Commercial Standards Research Articles

Multidimensional assessment of yield and quality of starchy potato cultivars

Tubers destined for starch production in potato industry need to meet certain commercial quality standards. The objective of the work was to conduct a multivariate assessment of yield potential and tuber quality of starchy potato cultivars. An analysis was performed of data describing potato cultivars listed in the National List of Potato Varieties (KRO) in Poland published by the Plant Breeding and Acclimatization Institute – National Research Institute at Radzików. Very early and early as well as medium late and late starchy potato cultivars were analysed in terms of 13 quantitative characteristic using principal component analysis and cluster analysis. It was demonstrated that, regardless of earliness group, the following traits had the greatest share in the total variation of starchy potato cultivars: tuber yield, starch content, starch yield and bioethanol yield. Cluster analysis allowed the division of very early and early cultivars into 3 groups. The cultivars Szyper, Zuzanna, Kuba and Jubilat, included in the first group, produced superior yields, the highest bioethanol yield and were the most resistant to potato blight. Medium late and late cultivars were divided into two groups. The first group (Pokusa, Gandawa, Rudawa, Hinga, Inwestor, Pasja, Pomorska and Ikar) gave poorer yields and lower bioethanol yields but were more resistant to potato blight in comparison with the second group (Sonda, Kuras, Jasia, Bzura, Skawa and Danuta). The multidimensional methods applied allowed a simultaneous assessment of starchy potato cultivars in terms of many characteristics, and grouping into clusters sharing similar traits.

A strong, silk protein-inspired tissue adhesive with an enhanced drug release mechanism for transdermal drug delivery

In transdermal drug delivery system (TDDS) patches, achieving prolonged adhesion, high drug loading, and rapid drug release simultaneously presented a significant challenge. In this study, a PHT-SP-Cu2+ adhesive was synthesized using polyethylene glycol (PEG), hexamethylene diisocyanate (HDI), trimethylolpropane (TMP), and silk protein (SP) as functional monomers which were combined with Cu2+ to improve the adhesion, drug loading, and drug release of the patch. The structure of the adhesion chains and the formation of Cu2+-p-π conjugated network in PHT-SP-Cu2+ were characterized and elucidated using different characterization methods including FT-IR, 13C NMR, XPS, SEM imaging and thermodynamic evaluation. The formulation of pressure-sensitive adhesive (PSA) was optimized through comprehensive research on adhesion, mechanics, rheology, and surface energy. The formulation of 3 wt.% SP and 3 wt.% Cu2+ provided superior adhesion properties compared to commercial standards. Subsequently, the peel strength of PHT-SP-Cu2+ was 7.6 times higher than that of the commercially available adhesive DURO-TAK® 87–4098 in the porcine skin peel test. The adhesion test on human skin confirmed that PHT-SP-Cu2+ could adhere to the human body for more than six days. Moreover, the drug loading, in vitro release test and skin permeation test were investigated using ketoprofen as a model drug, and the results showed that PHT-SP-Cu2+ had the efficacy of improving drug compatibility, promoting drug release and enhancing skin permeation as a TDDS. Among them, the drug loading of PHT-SP-Cu2+ was increased by 6.25-fold compared with PHT, and in the in vivo pharmacokinetic analysis, the AUC was similarly increased by 19.22-fold. The mechanism of α-helix facilitated drug release was demonstrated by Flori-Hawkins interaction parameters, molecular dynamics simulations and FT-IR. Biosafety evaluations highlighted the superior skin cytocompatibility and safety of PHT-SP-Cu2+ for transdermal applications. These results would contribute to the development of TDDS patch adhesives with outstanding adhesion, drug loading and release efficiency. Statement of significanceA new adhesive, PHT-SP-Cu2+, was created for transdermal drug delivery patches. Polyethylene glycol, hexamethylene diisocyanate, trimethylolpropane, silk protein, and Cu2+ were used in synthesis. Characterization techniques confirmed the structure and Cu2+-p-π conjugated networks. Optimal formulation included 3 wt.% SP and 3 wt.% Cu2+, exhibiting superior adhesion. PHT-SP-Cu2+ showed 7.6 times higher peel strength than DURO-TAK® 87–4098 on porcine skin and adhered to human skin for over six days. It demonstrated a 6.25-fold increase in drug loading compared to PHT, with 19.22-fold higher AUC in vivo studies. α-helix facilitated drug release, proven by various analyses. PHT-SP-Cu2+ showed excellent cytocompatibility and safety for transdermal applications. This study contributes to developing efficient TDDS patches.

Evaluation of mesoporous silica particles as a support for lipase immobilization in biodiesel production: Enhanced ethyl ester synthesis from algal oil

The utilization of novel materials in the biofuel production domain has been regarded as a significant advancement in catalyst development. Incorporating lipases in biodiesel manufacturing is often viewed as a cost-restrictive phase since the expenses associated with recovering these catalysts can render market expectations unfeasible. Within this investigation, mesoporous silica (MPS) particles were assessed as a supporting medium for immobilizing commercial lipase, subsequent to their utilization in ethyl ester synthesis. Initially, the production of mesoporous silica was achieved through the co-precipitation technique at a consistent pH and was subsequently chosen as an immobilization support for the enzyme. The characterization of the biocatalyst support materials produced was performed using various analytical methods including X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and BET analysis. The Novozym 435 lipase was then immobilized within the matrices, followed by the transesterification process of algal oil derived from Nannochloropsis. The resulting biodiesel samples demonstrated compliance with commercial standards, exhibiting an ester conversion rate exceeding 94.8 %. Additionally, properties such as density (0.93 g cm−3) and viscosity (5.01 mm2 s−1) satisfied the specifications mandated by ASTM for biofuel application. Experimental planning techniques showed that increasing lipase loading and using temperatures between 38 and 48 °C resulted in higher conversion rates of ethyl esters. This confirms the effectiveness of the enzymatic catalyst in generating primary fatty acid esters, even with residual lipid feedstocks.

Study on Al Evaporation during AlV55 Melting and Alloy Preparation

Vacuum induction melting is a commonly used method for preparing AlV55 alloys. However, this method results in high Al evaporation losses, leading to poor cost control. Moreover, the influence of the process parameters on the alloy composition remains unclear. In this study, the evaporation pattern of Al in the melting and preparation processes of AlV55 alloys is studied, and measures for controlling the system pressure are proposed to effectively reduce Al evaporation. The experimental results show that smelting under an Ar gas atmosphere of 2000 Pa can reduce the evaporation loss of Al from 11.48% under vacuum conditions (60 Pa) to 0.58% of the amount of raw material added, effectively improving the metal utilization rate and reducing production costs. The influence of various process parameters on the alloy composition and Al volatilization are investigated to enable the effective control of the compositional uniformity and impurity content of the resulting alloys. Under optimal conditions, the impurity contents of C, O, and N are 0.03%, 0.0073%, and 0.013%, respectively; this reduces the amount of Al lost by evaporation compared to conventional methods, and the alloy produced meets commercial standards.

Improved lipid analysis using a 2D-LC-MS system with a novel injection procedure

The aim of this study was to improve analysis of nonpolar lipidomics sample extracts using reversed phase (RP) chromatography. A 4/3/3 (v/v/v) mixture of methanol/methyl tert-butyl ether/chloroform (MeOH/MTBE/CHCl3, MMC) was chosen for sample extraction solvent based on its proven extraction capability for several lipid classes. To avoid carry over, loss of analytes and peak distortion the loops and all capillaries of the presented LC system were flushed and filled up with methanol until the analytical column. The choice of methanol was due to its weak elution strength and being infinitely miscible with MMC and several other nonpolar solvents. This allowed injection of a 100 μl sample that was 20 μl nonpolar extraction solvent diluted fivefold with methanol. All lipids of 25 lipid classes were transferred quantitatively to the column head where the online dilution of methanol was carried out with aqueous eluent for focusing the lipid analytes. The weak elution strength of methanol prevented peak distortions. The consecutive reversed phase elution resulted in remarkably narrow peaks (full width at half maximum was 0.07–0.08 min typically) and enhanced sensitivity (limit of detection usually in sub nM region) because of increased sample injection volume and narrow peaks. Calibration and quality control samples made by diluting commercial lipid standards 200–50000 times confirmed the applicability of this approach both for targeted lipid quantification and for untargeted quantitative comparison of lipids from different sources.

Microsatellite Instability Detection in Cancer: A Multiplex qPCR Approach that Obviates the Need for Matching Normal Samples.

Microsatellite instability (MSI) indicates DNA mismatch repair deficiency in certain types of cancer, such as colorectal cancer. The current gold standard technique, PCR-capillary electrophoresis (CE), requires matching normal samples and specialized instrumentation. We developed VarTrace, a rapid and low-cost quantitative PCR (qPCR) assay, to evaluate MSI using solely the tumor sample DNA, obviating the requirement for matching normal samples. One hundred and one formalin-fixed paraffin-embedded (FFPE) tumor samples were tested using VarTrace and compared with the Promega OncoMate assay utilizing PCR-CE. Tumor percentage limit of detection was evaluated on contrived samples derived from clinical high MSI (MSI-H) samples. Analytical sensitivity, specificity, limit of detection, and input requirements were assessed using synthetic commercial reference standards. VarTrace successfully analyzed all 101 clinical FFPE samples, demonstrating 100% sensitivity and 98% specificity compared to OncoMate. It detected MSI-H with 97% accuracy down to 10% tumor. Analytical studies using synthetic samples showed a limit of detection of 5% variant allele frequency and a limit of input of 0.5 ng. This study validates VarTrace as a swift, accurate, and economical assay for MSI detection in samples with low tumor percentages without the need for matching normal DNA. VarTrace's capacity for highly sensitive MSI analysis holds potential for enhancing the efficiency of clinical work flows and broadening the availability of this test.

Impact of densification process on unprocessed biomass and post-hydrothermal carbonization

The pulp and paper industry use biomass residues, such as paper sludge and bark as fuel to provide energy for their plants. However, issues such as high-water content or low heating value limit the amount of energy that can be utilized. Processes to improve heat generation include biomass densification, which facilitates transportation and handling and can increase energy yield. However, the technical feasibility of briquetting is a function of the feedstock and preprocessing. This study introduces a novel approach to briquette production from biomass residues by utilizing wet biomass with water as a natural binder, contrasting with conventional methods that require forced drying and/or the addition of binders. The objective of this research was to investigate the impact of briquetting both unprocessed biomass and post-hydrothermal carbonization. The study focused on manufacturing briquettes derived from different sources, including bark (Balsam fir), paper sludge, and hydrochar of paper sludge. The feedstock was characterized for ash content and higher heating value. Biomass particle size (range), moisture content (range), process temperature (range), process pressure (range), and process residence time (range) were varied in briquetting experiments to determine conditions to produce high-quality briquettes with minimal energy input. Moisture content as high a 50 wt% in feedstock produced technically feasible briquettes, with appropriate physical-mechanical properties (durability, volumetric expansion and apparent density), and energetic potential (calorific value). The addition of heat (pressing temperature of 150 °C) during the pressing process resulted in briquettes with enhanced physical-mechanical, and energetic properties, surpassing those produced at room temperature. Further tests with additional steps in the production process are required to meet commercialization standards in Canada, but the treatments conducted in this study effectively improved the energy potential of biomass for internal industrial energy gains.

Characterization of genetic diversity of greens‐type hybrid bermudagrass selections through SSR markers and morphological analysis

AbstractThe development of Tifgreen bermudagrass, and the subsequent mutations of this cultivar, has revolutionized the game of golf in the southern United States as superintendents have access to high‐quality putting surface capable of withstanding hot summers. However, the lack of genetic diversity may make them vulnerable to various pests and the low tolerance to freeze temperatures may make them susceptible to winterkill. In recent years, Oklahoma State University and other universities have begun to create new interspecific F1 hybrids between common (Cynodon dactylon) and African bermudagrasses (C. transvaalensis) for putting greens. The objectives of this study were to investigate the genetic diversity and variation among 14 experimental genotypes and two standard cultivars (TifEagle and Tifdwarf). Simple sequence repeat (SSR) markers and morphological characteristics were used to evaluate the genetic relationships and variation among the 16 genotypes. Results showed significant variation for 11 vegetative traits and two reproductive traits. The phenotypic coefficient of variation was greatest for the third internode length and the least for the first leaf angle for both the field and greenhouse trials. The morphological cluster analysis also showed variation between the two trial environments. The SSR marker cluster analysis showed the 16 genotypes were grouped into four major groups, with a similarity coefficient ranging from 0.44 to 1. The highest similarity was found among the two commercial standards and an experimental ultradwarf from Florida. Several new genotypes (OKC3920, 5 × 23, 11 × 2, 19 × 19, and 34 × 20) were also grouped with the ultradwarf genotypes in the morphological cluster analysis, showing the possibility of achieving similar morphological traits with new genetics. Further field evaluations are needed to determine the performance of these genotypes under low mowing heights.

UPLC-TQD-MS/MS Method Validation for Quality Control of Alkaloid Content in Lepidium meyenii (Maca)-Containing Food and Dietary Supplements.

Lepidium meyenii Walp. (Brassicaceae), also known as Maca or Peruvian ginseng, is a common ingredient in food supplements with many claimed health benefits, such as improved endurance, increased energy level, and enhanced sexual properties. Due to potential toxicity of its chemicals, including alkaloids, some regulatory authorities, e.g., in Belgium, Germany, the United States, expressed concerns about the safe consumption of Maca root. However, due to the lack of commercial standards, no established analytical method currently exists for this purpose. The current project focuses on the quantitative determination of potentially toxic alkaloids from Maca. The current study presents the first analytical method for quality control of alkaloid content in Maca-containing food and dietary supplements, assessing the presence of 11 major compounds belonging to three different classes, i.e., imidazole, β-carboline, and pyrrole alkaloids. An accurate, rapid, and sensitive UPLC-TQD-MS/MS method is reported, which was fully validated according to the International Council for Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) and SANTE/11312/2021 guidelines. To ensure the method's applicability and practicability in the absence of primary standards, validation of secondary standards (SSs) alongside primary standards (PSs) was also conducted for imidazole alkaloids. As a result, in Maca raw powder, total alkaloid content was found to vary from 418 to 554 ppm (mg/kg). Furthermore, all quantified imidazole alkaloids were ascertained to be the major alkaloids with the total content from 323 to 470 ppm in Maca raw powder, followed by the β-carboline and pyrrole alkaloids. It was also observed that the commercial preparation of finished products affects the total alkaloid content, evidenced by the large variation from 56 to 598 ppm. Ultimately, from a regulatory point of view, it seems advisible not to request the complete absence of the alkaloids but to impose a maximum level based on safety considerations. In addition to the analytical method, a low-cost, simple, and scalable synthetic scheme of macapyrrolins A, C, and G was reported for the first time.

ASSESSING 14C BLANKS IN THE SMALL-SCALE ANALYSIS OF N-ALKANE COMPOUND-SPECIFIC-RADIOCARBON-ANALYSIS

ABSTRACTCompound-specific radiocarbon analysis (CSRA) provides the possibility to date sample material at a molecular level. N-alkanes are considered as specific compounds with high potential to CSRA. As these compounds originate from plant waxes, their radiocarbon (14C) analysis can provide valuable information about the age and origin of organic materials. This helps to reconstruct and understand environmental conditions and changes in vegetation in the past. However, CSRA has two main challenges: The small sample size of CSRA samples, making them extremely sensitive to blank effects, and the input of unknown amounts of extraneous carbon during the analytical procedure. According to the previous study from Sun and co-workers, we used different-sized aliquots of leaves Fagus sylvatica (nC27, nC29) and Festuca rubra agg (nC31, nC33) as modern standards and two commercial standards (nC26, nC28) as fossil standards for blank determination. A third commercial standard (nC27) with predetermined radiocarbon content of F14C = 0.71 (14C age of 2700 BP) serves to evaluate the blank correction. We found that the blank assessment of Sun and co-workers is also applicable to n-alkanes, with a minimum sample size of 15 µg C for dependable CSRA dates. We determined that the blank introduced during the analytical procedure has a mass of (4.1 ± 0.7) µg carrying a radiocarbon content of F14C = 0.25 ± 0.05. Applying the blank correction to a sediment sample from Lake Holzmaar (Germany) shows that all four isolated n-alkanes have similar 14C ages. However, the bulk material of the sediment and branches found in the sediment core are younger than the CSRA dates. We conclude that the disparity between the actual age of analysed organic material and the age inferred from radiocarbon results, which can occur in sediment traps due to delayed deposition, is the reason for the CSRA age.

Abstract 5016: Building better contrived samples to properly evaluate Next-generation MRD and LBx assays

Abstract Circulating tumor DNA (ctDNA) is a component of cell-free DNA (cfDNA) that originates from tumor tissue in the plasma of cancer patients. Although ctDNA is a broadly applicable tumor biomarker, the absolute amount of ctDNA varies across indication and stage, with the level of ctDNA present reflective of tumor volume. As novel methods for the characterization of ctDNA develop, there is need to evaluate these assays with appropriate samples. But current commercial reference standards, generated from modified cell lines or oligonucleotides lack important features such as DNA methylation, fragmentation pattern and nucleosome positioning, whilst clinical trial samples lack the required volume to perform multiple tests and often lack proper consent. We have created a framework for generating contrived samples containing the biological features of clinical samples and the attributes of a reference standard. The plasma-in-plasma contrived samples are generated from commercially purchased and fully consented matched tumor and plasma from cancer patients with age and gender matched healthy donor plasma. Samples are characterized by an internally validated 700 gene NGS panel to identify somatic variants and copy number alterations, which establishes ‘ground truth’. A contrived plasma dilution range based on the mean variant allele frequency (VAF) of the concordant somatic variants identified is generated. Using these methods, we have been able to generate sample sets for pan-cancer and disease specific evaluations. We have tested these samples through many novel high sensitivity assays that utilize both tumor-informed and tumor agnostic methods. We have confirmed that plasma-in-plasma contrived samples are amenable to all evaluated assays to date. The FFPE tumor tissue provide results matching clinical trial samples and the extraction yields of cfDNA are within the range of plasma samples from clinical trial data. Each dilution can be generated with replicates for reproducibility metrics. Current models of the sample dilutions have been generated to increase the number of replicates at relevant levels of tumor burden (i.e., 0.01% VAF). Negative samples consisting of the background plasma were also generated for each sample used. These plasma-in-plasma contrived samples have greater commutability to clinical samples than other commercial reference standards, however there are limitations. The complexity of generating these samples restrict the number of unique patients that can be utilized. Also, due to the volume of healthy plasma used as diluent, it is difficult to generate volumes greater than 4ml. To our knowledge, this is the first report examining the generation and usage of a contrived sample set that can be applied to evaluating novel high sensitivity MRD assays with clinical sample commutability. Citation Format: Paul Labrousse, Hugh Russell, David Shera, Daniel Stetson, Barrett Nuttall, Brian Dougherty, Darren Hodgson, James Hadfield. Building better contrived samples to properly evaluate Next-generation MRD and LBx assays [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 5016.

Optimization of Fermentation and Sensory Quality of Mango Yogurt Using Various Sucrose Concentration Fermented by Lacticaseibaciluus paracasei Strain Shirota

This research explores the optimization of mango yogurt production, leveraging mango as the primary fermentation ingredient and Lacticaseibacillus paracasei strain Shirota (LcS) as the probiotic inoculum. Traditional yogurt, typically derived from animal milk, faces competition from plant-based alternatives. The research objective is to investigate the impact of inoculum ratios and sucrose concentrations on LcS density and sensory attributes, with a focus on the Substrate to Inoculum Ratio (S/I) as a critical parameter influencing microbial metabolism and population dynamics. Various inoculum ratios (1:1, 1:2, 1:4, 1:8 v/v) and sucrose concentrations (0%, 2.5%, 5%, 7.5%) were applied in mango yogurt production. Results from ANOVA analysis indicated significant differences in LcS density among inoculum ratios (F3,16 = 37.01, P = 0.000) and sucrose concentrations (F3,16 = 19.07, P = 0.000). The 1:2 inoculum ratio and 7.5% sucrose concentration emerged as optimal, as evidenced by stable pH conditions and lactic acid profiles within recommended standards. Sensory analysis, employing a 5-point hedonic scale for color, odor, taste, and texture evaluation, revealed moderate acceptance. In conclusion, this study introduces an innovative approach to mango yogurt production, highlighting the potential of specific inoculum ratios and sucrose concentrations for optimal results. The findings contribute to the broader landscape of plant-based yogurt alternatives, underscoring the need for ongoing refinement to meet commercial standards and ensure consumer satisfaction.

Physiological Quality of Treated and Stored Barley Seeds

Industrial seed treatment (IST) is used in some grain crops. However, the products used often impair the quality of seeds, especially insecticides. In the case of barley seeds, investigative studies on the use of IST are scarce. The present study aimed to evaluate the influence of IST with the fungicide (Iprodione) and insecticide (Thiamethoxan) products, mixed or not, on the physiological quality of barley seeds, before and after storage for two months. A completely randomized design was used, in a 4x2 factorial scheme, with four replications. The treatments consisted of four combinations of applications carried out via IST on barley seeds, of chemical pesticides (fungicide/insecticide), alone or in mixtures, as follows: {T1 – fungicide Iprodione (Rovral); T2 – Thiamethoxan insecticide (Cruizer); T3 – mixture of fungicide/insecticide products (Iprodione + Thiamethoxan); T4 – Control)}, submitted to storage for two months, with evaluations carried out at T0 (treated and analyzed seeds) and T1 (treated seeds stored for 60 days). The following tests were carried out: water content, germination, first count, accelerated aging, seedling length, seedling dry mass. It was concluded that the germination of barley seeds treated with the fungicide Iprodione (Rovral®) and the insecticide Thiamethoxan (Cruizer®), alone and in a mixture applied via IST, maintained the physiological quality of the seeds within the standards for commercialization until 60 days of storage. The use of the insecticide Thiamethoxan (Cruizer®) via IST showed greater damage to the physiology of barley seeds during storage (60 days), applied alone or in a mixture with the fungicide Iprodione (Rovral ®).

Hydrocracking of a HDPE/VGO Blend: Influence of Catalyst-to-Feed Ratio on Fuel Yield and Composition

The effects that the catalyst-to-feed ratio have on the yields of products and composition of the naphtha and light cycle oil (LCO) fractions in the hydrocracking of a blend composed of high-density polyethylene (HDPE) and vacuum gasoil (VGO) using a PtPd/HY catalyst were assessed. The hydrocracking runs were carried out in a batch reactor fixing the following operation conditions: 420 °C, 80 bar, 120 min and an HDPE-to-VGO ratio of 0.2 gHDPE gVGO−1, varying the catalyst-to-feed mass ratio within the 0.05–0.1 gcatalyst gfeed−1 range. The obtained results exposed that a catalyst-to-feed mass ratio of 0.075 gcatalyst gfeed−1 provided the best results, since the conversion of the heavy cycle oil (HCO) fraction and of the HDPE offered quite high values (73.1 and 63.9%, respectively) without causing an excessive overcracking in the form of gas products (the yield of gases was of 25%). Moreover, an interesting yield of naphtha (37.0 wt%) with an RON within the commercial standards (92.5) was obtained. With regard to coke formation, not-so-developed structures were formed for a catalyst-to-feed mass ratio of 0.075 gcatalyst gfeed−1, easing their combustion and presumably extending the lifespan of the catalyst.

Phenotypic characterization and quality perception of unsulfurated dried apricots in a panel of European accessions and breeding selections

Dried apricots are a nutrient-rich food increasingly attracting consumer's interest, especially when processed without preservative substances. Despite a certain increase of market demand, dried apricot production still relies on a few varieties with poorly differentiated taste and aroma. This study evaluates several quality-related features in fresh apricots and their impact on taste after drying in a set of fourteen accessions and breeding selections and includes three commercial standards to corroborate the results. The characterization of European apricot germplasm could allow the identification of novel materials that possess superior organoleptic characteristics after hot-air drying in order to renew the current varietal landscape.Apricot fruits were collected at full-physiological ripening stage in two harvesting seasons (2021 and 2022) in Italy and were characterized for several physical (fruit weight, flesh firmness and dry matter) and chemical (content of total polyphenols, soluble solids, titratable acidity and ten organic acids) attributes. The whole apricot accessions showed a phenotypic variation extremely valuable in ongoing breeding programmes that try to enhance fruit quality. Among the totality of apricot advanced selections, ‘BO02611038’, ‘BO10619011’, ‘BO11618023’ and ‘BO12607228’ were the most ranked for their high aroma, medium sourness and low bitterness. Citrate and malate were the most abundant organic acids found in fruit flesh and skin but only quinate seemed to enhance the sour taste and impact the sweetness. Interestingly, no differences were perceived by panelists in sweet taste perception leading to consider it an already-achieved breeding target in the European accessions included in our study. In addition, fruit dry matter content seemed to affect both textural properties and taste advancing it as a reliable selection criterion in novel apricot accessions meant for drying.The majority of the dried selections analyzed in this study revealed a superior organoleptic profile compared to commercial standards. A detailed characterization of fresh fruit quality attributes indicated that some parameters might be used to predict the sensory potential of dried apricots, while the aromatic profile seemed the next breeding target to improve the overall taste and further increase the degree of liking in consumers.

A 10 V Transfer Standard Based on Low-Noise Solid-State Zener Voltage Reference ADR1000

Voltage standards are widely used to transfer volts from Josephson voltage standards (JVSs) at national metrology institutes (NMIs) into calibration labs to maintain the volts and to transfer them to test equipment at production lines. Therefore, commercial voltage standards based on Zener diodes are used. Analog Devices Inc. (San Jose, CA, USA), namely, Eric Modica, introduced the ADR1000KHZ, a successor to the legendary LTZ1000, at the Metrology Meeting 2021. The first production samples were already available prior to this event. In this article, this new temperature-stabilized Zener diode is compared to several others as per datasheet specifications. Motivated by the superior parameters, a 10 V transfer standard prototype for laboratory use with commercial off-the-shelf components such as resistor networks and chopper amplifiers was built. How much effort it takes to reach the given parameters was investigated. This paper describes how the reference was set up to operate it at its zero-temperature coefficient (z.t.c.) temperature and to lower the requirements for the oven stability. Furthermore, it is shown how the overall temperature coefficient (t.c.) of the circuit was reduced. For the buffered Zener voltage, a t.c. of almost zero, and with amplification to 10 V, a t.c. of <0.01 µV/V/K was achieved in a temperature span of 15 to 31 °C. For the buffered Zener voltage, a noise of ~584 nVp-p and for the 10 V output, ~805 nVp-p were obtained. Finally, 850 days of drift data were taken by comparing the transfer standard prototype to two Fluke 7000 voltage standards according to the method described in NBS Technical Note 430. The drift specification was, however, not met.

Synthesis, characterization, antibacterial and antioxidant activity of 1,5-bis(6-chloro-1H-benzimidazol-2-yl)pentan-3-one and its Fe(III), Co(II), Cu(II), Zn(II) and Ru(II) complexes

A new bis-benzimidazole ligand, 1,5-bis(6-chloro-1H-benzimidazol-2-yl)pentan-3-one (L, C19H16Cl2N4O), and its complexes with Fe(III), Co(II), Cu(II), Zn(II) and Ru(II) chlorides are synthesized and characterized by elemental analysis, molar conductivity, magnetic moment, TGA, FT-IR, 1H-NMR, fluorescence and UV-visible spectroscopy. The spectral data suggest that the chelating ligand acted as tridentate towards to Cu(II) ion however bidentate in the other complexes. According to the molar conductance data, [Fe(L)2Cl2]Cl•2H2O and [Cu(L)Cl]Cl•2H2O complexes are 1:1 electrolytes whereas [Co(L)Cl2]•2H2O, [Zn(L)(Cl)2(H2O)]•H2O and [Ru(L)(DMSO)(H2O)Cl2] complexes are non-ionic. In addition, antibacterial and antioxidant activity of the compounds were tested. The Ru(II) and Co(II) complexes showed moderate activity against to all tested bacteria whereas the ligand itself had no activity. According to the 1,1-diphenyl-2-picrylhydrazyl radical (DPPH•) scavenging results, the Ru(II) complex of L had quite significant radical scavenging activity almost the same as that of 3,5-di-tert-4-butylhydroxytoluene (BHT), a commercial standard.

Evaluation of Porous (Poly(lactide-co-glycolide)-co-(ε-caprolactone)) Polyurethane for Use in Orthopedic Scaffolds.

To develop an orthopedic scaffold that could overcome the limitations of implants used in clinics, we designed poly(ester-urethane) foams and compared their properties with those of a commercial gold standard. A degradable poly(ester-urethane) was synthetized by polyaddition between a diisocyanate poly(ε-caprolactone) prepolymer (PCL di-NCO, Mn = 2400 g·mol-1) and poly(lactic-co-glycolic acid) diol (PLGA, Mn = 2200 g·mol-1) acting as a chain extender. The resulting high-molecular-weight poly(ester-urethane) (PEU, Mn = 87,000 g·mol-1) was obtained and thoroughly characterized by NMR, FTIR and SEC-MALS. The porous scaffolds were then processed using the solvent casting (SC)/particle leaching (PL) method with different NaCl crystal concentrations. The morphology, pore size and porosity of the foams were evaluated using SEM, showing interconnected pores with a uniform size of around 150 µm. The mechanical properties of the scaffolds are close to those of the human meniscus (Ey = 0.5~1 MPa). Their degradation under accelerated conditions confirms that incorporating PLGA into the scaffolds greatly accelerates their degradation rate compared to the gold-standard implant. Finally, a cytotoxicity study confirmed the absence of the cytotoxicity of the PEU, with a 90% viability of the L929 cells. These results suggest that degradable porous PLGA/PCL poly(ester-urethane) has potential in the development of meniscal implants.

Linear growth behaviour of intermetallic compound layer in electronic interconnections

We observed a linear behaviour of intermetallic compound (IMC) layer growth in electronic metallurgical interconnections, although the time required was twice that of commercial reliability standards for electronic packaging. This finding contradicts the classical parabolic growth law, which is widely reported to represent growth behaviour. We suggest that the parabolic growth law may be inadequate to thoroughly explain the IMC layer's growth by considering (a) one-directional growth and (b) reactions between elements for formation and growth. Further analysis has been carried out to analyse the logical judgment of the parabolic growth law and support our finding over linear IMC layer growth behavior.

Quantification of [99Tc]TcO4- in urine by means of anion-exchange chromatography–aerosol desolvation nebulization–inductively coupled plasma–mass spectrometry

To sensitively determine 99Tc, a new method for internal quantification of its most common and stable species, [99Tc]TcO4-\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext{O}}_{4}^{-}$$\\end{document}, was developed. Anion-exchange chromatography (IC) was coupled to inductively coupled plasma–mass spectrometry (ICP-MS) and equipped with an aerosol desolvation system to provide enhanced detection power. Due to a lack of commercial Tc standards, an isotope dilution-like approach using a Ru spike and called isobaric dilution analysis (IBDA) was used for internal quantification of 99Tc. This approach required knowledge of the sensitivities of 99Ru and 99Tc in ICP-MS. The latter was determined using an in-house prepared standard manufactured from decayed medical 99mTc-generator eluates. This standard was cleaned and preconcentrated using extraction chromatography with TEVA resin and quantified via total reflection X-ray fluorescence (TXRF) analysis. IC coupled to ICP-MS enabled to separate, detect and quantify [99Tc]TcO4-\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext{O}}_{4}^{-}$$\\end{document} as most stable Tc species in complex environments, which was demonstrated in a proof of concept. We quantified this species in untreated and undiluted raw urine collected from a patient, who previously underwent scintigraphy with a 99mTc-tracer, and determined a concentration of 19.6 ± 0.5 ng L−1. The developed method has a high utility to characterize a range of Tc-based radiopharmaceuticals, to determine concentrations, purity, and degradation products in complex samples without the need to assess activity parameters of 99(m)Tc.Graphical