Acidic Medium pH Research Articles

Anti-Obesity Effects of a Collagen with Low Digestibility and High Swelling Capacity: A Human Randomized Control Trial.

Collagen is a protein formed by very long amino acid chains. When conveniently treated, it can incorporate water into the net, thus increasing its volume and mass. The present work aimed to evaluate the potential anti-obesity effects of bovine collagen that has been technologically treated to increase its water retention capacity in an acid pH medium, with the objective of inducing satiation. Collagen's digestibility was tested with a pepsin digestion test. Its swelling capacity was tested in an acid pH medium simulating gastric conditions. Postprandial levels of ghrelin in response to collagen supplementation were tested in rats. In a randomized control trial, 64 subjects with overweight/obesity were allocated in two groups: supplemented daily with two protein bars enriched with collagen (20 g per day) for 12 weeks, or control group. Anthropometric and biochemical measurements were assessed in all the participants. This collagen showed a low digestibility (<60%) and high swelling capacity (>1900%) in vitro. In humans with overweight and obesity, this collagen significantly reduced body weight, body mass index (BMI), systolic blood pressure (SBP), and fatty liver index (FLI) and increased fat-free mass when compared with the control group. A significant reduction in the sarcopenic index; total, troncular, and visceral fat (measured by DEXA); and serum leptin levels were observed in the collagen group at the end of the intervention, with no differences with respect to controls. Collagen reduced the sensation of hunger and increased fullness and satisfaction. In male Wistar rats, collagen decreased postprandial blood ghrelin levels. Collagen supplementation (20 g per day for 12 weeks) reduced body weight, BMI, waist circumference, fat mass, FLI, and SBP in humans with overweight and obesity, which might be related to the increased sensation of fullness and satisfaction reported by the volunteers after the intake.

A quantitative review of the effects of biochar application on the reduction of Cu concentration in plant: a meta-analysis.

Contamination and toxicity of copper (Cu) in soils are global issues, particularly in regions where Cu-based fungicides are utilized. Elevated Cu concentrations can lead to soil contamination and pose significant risks to the ecosystem, including plant life, wildlife, and human health. The application of biochar has been proposed as a viable strategy to mitigate Cu accumulation in plants. However, there is no quantitative and data-based consensus on the impact of biochar on plant Cu accumulation. In this meta-analysis, 624 data records from 65 published literature were collected and the effects of various factors, including biochar properties, experimental conditions, and soil properties on Cu accumulation in plants, were examined through meta-subgroup analysis and meta-regression models. The results obtained indicate a significant dose-dependent effect of biochar in decreasing Cu concentration in plants by an average of 23.45%. Soils with acidic pH values and medium textures were more conducive for biochar to mitigate Cu accumulation in plant tissues. In addition, manure biochar and green waste biochar were found to be more successful in decreasing Cu concentrations in plants compared to other biochar types. Biochar types with pyrolysis temperatures of > 600°C and pH values of ≥ 10 resulted in greater decreases in plant Cu concentration. Regarding biochar application, biochar minimum range of 1% in potting experiments and 20 t/ha in field experiments have been recommended to effectively decrease Cu concentration in plants. Overall, these findings provide valuable insights into Cu transfer mitigation through food chain to human bodies and for policymakers to take preventive measures.

Delivery of Avocado Seed Extract Using Novel Charge-Switchable Mesoporous Silica Nanoparticles with Galactose Surface Modified to Target Sorafenib-Resistant Hepatocellular Carcinoma.

Sorafenib-resistant (SR) hepatocellular carcinoma (HCC) is a current serious problem in liver cancer treatment. Numerous phytochemicals derived from plants exhibit anticancer activity but have never been tested against drug-resistant cells. Avocado seed extract (APE) isolated by maceration was analysed for its phytochemical composition and anticancer activity. Novel design charge-switchable pH-responsive nanocarriers of aminated mesoporous silica nanoparticles with conjugated galactose (GMSN) were synthesised for delivering APE and their physicochemical properties were characterized. The drug loading efficiency (%LE) and entrapment efficiency (%EE) were evaluated. Anticancer activity of APE loaded GMSN was measured against HCC (HepG2, Huh-7) and SR-HCC (SR-HepG2). Anticancer activity of APE against non-resistant HepG2 (IC50 50.9 ± 0.83 μg mL-1), Huh-7 (IC50 42.41 ± 1.88 μg mL-1), and SR-HepG2 (IC50 62.58 ± 2.29 μg mL-1) cells was confirmed. The APE loaded GMSN had a diameter of 131.41 ± 14.41 nm with 41.08 ± 2.09%LE and 44.96 ± 2.26%EE. Galactose functionalization (55%) did not perturb the original mesoporous structure. The GMSN imparted positive surface charges, 10.3 ± 0.61mV at acidic medium pH 5.5 along with rapid release of APE 45% in 2h. The GMSN boosted cellular uptake by HepG2 and SR-HepG2 cells, whereas the amine functionalized facilitated their endosomal escape. Their anticancer activity was demonstrated in non-resistant HCC and SR-HCC cells with IC50 values at 30.73 ± 3.14 (HepG2), 21.86 ± 0.83 (Huh-7), 35.64 ± 1.34 (SR-HepG2) μg mL-1, respectively, in comparison to the control and non-encapsulated APE. APE loaded GMSN is highly effective against both non-resistant HCC and SR-HCC and warrants further in vivo investigation.

Impact of (nano ZnO/multi-wall CNTs) prepared by arc discharge method on the removal efficiency of stable iodine 127I and radioactive iodine 131I from water

Radioactive iodine isotopes especially 131I are used for diagnosis and treatment of different types of cancer diseases. Due to the leak of radioactive iodine into the patient’s urine in turn, the wastewater would be contaminated, so it is worth preparing a novel adsorption green material to remove the radioactive iodine from wastewater efficiently. The removal of 127I and 131I contaminants from aqueous solution is a problem of interest. Therefore, this work presents a new study for removing the stable iodine 127I− and radioactive iodine 131I from aqueous solutions by using the novel nano adsorbent (Nano ZnO/MWCNTs) which is synthesized by the arc discharge method. It is an economic method for treating contaminated water from undesired dissolved iodine isotopes. The optimal conditions for maximum removal are (5 mg/100 ml) as optimum dose with shacking (200 rpm) for contact time of (60 min), at (25 °C) in an acidic medium of (pH = 5). After the adsorption process, the solution is filtrated and the residual iodide (127I−) is measured at a maximum UV wavelength absorbance of 225 nm. The maximum adsorption capacity is (15.25 mg/g); therefore the prepared nano adsorbent (Nano ZnO/MWCNTs) is suitable for treating polluted water from low iodide concentrations. The adsorption mechanism of 127I− on to the surface of (Nano ZnO/MWCNTs) is multilayer physical adsorption according to Freundlich isotherm model and obeys the Pseudo-first order kinetic model. According to Temkin isotherm model the adsorption is exothermic. The removal efficiency of Nano ZnO/MWCNTs for stable iodine (127I−) from aqueous solutions has reached 97.23%, 89.75%, and 64.78% in case of initial concentrations; 0.1843 ppm, 0.5014 ppm and 1.0331 ppm, respectively. For the prepared radio iodine (131I−) solution of radioactivity (20 µCi), the dose of nano adsorbent was (10 mg/100 ml) and the contact time was (60 min) at (pH = 5) with shacking (200 rpm) at (25 °C). The filtration process was done by using a syringe filter of a pore size (450 nm) after 2 days to equilibrate. The removal efficiency reached (34.16%) after the first cycle of treatment and the percentage of residual radio iodine was (65.86%). The removal efficiency reached (94.76%) after five cycles of treatment and the percentage of residual radio iodine was (5.24%). This last percentage was less than (42.15%) which produces due to the natural decay during 10 days.

Ni/Co/Carbon nitride derived from ZIF-67 (MOF) nanocomposite: Enhanced light-driven photocatalytic degradation of methylparaben, mechanism & toxicity

A nickel oxide/cobalt/carbon nitride (Ni/Co/CN) nanocomposite synthesized via co-precipitation was used for the degradation of methylparaben (MEP). Various analytical techniques were used to ascertain the structural, optical, and electrochemical characteristics of the synthesized nanocomposite. The unique nature of the compound without any free particles over the CN was established. Photocatalytic degradation studies demonstrated the superiority of 3-Ni/Co/CN over bare NiO, Co/CN, 1-Ni/Co/CN, and 5-Ni/Co/CN. Near complete MEP degradation (100%) was achieved after 120 min of incubation with MEP 75 mg L−1 in acidic medium pH (3) for an initial concentration of 3-Ni/Co/CN (10 mg/100 mL). HPLC-MS/MS analysis was used to elucidate the degradation pathway, and the catalyst was found stable for four subsequent cycles. Hence, our nanocatalyst effectively degraded MEP. Furthermore, microbial, aquatic, and animal studies demonstrated the environmental efficiency of the synthesized nanomaterials.

INTERACTION OF PECTIN WITH THE ANTIBACTERIAL DRUG NITROXOLINE

The process of macromolecular complexation of natural polymer pectin with nitroxoline, which has antibacterial activity, was studied in order to increase the solubility of the drug and, consequently, its therapeutic efficiency. By potentiometric titration it has been shown that in dilute aqueous solutions in a wide range of slightly acidic, neutral, and alkaline pH medium, the electrostatic binding of nitroxoline with pectin occurs. In the most optimal for medical preparations neutral region pH 7 the conversion depth of this reaction was calculated. The depth of conversion of pectin carboxyl groups ɵ1 for various studied ratios P : NOC=10 : 1, 5 : 1, 3 : 1 is 0.052, 0.076, and 0.095, respectively. The corresponding values of the conversion depth for nitroxoline ɵ2 are somewhat larger and amount to 0.52, 0.38, 0.32, respectively, for the studied ratios. That is, the calculation shows that not all reactive carboxyl groups of pectin and amino groups of the medicinal substance participate in electrostatic interaction.&#x0D; By the viscometry method it has been established the decrease of the pectin solution viscosity in the presence of nitroxoline. This indicates that electrostatic bonding of the low molecular weight medicinal substance NOC leads to the hydrophobization of the pectin macromolecule.&#x0D; Comparative data, obtained by the method of derivatographic analysis, indicate, that the thermal characteristics of the studied complex of nitroxoline with pectin differ from the thermal parameters of the initial components and is thermally more stable. This confirms the formation of the product of chemical interaction - the complex of pectin with NOC.

Surface Modification of Tea-Waste-Based Biochar Adsorbent: Synthesis, Characterization, and Batch Adsorption for the Removal of Zidovudine ARV Drug and Phenol

Domestic, agricultural, and industrial waste has been investigated as a substitute for activated carbon adsorbents. For instance, the transformation of tea waste to biochar can be utilized as a substitute for activated carbon adsorbents. In this study, tea waste-based biochar adsorbents (biochar, biochar/reduced graphene oxide (biochar/rGO), biochar/reduced graphene oxide/deep eutectic solvent-cetyltrimethylammonium bromide (biochar/rGO/DES-CTAB), and biochar/reduced graphene oxide/deep eutectic solvent-glycerol (biochar/rGO/DES-glycerol)) were synthesized by simple thermal treatment of tea waste and sucrose followed by modification with reduced graphene oxide and deep eutectic solvents. The obtained materials were characterized using a range of spectroscopy techniques, Fourier Transformed Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), Scanning Electron Microscopy–Energy-Dispersive X-ray Spectroscopy (SEM–EDS), Brunauer, Emmett, and Teller (BET) surface area analysis, and pH at point of zero charge (pH PZC). The obtained results showed that the principal material, i.e., biochar was modified, and FTIR results confirmed the presence of added functional groups. SEM images revealed surface structural changes, and BET showed a decrease in pore size from 10.16 nm to 6.87 nm. The synthesized materials were applied for the removal of ZDV and phenol from the aqueous medium. Batch adsorption studies were conducted to optimize operating parameters such as the adsorbent dose, solution pH, contact time, and initial concentration. Pseudo-first-order (PFO), Pseudo-second-order (PSO), and intraparticle diffusion (IPD) kinetic models were determined to investigate the mechanism of the adsorption process. The coefficient of correlation, R2, was used to determine the best fit of the kinetic models. The adsorption results showed that the DES-glycerol-modified adsorbent was more efficient in removing the pollutants ZDV and phenol than biochar, biochar/rGO, and biochar/rGO/DES-CTAB adsorbents. In addition, the results showed that an acidic medium of pH 2.00 and a contact time of 1 h 30 min and 30 min is sufficient for removing ZDV and phenol, respectively, from an aqueous medium.

Ethylenediamine functionalized waste polyethylene terephthalate-derived metal-organic framework for adsorption of palladium ions from aqueous solutions

The recovery of palladium metal is essential in order to meet its growing global demand and also to address water pollution crisis. Herein, MIL-101(Cr)/ED was fabricated from waste polyethylene terephthalate (PET) bottles and modified using ethylenediamine (ED) to retrieve divalent palladium (Pd(II)) metal ions from aqueous environment. The successful grafting of ED moieties onto MIL-101(Cr) was established by the appearance of broad bands at around 2800–3300 cm−1 on the Fourier transform infrared spectrum which was supported by the increase in binding energy using density functional theory. The adsorption experiments revealed that higher Pd(II) ion intake occurred using 30 mg of MIL-101(Cr)/ED in acidic media of pH = 3.0. The data fit better on the Langmuir isotherm with the correlation coefficient (R2) 0.9089. At 25 °C, the MIL-101(Cr)/ED achieved a substantial enhancement in the intake capacities of 454.2 mg.g−1. Kinetics data demonstrated to comply with pseudo-second order, achieving a rapid rate of Pd(II) adsorption by the MIL-101(Cr)/ED in less than 3 min given by the rate constant k2 = 0.02065 g.mg−1.min−1. The MIL-101(Cr)/ED has high affinity for Pd(II) ions as more than 80% removal was achieved even in presence of other ions. These observations revealed the potential utilization of MIL-101(Cr)/ED as an adsorbent to efficiently extract Pd(II) ions from wastewater.

Exploring in vitro solubility of lamotrigine in physiologically mimetic conditions to prospect the in vivo dissolution in pediatric population

Pediatric drugs knowledge still leaves several gaps to be filled, all the while many biopharmaceutic properties applied to adults do not work in pediatrics. The solubility in many cases is extrapolated to pediatrics; however, sometimes it may not represent the real scenario. In this context, the aim of this study was to assess the possibility of the extrapolation of the solubility data assumed for adults to children aged 2-12years using lamotrigine (LTG) as a model. LTG showed that its solubility is dependent on the pH of the medium, no precipitate formation was seen, and biomimetic media showed a greater capacity to solubilize it. Based on the dose number (D0 ) in adults, the LTG was soluble in acidic pH media and poorly soluble in neutral to basic. Similar behavior was found in conditions which mimic children aged 10-12years at a dose of 5 and 15mg/kg. The D0 for 5-year-old children at a dose of 15mg/kg showed different behaviors between biorelevant and pharmacopeial buffers media. For children aged 2-3years, LTG appeared to be poorly soluble under both gastric and intestinal conditions. Solubility was dependent on the volume of fluid calculated for each age group, and this may impact the development of better pharmaceutical formulations for this population, better pharmacokinetic predictions in tools as PBPK, and physiologically-based biopharmaceutics modeling, greater accuracy in the justifications for biowaiver, and many other possibilities.

Photocatalytic Removal of Thiamethoxam and Flonicamid Pesticides Present in Agro-Industrial Water Effluents

Pesticide residues, when present in agricultural wastewater, constitute a potential risk for the environment and human health. Hence, focused actions for their abatement are of high priority for both the industrial sectors and national authorities. This work evaluates the effectiveness of the photocatalytic process to decompose two frequently detected pesticides in the water effluents of the fruit industry: thiamethoxam-a neonicotinoid compound and flonicamid-a pyridine derivative. Their photocatalytic degradation and mineralization were evaluated in a lab-scale photocatalytic batch reactor under UV-A illumination with the commercial photocatalyst Evonik P25 TiO2 by employing different experimental conditions. The complete degradation of thiamethoxam was achieved after 90 min, when the medium was adjusted to natural or alkaline pH. Flonicamid was proven to be a more recalcitrant substance and the removal efficiency reached ~50% at the same conditions, although the degradation overpassed 75% in the acidic pH medium. Overall, the pesticides’ degradation follows the photocatalytic reduction pathways, where positive charged holes and hydroxyl radicals dominate as reactive species, with complete mineralization taking place after 4 h, regardless of the pH medium. Moreover, it was deduced that the pesticides’ degradation kinetics followed the Langmuir-Hinshelwood (L-H) model, and the apparent rate constant, the initial degradation rate, as well as the L-H model parameters, were determined for both pesticides.

Application of salts of chaotropic anions in the development of hplc methods for the determination of meldonium in dosage forms

The aim of the work was to create an approach for the development of HPLC methods for the determination of meldonium in dosage forms with the usage of salts of chaotropic anions in mobile phases.&#x0D; Material and methods. Analytical equipment: Shimadzu UPLC system LC-40 PDA; Shimadzu Nexera-i LC-2040C 3D-Plus, controlled by software Lab Solution version 5.97, electronic laboratory balance RAD WAG AS 200/C, pH-meter I-160MI. Meldonium dihydrate (purity 99.3 %) was purchased from Sigma-Aldrich (Switzerland), and Vasopro capsules 500 mg were purchased from a local pharmacy. Chromatographic conditions: Agilent Zorbax C-18 SB 150 mm x 4.6 mm 3.5 μm column was used (Agilent Technologies, USA). Mobile phases: 1) 0.25 % KPF6 w/v – 0.1 % v/v 85 %H3PO4 95 % – 5 % ACN, 2) 0.3 % bis-(trifluoromethane)sulfonimide lithium salt 97 % w/v – 0.1 %v/v 85 % H3PO4 80 % – 20 % acetonitrile. Flow rate - 1mL/min, T=32 °C, detection UV=at 4 channels - 190 nm, 195 nm, 200 nm, 205 nm.&#x0D; Results and discussion. We have proposed two approaches using two different salts of chaotropic anions - potassium hexafluorophosphate and bis-(trifluoromethane)sulfonimide lithium salt – for the HPLC method development. The chaotropic effects of these anions toward meldonium strongly influenced the analyte migratory behaviour. Both mobile phases involved, in addition to the use of a chaotrope, also the use of acetonitrile and pH adjustment with 0.1 % v/v 85 % H3PO4 solution. The detection wavelength (190 nm, 195 nm, 200 nm, 205 nm) was selected experimentally. The results were obtained for 8 concepts. Parameters of the chromatographic system confirm the conclusions and results of this investigation for the influence of chaotropic salts on N-containing molecules in an acidic pH medium, by increasing their retentivity and improving peak shape and uniformity homogeneity, even on the column without end-capping and base-deactivating. Validation of the analytical method was carried out following the requirements of SPhU. Conclusions. HPLC methods for the determination of meldonium in dosage forms have been developed, using positive impacts of chaotropic salts on the molecules containing N-atoms in their molecule on their retentions and peak symmetries on the chromatogram. The validation of the analytical methods showed their suitability for pharmaceutical analysis

Development of eplerenone nano sono-crystals using factorial design: enhanced solubility and dissolution rate via anti solvent crystallization technique

Objective The purpose of this work was to improve EP solubility by using a sono-crystalization approach to reduce particle size and hence, increase the dissolution rate. Significance Eplerenone (EP) is an antagonist of the aldosterone receptor and is used for the treatment of hypertension and chronic heart failure. EP was classed as biopharmaceutical classification (BCS) class II because of its poor solubility and high permeability, which retards dissolution rate and drug absorption, and decreases bioavailability. Methods Three-factors and two-level (23) multifactorial design have been employed to study the effect of independent variables which are drug concentration; (X1), stabilizer type (X2), and stabilizer concentration (X3) on responses; saturated solubility of EP in distilled water (Y1), saturated solubility in acidic media pH 1.2 (Y2), particle size (Y3), and polydispersity index, PDI (Y4). Also, they were characterized by Fourier transformed infrared spectroscopy (FTIR), Powder X-ray diffraction (PXRD), Differential scanning calorimetry (DSC), and yield percentage. The optimum formula was further subjected to an in-vitro release study. Results The optimized formulation showed a saturated solubility of EP as 1.29, and 1.86 (mg/ml) in distilled water and acidic media (pH 1.2) respectively. Also, the particle size of 133 nm, and PDI of 0.824 with a small percentage of the difference between the observed and predicted values. Ninety-one percent of EP was released within 10 min., and it was completely released within 45 min. with a significantly higher release rate compared to raw drug. Conclusion This work resulted in a satisfactory enhancement of solubility and dissolution rate which, is suitable for further in-vivo analysis.

Enzymatic PCL-grafting to NH2-end grouped silica and development of microspheres for pH-stimulated release of a hydrophobic model drug

This study set out to evaluate novel PCL-based silica containing nanohybrids as the polymer matrix in a hydrophobic drug-loaded microsphere system. Nanohybrids were synthesized by PCL-grafting to NH2-end grouped silica by in situ enzymatic ring opening polymerization of ε-caprolactone. Molecular weight and monomer conversion, PCL grafting percentage, thermal properties and crystallinity of the nanohybrids were determined by 1H NMR, TGA, DSC and XRD. Synthesized nanohybrids had low crystallinity percentage (32 and 39 %) and molecular weight (4800 and 8700 g/mol), promising for controlled drug release applications. The nanohybrids were used for fabrication of trans-chalcone-loaded microspheres by O/W single emulsion solvent evaporation. Mean particle diameter of the microspheres were between 15 and 30 µm. The result of release studies showed that optimum microsphere formulations (AP4 and A2, respectively) had 61 and 64 % encapsulation efficiency. One of the more significant findings to emerge from this investigation is that TC release was extended to 16 and 37 days, in a controlled manner. TC release was significantly enhanced in acidic pH media (pH 3.6 and 5.6) indicating pH-dependent release from nanohybrid microspheres; releasing 80–100 % of the loaded drug in 4–14 days. Drug/polymer interactions and molecular structures were investigated by FT-IR spectroscopy and DSC analysis. According to the results obtained, enzymatically synthesized nanohybrids have potential for pH-dependent release of the model drug, trans-chalcone.

Preparation of pH-Responsive Hydrogels Based on Chondroitin Sulfate/Alginate for Oral Drug Delivery.

This study investigates pH-sensitive hydrogels based on biocompatible, biodegradable polysaccharides and natural polymers such as chondroitin sulfate and alginate in combination with synthetic monomer such as acrylic acid, as controlled drug carriers. Investigations were conducted for chondroitin sulfate/alginate-graft-poly(acrylic acid) hydrogel in various mixing ratios of chondroitin sulfate, alginate and acrylic acid in the presence of ammonium persulfate and N′,N′-Methylene bisacrylamide. Crosslinking and loading of drug were confirmed by Fourier transform infrared spectroscopy. Thermal stability of both polymers was enhanced after crosslinking as indicated by thermogravimetric analysis and differential scanning calorimeter thermogram of developed hydrogel. Similarly, surface morphology was evaluated by scanning electron microscopy, whereas crystallinity of the polymers and developed hydrogel was investigated by powder X-ray diffraction. Furthermore, swelling and drug-release studies were investigated in acidic and basic medium of pH 1.2 and 7.4 at 37 °C, respectively. Maximum swelling and drug release were detected at pH 7.4 as compared to pH 1.2. Increased incorporation of hydrogel contents led to an increase in porosity, drug loading, and gel fraction while a reduction in sol fraction was seen. The polymer volume fraction was found to be low at pH 7.4 compared to pH 1.2, indicating a prominent and greater swelling of the prepared hydrogels at pH 7.4. Likewise, a biodegradation study revealed a slow degradation rate of the developed hydrogel. Hence, we can conclude from the results that a fabricated system of hydrogel could be used as a suitable carrier for the controlled delivery of ketorolac tromethamine.

Using of eosin Y as a facile fluorescence probe in alogliptin estimation: Application to tablet dosage forms and content uniformity testing

New simple sensitive and reliable spectrofluorimetric approach was established for the determination of the antidiabetic drug; Alogliptin (ALG) in its pure and tablet forms. The developed approach is depended on the suppressive action of ALG on the eosin Y native fluorescence. The quenching action of ALG on the eosin Y native fluorescence was measured at acidic medium pH: 3.5, emission wavelength 541 nm (λex. 260 nm). The relative fluorescence intensity (RFI) was measured, and it was directly proportional to ALG concentration in the concentration range of (15–110) μg/mL. The developed and optimized approach was entirely validated regarding to ICH guidelines. The developed method application was successfully extended for ALG content uniformity test (CU). The distribution fraction (DF), rate constants (K), and free energy changes (ΔG°) were calculated. The results obtained were compared to that of the published spectrophotometric one.

Removal of hexavalent chromium via biochar-based adsorbents: State-of-the-art, challenges, and future perspectives

Chromium originates from geogenic and extensive anthropogenic activities and significantly impacts natural ecosystems and human health. Various methods have been applied to remove hexavalent chromium (Cr(VI)) from aquatic environmental matrices, including adsorption via different adsorbents, which is considered to be the most common and low-cost approach. Biochar materials have been recognized as renewable carbon sorbents, pyrolyzed from various biomass at different temperatures under limited/no oxygen conditions for heavy metals remediation. This review summarizes the sources, chemical speciation & toxicity of Cr(VI) ions, and raw and modified biochar applications for Cr(VI) remediation from various contaminated matrices. Mechanistic understanding of Cr(VI) adsorption using different biochar-based materials through batch and saturated column adsorption experiments is documented. Electrostatic interaction and ion exchange dominate the Cr(VI) adsorption onto the biochar materials in acidic pH media. Cr(VI) ions tend to break down as HCrO4-, CrO42-, and Cr2O72- ions in aqueous solutions. At low pH (∼1-4), the availability of HCrO4- ions attributes the electrostatic forces of attraction due to the available functional groups such as -NH4+, -COOH, and -OH2+, which encourages higher adsorption of Cr(VI). Equilibrium isotherm, kinetic, and thermodynamic models help to understand Cr(VI)-biochar interactions and their adsorption mechanism. The adsorption studies of Cr(VI) are summarized through the fixed-bed saturated column experiments and Cr-contaminated real groundwater analysis using biochar-based sorbents for practical applicability. This review highlights the significant challenges in biochar-based material applications as green, renewable, and cost-effective adsorbents for the remediation of Cr(VI). Further recommendations and future scope for the implications of advanced novel biochar materials for Cr(VI) removal and other heavy metals are elegantly discussed.

Adsorption of anionic dyes from textile wastewater utilizing raw corncob

Toxic dyes are irrefutable effluent components of textile wastewater, so they have become a major economic and health concern. With the purpose of efficient removal of textile dyes, multiple nature-inspired adsorbents have been applied. Herein, raw corncob is proposed as a novel highly efficient, low-price, and abundantly attainable adsorbent with the potential for uptake of methyl red and methyl orange. Multiple experiments were carried out to optimize parameters including pH, primary concentration, adsorbent dosage, temperature, and contact time. The adsorption was raised with the mounting of the contact time and it was alleviated with the addition of initial concentration. The foremost uptake of dye was apperceived at an acidic medium pH 4 for methyl red and pH 1 for methyl orange. Scanning Electron Microscopy and Fourier Transform Infrared Spectroscopy were employed to characterize the surfaces of corncobs. The well-fitted Langmuir and Freundlich models (methyl red: R2 = 0.9956 and methyl orange: R2 = 0.9883) confirmed the homogeneous monolayer adsorption process on the raw corncob surface. The obtained results disclose that corncob is an effectual biosorbent for eliminating anionic dyes without the necessity for any prior modifications.

Adsorption and Reusability Performances of Ni/Al Layered Double Hydroxide for the Removal of Eriochrome Black T dye

This work deals with the synthesis, characterization, and adsorptive removal performances for eriochrome black T (EBT) dye of Ni/Al lamellar double hydroxides (Ni-Al-LDH). The characterization results showed that the material exhibited excellent crystallinity and an excess of hydroxyl groups on its surface with better textural properties. Also, after interaction with EBT, FT-IR spectroscopy showed that EBT was on both surfaces adsorbed and intercalated by the material. Adsorption experiments results showed higher adsorption in an acidic pH medium. The adsorption process followed the pseudo-first-order kinetic model, and the Langmuir equation adequately described the equilibrium data. The maximum adsorption capacity was 37.71 mg/g at an initial dye concentration of 20 mg/L, contact time of 120 min, and temperature of 298 K. The thermodynamic parameters indicate spontaneous and exothermic physisorption process. Finally, the adsorption performance after three successive regeneration cycles shows that Ni-Al-LDH has superior adsorption and reuse performance for EBT dye, indicating that the material could be used as an effective adsorbent for the decontamination of anionic dyes in wastewaters.

PH-sensitive carbon nanotubes graft polymethylacrylic acid self-assembly nanoplatforms for cellular drug release.

pH-Sensitive carbon nanotubes graft polymethylacrylic acid hybrids (CNTs-g-PMAA) were prepared through a three-step process, and self-assembled into core-shell micelle nanoparticles. The chemical structure of the hybrids were characterized by FTIR, 1H NMR and TGA. The critical micelle concentration (CMC) was measured by surface tension, and the value hinged on the Mn values or chain lengths of PMAA segments. The UV-vis transmittance, dynamical light scattering (DLS), and zeta potential measurements indicated that the hybrid self-assembly exhibited pH-sensentive responsiveness. The self-assembly was used to load an anticancer drug, paclitaxel (PTX), with an encapsulation efficiency of 77%. The PTX-loaded hybrid drug preparations were applied for cancer-cellular drug release, finding that the release rate was dependent on pH environments, and faster in acidic media of pH < 6.8 than in pH 7.4. MTT and hemolysis assays manifested that the blank hybrid drug carriers were nontoxic and safe, whereas the PTX-loaded drug preparations possessed comparable and even higher anticancer activity in comparison with free PTX. Consequently, the developed hybrid drug nanocarriers can be used for cancer therapy as a promising candidate.

Rutin-Loaded Stimuli-Responsive Hydrogel for Anti-Inflammation.

An active flavonoid compound rutin was incorporated into a guanosine phenylborate hydrogel (GBR) by a stimuli-responsive borate ester linkage for the treatment of inflammatory bowel disease (IBD). The components and morphology of the drug delivery system were characterized by NMR, UV-vis spectroscopy, and AFM. Rheological measurements revealed the required injectability and self-healing ability, which contributed to its application in rectal administration. The cell assays proved the excellent compatibility and safety of the system, and a possible pathway to form multicellular aggregates. In vitro drug-release studies showed that the hydrogel exhibited good stability in physiological medium, and the drug was almost completely released (more than 90 wt % after 24 h of incubation) in acidic pH and excessive ROS-containing medium, realizing the dual-responsive release of pH/ROS. In vivo activities of the GBR hydrogel showed higher therapeutic efficacy than free rutin in a colitis mice model, and it could significantly inhibit overexpressed inflammatory cytokines, including TNF-α and IL-6. Degradation studies of the hydrogel provided further evidence for the safety of its in vivo application. The work provided a simple strategy to prepare a G-quadruplex drug carrier, which was expected to achieve multi-drug delivery.