Sodium Phosphate Research Articles

Effect of phosphate nature on the inhibitory capability of phosphate compositions

Corrosion inhibitors find ubiquitous application across diverse sectors to formulate robust coatings and chemical compounds. Serving as pivotal additives in compositions, they play a vital role in crafting coatings for circulating water systems, water supply networks, oil refining, petrochemical industries, and power plants. Incorporation extends to fuels, oils, lubricants, and construction materials. In industries oxidation inhibitors is particularly high as chemical, electrochemical, petrochemical, and gas, as well as in water supply networks and circulating water systems. The utilization of inhibitors obviates the necessity for treating metal surfaces with protective enamels and mastics. Effectively preventing oxidation involves the introduction of chemical contributions into aggressive ecology, thereby neutralizing or retarding the oxidation processes. This article explores the anti-oxidation properties of inhibitors in compositions related to St-3 steel. The study includes factors such as the pH of the medium, the nature and concentration of phosphate in compositions simulating reservoir water under stationary and aerated conditions. Investigation methods as potentiometry and photocolorimetry used in research. Experimental data, quantitative parameters of the oxidation process, oxidation rate, and degree of protection, depth index, and stability of the film formed were determined. These indicators were assessed on the oxidation resistance scale relative to steel. Analysis of the data shows that out of 63 compositions, seven systems demonstrate the most significant protective effects, with five containing sodium orthophosphate and two containing sodium hydroorthophosphate. The effective, surrounding friendly and cost-effective steel oxidation inhibitors using materials from Kazakhstan will contribute to the development of industry,

Reversible opening of the blood-labyrinth barrier by low-pressure pulsed ultrasound and microbubbles for the treatment of inner ear diseases

Systemic drug administration provides convenience and non-invasive benefits for preventing and treating inner ear diseases. However, the blood-labyrinth barrier (BLB) restricts the transport of drugs to inner ear tissues. Ultrasound can stimulate specific areas and penetrate tissues, with the potential to overcome physiological barriers. We present a novel strategy based on low-pressure pulsed ultrasound assisted by microbubbles (USMB) to transiently open the BLB and deliver therapeutics into the inner ear. A pulsed ultrasound device with adjustable pressure was established; the generated ultrasound was transmitted through the external auditory canal into the guinea pig's inner ear. We observed that the application of microbubbles allowed the use of safe and efficient ultrasound conditions to penetrate the BLB. We found that USMB-mediated BLB opening seemed to be associated with a reduced expression of the tight junction proteins zonula occludens-1 and occludin. Following intravenous administration, hydrophilic dexamethasone sodium phosphate (DSP), hydrophobic curcumin (CUR), as well as drug-loaded nanoparticles (Fe3O4@CUR NPs) could be efficiently delivered into the inner ear. We observed better drug accumulation in the perilymph of the inner ear, resulting in less drug (cisplatin)-induced ototoxicity. Furthermore, physiological, hematological, and histological studies showed that the modulation of the BLB by low-pressure USMB was a safe process without significant adverse effects. We conclude that USMB could become a promising strategy for the systematic delivery of therapeutics in the treatment of inner ear diseases.

Study the Stability of Pharmaceutical eye drop composed of Chloramphenicol and Dexamethasone Sodium Phosphate stored in non-recommended ‎conditions

Study the Stability of Pharmaceutical eye drop composed of Chloramphenicol and Dexamethasone Sodium Phosphate stored in non-recommended ‎conditions

Adequate Colon Preparation in Screening Colonoscopy

Colorectal cancer (CRC) is one of the most common forms of cancer worldwide, being the fourth most prevalent cancer and the third most common in terms of mortality. A decrease in the incidence and mortality of CRC has been observed among adults over 50 years of age, screening colonoscopy being a contributory factor for this improvement. Adequate preparation of the colon is essential for obtaining accurate results and minimizing the risks associated with the colonoscopy procedure. Both ESGE (European Society of Gastrointestinal Endoscopy) and UEG (United European Gastroenterology) recommend adequate preparation in at least 90% of cases, calculated both at the endoscopy center level and for each individual endoscopist. The purpose of our article is to review the literature on different bowel preparation products for colonoscopy and demonstrate the non inferiority of low-volume preparations over the standard PEG 4L. Preparations containing PEG are the most common in preparation for colonoscopy. A recent meta-analysis suggests that high-volume, mutiple-dose regimens are superior in terms of efficacy to low-volume, multiple- dose regimens, including low-volume PEG with various adjuvants and sodium phosphate, although with lower tolerability. Due to low levels of compliance, tolerability and acceptability, standard 4L single-dose regimens of PEG have been gradually and successfully replaced by newer regimens that include low-volume solutions. An eample of low-volume split-dose preparation is the solution of low-volume PEG4000, sodium sulphate, citric acid, sodium citrate, sodium chloride, potassium chloride and simethicone. In several studies this 2 L low volume preparations ehibit similar effectiveness with safety profiles that are comparable to classic 4 L PEG, with lower incidence of adverse effects and good tolerability. In conclusion, adequate preparation increases the quality of colonoscopy procedures as proper patient preparation is essential to obtain an optimal visualization of the intestinal mucosa. Low-volume bowel preparation is effective, safe and well tolerated by the patients, with higher acceptability compared to the standard volume PEG.

Recovery of Proteases and Protease Inhibitors from Ganoderma spp. Cultivated in Amazonian Lignocellulose Wastes.

Ganoderma spp. are a great source of bioactive molecules. The production and recovery of bioactive molecules vary according to strain, growth substrate, and extraction solution. Variations in protease and their inhibitors in basidiomata from a commercial strain (G. lingzhi) and an Amazonian isolate (Ganoderma sp.) cultivated in Amazonian lignocellulosic wastes and extracted with different solutions are plausible and were investigated in our study. Basidiomata from cultivation in substrates based on açaí seed, guaruba-cedro sawdust and three lots of marupá sawdust were submitted to extraction in water, Tris-HCl, and sodium phosphate. Protein content, proteases, and protease inhibitors were estimated through different assays. The samples were characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Fourier transform infrared spectroscopy with attenuated total reflectance (FTIR-ATR). Tris-HCl provided higher protein extraction from Ganoderma sp. and higher caseinolytic, gelatinolytic, and fibrinolytic activity for G. lingzhi cultivated in açaí. Water extracts of Ganoderma sp., in general, exhibited higher trypsin and papain inhibitor activities compared to G. lingzhi. Extracts in Tris-HCl and sodium phosphate showed more intense protein bands in SDS-- PAGE, highlighting bands of molecular weights around 100, 50, and 30 kDa. FTIR spectra showed patterns for proteins in all extracts, with variation in transmittance according to substrate and extractor. Water extract from Amazonian Ganoderma sp. cultivated in marupá wastes are promising as a source of protease inhibitors, while the Tris-HCL extract of G. lingzhi from açaí cultivation stands out as a source of proteases with fibrinolytic, caseinolytic, and gelatinolytic activities.

Correlating Material Properties to Osteoprotegerin Expression on Nanoparticulate Mineralized Collagen Glycosaminoglycan Scaffolds.

Precision material design directed by cell biological processes represents a frontier in developing clinically translatable regenerative technologies. While understanding cell-material interactions on multipotent progenitor cells yields insights on target tissue differentiation, equally if not more important is the quantification of indirect multicellular interactions. In this work, the relationship of two material properties, phosphate content and stiffness, of a nanoparticulate mineralized collagen glycosaminoglycan scaffold (MC-GAG) in the expression of an endogenous anti-osteoclastogenic secreted protein, osteoprotegerin (OPG) by primary human mesenchymal stem cells (hMSCs) is evaluated. The phosphate content of MC-GAG requires the type III sodium phosphate symporter PiT-1/SLC20A1 for OPG expression, correlating with β-catenin downregulation, but is independent of the effects of phosphate ion on osteogenic differentiation. Using three stiffness MC-GAG variants that do not differ significantly by osteogenic differentiation, it is observed that the softest material elicited ≈1.6-2 times higher OPG expression than the stiffer materials. Knockdown of the mechanosensitive signaling axis of YAP, TAZ, β-catenin and combinations thereof in hMSCs on MC-GAG demonstrates that β-catenin downregulation increases OPG expression by 1.5-fold. Taken together, these data constitute a roadmap for material properties that can used to suppress osteoclast activation via osteoprotegerin expression separately from the anabolic processes of osteogenesis.

β-galactosidase immobilization on ceramic ultrafiltration membrane for simultaneous lactose hydrolysis and protein separation

Protein and lactose of cheese whey can be separated using ultrafiltration membranes and lactose can be hydrolyzed by β-galactosidase. This study investigated the integration of ultrafiltration and enzymatic hydrolysis for simultaneous protein concentration and lactose hydrolysis. β-galactosidase was immobilized on ceramic membrane via surface activation with gelatin and subsequent enzyme cross-linking with glutaraldehyde. Membrane geometries, buffer types, gelatin and enzyme concentrations were optimized. The optimal results yielded a 63 % enzyme immobilization efficiency and a 93 % lactose hydrolysis rate by using disc membrane, sodium acetate buffer (pH 4.8), sodium phosphate buffer (pH 7.5), 0.1 g/L gelatin concentration, and 5.0 g/L enzyme concentration. The optimized enzymatic membrane was evaluated with synthetic and real whey. In synthetic whey, 85 % lactose hydrolysis and 89 % protein rejection were achieved. While in real whey, 72 % lactose hydrolysis and 83 % protein recovery were obtained. This approach offers a single-step, efficient, and scalable method for whey valorization with potential for industrial applications.

Validation of a novel alcohol-free preservative solution in comparison with conventional prefixation on quality of serous body fluid smears.

We describe a novel alcohol-free preservative composed of glucose, mannitol, disodium hydrogen orthophosphate, thymol, and distilled water (glucose-mannitol-disodium dihydrogen orhtophosphate-thymol [GMDT] preservative) in appropriate proportion as an alternative to alcohol prefixation (APF) of body fluids. To assess the cytomorphologic preservation and staining quality of serous body fluid smears generated by GMDT preservative and compare it with smears processed by standard 50% APF. The study comprised 151 effusion samples. Each sample was equally divided into four tubes. Equal volumes of APF and GMDT preservatives were added to the first two tubes and left at room temperature for 24 h. Similarly, the corresponding preservatives were added to the third and fourth tubes and stored for 48 h. Two smears were prepared from the centrifuged sediments of each tube (all four tubes) and stained with May-Grünwald Giemsa and Papanicolaou (Pap) stains. Using a three-tiered scoring system, the smear examination was blinded to assess the extent of cellular preservation and the staining quality by two cytotechnologists and two cytopathologists. Statistical analysis was performed by STATA 16.0. Samples processed with the GMDT preservative at 24 h showed better cytoplasmic preservation and smear background, while nuclear features and staining quality showed no difference between the two preservatives. Mild cytoplasmic and nuclear degenerative changes were noted with the GMDT at 48 h, while all four parameters remained similar with APF at 24 and 48 h. The newly developed alcohol-free, GMDT preservative, could be a feasible and cost-effective alternative to 50% APF, preferably when samples are processed within 24 h.

Active release of diatomite-MgAl-layered double hydroxide nanostructures on corrosive inhibitors to effectively suppresses corrosion of LA51 alloy

Two-dimensional (2D) materials have been potentially applicable for the corrosive resistance of alloys in corrosive media. Nevertheless, a challenge remains in adapting the 2D nanomaterial layered double hydroxide (LDH) with diatomaceous earth (DE) as two inorganic nanocontainers homogeneously combined and loaded with controlled release corrosion inhibitors. In this research, the high-efficiency anti-corrosion nanofiller for LA51 alloy protection was obtained by integrating MgAl-LDH with Sodium phosphate (SP) utilizing the unique hollow porous structure of DE as a template. As a result, the incorporation of DE-LDH-P provides a 3-order of magnitude enhancement in coating immersion in 3.5 wt% NaCl solution for 40 days compared to pure epoxy. Furthermore, two nanocontainers of DE and LDH with corrosion inhibitor loading up to 15 wt% still demonstrated excellent corrosive protection after 120 h of salt spray. The key to its protective performance is promoting controlled corrosion inhibitor release through a scientific approach that fully utilizes the slow-release properties of DE and LDH. This strategy offers a straightforward and effective approach for formulating anti-corrosion additives tailored for use in corrosive settings, with potential applications across various industrial sectors. Specifically, we advocate for the utilization of maritime instrumentation, underwater armaments, and seawater-based power sources within the domains of ship construction and marine engineering.

A better understanding of the effectiveness of placed phosphorus fertilisation with struvite for silage maize: A pot experiment

Struvite is emerging as a circular, slow-release phosphorus (P) fertiliser. However, its effectiveness for crops and its impact on soil P tests still remain largely unclear. We analysed the effectiveness of struvite as a row fertiliser in a pot experiment with maize in a sandy soil and a loamy soil, both exhibiting a low agronomic soil P status. Maize was seeded in both soils, amended with either granular struvite or water-soluble di-ammonium phosphate (DAP) as row fertilisers. A positive control received an excess of sodium phosphate, mixed homogeneously through both soils; a negative control did not receive additional P. We measured the agronomic maize performance at the end of the vegetative growth stage (V10) and assessed the suitability of two established agronomic soil P tests (i.e. P-CaCl2 and P-AL) to predict plant-available P in the soils amended with struvite. Furthermore, we performed an additional batch experiment to better understand the dissolution dynamics of struvite during a prolonged period of extraction of soil in 0.01 M CaCl2. Placed struvite application led to a lower performance of maize in comparison to DAP in terms of biomass production as well as P uptake (53 and 71 % lower, respectively). Yet the agronomic performance of struvite in general was higher than the performance of the negative control, confirming the potential of struvite as an emerging P fertiliser. Surprisingly, both soils fertilised with struvite showed a significantly higher soil P test than any other P treatment in our pot experiment. This was an artefact due to the dissolution of residual struvite granules during the soil extraction procedures. These results call for a reconsideration of how to interpret P-CaCl2 and P-AL as a basis for P fertiliser recommendations for soils receiving struvite as a P fertiliser.

Formation of left-handed helices by C2'-fluorinated nucleic acids under physiological salt conditions.

Recent findings in cell biology have rekindled interest in Z-DNA, the left-handed helical form of DNA. We report here that two minimally modified nucleosides, 2'F-araC and 2'F-riboG, induce the formation of the Z-form under low ionic strength. We show that oligomers entirely made of these two nucleosides exclusively produce left-handed duplexes that bind to the Zα domain of ADAR1. The effect of the two nucleotides is so dramatic that Z-form duplexes are the only species observed in 10 mM sodium phosphate buffer and neutral pH, and no B-form is observed at any temperature. Hence, in contrast to other studies reporting formation of Z/B-form equilibria by a preference for purine glycosidic angles in syn, our NMR and computational work revealed that sequential 2'F…H2N and intramolecular 3'H…N3' interactions stabilize the left-handed helix. The equilibriumbetween B- and Z- forms is slow in the 19F NMR time scale (≥ms), and each conformation exhibited unprecedented chemical shift differences in the 19F signals. This observation led to a reliable estimation of the relative population of B and Z species and enabled us to monitor B-Z transitions under different conditions. The unique features of 2'F-modified DNA should thus be a valuable addition to existing techniques for specific detection of new Z-binding proteins and ligands.

Electrolyte‐gated organic field‐effect transistors with high operational stability and lifetime in practical electrolytes

AbstractA key component of organic bioelectronics is electrolyte‐gated organic field‐effect transistors (EG‐OFETs), which have recently been used as sensors to demonstrate label‐free, single‐molecule detection. However, these devices exhibit limited stability when operated in direct contact with aqueous electrolytes. Ultrahigh stability is demonstrated to be achievable through the utilization of a systematic multifactorial approach in this study. EG‐OFETs with operational stability and lifetime several orders of magnitude higher than the state of the art have been fabricated by carefully controlling a set of intricate stability‐limiting factors, including contamination and corrosion. The indacenodithiophene‐co‐benzothiadiazole (IDTBT) EG‐OFETs exhibit operational stability that exceeds 900 min in a variety of widely used electrolytes, with an overall lifetime exceeding 2 months in ultrapure water and 1 month in various electrolytes. The devices were not affected by electrical stress‐induced trap states and can remain stable even in voltage ranges where electrochemical doping occurs. To validate the applicability of our stabilized device for biosensing applications, the reliable detection of the protein lysozyme in ultrapure water and in a physiological sodium phosphate buffer solution for 1500 min was demonstrated. The results show that polymer‐based EG‐OFETs are a viable architecture not only for short‐term but also for long‐term biosensing applications.

Study on harmless treatment of electrolytic manganese residue by low temperature thermochemical method.

The Electrolytic Manganese Residue (EMR) is a by-product of the electrolytic manganese metal (EMM) industry, containing high concentrations of potential pollutants such as NH4+-N and soluble Mn2+. These components pose a serious threat to the ecological environment. To explore accurate, efficient, and harmless treatment methods for EMR, this study proposes a low-temperature thermochemical approach. The orthogonal experiment design investigates the effects of reaction temperature, reaction time, quicklime (CaO), sodium carbonate (Na2CO3), sodium phosphate (Na3PO4) (Reviewer #3), and water consumption on manganese solidified and ammonia removal from EMR. The results indicate that optimal conditions are a reaction temperature of 60 ℃ (Reviewer #3) and a reaction time of 10min. CaO precipitates Mn2+ as manganese hydroxide (Mn(OH)2) (Reviewer #3), achieving effective manganese solidified and ammonia removal. The addition of Na2CO3 causes Mn2+ to form manganesecarbonate (MnCO3) (Reviewer #3)precipitate, while Na3PO4 makes Mn2+ form Manganese phosphate trihydrate (Mn3(PO4)2·3H2O) (Reviewer #3). Increased water consumption enhances the interaction adequacy between ions. Under optimal conditions (CaO 10%, Na2CO3 1%, Na3PO4 0.5%, and 80% water consumption), the removal rate of ammonium ions reaches 98.5%, and the solidification rate of soluble Mn2+ is 99.9%. The order of influence on ammonium ion removal is CaO > water consumption > Na3PO4 > Na2CO3. Therefore, this study provides a new method for low-cost process disposal and efficient harmless treatment of EMR (Reviewer #3).

A soft carbon materials with engineered composition and microstructure for sodium battery anodes

Sodium-ion batteries (SIBs) have advantages in high sodium resources, providing powerful supplement to the current energy storage system. However, the lack of low-cost and high-performance anode materials still limits its practical application. Herein, a soft carbon anode derived from petroleum coke was successfully synthesized by engineering its composition and microstructure through resin and sodium phosphate compositing with optimal heat treatment process, delivering significant merits over existing composite anode in term of price density, initial Coulombic efficiency (ICE) and carbon yield. Resin helps to increase micropores and inhibit graphitization. Na3PO4 contributes to expand layer spacing and increase reversible groups, meanwhile facilitates the cross-linking of graphite microcrystalline and provides additional sodium supplement with improved ICE and conductivity. Through the synergistic effect by the additives, the optimized sample (P-ONH-1200) exhibits a superior reversible charge specific capacity of 311.9 mAh g−1 with high cycling stability, ICE (90.7 %) in SIBs, and high carbon yield (70 %). It also gains rate performance of 209.7 mAh g−1 at 4 C with 98 % retention after 1000 cycles. The full cell with Na3V2(PO4)3 (NVP) cathode at 1.05 N/P ratio exhibits an excellent stability with a capacity retention of 70 % after 500 cycles at 1 C. It provides a model reference for the microstructure regulation of petroleum coke and a revenue for preparation high-performance soft carbon anode for SIBs.

Comparative study on the preparation of phosphate-based geopolymers using different activators

Fly ash has the potential to be used as the precursor in the acid-activated geopolymer preparation, fly ash can react with phosphorus-containing activators to form geopolymers, but different types of activators present different activation effects on fly ash. In this study, common liquid phosphoric acid (PA), liquid aluminum dihydrogen phosphate (ADP), solid sodium dihydrogen phosphate (SDP) and solid potassium dihydrogen phosphate (PDP) are used as a single-component or composite activators and fly ash as raw material to prepare phosphate-based geopolymers (PGEOs). The effect of different activators on setting time, pH, electrical conductivity (EC) and compressive strength of PGEOs were assessed. Moreover, the activation mechanism of different activators on fly ash was revealed by using X-ray diffraction, Fourier transform infrared spectroscopy, Mercury Intrusion Porosimetry, X-ray Photoelectron Spectroscopy and Scanning Electron Microscopy-Energy Dispersive Spectroscopy. The results showed that geopolymer prepared using ADP exhibited the highest compressive strength among the different activators, but combining ADP and PA would prolong setting time. However, the unreacted SDP and PDP particles were detected in geopolymers activated by PA+SDP and PA+SDP composite activator due to insufficient geopolymerization. Nonetheless, combining PDP or SDP with PA as composite activator is more effective than the single-component PDP or SDP activator in improving compressive strength. The pH values of the geopolymers increased with the curing time while EC showed a decreasing trend which was independent of the activator type. AlPO4 phase was found in all samples, and Al-containing phases are the main strength-given component of PGEOs.

Interaction of Lyophilic Zinc(II) Porphyrins with Bovine Serum Albumin

Palladium-catalyzed heterylation of monobromophenyl-substituted zinc(II) porphyrin with small heterocycles (benzothiazole, benzoxazole, and N-methylbenzimidazole) was carried out. As a result, unsymmetrical heterylphenyl-substituted zinc(II) porphyrins soluble in organic solvents were obtained. The interaction of heteryl-substituted zinc(II) porphyrins with alpha-helical proteins was studied by spectral methods using bovine serum albumin in aqueous organic solvents. It was found that the titration of the zinc(II) porphyrins with albumin in a sodium phosphate buffer involves a number of equilibria including complexation and aggregation. In the case of porphyrins containing N-methylbenzimidazole and benzoxazole residues, self-aggregation processes initiated by absorption of organic solvent molecules by the protein predominate. It was found that more hydrophobic nature of zinc(II) porphyrin with benzothiazole residue promotes the complex formation with the protein. The photochemical properties of zinc(II) porphyrin with a benzothiazole residue, capacity for the photooxidation of the alpha-helical protein, and the high affinity of protein to this porphyrin make it a promising candidate for the potential applicability for photodynamic inactivation.

Influence of calcium sequestering salt type and concentration on the characteristics of processed cheese made from Gouda cheese of different ages

The effect of 90, 180 and 270 mEq/kg of the calcium sequestering salts (CSS) disodium phosphate (DSP), trisodium citrate (TSC) and sodium hexametaphosphate (SHMP) on the solubilisation of proteins and minerals and the rheological and textural properties of processed cheese (PC) prepared from Gouda cheese ripened for 30–150 d at 8°C was studied. The solubilisation of individual caseins and Ca and the maximum loss tangent during temperature sweeps of PC made from Gouda cheese increased, while hardness of PC decreased with ripening duration of the Gouda cheese. Levels of soluble Ca in PC increased with increasing concentration of TSC and SHMP, but decreased with increasing concentration of DSP. The solubilisation of casein and Ca due to ripening of Gouda cheese used for manufacturing PC could explain the changes in texture and loss tangent of PC. The results suggest that DSP, TSC or SHMP in PC formulation can form insoluble Ca-phosphate, soluble Ca-citrate or insoluble casein-Ca-HMP complexes, respectively, that influence casein solubilisation differently and together with levels of residual intact casein determine the functional attributes of PC.

Effect of the calcium silicate and sodium phosphate remineralizing products on bleached enamel.

This study evaluated the effect of calcium silicate and sodium phosphate (CSSP) dentifrice and serum on the surface of enamel bleached with hydrogen peroxide (H2O2). A total of 160 bovine enamel slabs were bleached with 35% H2O2 and treated with sodium fluoride (NaF) dentifrice-GI, CSSP dentifrice-GII; CSSP dentifrice + CSSP serum-GIII, or NaF dentifrice + NaF gel-GIV. The dentifrices were applied using a brushing machine three times daily for 7 days. After brushing, sodium phosphate gel and CSSP serum were applied. The microhardness (KNH, n = 14), surface roughness (Ra, n = 14), energy dispersive spectroscopy (n = 6), and scanning electron microscopy (n = 6) were assessed at t0 (before bleaching), t1 (after bleaching), and t2 (after postbleaching treatments). The data were subjected to a two-way analysis of variance and Bonferroni's test. The KNH decreased at t1 (P < 0.001) but recovered at t2 for all treatments, although only GII showed restored baseline values (P = 0.0109). The surface roughness increased at t1 (P < 0.001) and reduced at t2 (P < 0.001) for all groups, with no significant differences among groups. Enamel composition and morphology did not differ after the treatments, except for silicon accumulation in GIII. Postbleaching treatment with CSSP dentifrice and serum yielded superior remineralizing effects on bleached enamel.

Formation of quercetin from taxifolin and quercetin 7-O-glucoside from taxifolin 7-O-glucoside by cooking sorghum grains: Possible mechanisms of their formation

Sorghum grains contained taxifolin (dihydroquercetin) and taxifolin 7-O-glucoside (T7G). Quercetin and its 7-O-glucoside (Q7G) were formed by heating sorghum grains in distilled water. The formation of the above components was also observed by heating an extract of the grains prepared using 0.1 M sodium phosphate with 0.15 M NaCl (pH 7.0). It was shown that quercetin and Q7G could be formed from taxifolin and T7G, respectively, which were isolated from sorghum grains, by heating around pH 7. The formation of quercetin was accompanied by the formation of two taxifolin isomers, namely, taxifolin 2,3-cis isomer and alphitonin. Two isomers were also formed from T7G accompanying the formation of Q7G, and the characteristics of the isomers were similar to the taxifolin isomers. Taking the mechanism of the isomer formation into account, it is discussed that quercetin and Q7G might be formed by the oxidation of chalcones, which were formed via quinone methides of taxifolin and T7G, respectively.

Transcutaneous Delivery of Dexamethasone Sodium Phosphate Via Microneedle-Assisted Iontophoretic Enhancement - A Potential Therapeutic Option for Inflammatory Disorders.

This study aimed to fabricate dexamethasone sodium phosphate loaded microneedle arrays (MNA) and investigate their efficiency in combination with iontophoresis for the treatment of hind paw oedema in rats. Drug loaded polyvinyl alcohol, polyvinyl pyrrolidone and D-sorbitol-based MNA11 were fabricated by vacuum micromolding. Physicochemical, morphological, thermal, in-silico, in-vitro insertion ability (on parafilm) and drug release studies were performed. Ex-vivo permeation, in-vivo insertion and anti-inflammatory studies were performed in combination with iontophoresis. MNA11 displayed sharp-tipped projections and acceptable physicochemical features. Differential scanning calorimetry results indicated that drug loaded MNA11 were amorphous solids. Drug interacted with PVP and PVA predominately via hydrogen bonding. Parafilm displayed conspicuously engraved complementary structure of MNA11. Within 60min, 91.50 ± 3.1% drug released from MNA11. A significantly higher i.e., 95.06 ± 2.5% permeation of drug was observed rapidly (within 60min) from MNA11-iontophoresis combination than MNA11 i.e., 84.07 ± 3.5% within 240min. Rat skin treated using MNA11 and MNA11-iontophoresis showed disruptions / microchannels in the epidermis without any damage to underlying anatomical structures. MNA11-iontophoresis combination led to significant reduction (83.02 ± 3.9%) in paw oedema as compared to MNA11 alone (72.55 ± 4.1%). MNA11-iontophoresis combination can act as a promising candidate to deliver drugs transcutaneously for treating inflammatory diseases.