ChlorTox scale assessment, greenness, and whiteness evaluation of selective spectrophotometric analysis of dimenhydrinate and cinnarizine.

Nausea and vomiting are considered common series side effects induced by chemotherapy treatment in cancer patients. This annoying side effect can impair the patient's compliance to cancer treatment and affect their quality of life. Dimenhydrinate and cinnarizine in combined pharmaceutical dosage form is used to control chemotherapy induced nausea and vomiting in cancer patients. For safety, selective spectrophotometric methods based on novel dual resolution strategies were introduced to estimate dimenhydrinate and cinnarizine in presence of their harmful impurities namely benzophenone and 1- (diphenylmethyl)piperazine, respectively. These methods namely, dual ratio difference (DRD), dual ratio extraction (DRE) and dual absorbance extraction coupled with dual ratio extraction (DAE-DRE) were successfully performed to simultaneously analyze the drug of interests dimenhydrinate and cinnarizine in their pure form, synthetic mixtures and in market dosage form. Linearity ranges were 6.0-60.0 µg/mL and 3.0-30.0 µg/mL for dimenhydrinate and cinnarizine, respectively with good recovery% of Mean ± SD for all the proposed methods 99.82 ± 0.48, 99.79 ± 0.40, 100.14 ± 0.82, 100.03 ± 0.69, respectively. ICH guidelines were adhered in accordance with confirming validation of the proposed methods where fulfilling results were accomplished. Various unified greenness and whiteness assessment tools, such as the chlorTox scale, greenness index via spider chart, AGREE (The Analytical Greenness Metric), green certificate, and the RGB12 algorithm were employed in this research to assess the greenness and sustainability of the introduced UV-spectrophotometric methods in comparison to the reported HPLC method. As a result, these methods hold significant potential for utilization in the quality control department of pharmaceutical companies, contributing to enhanced pharmaceutical product analysis and overall sustainability practices.

Synthesis and characterization of a novel ionic liquid for preconcentration of Brilliant Blue FCF (E 133) from some foods by ultrasound assisted temperature controlled ionic liquid dispersive liquid liquid microextraction method prior to spectrophotometric analysis; A comparative study.

In this study, a novel ionic liquid (3-(3-chloro-2-hydroxypropyl)-1-butyl-1H-imidazol-3-ium hexafluorophosphate, (IL-2) was synthesized and characterized by FT-IR, NMR (1H,13C,31P) spectroscopy, and TGA. Two microextraction methods, ultrasonic assisted ionic liquid dispersive liquid liquid microextraction (USA-IL-DLLME) and ultrasonic assisted-temperature controlled ionic liquid DLLME, have been developed for preconcentration of Brilliant Blue FCF (E133) from some food products by the sythesized IL-2. For optimization of the both methods, several parameters such as volume of IL-2, pH, temperature, ultrasonication time, extraction time, centrifugation time, and salt effect were investigated. The obtained results for both methods under optimum conditions were compared. According to these results, the best limit of detection (4.55 µg L -1), enrichment factor (58), preconcentration factor (50), linear range (15-80 µg L -1), relative standard deviation % (1.15 %) were obtained by use of USA-TC-IL-DLLME method. Furthermore, the developed USA-TC-IL-DLLME method was succesfully applied to real samples for the preconcentration of Brilliant Blue FCF.

Novel reusable and switchable deep eutectic solvent for extraction and determination of curcumin in water and food samples.

For the first time, a fast and easy extraction method based on a unique reusable and switchable deep eutectic solvent (made of octylamine, succinic acid, and water as precursors) was presented and utilized for the microextraction and determination of curcumin as a model analyte. The main factors used to induce a phase transition in the as-prepared deep eutectic solvent were solutions of NaOH and HCl. Among the standout characteristics of the suggested deep eutectic solvent are the removal of toxic organic solvents like THF, the lack of a need for centrifugation, and the ability to be reused in subsequent extractions. The influence of effective parameters (i.e., proportions of deep eutectic solvent structure components, volume of prepared deep eutectic solvent, volume and concertation of NaOH, volume of HCl, and salt effect) on the extraction procedure were investigated. The calibration curve also was linear in the range of 35-500 µg L-1 with coefficients of determination (R2) of 0.9976. Limit of detection (S/N = 3) 10.0 µg L-1, the limit of quantification (LOQ) of 35.0 µg L-1, the relative standard deviations (RSDs %) composed of intra-day RSD (4.7) and inter-day RSD (6.4), preconcentration factor of 40.0, enrichment factor of 38.68, and relative recovery of 92.6%-100.3 % were achieved. The reusable and switchable deep eutectic solvent based-dispersive liquid-liquid microextraction technique was proficiently employed to expedite easy and fast extraction of curcumin from water and food samples.

Spectrophotometric Analysis of Color Stability Induced by Various Calcium Silicate Cements in Full Pulpotomy of Permanent Molars: Theracal PT, Biodentine, and ProRoot MTA.

AIM: The objective of this study was to assess the color stability induced by Theracal PT, Biodentine, and ProRoot MTA in teeth subjected to full pulpotomy, over a span of 6 months. MATERIALS AND METHODS: The study employed a total of 48 freshly extracted intact human third molar teeth. Samples were randomly assigned into four groups (n = 12). All teeth, with the exception of the control group, underwent endodontic access. All materials were mixed in accordance with the manufacturer's guidelines and applied at a thickness of 3 mm at the orifice level before they set. The study groups were negative control (was not prepared), positive control (ProRootMTA), Biodentine, and Theracal PT. Glass ionomer and composite resin material was applied to the cavities. The color measurements were performed using the VITA Easy Shade spectrophotometer. All measurements were repeated 3 times in the determined area on the middle buccal surface of the tooth at baseline that (T0); after access preparation and material placement and setting) and then subsequently at 7 (T1), 30 (T2), 90 (T3), and T4 (180) days later. Data were statistically analyzed by using Kruskal-Wallis H at a confidence level of 95% (P < .05). RESULTS: Compared with the negative control group, Biodentine and Theracal PT showed color stability (ΔE ≤ 3.7). The teeth treated with MTA showed clinically observable discoloration (ΔE ≥ 3.7) at T0, T1, T2, T3, and T4 intervals. At all-time intervals, the MTA group induced more discoloration than Biodentine and Theracal PT (P < .05). CONCLUSIONS: Theracal PT and Biodentine caused least discoloration compared to PMTA even 6 months after its application in teeth undergoing pulpotomy, thereby offering clinicians a reliable alternative for use in the esthetic zone.

Spectrophotometric Analysis of Coronal Discoloration In Vitro Induced by Bioceramic Cements.

The aim of this study was to evaluate and quantify, in vitro, the extent of coronal discoloration induced by bioceramic materials over time. In total, 44 human monoradicular teeth were divided into four groups (n = 11), according to the applied material: Negative control (NC); White MTA ProRoot® (WMTAP); Biodentine™ (BD); and TotalFill® BC RRM™ Putty (TF). Teeth were immersed in saline solution and incubated at 37 °C; the following periods of time were defined: before incubation: [t0]-without bioceramic material, t1-immediately after the bioceramic material placement; after incubation: t24h-24 h, t7d-7 days, and 30d-30 days. Descriptive and inferential statistical analysis were performed. Cochran's Q test was used to evaluate coronal discoloration across the different groups, while the Kruskal-Wallis test was employed to determine differences in discoloration among the groups at each time interval. Additionally, the Friedman test was applied to analyze the variations in discoloration within each group over time. A significance level of 5% was set. All experimental groups revealed coronal discoloration over time: NC (p = 0.001), WMTAP (p < 0.001), BD (p = 0.001), and TF (p = 0.006). No significant differences were observed between groups for each time interval (p > 0.05). The WMTAP group varied the most considering the intervals [t0-t1] and [t24h-t7d] (p = 0.037) compared to the remaining experimental groups.

Estimation of the Controlled Release of Antioxidants from ß-Cyclodextrin/Chamomile (Matricaria chamomilla L.) or Milk Thistle (Silybum marianum L.), Asteraceae, Hydrophilic Extract Complexes through the Fast and Cheap Spectrophotometric Technique.

This is the first study on the modeling of the controlled release of the estimated antioxidants (flavonoids or flavonolignans) from ß-cyclodextrin (ß-CD)/hydrophilic vegetable extract complexes and the modeling of transdermal pharmaceutical formulations based on these complexes using an overall estimation by the spectrophotometric method. The Korsmeyer-Peppas model was chosen for evaluating the release mechanisms. ß-CD/chamomile (Matricaria chamomilla L., Asteraceae) ethanolic extract and ß-CD/milk thistle (Silybum marianum L., Asteraceae) ethanolic extract complexes were obtained by the co-crystallization method with good recovering yields of 55-76%, slightly lower than for ß-CD/silibinin or silymarin complexes (~87%). According to differential scanning calorimetry (DSC) and Karl Fischer water titration (KFT), the thermal stability of complexes is similar to ß-CD hydrate while the hydration water content is lower, revealing the formation of molecular inclusion complexes. In the Korsmeyer-Peppas model, ß-CD/M. chamomilla flower extract complexes reveal Case II transport mechanisms, while the corresponding complexes with leaf extracts indicate non-Fickian diffusion for the controlled release of antioxidants in ethanol 60 and 96%. The same non-Fickian diffusion was revealed by ß-CD/S. marianum extract and ß-CD/silibinin complexes. On the contrary, almost all model transdermal pharmaceutical formulations based on ß-CD/M. chamomilla extract complexes and all those based on ß-CD/S. marianum extract complexes revealed non-Fickian diffusion for the antioxidant release. These results indicate that H-bonding is mainly involved in the diffusion of antioxidants into a ß-CD based matrix, while the controlled release of antioxidants in model formulations is mainly due to hydrophobic interactions. Results obtained in this study can be further used for studying the particular antioxidants (namely rutin or silibinin, quantified, for example, by liquid chromatographic techniques) for their transdermal transport and biological effects in innovatively designed pharmaceutical formulations that can be obtained using "green" methods and materials.

A simplified methodology for the activation of organic charcoal.

One in three people globally are challenged to live on hazardous, unsanitary water, and this relates to higher risks of death and development of diseases. According to scientific research, activated charcoal can be used to clean water contaminants to help make water safer.•Carbonization: this study demonstrates an inexpensive method of producing activated charcoal that can be performed in any setting using locally available biomass materials.•Activation: thermal air oxidation between moderate temperatures of 450-550 °C. Our data indicate that this technique produces charcoal with an adsorptive capacity near to that of commercial-grade charcoal as demonstrated by spectrophotometric analysis. This simple approach to charcoal activation may benefit rural communities where sources of sanitary water are low or nonexistent.

Tooth discoloration induced by endodontic sealers and cervical limit: 1-year in vitro evaluation

Abstract This laboratory study aimed to evaluate the influence of endodontic sealer and cervical limit of root filling on the discoloration of root canal treated teeth. Bovine incisors were randomly distributed into six experimental groups and control (n=21/group), according to the endodontic sealer used [AH Plus (AP); MTA Fillapex (MF) and Sealer Plus BC (SPB)] and the cervical limit of root filling [dental cervix (DC) or 2 mm in apical direction (2mm-AD)]. Tooth discoloration (ΔE) was evaluated by a digital spectrophotometer using the CIED2000 method. Color assessments were performed immediately before (baseline), 1 week, 1, 3, 6 months, and 1 year after obturation. Data were analyzed by ANOVA and Tukey's post-hoc tests (α=5%). Teeth filled with the three sealers showed perceptible tooth discoloration (ΔE≥2.7) in 1 week, maintaining similar values over time. There was a significant difference between MF and SPB sealers in the 2mm-AD groups. In addition, 2mm-AD groups promoted significantly lower discoloration than DC groups for AH (3 months) and SPB (1 and 3 months) sealer,s. Teeth filled with AP, MF, and SPB sealers displayed discoloration from 1 week to one year, with differences between MF and SPB sealers. A cervical limit of filling material at 2 mm from the dental cervix seems more advisable, promoting lower crown discoloration.

Resumo O presente estudo laboratorial teve como objetivo avaliar a influência do cimento endodôntico e do limite cervical da obturação radicular na alteração de cor de dentes tratados endodonticamente. Incisivos bovinos foram distribuídos aleatoriamente em seis grupos experimentais e um controle (n=21/grupo), de acordo com o cimento endodôntico utilizado [AH Plus (AP); MTA Fillapex (MF) e Sealer Plus BC (SPB)] e o limite cervical da obturação [Colo dentário (CD) ou 2mm na direção apical (2mm-DA)]. A alteração de cor (ΔE) foi avaliada por um espectofotômetro digital usando o método CIED2000. As avaliações de cor foram realizadas imediatamente antes (baseline), 1 semana, 1, 3, 6 meses e 1 ano após a obturação. Os dados foram analisados pelos testes ANOVA e post-hoc de Tuckey (α=5%). Dentes obturados com os três cimentos apresentaram alteração de cor perceptível (ΔE≥2.7) em 1 semana, mantendo valores semelhantes ao longo do tempo. Houve uma diferença significativa entre os cimentos MF e SPB nos grupos 2mm-DA. Além disso, os grupos 2mm-DA promoveram uma alteração de cor significativamente menor do que o grupos CD para os cimentos AH (3 meses) e SPB (1 e 3 meses). Os dentes obturados com os cimentos AH, MF e SPB apresentaram alteração de cor entre 1 semana a um ano, com diferenças entre os cimentos MF e SPB. O limite cervical do material obturador a 2mm do colo dentário parece mais aconselhável, promovendo menor alteração de cor da coroa dentária.

Ultrasound-Assisted Dispersive Liquid-Liquid Microextraction Using Deep Eutectic Solvents (DESs) for Neutral Red Dye Spectrophotometric Determination.

Deep eutectic solvents (DES), which have low toxicity and are low cost, biodegradable, and easily synthesized, were used for the extraction of neutral red (NR) dye before its spectrophotometric analysis. DES, containing choline chloride as a hydrogen bond acceptor and phenol as a hydrogen bond donor with a molar ratio of 1:2, was used for the extraction of NR dye from aqueous media. The possible interaction of different DESs with NR was studied using density functional theory (DFT) calculations. Experimentally, a UV-visible spectrophotometer was used for the quantitative analysis. The most important parameters affecting method performance, such as pH, extraction temperature, DES type, its volume, THF volume, sonication time, and centrifugation time, were optimized. The developed method provides exceptional sensitivity in terms of LOD and LOQ, which were 2.2 and 7.3 µg/L respectively. The relative standard deviation was 1.35−1.5% (n = 10), and the pre-concentration factor was 40. The method was found to be linear in the range of 2−300 µg/L (R2 = 0.9967). The method was successfully used for the determination of NR in wastewater samples. Finally, the DES-based method presents operational simplicity, high sensitivity, and rapid determination (<5 min) compared with other analytical procedures.

Carotenoids from Haloarchaea: Extraction, Fractionation, and Characterization.

Carotenoids are bioactive molecules known to promote human health. Many extreme halophilic archaea synthesize carotenoids, mainly represented by C50 bacterioruberin (BR) and its derivatives. BR has a potent antioxidant capacity, even higher than that of ß-carotene, thus, there is an increasing interest to advance the study of its biological properties as well as to extend its current applications. Here, we describe a procedure to extract and characterize carotenoids (enriched in BR) from haloarchaea using a "hyperpigmented" genetically modified strain of Haloferax volcanii.

Spectrophotometric analysis of post-mortem lividity: A new objective measure to define time of death.

The correct definition of time of death often represents a key to solving judicial cases. One of the methods for determination of the time interval since death is at present the quantitative and qualitative characteristics of hypostases. However, the simple observation of the degree and fixation of hypostases is based on nonobjective parameters, and is therefore characterized by an intrinsic variability that can compromise their reliability. The purpose of the present study was to define an objective and standardizable method that allows estimation of time since death with good approximation. To achieve this, the instrument used was based on spectrophotometry, to analyze only the hemoglobin contribution to skin color, while excluding the role of melanin. This made it possible to analyze a hypostatic area, with a numerical value defined as a measure of the hemoglobin content before and after application of standardized pressure for a defined time interval. The study was conducted on 100 cadavers in various wards. The variables considered in the study were: Hb-pre (mean hemoglobin measure before weight force application); Hb-post (mean hemoglobin measure after weight force application), ΔHb (change in mean hemoglobin measures from before to after weight force application); and red% Hb (percentage reduction in hemoglobin after weight force application, compared to the mean measure of hemoglobin before weight force application). The analysis showed statistically significant correlations between red% Hb in the skin area analyzed and time from death to examination. This provided a mathematical formula to estimate time since death with good reliability ( ± 4 h, 50 min).

Non-destructive, spectrophotometric analysis of the thickness of the cell-multilayered periosteal sheet.

BACKGROUND: Autologous tissue-engineered periosteal sheets, which have been clinically applied for periodontal regeneration, sinus lift, and alveolar ridge augmentation, are enriched with osteoblast precursor cells and the abundant deposition of collagen type I in the extracellular spaces. Their quality is inspected prior to clinical use; however, most criteria cannot be evaluated without sacrificing samples. To reduce such losses, we developed a non-destructive optical method that can quantitatively evaluate the thickness of the periosteal sheet. METHODS: Dispersed periosteal cells were inoculated into small pieces of collagen sponge (Terudermis®) and plated into 60-mm dishes for further explant culture using a conventional medium and a stem-cell culture medium. The thickness of periosteal sheets was evaluated using inverted microscopic, histological, labeling (CellVue®)-based imaging and spectrophotometric (Spectro-1®) methods. RESULTS: The three-dimensional growth of periosteal sheets did not necessarily correlate with two-dimensional growth. The periosteal sheet prepared with the stem-cell medium formed cell multilayers, a phenomenon that could be observed qualitatively by inverted microscopy. The spectrophotometric analysis enabled the quantitative evaluation of the thickness of the cell multilayer without sacrificing the samples processed for scheduled cell therapy. CONCLUSIONS: The growth of periosteal sheets is influenced by several major factors, including the basic quality of the individual original periosteal tissue segments, the technical expertise of doctors and operators involved in tissue harvesting and processing, and culture conditions. This newly developed spectrophotometric analysis can quantify the thickness of cell-multilayered periosteal sheets for quality assurance in a non-destructive manner, thereby contributing to better bone augmentation prior to implant therapy.

Indirect spectrophotometric determination of aqueous ferrate(VI) based on its reaction with iodide in acidic media.

Ferrate(VI) (Fe(VI)) is utilized as an efficient and environmentally friendly water treatment agent that can be widely used for degradation of (in)organic pollutants in practical applications. However, only a few spectrophotometric methods for Fe(VI) determination were reported. In this study, a novel method for determining trace levels of aqueous Fe(VI) was developed based on the fact that Fe(VI) reacts with iodide at acidic pH to form iodine, which subsequently is treated with starch to yield the blue starch-iodine complex measured spectrophotometrically at 590 nm. The key measurement parameters, including acidic medium, starch dosages, temperature, time, and addition order were optimized to improve the sensitivity of detection. The increase in absorbance at 590 nm was linear with respect to Fe(VI) added (0.022-50 µM). Its sensitivity was determined as (4.61 ± 0.05) × 104 M-1 cm-1, which was higher than that of existing spectrophotometric methods. The principle for Fe(VI) determination was studied by investigating stoichiometry, kinetics, and mechanism of Fe(VI) reaction with iodide. The molar stoichiometry of Fe(VI) with I3- species was determined to be 1:2. The reaction of Fe(VI) with iodide followed a second-order rate law with first order in each reactant and displayed apparent anti-Arrhenius kinetics, then its reaction pathway was proposed as well. Furthermore, the established method was successfully applied to measure Fe(VI) in various environmental water samples. The results show that the proposed approach is simple, convenient, highly reproducible and extremely sensitive, and is also expected to be of use for kinetic studies of Fe(VI) reaction with (in)organic compounds under acidic conditions.

Development of an Optical Method to Monitor Nitrification in Drinking Water.

Nitrification is a common issue observed in chloraminated drinking water distribution systems, resulting in the undesirable loss of monochloramine (NH2Cl) residual. The decay of monochloramine releases ammonia (NH3), which is converted to nitrite (NO2-) and nitrate (NO3-) through a biological oxidation process. During the course of monochloramine decay and the production of nitrite and nitrate, the spectral fingerprint is observed to change within the wavelength region sensitive to these species. In addition, chloraminated drinking water will contain natural organic matter (NOM), which also has a spectral fingerprint. To assess the nitrification status, the combined nitrate and nitrite absorbance fingerprint was isolated from the total spectra. A novel method is proposed here to isolate their spectra and estimate their combined concentration. The spectral fingerprint of pure monochloramine solution at different concentrations indicated that the absorbance difference between two concentrations at a specific wavelength can be related to other wavelengths by a linear function. It is assumed that the absorbance reduction in drinking water spectra due to monochloramine decay will follow a similar pattern as in ultrapure water. Based on this criteria, combined nitrate and nitrite spectra were isolated from the total spectrum. A machine learning model was developed using the support vector regression (SVR) algorithm to relate the spectral features of pure nitrate and nitrite with their concentrations. The model was used to predict the combined nitrate and nitrite concentration for a number of test samples. Out of these samples, the nitrified sample showed an increasing trend of combined nitrate and nitrite productions. The predicted values were matched with the observed concentrations, and the level of precision by the method was ± 0.01 mg-N L-1. This method can be implemented in chloraminated distribution systems to monitor and manage nitrification.

Trichromatic Vat Dyeing of Cationized Cotton.

This article deals with cationization of cotton during mercerization and its effects on trichromatic vat dyeing. If cationization is carried out during the after-treatment, regardless of cotton pretreatment, the reaction takes place on the surface and blocks cellulose groups, subsequently resulting in uneven coloration. However, when cationization is carried out with an epihalohydrin during the mercerization process, new cellulose is formed in which the cationic compound is uniformly distributed and trapped between cellulose chains, resulting in uniform coloration after the dyeing process. The reaction time for the process during mercerization is 24 h, thus a more favorable process was researched. Based on electrokinetic analysis, it was found that 5 h was sufficient for the reaction with 3-chloro-2-hydroxypropyltrimethyl ammonium chloride (CHPTAC). The cationization of cotton contributed to the processes of vat dyeing. The change in charge upon cationization resulted in very high adsorption of vat-dye anions, indicating that ionic bonding occurred in addition to van der Waals forces. The color depth improved by more than 10 times. It should be emphasized that the colors with higher chroma and targeted color hue, especially in trichromatic dyeing, were obtained on cationized cotton, in contrast to standard cotton fabrics. The color differences obtained under the different light sources indicate the occurrence of metamerism. Considering the color fastness to laundering, vat-dyed cationized fabrics of all colors may be used in hospitals or other environments where high hygiene and oxidative bleaching are required.

Study on Extra Virgin Olive Oil: Quality Evaluation by Anti-Radical Activity, Color Analysis, and Polyphenolic HPLC-DAD Analysis.

This study aimed to evaluate the quality of oils available on the Italian market and purchased directly from the mill or in the supermarket and labelled as extra virgin olive oils (EVOOs). As one of the most relevant foods of the Mediterranean diet and recognized as a functional food if regularly consumed, the quality of EVOO needs to be continuously monitored. Different analytical protocols were applied. The spectrophotometric parameters used to classify the extra virgin olive oils-a CIEL*a*b*color analysis and the quali-quantitative analysis of bioactive molecules by HPLC-DAD detection and the anti-radical activity, by the DPPH method, were evaluated and compared among the samples. This study confirmed a very high variation in terms of quality, both in oils purchased directly from mills throughout Italy, but also in oils labeled as "100% of Italian origin". Due to the high variability reconfirmed in the monitored samples, it is necessary to carry out a capillary control, not limited only to the parameters indexed by law. A useful complementary method could be represented by reflectance colorimetric analysis.

Carmines (E120) in coloured yoghurts: a case-study contribution for human risk assessment.

Carmines (E120) are used worldwide as natural food colouring agents of animal origin, with a widespread application, including yoghurts. Despite being considered safe for human health, carmines are known to cause allergic reactions. Our goal was to evaluate the presence of carmines in different yoghurts with a label declaration of E120, purchased in Portugal, and, for the first time, to assess the human risk. The analytical methodology, recommended by JECFA, was based on acid hydrolysis of the samples followed by spectrophotometric UV-Vis analysis at 494 nm. This methodology allowed for a limit of quantification (LOQ) of 39.0 mg/kg and recovery rates higher than 97.7%. All the samples had carmines at levels above the LOQ, ranging between 43.8 and 193.8 mg/kg, with an average of 125.2 ± 34.5 mg/kg. In total, 8 (26.7%) samples exceeded the European Union (EU) maximum permitted level (MPL) established for carmines in this foodstuff, 150 mg/kg. Solid yoghurts presented higher average levels, 137.2 mg/kg, when compared to liquid samples, 107.2 mg/kg, with a significant statistical difference (p= 0.0236) being observed. No significant statistical difference was observed between white and private labels, whose average levels were very similar, 125.4 vs 125 mg/kg, respectively. Although some samples were above the allowable values, the estimated daily intake (EDI), designed for the different scenarios of different yoghurt types, did not exceed the established ADI, 5 mg/kg bw/day. According to the obtained results, carmine ingestion through the consumption of yoghurt poses low risk to the Portuguese consumers. However, children were the most vulnerable population group with a calculated risk value of up to 10% considering the mean content scenario. These first findings point out the need to reinforce surveillance programmes and monitoring studies, contributing to an increased awareness regarding carmine exposure, however it must be emphasised that yoghurt has evident nutritional benefits depending on a healthful consumer choice.

Simple and efficient spectroscopic-based univariate sequential methods for simultaneous quantitative analysis of vandetanib, dasatinib, and sorafenib in pharmaceutical preparations and biological fluids.

Six sequential spectrophotometric-based univariate methods were developed and validated for the simultaneous estimation of three novel anticancer drugs vandetanib (VAN), dasatinib (DAS), and sorafenib (SOR) in a mixture, without the requirement for separation. These methods are novel, simple, precise, and accurate. Different steps including zero crossing, ratio-based, and/or derivative spectra were utilized to develop these analytical methods, namely, ratio difference spectrophotometric method, constant center method, successive derivative ratio method, isoabsorptive method, mean centering of the ratio spectra method, and derivative ratio spectrum-zero crossing method. The calibration curve linearity was ranged from 2 to 9, 2-9, and 3-9 µgmL-1 for VAN, DAS, and SOR, respectively. These established methods were applied for the quantification of the three selected drugs in different biological fluids (spiked human plasma and urine) and pharmaceutical preparations. The aforementioned methods were established for the concurrent estimation of ternary and binary mixtures to enhance the signal-to-noise ratio. The results did not statistically differ from the other reported methods, indicating no significant difference in accuracy and precision at p = 0.05.

Spectrophotometric determination of Metronidazole antibacterial drug via oxidation with alkaline potassium permanganate.

Highly simple, sensitive and selective method is developed for the spectrophotometric determination of Metronidazole (MDZ) antibacterial drug either in pure form or in pharmaceutical formulations. This method is based on reduction of potassium permanganate by Metronidazole drug in sodium hydroxide solution to give green manganate ion which recorded at 610 nm. The method produced linear responses in the concentration range 4.28 - 59.91 µg mL-1 with limit of detection (LOD) and limit of quantification (LOQ) 0.21 and 0.69 µg mL-1 for Metronidazole drug respectively. The apparent molar absorptivity is 0.865 × 104 L mol-1 cm-1, Sandell sensitivity is 0.019 µg cm-2 and correlation coefficient is 0.951. The method is highly reproducible and has been applied to a wide variety of pharmaceutical formulations and the results compare favourably with those of official methods.

Anthropogenic nitrogen pollution in mangrove ecosystems along Dar es Salaam and Bagamoyo coasts in Tanzania.

Mangroves are among the most productive coastal ecosystems; however, they are prone to anthropogenic pollution due to their land-sea interface position. We used stable nitrogen isotopes and spectrophotometric nitrate analysis to study the anthropogenic pollution in five mangrove ecosystems in Tanzania, including two polluted (Mzinga and Kizinga), one moderate (Kunduchi) and non-polluted (Mbegani and Ras Dege) sites. Also, we tested the suitability of mangrove leaves, roots, sediment, and gastropod as indicators of anthropogenic nitrogen pollution using stable δ15N isotope analysis. Results revealed higher than 10‰ δ15N values in all analysed components and the highest nitrate concentrations of 16.44 mg L-1 in the interstitial waters at the polluted sites, indicating anthropogenic nitrogen inputs. The δ15N enrichment increased in the order: non-polluted < moderate < polluted. The polluted sites are fed by freshwater creeks and probably receive high loads of domestic sewage from the surrounding communities, industries, and agricultural effluents. Therefore, to protect mangrove ecosystems, proper waste and wastewater management upstream are recommended.