finally, the future development direction was proposed, namely, coupling membrane treatment technology with intellectual development, which will help realize the scale and industrialization of source-separated urine treatment. Full article

The new direct oral anticoagulants (DOACs) are increasingly used to treat and prevent thromboembolic disorders, and monitoring concentrations may be valuable in some special scenarios to prevent clinical adverse events. This study aimed to develop generic methods for the rapid and simultaneous analysis of four DOACs in human plasma and urine. Protein precipitation and one-step dilution were used to prepare the plasma and urine; the extracts were injected to ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) for analysis. Chromatographic separation was performed on an Acquity™ UPLC BEH C₁₈ column (2.1 × 50 mm, 1.7 μm) with gradient elution of 7 min. A triple quadrupole tandem mass spectrometer with an electrospray ionization source was employed to analyze DOACs in a positive ion mode. The methods showed great linearity in the plasma (1~500 ng/mL) and urine (10~10,000 ng/mL) for all analytes (R² ≥ 0.99). The intra- and inter-day precision and accuracy were within acceptance criteria. The matrix effect and extraction recovery were 86.5~97.5% and 93.5~104.7% in the plasma, while 97.0~101.9% and 85.1~99.5% in the urine. The stability of samples during the routine preparation and storage were within the acceptance criteria of less than ±15%. The methods developed were accurate, reliable, and simple for the rapid and simultaneous measurement of four DOACs in human plasma and urine, and successfully applied to patients and subjects with DOACs therapy for anticoagulant activity assessment. Full article

The impact of nutrients on the environment, particularly on water bodies, has led to extensive studies for nutrient control. Within this context, studies have been focused on source separation of human urine from domestic wastewater to recover nutrients. Potassium is one of the most important components of human urine. However, data on potassium removal or recovery are quite limited except for some indirect information through use of zeolites for mostly ammonia removal. Potassium struvite or K-struvite (MgKPO₄·6H₂O) is a sparingly soluble salt belonging to the struvite family that has the potential of being used as a means of potassium and phosphate recovery from segregated human urine. This study aimed to assess the potential of K-struvite precipitation for control and recovery of nutrients. Within this context, K-struvite precipitation experiments were performed on both synthetically prepared samples and synthetic human urine solution to determine effect of operation parameters i.e., pH, stoichiometry, and temperature on potassium recovery performance. Results indicated that process performance as well as type of solid phases co-precipitated with K-struvite were closely related to initial potassium concentration, pH, and reaction stoichiometry. At pH 10, the potassium recovery efficiency was maximized up to 87% by application of 100% excess dose of Mg and P for both synthetic samples and synthetic human urine solution. On the other hand, application of excess dose of K did not provide any improvement in K recovery efficiency. The effect of temperature on solubility of K-struvite was insignificant at the temperature range of 24–90 °C. Solid phase analyses confirmed that K-struvite was co-precipitated with either Mg₃(PO₄)₂, MgNaPO₄·7H₂O, or MgHPO₄·7H₂O depending on pH and stoichiometry instead of a pure compound. Full article

Analysis of amino acids by gas chromatography-mass spectrometry (GC–MS) requires at least one derivatization step to enable solubility in GC–MS-compatible water-immiscible organic solvents such as toluene, to make them volatile to introduce into the gas chromatograph and thermally stable enough for separation in the GC column and introduction into the ion-source, and finally to increase their ionization by increasing their electronegativity using F-rich reagents. In this work we investigated the long-term stability of the methyl esters pentafluoropropionic (Me-PFP) derivatives of 21 urinary amino acids prepared by a two-step derivatization procedure and extraction by toluene. In situ prepared trideuteromethyl ester pentafluoropropionic derivatives were used as internal standards. GC–MS analysis (injection of 1 µL aliquots and quantification by selected-ion monitoring of specific mass fragments) was performed on days 1, 2, 8, and 15. Measured peak areas and calculated peak area ratios were used to evaluate the stability of the derivatives of endogenous amino acids and their internal standards, as well as the precision and the accuracy of the method. All analyses were performed under routine conditions. Me-PFP derivatives of endogenous amino acids and their stable-isotope labelled analogs were stable in toluene for 14 days. The peak area values of the derivatives of most amino acids and their internal standards were slightly higher on days 8 and 15 compared to days 1 and 2, yet the peak area ratio values of endogenous amino acids to their internal standards did not change. Our study indicates that Me-PFP derivatives of amino acids from human urine samples can easily be prepared, are stable at least for 14 days in the extraction solvent toluene, and allow for precise and accurate quantitative measurements by GC–MS using in situ prepared deuterium-labelled methyl ester as internal standard. Full article

Oxandrolone, a synthetic testosterone analog, is used for the treatment of several diseases associated with weight loss. Unfortunately, oxandrolone is abused by many athletes and bodybuilders due to its strong anabolic effect. We have developed and validated a highly sensitive and rapid on-line SPE-UHPLC-MS/MS method for the determination of oxandrolone and simultaneous identification of its major metabolite 17-epi-oxandrolone in urine matrices. Enrichment of the analytes via an integrated solid-phase extraction was achieved using an Acquity UPLC BEH C18 Column. Subsequently, the chromatographic separation of the on-line preconcentrated sample fraction was achieved using an Acquity HSS T3 C18 Column. For the structural identification of these analytes, a high-resolution mass spectrometer Synapt-G2Si coupled to the Acquity M-class nano-LC system with ionKey source was used. A highly sensitive determination of oxandrolone was achieved using a tandem quadrupole mass spectrometer XEVO TQD. The method was successfully validated in the linear range of oxandrolone from 81.63 pg·mL⁻¹ (limit of quantification, LOQ) to 5000 pg·mL⁻¹ in the human urine matrix. It was applied to the analysis of real urine samples obtained from a healthy volunteer after the oral administration of one dose (10 mg) of oxandrolone. Concentration vs. time dependence was tested in the time interval of 4 h–12 days (after oral administration) to demonstrate the ability of the method to detect the renal elimination of oxandrolone from the human body. Favorable performance parameters along with successful application indicate the usefulness of the proposed method for its routine use in antidoping control labs. Full article

Bone is a major storage site as well as an endogenous source of lead in the human body. Dietary sodium and potassium intake may play a role in the mobilization of lead from bone to the circulation. We examined whether association between bone lead and urinary lead, a marker of mobilized lead in plasma, was modified by dietary intake of sodium and potassium among 318 men, aged 48–93 years, in the Veterans Affairs (VA) Normative Aging Study. Dietary sodium and potassium were assessed by flame photometry using 24-h urine samples, and a sodium-to-potassium ratio was calculated from the resulting measures. Patella and tibia bone lead concentrations were measured by K-shell-x-ray fluorescence. Urinary lead was measured by inductively coupled plasma mass spectroscopy in 24-h urine samples. Linear regression models were used to regress creatinine clearance-corrected urinary lead on bone lead, testing multiplicative interactions with tertiles of sodium, potassium, and sodium-to-potassium ratio, separately. After adjustment for age, body mass index, smoking, vitamin C intake, calcium, and total energy intake, participants in the highest tertile of sodium-to-potassium ratio showed 28.1% (95% CI: 12.5%, 45.9%) greater urinary lead per doubling increase in patella lead, whereas those in the second and lowest tertiles had 13.8% (95% CI: −1.7%, 31.7%) and 5.5% (95% CI: −8.0%, 21.0%) greater urinary lead, respectively (p-for-interaction = 0.04). No statistically significant effect modification by either sodium or potassium intake alone was observed. These findings suggest that relatively high intake of sodium relative to potassium may play an important role in the mobilization of lead from bone into the circulation. Full article

Nutrient recovery from source-separated human urine has been identified by many as a viable avenue towards the circular economy of nutrients. Moreover, untreated (and partially treated) urine is the main anthropogenic route of environmental discharge of nutrients, most concerning for nitrogen, whose release has exceeded the planet’s own self-healing capacity. Urine contains all key macronutrients (N, P, and K) and micronutrients (S, Ca, Mg, and trace metals) needed for plant growth and is, therefore, an excellent fertilizer. However, direct reuse is not recommended in modern society due to the presence of active organic molecules and heavy metals in urine. Many systems have been proposed and tested for nutrient recovery from urine, but none so far has reached technological maturity due to usually high power or chemical requirements or the need for advanced process controls. This work is the proof of concept for the world’s first nutrient recovery system that powers itself and does not require any chemicals or process controls. This is a variation of the previously proposed microbial electrochemical Ugold process, where a novel air cathode catalyst active in urine conditions (pH 9, high ammonia) enables in situ generation of electricity in a microbial fuel cell setup, and the simultaneous harvesting of such electricity for the electrodialytic concentration of ionic nutrients into a product stream, which is free of heavy metals. The system was able to sustain electrical current densities around 3 A m^–2 for over two months while simultaneously upconcentrating N and K by a factor of 1.5–1.7. Full article

Yellow water is a segregated domestic wastewater stream resulting from Ecological Sanitation (ECOSAN). It is mainly source separated human urine which is rich in nutrients. The potential contribution of yellow water as fertilizer to food security is considerable. The use of this potential however is related to the acceptance of the consumers towards urine based fertilizers (UBF). This work aims to assess acceptance of consumers towards UBF and urine diverting toilets (UDT) for separation of urine, through questionnaires with 444 participants from Egypt, Iraq and Turkey with different age groups, genders, educational backgrounds and occupations. The overall acceptance for UDTs and UBF was 62% and 56%, respectively. All-in-all, public opinion regarding the use of UDT/UBF is promising. Full article

A novel method for the simultaneous determination of enniatins A, A1, B and B1 and beauvericin, both in human urine and plasma samples, was developed and validated. The method consisted of a simple and easy pretreatment, specific for each matrix, followed by solid phase extraction (SPE) and detection by high performance liquid chromatography-tandem mass spectrometry with an electrospray ion source. The optimized SPE method was performed on graphitized carbon black cartridges after suitable dilution of the extracts, which allowed high mycotoxin absolute recoveries (76%–103%) and the removal of the major interferences from the matrix. The method was extensively evaluated for plasma and urine samples separately, providing satisfactory results in terms of linearity (R² of 0.991–0.999), process efficiency (>81%), trueness (recoveries between 85% and 120%), intra-day precision (relative standard deviation, RSD < 18%), inter-day precision (RSD < 21%) and method quantification limits (ranging between 20 ng·L⁻¹ and 40 ng·L⁻¹ in plasma and between 5 ng·L⁻¹ and 20 ng·L⁻¹ in urine). Finally, the highly sensitive validated method was applied to some urine and plasma samples from different donors. Full article