Reaction Components Research Articles

Utilizing Alkyne-Nitrone Cycloaddition for the Convenient Multi-Component Assembly of Protein Degraders and Biological Probes.

Proteolysis-targeting chimeras (PROTACs) have become a popular therapeutic strategy, and the development of multi-functional PROTACs has added complexity to their synthetic process. Although click reactions have been widely applied to prepare highly functionalized biomolecules, most of them are limited to two-component reactions, restricting the creation of more complex structures. Here, we developed a convenient multi-component assembly strategy via strain-promoted alkyne-nitrone cycloaddition (SPANC), which can be extended to a 3-component reaction when combined with nitrone formation. Using the 2-component assembly, we demonstrated the targeted protein degradation with both preassembled and in-cell assembled PROTACs. This strategy was also applied to facilitate the screening of E3 ligases in PROTACs and the preparation of various biological probes. Moreover, the 3-component assembly, via sequential nitrone formation and SPANC, enabled the synthesis of trifunctional 3-component PROTACs. The N-substituent, serving as an additional functional moiety, was designed as a photocage for sterically controlling PROTAC activity. The 3-component assembly can be further modified to provide additional control or enhance the cell-targeting ability of PROTACs. In short, our multi-component SPANC assembly strategy offers a modular and versatile synthetic platform for creating multi-functional PROTACs and biological probes.

The suppression and CO elimination performance of Co3O4 dust cloud for methane-air mixture explosion

This paper experimentally studied the effect of Co3O4 dust clouds on the methane-air mixture explosion characteristics and post-explosion CO concentration, aiming to propose a novel method for simultaneously suppressing explosion and eliminating CO product. The Co3O4 catalyst was synthesized utilizing the co-precipitation method. We varied the methane concentration and Co3O4 dust cloud concentration to investigate their effects on the flame propagation behavior, maximum explosion overpressure (Pm), flame combustion time (tc), and the gaseous product concentration. The hazard of the gaseous product was evaluated by the effective escape time (te) based on the Fraction Effective Dose (FED) mathematical model. The results demonstrated that the Co3O4 dust cloud could significantly reduce the explosion severity and CO concentration. Furthermore, the higher the concentration of Co3O4 dust clouds, the more significant the explosion suppression and CO elimination performance, which was as a result of the significant increase in the contact area and collision probability between the Co3O4 particles and the reaction components increased. Compared to traditional inhibitors that only reduce the severity of an explosion, Co₃O₄ could not only significantly reduce the explosion severity, but also quickly eliminate post-detonation CO. The method proposed in this paper could effectively reduce the hazard of methane-air mixture explosion, which was of great practical significance for ensuring the safety of personnel involved in the risk.

A novel neutralization process for improving dehydration performance of industrial by-product gypsum

By-product gypsum, produced through the traditional neutralization precipitation method for treating industrial acidic wastewater, is difficult to recycle due to its high moisture content. In this study, we proposed a novel neutralization process i.e. the two-stage neutralization method. By-product gypsum was used as an alkaline neutralizer and recycled as seed crystals for the first time. The original by-product gypsum has the poor dehydration performance due to its small particle size and the presence of colloids on its surface. After adding the by-product gypsum to the acidic wastewater, the ratio of CaO/SO3 in the system descended and colloids were dissociated. On the one hand, the alkaline component of the incomplete reaction continues to play a neutralizing role. On the other hand, CaSO4·2H2O particles act as seed crystals, promoting rapid growth of new crystals along their surface, which effectively improved crystallization performance and dehydration performance of the neutralization slag (outward discharge of slag). Compared with the original method, the wet weight of the neutralization slag is decreased from 186.0 g/L to 88.8 g/L, and the water cut is declined from 64.5% to 34.1%. The utilization ratio of the carbide slag augmented from 63.0% to 99.47%.

Tribological Properties of SPS Reactive Sintered Al/MoS2 Composites

In search of opportunities to improve mechanical properties and abrasion resistance, composites based on aluminum reinforced with MoS2 particles were produced. The authors’ previous research indicated the possibility of obtaining hard dispersion precipitates of the Al12Mo intermetallic phase as a result of the reaction of the composite components at a temperature exceeding 550 °C during the SPS (Spark Plasma Sintering) process. This work focused on optimizing the SPS consolidation process and assessing the microstructure and mechanical properties of the obtained materials. A series of experiments proved that by increasing the amount of the strengthening phase and increasing the process temperature, a significant amount of Al12Mo and Al5Mo strengthening phases is produced. Exceptionally good dispersion of reinforcing particles and the presence of layered MoS2 crystals, while ensuring optimal parameters of the synthesis process, lead to a change in friction mechanisms and improved abrasion resistance through an approximately 30-fold decrease in the wear factor.

Preparation of New Aminodimethyl(Methylsulfonyl)Dihydropyrido[2,3-d]Pyrimidinedione Derivatives in the Presence of Fe3O4@SiO2@[O-(CH2)2-NH2][CH3CO2H] as Novel Nanocatalyst

An efficient synthesis of new aminodimethyl(methylsulfonyl)dihydropyrido[2,3-d]pyrimidinedione derivatives via the three components reaction of 2-methanesulfonylacetonitrile, 1,3-dimethyl-6-amino-uracil, and aromatic aldehydes in the presence of [HO-(CH2)2-NH2][CH3CO2H] and Fe3O4@SiO2@[O-(CH2)2-NH2][CH3CO2H] as novel heterogeneous magnetic nanocatalyst was described. The Fe3O4@SiO2@[O-(CH2)2-NH2][CH3CO2H] as nanocatalyst can be easily separated from the reaction mixture by an external magnet, recycled, and reused several times without any significant decrease in catalytic activity. These methods showed several advantages, including high yields, easy operation, and environment-friendly protocols.

A Novel Banana-Shaped Mixed-Metal Co/Fe Polyoxometalate Cluster.

The synthesis and characterization of a Co/Fe mixed-metal banana-shaped polyoxometalate with the formula [(Co2.5Fe0.5(H2O)PW9O34)2(PW6O26)]16- (Co5Fe) is reported. This transition-metal-substituted polyoxometalate readily assembles from its components in a one-pot reaction and crystallizes in the monoclinic space group P21/c. The structure of Co5Fe can be considered a double sandwich composed by two B-α-{Co2.5Fe0.5PW9O40} Keggin units, in which one coordinatively saturated octahedral metal position is equally occupied by Co(II) and Fe(III) ions with a 50 % of site occupancy. These Keggin units are linked via a hexalacunary Keggin unit {PW6O26}. Single crystal X-ray diffraction and magnetic measurements support the proposed atom arrangement within the crystal structure. Magnetic measurements of these double trimeric unit {Co2.5Fe0.5O13}2 show a combination of antiferromagnetic interactions, the presence of spin frustration, and the first-order spin-orbit coupling of Co(II) ions. Electrocatalytic water oxidation measurements show that Co5Fe displays low stability in both homogeneous and heterogeneous conditions. This is evidenced by the constant increase on the catalytic currents over time together with the appearance of polyoxometalate-derived electrode-bound species that can be responsible for the observed catalytic activity.

Visible light-induced photocatalytic oxidation of gaseous ammonia on C surface-coated N-TiO2 catalyst: synthesis, properties and mechanism

This paper explores an eco-friendly and efficient photocatalytic oxidation (PCO) technology aimed at converting NH3 into N2, which holds considerable importance for environmental conservation and human well-being. Building upon previous investigations of N-TiO2 catalysts, the research group successfully synthesized an N-TiO2 catalyst featuring a carbon layer on its surface via mechanical mixing followed by calcination at 400 °C (denoted as C/N-TiO2(1), 1 represents the molar ratio of N and Ti). The analysis concentrated on the influence of C content on the PCO efficiency of NH3, revealing a peak performance correlated with increasing C levels. Notably, the C/N-TiO2(1) catalyst with 3.0 wt% C exhibited remarkable catalytic performance, achieving a conversion rate of 94 % and selectivity of 98 %. The enhancement of catalytic activity and selectivity is primarily attributed to the co-doping of C and N elements. Experimental results indicate that doping with N alone effectively suppresses the recombination of photogenerated carriers under visible light. Furthermore, the simultaneous doping of C and N significantly reduces the band gap energy of TiO2 (3.18 to 2.90 eV), thereby broadening its photoresponse range. Concurrently, more Ov (Oxygen vacancy) are formed under visible light irradiation, which enhances the PCO performance. More importantly, more acidic sites are introduced to improve the catalyst’s adsorption capacity for NH3. Additionally, the impact of various reaction components on the PCO capability of the 3.0 wt% C/N-TiO2(1) catalyst is examined further. The findings indicate that oxygen anion radicals produced from O2 play a critical role in facilitating NH3-PCO. However, the presence of CO2 and extra H2O could hinder the approach of NH3 molecules to the active sites and decrease the longevity of photogenerated ·OH, consequently reducing catalytic effectiveness. This research introduces fresh insights and optimization approaches for enhancing the activity, selectivity, and stability of catalysts.

Molybdenum Complex-Catalyzed N-Alkylation of Bulky Primary and Secondary Amines.

Aliphatic allylic amines are present in a large number of complex and pharmaceutically relevant molecules. The direct amination of allylic electrophiles serves as the most common method toward the preparation of these motifs. However, the use of feedstock reaction components (allyl alcohol and aliphatic amine) in these transformations remains a great challenge. Such a challenge primarily stems from the high Lewis basicity and large steric hindrance of aliphatic amines, in addition to the low reactivity of allylic alcohols. Herein, we report a general solution to these challenges. The developed protocol allows an efficient allylic amination of allyl alcohols with sterically bulky aliphatic amines in the presence of an inexpensive earth-abundant molybdenum complex. This simple and economic protocol also enables regioselective branched amination; the practicality of the reaction was shown in an efficient, scaled-up synthesis of several drugs.

A Cytochrome P450 TxtE Model System with Mechanistic and Theoretical Evidence for a Heme Peroxynitrite Active Species.

The cytochrome P450 homolog, TxtE, efficiently catalyzes the direct and regioselective aromatic nitration of the indolyl moiety of L-tryptophan to 4-nitro-L-tryptophan, using nitric oxide (NO) and dioxygen (O2) as co-substrates. Pathways for such direct and selective nitration of heteroaromatic motifs present platforms for engineering new nitration biocatalysts for pharmacologically beneficial targets, among a medley of other pivotal industrial applications. Precise mechanistic details concerning this pathway are only weakly understood, albeit a heme iron(III)-peroxynitrite active species has been postulated. To shed light on this unique reaction landscape, we investigated the indole nitration pathway of a series of biomimetic ferric heme superoxide mimics, [(Por)FeIII(O2 -⋅)], in the presence of NO. Therein, our model systems gave rise to three distinct nitroindole products, including 4-nitroindole, the product analogous to that obtained with TxtE. Moreover, 15N and 18O isotope labeling studies, along with meticulously designed control experiments lend credence to a heme peroxynitrite active nitrating agent, drawing close similarities to the tryptophan nitration mechanism of TxtE. All organic and inorganic reaction components have been fully characterized using spectroscopic methods. Theoretical investigation into several mechanistic possibilities deem a unique indolyl radical based reaction pathway as the most energetically favorable, products of which, are in excellent agreement with experimental findings.

A Cytochrome P450 TxtE Model System with Mechanistic and Theoretical Evidence for a Heme Peroxynitrite Active Species

AbstractThe cytochrome P450 homolog, TxtE, efficiently catalyzes the direct and regioselective aromatic nitration of the indolyl moiety of L‐tryptophan to 4‐nitro‐L‐tryptophan, using nitric oxide (NO) and dioxygen (O2) as co‐substrates. Pathways for such direct and selective nitration of heteroaromatic motifs present platforms for engineering new nitration biocatalysts for pharmacologically beneficial targets, among a medley of other pivotal industrial applications. Precise mechanistic details concerning this pathway are only weakly understood, albeit a heme iron(III)‐peroxynitrite active species has been postulated. To shed light on this unique reaction landscape, we investigated the indole nitration pathway of a series of biomimetic ferric heme superoxide mimics, [(Por)FeIII(O2−⋅)], in the presence of NO. Therein, our model systems gave rise to three distinct nitroindole products, including 4‐nitroindole, the product analogous to that obtained with TxtE. Moreover, 15N and 18O isotope labeling studies, along with meticulously designed control experiments lend credence to a heme peroxynitrite active nitrating agent, drawing close similarities to the tryptophan nitration mechanism of TxtE. All organic and inorganic reaction components have been fully characterized using spectroscopic methods. Theoretical investigation into several mechanistic possibilities deem a unique indolyl radical based reaction pathway as the most energetically favorable, products of which, are in excellent agreement with experimental findings.

Immuno-RCA for highly sensitive detection of the antigen-antibody complex in the blood group antigen model

The problem of detecting tiny quantities of analytes by immunochemical methods has been tried for a long time. One approach is to use nucleic acid amplification methods to amplify the signal from a single antigen-antibody interaction. An amplification method suitable for microarrays is the rolling circle amplification reaction. The principle of the method is usage of a conjugate of a detecting antibody with a primer and subsequent isothermal amplification. The generation of a huge single-stranded reaction product starts after adding the necessary components for amplification reaction: circular oligonucleotides, which serves as a template for amplification and phage phi29 polymerase with the other components. This reaction product consists of a lot of repeats of a nucleotide sequence, that is complementary to the circular template. The fluorescent DNA probe can hybridize to each repeat on the product molecule, resulting in a significantly higher level of fluorescence than with fluorescently labeled antibody or streptavidin development systems. In addition, the reaction product remains immobilized on the surface, allowing usage of this approach for the detection of antigen-antibody interactions in other solid-phase analysis systems, such as microarrays. A common problem with such approaches is the nonspecific sorption of components of the immunochemical reaction or amplification reaction, leading to a high background. It is obvious that no matter how highly sensitive the analysis is in theory, a high background will reduce the entire potential of the method to nothing. Herein, we have developed a method that makes it possible to detect small amounts of antibodies to glycans in blood serum and in swabs from tumor cells in a microarray format using a model of blood group antigens. It was possible to obtain a 30 to 70-fold increase of fluorescence level from a specific interaction compared to the use of fluorescently labeled streptavidin. The method we are developing is promising, as it allows us to significantly increase the signal from the specific antigen/antibody interaction in the glycochip format, which will make it possible to detect antibodies to glycans in samples with a very low concentrations of antibodies, for example, in washes from tumor cells.

Design, synthesis and antioxidant studies of thiopyrimidine-based Passerini reaction: sulfur linked derivatives

Researchers have shown that sulfur-based heterocyclic frameworks form the backbone of a wide variety of synthetic analogues with a wide variety of medicinal actions. In this study, Passerini 3-component condensation reaction (P-3-CCR) approach has been used for the design strategy for imparting sulfur-based starting material, synthesis and antioxidant potential of sulfur containing pyrimidine (α-acyloxy amide) derivatives. The thorough assessment of antioxidant activities with a reference drug allows a proficient assessment of the structure–activity relationships (SARs) of the diversely synthesized molecules of the series. Compounds 4f with 3,4-(OMe)2 [17.35 ± 0.14 µM] and 4h with 4-NO2 [19.21 ± 0.14 µM] functionalities were identified as lead scaffolds with minimum IC50 values. A molecular docking investigation was also performed to compute the binding free energy of 4h and 4f to 1F9G. The results revealed a strong binding affinity (-7.1 kcal/mol) of both compounds as compared to that of ascorbic acid (-6.2 kcal/mol). A design strategy though molecular docking followed by MCRs approach to identify new α-acyloxy amides provided an outstanding approximation and shedded light on the sites of binding for their better use in medicinal field.

To Evaluate Structured Competency-Based Curriculum for Health Programs among Community Medicine Postgraduates: Mixed Method Approach

Background: The postgraduate curriculum needs to be given a definite shape so as to make health programs more intensive and integrative. In the present scenario, most of the information is unclear and infrequent. A structured public health competency-based education is an important aspect to consider for integrative health care. Evaluate the structured competency-based curriculum (SCBC) prepared on health program matters. Methods: Mixed method model involving postgraduate students, faculties in community medicine departments of selected medical colleges and stakeholders from district administration. The SCBC was piloted and validated for use. The evaluation was then done based on pre- and posttest performance analysis, satisfaction survey, and questionnaires for reaction and learning components. Results: For a complete understanding of the program, students had to invest 52 hours of stipulated time. CBC assessment mean scores for a) problems in PHC and programmatic evaluation (78.9%) and b) identification of success and failure of programs (78.2%) were more than 75% mean score; whereas, assessment scores for topics on a) resource allocation and b) evaluation of program as write-up was 65% and 52%, respectively. As compared to the conventional method, the SCBC showed a critical evaluation score of 70% with a 0.001 significance level. Discussion and Conclusion: Students’ narratives were that they could understand as well as integrate them better on the field. There was enhanced satisfaction and encouragement. Structured curriculum will also help in making learning more student-centric and go a long way in boosting their creativity.

Antioxidant activity of extracts of oregano and marsh cinquefoil, growing in the Altai region, in connection with their content of favonoids

Drugs based on medicinal plants have such advantages over synthetic analogues as low toxicity, better tolerability and reduced risk of addiction. Antioxidant agents in medicinal plants include substances from the flavonoid group, due to their ability to inactivate free radical processes, due to the mechanism of electron transfer between reaction components to neutralize free radicals. Among the medicinal plants of Western Siberia and the Altai Territory, oregano and marsh cinquefoil have a high content of flavonoids. The purpose of the study was to evaluate the antioxidant activity of alcohol-free extracts of oregano and marsh cinquefoil growing in the Altai region in connection with the content of flavonoids (flavonols and proanthocyanidins). To conduct the study, alcohol-free extracts of the studied plants were prepared using patented technology. The content of flavonols and proanthocyanidins was studied by arbitration techniques using spectrophotometry. The antioxidant activity of the extracts was measured using cathodic voltammetry method. The results showed that the average flavonol content in oregano extract was 866.5 μg/ml, while only traces were found in the extract of cinquefoil (60.0 μg/ ml). The average content of proanthocyanidins in the extract of cinquefoil was 4.05%, in the extract of oregano content of proanthocyanidins was 0.43%. The average coefficient of antioxidant activity for cinquefoil extract was 11.63 mmol/l×min and 3.81 mmol/l×min for oregano extract. From the results obtained, we can conclude that it is advisable to use extracts of marsh cinquefoil and oregano, growing in the Altai Territory, in the composition of biologically active antioxidant additives.

Optimization of loop-mediated isothermal amplification assay for sunflower mildew disease detection

Loop-Mediated Isothermal Amplification (LAMP) represents a valuable technique for DNA/RNA detection, known for its exceptional sensitivity, specificity, speed, accuracy, and affordability. This study focused on optimizing a LAMP-based method to detect early signs of Plasmopara halstedii, the casual pathogen of sunflower downy mildew, a severe threat to sunflower crops. Specifically, a set of six LAMP primers (two outer, two inner, and two loop) were designed from P. halstedii genomic DNA, targeting the ribosomal Large Subunit (LSU). These primers were verified by in silico analysis and experimental validation using both target and non-target species' DNAs. Optimizations encompassing reaction conditions (temperature, time) and component concentrations (magnesium, Bst DNA polymerase, primers, and dNTP) were determined. Validation of these optimizations was performed by agarose gel electrophoresis. Furthermore, various colorimetric chemicals (Neutral Red, Hydroxynaphthol Blue, SYBR Safe, Thiazole Green) were evaluated to facilitate method analysis, and the real-time analysis has been optimized, presenting multiple approaches for detecting sunflower downy mildew using the LAMP technique. The analytical sensitivity of the method was confirmed by detecting P. halstedii DNA concentrations as low as 0.5 pg/μl. This pioneering study, establishing P. halstedii detection through the LAMP method, stands as unique in its field. The precision, robustness, and practicality of the LAMP protocol make it an ideal choice for studies focusing on sunflower mildew, emphasizing its recommended use due to its operational ease and reliability.

In-suit cemented strategy enables intumescent flame retardant transition from hyper-hydrophilic to hydrophobic and aggregation flame retardant effect simultaneously in polypropylene

To meet the stringent requirements of specific high-end manufacturing applications involving flame retardant polypropylene (PP) materials, it's imperative to overcome the inherent superhydrophilicity of intumescent flame retardants (IFR) while simultaneously further enhancing flame retardant efficiency. In addressing this challenge, novel in-situ cemented MVC-IFR microparticles characterized by a microparticle-aggregation effect and hydrophobic structure were successfully synthesized. The micro-aggregated MVC-IFR particles not only bolstered the hydrophobicity and charring flame retardancy of PP composites compared to conventional IFR but also exhibited superior resistance to water erosion. The water contact angle (WCA) of 3MVC-22IFR reached an impressive 159°, whereas the WCA of IFR stood at 0°. Moreover, when MVC-IFR and IFR were incorporated into PP, 3MVC-22IFR/PP displayed a WCA of 108° which was a hydrophobic composite, while 25IFR/PP exhibited a WCA of 81° which was a hydrophilic composite. Notably, the hydrophobic MVC-IFR showcased greater resistance to water exposure than hydrophilic IFR, thereby maintaining its flame retardant efficacy in practical applications. Furthermore, MVC-IFR microparticles with aggregation of acid, carbon, and gas sources, facilitated the charring reactions of different components, thereby enhancing its charring flame retardant effect in PP. Remarkably, 1MVC-24/PP not only attained a UL 94V-0 rating but also achieved a glow wire flammability index (GWFI) of >960 °C, a glow wire ignition temperature (GWIT) of 850 °C, and an LOI value of 28.7 %. In contrast, 25IFR/PP failed to secure a UL 94 rating and exhibited lower GWIT and LOI values. Crucially, the peak heat release rate and total smoke release of 1MVC-24IFR/PP were markedly reduced by 76 % and 41 %, respectively, compared with those of neat PP. In summary, this study presented a novel design concept and rules for flame retardant morphology, to find a way for the development of polyolefin materials boasting both high hydrophobicity and superior flame retardancy.

A simple and highly efficient catalyst-free for the synthesis of dihydro pyrido[1, 2-a]quinoxaline derivatives by four component reactions and evaluation of their antibacterial activity

In the current work, a new series of methyl-10-amino-9-cyano-6-oxo-8-aryl-6,8-dihydro-5H-pyrido[1,2-a]quinoxaline-7-carboxylate derivatives were efficiently designed and prepared using a convenient route in excellent yields by four-component reactions among benzene-1,2-diamine, dimethyl acetylenedicarboxylate, various aromatic aldehydes and malononitrile. These reactions were carried out in acetonitrile at ambient temperature under catalyst-free conditions for 7 h. The structures of the new obtained compounds were confirmed by NMR, IR, EI-MS and elemental analysis. The antibacterial activity of the synthesized products was studied using bacterial strains: Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. The results showed that all the synthesized compounds are effective against Staphylococcus aureus, Bacillus subtilis and Escherichia coli bacteria.

Interactions of 3‐Acylisocoumarins with Ethane‐1,2‐diamines: A Simple Route to 3,4‐Dihydro‐6H‐pyrazino[1,2‐b]isoquinolin‐6‐ones and Their Hydrogenated Derivatives

AbstractThe recyclization of isocoumarins under the N‐nucleophile action is a well‐known route to different isoquinolones. But addition of functional groups in such substrates can provide more complicated nitrogen‐containing heterocycles. In this study, the easy formation of 3,4‐dihydro‐6H‐pyrazino[1,2‐b]isoquinolin‐6‐one system via the interaction of 3‐acylisocoumarins and ethane‐1,2‐diamines is demonstrated. As the acyl component of reaction, 3‐acetyl‐ and 3‐benzoylisocoumarins, 2,3‐dihydro‐1H‐benzo[c]chromene‐4,6‐dione, and heteroanalogs of 3‐acetylisocoumarin were successfully used; and the amino component was represented by ethane‐1,2‐diamine, some cyclic vicinal diamines, methyl 2,3‐diaminopropanoate, and N1‐methylethane‐1,2‐diamine. The variation of substrates gave different structures with 3,4‐dihydro‐6H‐pyrazino[1,2‐b]isoquinolin‐6‐one core; and the number of products can grow extremely because of this core's aptitude to reduction. Thus, 1,2,3,4‐tetrahydro‐6H‐pyrazino[1,2‐b]isoquinolin‐6‐ones, 1,2,3,4,11,11a‐hexahydro‐6H‐pyrazino[1,2‐b]isoquinolin‐6‐ones and 1,3,4,6,11,11a‐hexahydro‐2H‐pyrazino[1,2‐b]isoquinolines were synthetized by using various reduction methods for separate 3,4‐dihydro‐6H‐pyrazino[1,2‐b]isoquinolin‐6‐ones.

Experimental and simulation study of magnesium phosphate cement two-liquid grouting materials

Magnesium phosphate cement (MPC) has a promising application in grouting. This study drew on the traditional cement-waterglass two-liquid grouting model. Creatively, the two main reaction components of MPC, dead-burned magnesium oxide and phosphate, were applied to the grouting field in a two-component liquid form. At the same time, through proportioning adjustment and experimental testing, we obtained A\B liquid components, which can be stabilized. In addition, MPC slurry was compared with the traditional grouting material, silicate cement slurry, to demonstrate its superiority. Finally, we simulated the grout diffusion process of the mixed slurry using the two-phase Darcy's law module of COMSOL Multiphysics subsurface fluids. The results show that the mixed slurry with a magnesium phosphate ratio of 1/3, a magnesium–boron ratio between 5% and 10%, and a water–cement ratio of 0.2–0.5 has better stability and mobility. Under the same fluidity, its strength is much higher than that of common silicate cement slurry and has good injectability. MPC was subjected to two-fluid grouting to take advantage of its fast-hardening and early-strengthening properties, while also improving its stability and fluidity. This study provided a theoretical foundation for the application of MPC.

Molecular Detection of Human parvovirus B19 in Patients with Thalassemia in Wasit Province, Iraq

Background: Human B19 (PVB19) isssmall, non-envelope single strand DNA viruses from family of "Parvoviridae" it cause infections in human. In thalassemia are a heterogeneous grouping of genetic disorders that result from a decreased synthesis of alpha or beta chains of hemoglobin (Hb). Numerous factors contribute to functional abnormality found in βeta thalassemia patient like decrease red cells life span, rapidsiron turnover, and tissue deposition of excess iron B19 targets the erythroid progenitors in the bone marrow by binding to the glycosphingolipid. Materials and Methods: This case cross sectional study and the patients aged between (5-40) years , study has been carried outsin Al-Kut teaching hospitals in Al-Iraq-Wasit in a period between September 2023 and March 2024. This study followed the cross-sectional design. The populations of our study included 120 patients’ samples with thalassemia infected by Human Parvovirus B19 in blood transfusion patients 64 male and 56 female. Nested-PCR used to detect of B19V by using primers. PCR reaction was done by using special sets of primers mentioned previously and special components and specific program and procedure according to components of PCR reaction. Result: Human parvovirus 19 Positive case percentage using polymerase chain reaction indicated that the positive cases was reported according to polymerase chain reaction (PCR) as a percentage of case related to the main characteristic of patients, current study data has been indicated as following: in total of 120 patient sample with thalassemia has been included in this study, PCR positive case was 17 (14.2%), 6 (5%), 2 (1.7%) and 0 (0%) in the age groups (5-15), (16-25), (26-35) and (36-45) respectively. Male was more prevalent 17 (14.2%), than female 8 (6.7%), So as to records of major type in comparision to intermediate 19 (15.8%) and 6 (5%). All positive cases were 25 cases. Conclusion: Current data showed prevalence of Human parvovirus 19 in Iraqi patients. This prevalence should be alarming public health.