RESUMEN

The aim of this study was to investigate the relation between residual α- and ß-punicalagin in Punica granatum L.; PPE and rosmarinic acid, carnosol, and carnosic acid in Salvia eremophila (SE) with residual nitrites, biogenic amines (cadaverine, putrescine, and histamine), N-nitrosodimethylamine (NDMA), microbial counts, lipid oxidation indices, and color values in extract-treated sausage over 14 days of storage. Sausage containing SE + nitrite 60 ppm (SSN) showed minimum levels of the residual nitrites (13.14 mg/kg), NDMA (0.74 ± 0.05 µg/kg), and biogenic amine (histamine, 1.8 mg/kg; cadaverine, 3.7 mg/kg; and putrescine, 4.3 mg/kg) due to retarded degradation rate of 285.84-216.44 mg/kg; rosmarinic acid, 41.62-33.16 mg/kg; carnosol, and 88.70-76.73 mg/kg; carnosic acid over storage time. The first-order kinetic model fitted well for the degradation of rosmarinic acid and carnosol acid in SSN sample. TBA value remained below the threshold limit (0.32 mg kg-1) through 14 days for SSN. Second-order and zero-order reaction models had the best agreement with sausages' PV and TBA values, respectively. After 2 weeks of storage, E. coli and Cl. perfringens counts in the SN120 (sausage containing 120 ppm nitrite) and SSN were significantly lower than the other samples (p < .05), with the values 2.1 and 1.5 log cfu/g for SN120 and 2.2 and 1.6 log cfu/g for SSN formulation. Conversely, oxidation indices, residual nitrites, NDMA, and biogenic amine increased in sausage samples containing PPE extracts (SPN) owing to total degradation of α- and ß-punicalagin during storage. The results indicated that SE can be used as potential co-preservative by reducing the levels of required nitrite in food industry.

RESUMEN

This study aimed to determine how different forms of lutein found in nature affected their thermal stability, degradation, and antioxidant activities. The findings show that commercial lutein (CL) degraded faster than silk luteins (SLs) at ≤ 4 °C. The two-stage first-order kinetics of thermal degradation showed that Ea for SLs was 4.6-9.5 times higher than CL. However, at ≥ 25 °C, both the CL and SLs degraded rapidly within one month. SLs had half-life at 4 °C from 10 to 104 wks. FTIR and HRMS analysis revealed that their oxidation products were similar (C18H26O2: 297 m/z). Based on IC50, antioxidant activities of SLs were superior to CL. The stability and antioxidant capacity of lutein may be influenced by its naturally occurring forms. The naturally occurring forms and unpurified state of lutein can affect its stability and antioxidant activity, which must be considered when storing lutein at different temperatures.

RESUMEN

Phenolic compounds are the major contaminants identified from various industrial effluents, which pose an extreme threat to the environment. Therefore, investigating an effective technique to remove these toxic phenolic compounds from the contaminated environment is very essential. In the present investigation, batch tests were performed to assess the biodegradation of phenol using an indigenous Rhodococcus pyridinivorans strain PDB9T NS-1 encapsulated in a calcium alginate bead system. In order to improve the mechanical stability, silica was added to the cell-embedded Ca-alginate beads. The impact of experimental conditions such as contact time, pH, and initial phenol doses was investigated. The biodegradation of phenol was examined over a wide range of phenol, and the results showed that more than 99.6% degradation was achieved at an initial phenol dose of 1000 mg/L in 70 h at 30 °C. Among the various sorption isotherm tested, the Freundlich isotherm was the best fitted to the experimental data. This behavior indicated a multilayer biosorption process and was controlled by heterogeneous surface energy. Based on an intra-particle diffusion model, internal mass transfer or pore diffusion predominated over exterior mass transfer in controlling the entire phenol biosorption process. The biosorption of phenol onto the cell encapsulated in the Ca-alginate bead follows pseudo-first-order kinetics with a superior phenol biosorption capacity of 155 mg/g of Ca-alginate. Further stability study revealed that the bead could be recycled successfully without any substantial decline in phenol degradation efficiency, indicating that the immobilized microbe possesses exceptional operating stability.

RESUMEN

Tetracycline (TC) is an antibiotic that is recently found as an emerging pollutant with low biodegradability. Biodegradation shows great potential for TC dissipation. In this study, two TC-degrading microbial consortia (named SL and SI) were respectively enriched from activated sludge and soil. Bacterial diversity decreased in these finally enriched consortia compared with the original microbiota. Moreover, most ARGs quantified during the acclimation process became less abundant in the finally enriched microbial consortia. Microbial compositions of the two consortia as revealed by 16 S rRNA sequencing were similar to some extent, and the dominant genera Pseudomonas, Sphingobacterium, and Achromobacter were identified as the potential TC degraders. In addition, consortia SL and SI were capable of biodegrading TC (initial 50 mg/L) by 82.92% and 86.83% within 7 days, respectively. They could retain high degradation capabilities under a wide pH range (4-10) and at moderate/high temperatures (25-40 °C). Peptone with concentrations of 4-10 g/L could serve as a desirable primary growth substrate for consortia to remove TC through co-metabolism. A total of 16 possible intermediates including a novel biodegradation product TP245 were detected during TC degradation. Peroxidase genes, tetX-like genes and the enriched genes related to aromatic compound degradation as revealed by metagenomic sequencing were likely responsible for TC biodegradation.

Asunto(s)

RESUMEN

The oral delivery of medicines is the most popular route of administration for patients. However, thymopentin (TP5) is only available in the market in forms for parenteral administration. In large part, this is because of extensive peptidolytic degradation in the gastrointestinal tract (GIT), which decreases the amount of TP5 available for absorption. This study aims to understand the extent of TP5 peptideolysis and determine effective inhibitors and suitable lipid-based nanocarriers to aid in the development of an effective oral delivery formulation. Enzymatic degradation kinetics of TP5 was investigated in the presence or absence of mucosal and luminal components extracted from various parts of the rat intestine, including the duodenum, jejunum, ileum, and colon. Inhibition of TP5 enzymatic peptidolysis was screened in the presence or absence of EDTA, trypsin and chymotrypsin inhibitors from soybean (SBTCI), and bestatin. TP5 with SBTCI was loaded into lipid-based nanocarriers, including microemulsions, niosomes and solid lipid nanoparticles. These TP5-loaded nanocarriers were investigated through characterization of morphology, particle size, zeta potential, entrapment efficacy (EE%), and ex vivo rat intestinal degradation studies to select a lead formulation for a future oral drug delivery study. The degradation kinetics of TP5 followed pseudo-first-order kinetics, and the biological metabolism of TP5 was displayed in the presence of luminal contents, indicating that TP5 is sensitive to luminal enzymes. Notably, a considerable decrease in TP5 peptidolysis was found in the presence of SBTCI, bestatin, and EDTA. TP5 and SBTCI were loaded into three lipid-based delivery systems, displaying superior protection under ex vivo intestinal luminal contents and mucosal homogenates for 6 h compared with the pure drug solution. These findings suggest that using select inhibitors and lipid-based nanocarriers can decrease peptide degradation and may improve oral bioavailability of TP5 following oral administration.

Asunto(s)

RESUMEN

The widespread adoption of electrified carbon nanotube membranes (ECM) requires to better understand process effectiveness according to limiting phenomena of natural organic matters (NOMs). In this study, the influences of various NOM fractions were investigated on the oxidative degradation of Rhodamine B (RhB) in ECM. The results showed the decolorizing efficiencies of RhB in the presence of humic acid (HA) were still above 96%, while bovine serum albumin (BSA) reduced firstly and then increased the decolorizing efficiencies of RhB. The decolorizing efficiencies of RhB with alginate (AA) were over 98% at the first 15 min but decreased gradually to 76% after 150 min. These different performances of HA, BSA and AA were mainly due to their influences on the electrochemical reactivity characterization of ECM. ECM with the BSA depositing layer showed the highest exchange current density (j0), while the AA depositing layer restrained electron-transfer activity of ECM. Cyclic voltammetry (CV) experiments showed that the partial electrooxidation of BSA would occur in ECM with its degradation product observed in the effluent. The variation of electrochemical reactivity characterization of ECM resulted into its electri-oxidation and electri-adsorption rates to be the largest with BSA, followed by AA and HA.

Asunto(s)

RESUMEN

Binimetinib (BMT) has recently been approved by the USFDA for the treatment of melanomas. An extensive literature search revealed that degradation kinetics of BMT is not reported in any scientific report. Till date, no stability indicating analytical method (SIAM) is available for quantification of BMT in presence of its impurities. Moreover, information on degradation products (DPs) of BMT and the degradation pathway is not known. In this study, we have developed a SIAM for BMT and characterized its major DPs using LC-Q-TOF-MS/MS. The SIAM was validated according to the ICH guideline and subsequently used to study the degradation kinetics of BMT. The method was found to be useful for separating BMT and all its DPs formed during different stress conditions. Three new DPs have been identified and characterized. H1 (acid hydrolytic DP) and O1 (oxidative degradation product) were isolated and characterized by NMR (1H) spectroscopy. An in silico toxicity evaluation of the DPs was performed using ProTox-II toxicity prediction software. Data obtained from the degradation kinetic study revealed that BMT degradation follows first-order kinetics under acidic hydrolysis and oxidative stress conditions. The degradation kinetics mechanism and knowledge on the pathway of degradation established through this study can be useful to improve the stability profile of the drug and to propose a more appropriate storage condition. The degradation impurities we have identified and characterized can be useful in setting the quality control acceptance criteria of the drug after their required qualification. The quantitative assay method can be used for routine quality control and stability study analysis of BMT in pharmaceutical industries and research laboratories.

Asunto(s)

RESUMEN

Vortioxetine (VOR) is a new antidepressant drug used to treat major depressive disorder. In this work, a novel, simple, rapid, accurate, precise, selective, stability-indicating, and fully validated high-performance liquid chromatography method with diode array detection (HPLC-DAD) was developed to determine VOR in bulk and pharmaceutical formulations. A Polar-RP column was used, with a mobile phase consisting of acetonitrile (ACN), methanol (MeOH), acetate buffer pH 3.5, and addition of diethylamine (DEA) in the isocratic elution mode. Assessing the stability of the VOR is fundamental to guarantee the efficacy, safety, and quality of drug products. In this study, the VOR active pharmaceutical ingredient (API) and tablets were subjected to a detailed study of forced degradation, using several degrading agents (acid, alkaline, water, heat, light, and oxidation agents). The developed HPLC-DAD method allows the collection of all the essential data to determine degradation kinetics. It was found that the decomposition of vortioxetine is fragile towards oxidative conditions and photolysis, yielding the first-order and second-order kinetic reaction in the above stress conditions, respectively. The degradation products (DPs) were identified by the high-resolution liquid chromatography coupled with electrospray ionization-quadrupole-time of flight-mass spectrometry (LC-ESI-QTOF-MS) method. The HPLC-DAD method was successfully applied for the quantification of VOR in tablets. Additionally, in silico toxicity prediction of the DPs was performed.

Asunto(s)

RESUMEN

BACKGROUND: The SARS-CoV-2 pandemic has resulted in a dramatic rise of the demand for medical devices and drugs. In this context, an important shortage of programmable syringe pumps, used to administrate different drugs in intensive care units, was seen. The opportunity of administrating combinations of five intensive care units selected drugs (Sufentanil, Clonidine, Loxapine, Midazolam, and Ketamine) was considered. METHODS: The drug mixtures were studied in a pure form or diluted in NaCl 0.9% or G5%. Twenty-six possible combinations of the five drugs were produced in glass vials or polypropylene syringes and stored at 25 °C for 14 days. The LC method was implemented to study drugs combinations in the presence of the degradation products. The clearness and pH were also monitored. RESULTS: All the 26 possible combinations displayed adequate physicochemical stability at 25 °C: at least 3 days and 7 days, respectively, for the dilution in 0.9% NaCl or glucose 5%, and the pure drug products mixtures. CONCLUSIONS: The study provided sufficient stability results, covering the medication administration period of at least three days. The combination of more than two drugs offers the advantage of minimizing the individual doses and reduces unwanted side-effects. Hence, this study opens up the possibility of combining the five drugs in one single syringe, which is useful especially under the current circumstances associated with an important shortage of programmable syringe pumps and pharmaceuticals.

RESUMEN

Beetroot is a good source of natural food colorants given that it contains significant amount of betalain pigments. This study investigates the three-months storage stability of betalain extracts recovered from unsold beetroot by a specific enzymatic mix. The extract storability was evaluated by the kinetic degradation model of betacyanins and betaxanthins, as well as by pigment color attributes (CIELa*b* parameters) under dark and UV-light exposure at different temperatures (4, 25 and 40 °C). Considering all the tested storage conditions, betaxanthins appeared to be more stable than betacyanins in terms of degradation rate constant, half-life time and activation energy. The effect of UV-light was negligible if the pigment was not exposed to temperatures higher than the room one, since no relevant differences were found between the parameters studied at 4 and 25 °C. Taking into account the visual color, all the investigated color indexes (total color difference, chroma and hue) were mainly affected by temperature, even if mildly high (40 °C), and to a lesser extent by UV-light exposure.

Asunto(s)

RESUMEN

Recently, the growing environmental concerns and economic demands have driven the need to develop effective solutions for the treatment of vegetal fibers to be used as renewable source for various industrial applications. The present study aimed to explore pineapple crown fibers (PCs) as an alternative source of cellulose. The three treatments (alcohol-insoluble residue (AIR), alkaline (AT), and organosolv) evaluated promoted chemical and morphological changes to the PCs. Fresh and treated PCs were characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Scanning electron microscopy (SEM), thermogravimetric analysis (TG), and chemical composition. The XRD results showed that the Cellulose-I allomorph was not altered during extraction, and that the crystallinity index of the fibers treated with AT, first bleaching step, second bleaching step, and the second bleaching step followed by KOH treatment (2B_KOH) increased to 77.8; 83.2; 83.5 and 86% when compared with fresh PC (62.3%). Results from the thermal analysis revealed that thermal stability increased for the isolated cellulose, and the maximum degradation for (2B_KOH) is 350 °C. Chemical composition results showed a decrease in the content of hemicellulose, lignin and other soluble materials after alkaline treatment, suggesting high-quality 2B_KOH with 74.6% of cellulose. SEM revealed changes in the morphological structure on fibers. Alkaline treatment followed by H2O2 bleaching is an excellent alternative for the removal of non-cellulosic material and facilitates the isolation of cellulose. These results suggested that there is a potential to isolate cellulose from PC via the sequence of treatment of a methodology by chlorite-free.

Asunto(s)

RESUMEN

Di-(2-ethylhexyl) phthalate (DEHP) is a chemical plasticizer that has been commonly used in the manufacture of polyvinyl chloride. DEHP is one of the environmental pollution sources. In this study, a gram-negative strain RX bacterium utilizing DEHP as sole carbon source was isolated from activated sludge through screening test. This strain RX was identified as Achromobacter sp. RX based on its morphology, physiological properties and 16S rRNA gene sequence analysis. The results showed that the optimal conditions for the DEHP degradation were 30.0 °C and pH 7.0. The DEHP degradation induced by strain RX demonstrated nitrogen source dependent, while followed a decreasing degradation rate under the source of: NO3- > NH4+ > NO2-. The biodegradability of Achromobacter sp. RX was enhanced with Masson pine seed powder as a co-metabolic substrate and Tween-80 as a solubilizing agent. Meanwhile, the degrading kinetics analysis was performed in the condition of DEHP as sole carbon source. The DEHP degradation curves fitted well with the first-order kinetic model at 50-300 mg/L of DEHP, with the half-life ranging from 13.0 to 16.4 h. During the biodegradation of DEHP, mono-(2-ehtylhexyl) phthalate (MEHP) was firstly generated through de-esterification, followed by the formation of phthalic acid and benzoic acid after further de-esterification of MEHP. Benzoic acid was finally mineralized to CO2 and H2O. The decontamination of DEHP-contaminated soil by Achromobacter sp. RX was investigated using a rotating-drum bioreactor. Evolution of total organic carbon from the contaminated soil showed that 86.4%-91.7% of DEHP was mineralized at pH 7.0 and 30.0 °C within 96 h. Reusability of Achromobacter sp. RX and its lifetime were observed over six consecutive cycles. Thus, Achromobacter sp. RX possessed high DEHP biodegradability, which provided a good potential in dealing with DEHP-contaminated soil.

Asunto(s)

RESUMEN

Systematic kinetics of melt-blended Poly(lactic acid) (PLA)/Poly(butylene succinate) (PBS) and PLA/PBS/functionalized chitosan (FCH) nanobiocomposites with dicumyl peroxide (DCP) and chemical changes thereof at degradation temperatures are evaluated using thermogravimetry (TGA) and thermogravimetry coupled to Fourier transform infrared spectroscopy (TGA-FTIR). A comprehensive kinetic model is employed on above blended samples, including (i) Flynn-Wall-Ozawa, Kissinger, Kissinger-Akahira-Sunose methods to investigate the kinetic and thermodynamic variables, and (ii) Generalized master plots to propose the thermal-induced mechanism. The thermal stability of PLA/PBS reduced with increasing FCH loading up to 3 wt%, and improved for DCP treated PLA/PBS/1FCH at maximum degradation temperature (Tmax) is noticed. The activation energy estimated from Flynn-Wall-Ozawa method are (129-139 kJmol-1), (116-152 kJmol-1), (109-146 kJmol-1), (132-169 kJmol-1) and (120-166 kJmol-1) for PLA/PBS, PLA/PBS/1FCH, PLA/PBS/3FCH, PLA/PBS/1DFCH and PLA/PBS/3DFCH respectively. The generalized master plots depicts that the PLA/PBS blend exhibited L2-F1 mechanism whereas their nanobiocomposite with or without DCP followed L2-Dn and A2-L2-Dn mechanism respectively. Coupled TGA-FTIR highlights the similar kinds of products such as lactide, acetaldehyde, esters, CO2 and CO liberated during the thermal degradation of PLA/PBS blend and their nanobiocomposites. These crosslinked/branched structures are postulated by the rheological behavior which confirmed increase in the complex viscosity (η*) and storage modulus (G') of PLA/PBS/D/1FCH.

Asunto(s)

RESUMEN

In this study, the effect of various supports on activation of peroxymonosulfate and consequent degradation of Acid Orange 7 (AO7) in aqueous solutions was examined at the presence of LaFeO3 perovskite as catalyst. Results showed that the AO7 degradation efficiency by LaFeO3 supported on different supports was in an order of LaFeO3/Al2O3 (86.2%) > LaFeO3 (70.8%) > LaFeO3/CeO2 (59.0%) > LaFeO3/SiO2 (52.3%) > LaFeO3/TiO2 (32.2%). Moreover, the pseudo first-order rate constant for AO7 degradation by LaFeO3/Al2O3 was 3.2 times than that by LaFeO3. The enhancement was attributed to its large surface area, abundant chemisorbed surface-active oxygen, redox property and faster electron transfer. AO7 degradation and the leaching of iron ions decreased with the increase of pH. Data of electron spin resonance spectroscopy and quenching experiments revealed that sulfate and hydroxyl radicals were generated on LaFeO3/Al2O3 surface, while sulfate radicals were identified to be the main reactive species responsible for AO7 degradation. Mechanisms for peroxymonosulfate activation were consequently proposed. Furthermore, LaFeO3/Al2O3 catalyst exhibited a superior stability after five cycles. This work provides a new approach for design of iron-based perovskite catalysts with high and stable catalytic activity for removal of organic pollutants from aqueous solutions.

Asunto(s)

RESUMEN

Diclofenac (DCF), as an emerging contaminant in aquatic environments, has sparked increasing concerns about its impact on the environment. Nitrification in wastewater treatment processing has removed DCF to a large extent. However, the removal characteristics and mechanisms of DCF in the nitrification process are still poorly understood. In this study, enriched nitrifying sludge was used to investigate the transformation of DCF during the nitrification process. Elimination of DCF caused by volatilization, hydrolyzation and adsorption was limited. Abiotic nitration removal was confirmed as significant in enriched nitrifying sludge at a low pH and high nitrite concentration. Free nitrite acid was proposed as the reaction species participating in the DCF transformation process, and a regression equation was developed to predict the contribution of abiotic nitration on DCF removal in enriched nitrifying sludge. By slowly and continuously adding an ammonia stock solution and controlling the pH, we avoided the effect of abiotic nitration removal, and DCF biodegradation was positively correlated to specific ammonium oxidation rates (SAORs). The removal of DCF fit the first order kinetic model (R2 = 0.8285, p < 0.05) with an SAOR of 0.25 mg NH4+-N/(gMLSS·min). The high removal rate constant of k (0.1286 L/(gMLSS·h)) and short half-life (2.48 h) revealed the strong capability of nitrifying bacteria to transform DCF. Nine DCF transformation products were identified and three of them were quantified in the transformation process. The formation of kinetic profile 4-OH-DCF, 5-OH-DCF and DCF-Benzoic acid (DCF-BA) implied that hydroxylation may be the first reaction of DCF and DCF-BA may be a terminal product that resists further degradation. The postulated reactions concerning the transformation of DCF were hydroxylation, lactam formation and oxidation. Accordingly, a detailed degradation pathway was presented.

Asunto(s)

RESUMEN

The antibiotic tiamulin (TIA) is common and widely used medication for dysentery eradication in swine productions. Tiamulin persists in livestock manure, and its residues have been found in various environment. This work obtained four tiamulin-degrading enriched bacterial consortia from a covered anaerobic lagoon system and a stabilized pond system of swine farms. Tiamulin was efficiently removed by the enriched cultures at the concentrations between 2.5 and 200 mg/L, with a removal of 60.1-99.9% during 16 h and a degradation half-life of 4.5-15.7 h. The stabilized pond system cultured with taimulin solely could eliminate tiamulin at the highest rates. The logistic substrate degradation model fit most of the experimental data. Next-generation amplicon sequencing was conducted, and it was found that the bacterial community was significantly impacted by the inoculum source, nutrient addition, and high tiamulin concentrations. Principal coordinate analysis (PCoA) indicated the similarity of bacterial communities in the original enriched samples and the 2.5 mg/L tiamulin-removed cultures. The 200 mg/L consortia were rather different and became similar to the other 200 mg/L consortia from different sources and cultures without nutrient supplementation. Shannon and Simpson indices suggested a reduction in bacterial diversity at high concentrations. The microbes that had high growth in the most efficient enriched culture, or which were abundant in all samples, or which increased with higher tiamulin concentrations were likely to be the major tiamulin-degrading bacteria. This is the first report suggested the possible roles of Achromobacter, Delftia, Flavobacterium, Pseudomonas, and Stenotrophomonas in tiamulin degradation.

RESUMEN

Diclofenac was frequently found in various waters, indicating conventional wastewater treatment methods ineffective in its removal. In this study, LaFeO3 (LFO) was synthesized and its catalytic activity of LFO as the activator of different oxidants such as persulfate (PS), hydrogen peroxide and peroxylmonosulfate (PMS) was evaluated in terms of DCF degradation. The influence of calcination temperature was examined on the catalytic activity of LFO. The effects of various parameters including pH levels, PMS concentration, LFO dose and initial DCF concentration were investigated on DCF degradation rate. The marginal effects of PMS concentration and LFO dose were compared. Langmuir-Hinshelwood (LH) model was used to quantitatively describe DCF degradation reaction in LFO/PMS system. The two constants, k (Limiting reaction rate at maximum coverage) and K (Equilibrium adsorption constant), were determined on the basis of LH model. The performance of LFO/PMS process was also estimated in the presence of various inorganic anions. The potential toxicity of LFO and PMS were evaluated using phytoplankton and the toxicity evolution during DCF degradation was also investigated using luminescent bacteria. This contribution provides a basic study regarding the potential application of heterogeneous PMS activation by perovskite LFO for both DCF removal and toxicity elimination.

Asunto(s)

RESUMEN

A modified shrinking core model (MSCM) has been used to describe the mechanism for the degradation of Protein A resin particles taking place under continuous chromatographic operation. The model is based on the hypothetical shrinkage of the boundary layer of the resin particles, which house the active Protein A ligands within their pores. The caustic during the sanitization phase of chromatography has been determined to cause the Protein A ligand degradation. Protein A resins provided by manufacturers possess unique caustic stability, which has been used in MSCM to appraise the ligand degradation. The kinetic model utilized semiempirical parameters including diffusion constant, rate constant, stoichiometric factor, and reaction order. The parameters were estimated from column breakthrough experiments to simulate continuous Protein A chromatography for three distinct resins. The reaction order has been identified as the key parameter for predicting the degradation kinetics. The recorded reaction orders vary for three different resins with the resin B showing the highest reaction order of 4 and lowest being 1.65 for the resin C. The model can predict the effects of caustic on resin performance and displayed that minimal degradation of the resins A and B occurred, when exposed to 0.1 N and 0.2N NaOH, retaining up to 96% binding capacity after 240 cycles. The adsorption study conducted for the resin B demonstrated the dynamic physical and chemical changes transpiring through the life cycle of the resin, further supported the degradation model. The performance data demonstrate that the resin B exhibits the desirable performance, with higher reaction order indicating slower resin degradation, higher binding capacities, and increased sustenance of this binding capacity for extended duration. The degradation model can be extended to build effective cleaning strategies for continuous downstream processing.

Asunto(s)

RESUMEN

Over the past decade, the environment has been polluted by a wide spectrum of exogenous chemicals and environmental analysis has become one of the most progressive parts of analytical research. The aim of this work was to determine the kinetics of natural degradation, and to identify the degradation products of the massively used estrogenic drug, 17-α-ethinylestradiol. The photodegradation, oxidation and thermostability conditions were selected according to ICH requirements for pharmaceutical stability testing. A simple 72-h photodegradation study in purified water exhibited significant first-order kinetics with the kinetic constant k = 0.0303 h-1, and degradation halftime 22.8 h. The basic halftime could be reduced to 17.1 h by the addition of sea salt, and increase in temperature. Monohydroxy, dihydroxy and dehydrogenated derivatives of ethinylestradiol with intact steroidal structure were identified as major degradation products resulting from simple photodegradation. The addition of an oxidative agent significantly accelerated the degradation rate; combined with higher temperature, the degradation halftime was reduced to 1.1 h with the first-order kinetic constant k = 0.632 h-1. TOC analysis showed a notable decrease of organic mass (18% in 3 days) during oxidation experiments, and confirmed the degradation of steroidal structure.

Asunto(s)

RESUMEN

The aim of this study is to ascertain the degradation kinetic of anthocyanin in dehydration process of solid food system. Mulberry fruit was treated by hot air and vacuum drying at 60 and 75°C. The contents of cyanidin 3-O-glucoside and cyanidin 3-O-rutinoside were determined by using high performance liquid chromatography. Kinetic and thermodynamic parameters were calculated for analysing the degradation characteristics. Model fitting results showed monomeric anthocyanin degradations were followed the second-order kinetic. Vacuum drying presented high kinetic rate constants and low t1/2 values. Thermodynamic parameters including the activation energy, enthalpy change and entropy change appeared significant differences between hot air and vacuum drying. Both heating techniques showed similar effects on polyphenol oxidase activities. These results indicate the anthocyanin degradation kinetic in solid food system is different from that in liquid and the oxygen can be regarded as a catalyst to accelerate the degradation.

Asunto(s)