High-performance Liquid Chromatography Technique Research Articles

Release Kinetics of Sulfentrazone from Chitosan Clay Sulfentrazone Nanocomposite

Introduction: With a rational objective to reduce groundwater contamination from pesticides and thereby reducing ecotoxicological effect of pesticide, present research programme was carried out. Sulfentrazone is a well-known effective pesticide that is used for soybean crops. But at the same time, sulfentrazone is known for its high leaching potential through soil and could lead to ground water contamination. Methods: So we have synthesized a novel chitosan clay nanocomposites of sulfentrazone at three different concertations of sulfentrazone, 37.64%, 52.44% and 59.85% and its release pattern was studied at three different buffer systems like pH 2, pH 4 and pH 6. Release pattern of Sulfentrazone has been quantified by using High Performance Liquid Chromatography (HPLC) technique. Various mathematical tools have been applied to understand the release kinetics of chitosan clay sulfentrazone nanocomposites. Results: Correlation coefficient (R2) of many models has been plotted and the Huguchi model was found to be the most suitable for these nanocomposites. The salient finding of this study is that the release rates of sulfentrazone at pH 4 is 68.39%, 42.62% and 37.75% after 8 hours at three different loading. This release pattern is higher than the release pattern at pH 6 and pH 2. Conclusion: Based on these release data, it is very clear that chitosan clay sulfentrazone nanocomposite can control the release of sulfentrazone at regular soil pH conditions, which is pH 6.

Assessment of Pesticide Residues in Fruits and Vegetables Grown in Abidjan, Ivory Coast

Introduction: The presence of pesticide residues in primary and derived agricultural products raises serious health problems for consumers. The aim of this study was to assess the level of pesticide residues in commonly consumed vegetables. Methods: Pesticide residues were extracted from market garden products (Solanum lycopersicum, Capsicum sp, Cucumis sativus and Lactuca sativa) by the QuEchERS method and analyzed by high performance liquid chromatography (HPLC-UV) technique. Results: These analyzes made it possible to detect 32 pesticide residues. All market garden products contained pesticide residues, 12.82% of which exceeded the maximum residue limits (MRLs). The pesticide families found were triazines (34.34%), urea derivatives (31.25%), organophosphorus residues (9.37%), organochlorines (9.37%), triazinones (9.37%) and carbamates (6.25%). Among the market garden products, only lettuce was contaminated by residues from all families with concentrations of pesticide residues exceeding their limits of quantification at the level of 5 molecules: Chlorpropham (0.016 mg/kg), Linuron (0.02 mg/kg), Chlorfenvinphos (0.026 mg/kg) Parathion-ethyl (0.014) and Metolachlor (0.013 mg/kg) which is an organochlorine pesticide. Organochlorines are among the prohibited pesticides. Among agrochemicals used, some were not approved. Conclusion: The results indicate the presence of pesticide residues in commonly consumed vegetables and highlight the urgent need to develop comprehensive intervention measures to reduce the potential health risk to consumers. The need for regular monitoring of pesticide residues and raising farmers' awareness of better pesticide safety practices are actions to be taken for the health of consumers.

A REVIEW HPLC AND UV METHODS FOR THE ESTIMATION OF CIDOFOVIR IN PHARMACEUTICAL DOSAGE FORM

Cidofovir is an antiviral agent primarily used in the treatment of cytomegalovirus (CMV) infections, particularly in immunocompromised patients. This review summarizes the analytical methods developed for estimating Cidofovir, an antiviral used in treating cytomegalovirus (CMV) infections. Emphasis is placed on High-Performance Liquid Chromatography (HPLC) and related techniques, discussing method development, validation, and application across various pharmaceutical dosage forms such as tablets and injectables. The review also highlights the role of HPLC in pharmacokinetic studies and explores recent advancements like nanoparticle drug delivery systems to improve Cidofovir bioavailability. Challenges related to Cidofovir stability, solubility, and renal excretion are also discussed.

Phytochemical Analysis, Antioxidant Activity of Wild Medicinal Plants of Himalayan Range

Plants that are indigenous to the Himalayas have been exploited for their therapeutic properties for over 6,500 years. Using their deep knowledge of the local flora and fauna, traditional healers in the region are able to treat a wide variety of maladies with herbal treatments. People who live in rural areas of the Himalayas rely on wild medicinal plants for their health, and we need to do everything in our power to ensure that these plants continue to thrive in the harsh desert climate of the Himalayas. Raw materials that are obtained from wild plants are in high demand all around the world, particularly among pharmaceutical companies, ethnomedics, and practitioners of traditional medicine as well as other medical practitioners. India has been a top exporter of raw herbal medications all over the world. This is mostly due to the number of medicinal plants that can be found in the Himalayas. The aim of this study was to determine the Phytochemical analysis and antioxidant activity of various parts of 20 selected wild medicinal plants, found in the Himalayan regions in India, China, Nepal, Bhutan and Pakistan including Swertia bimaculate, Ficus neriifolia, Rubus treutleri, Periploca calophylla, G. depressa, Buddleja napaulensis, Habenaria edgeworthii, Pyracantha crenulate, Roscoea procera, Allium rubellum, Berberis chitria, Capsella bursa-pastoris, Artemisia maritima, C. glanduliferum, C. distans, Juniperus macropoda, Origanum vulgare, Valeriana jatamansi, Polygonatum verticillatum, Meconopsis aculeate and Fragaria nubicolais. There were several different parts of the species that were examined to determine their total polyphenol, flavonoid, alkaloid, saponin, and tannin concentrations. One fraction of the plant extracts was found to contain a higher quantity of phytochemicals when compared to the other portions. Through the utilisation of the DPPH and FRAP model systems, the antioxidant capacity of a number of different components was assessed. The high-performance liquid chromatography (HPLC) technique can be combined with the DPPH and/or ABTS tests in order to rapidly screen extracts for the presence of active chemicals.

Comparative metabolomics-based screening of fruit extracts of less-known melon (Cucumis melo var. agrestis) accessions collected from dry terrain of North India by using HPLC–DAD

Cucumis melo var. agrestis (Naudin) is an important wild crop that belongs to the family Cucurbitaceae. Fruits possess digestive, stomachic, vermifuge and febrifuge properties and possess analgesic, antioxidant, antibacterial and anti-inflammatory activities. Current research is aimed at screening diverse phytoconstituents present in the fruit extract of wild melon (C. melo var. agrestis) with the technique of high-performance liquid chromatography (HPLC). Our outcomes showed that fruit extract of C. melo var. agrestis has various phytochemicals such as glycosides, alkaloids, phenols, flavonoids, saponins, tannins, proteins, amino acids and carbohydrates. HPLC analysis revealed that naringenin and catechin were reported to have the highest concentrations among the all studied accessions. PCA and HCA multivariant analysis showed that, first two principal components, i.e. PC1 and PC2 contributed to 54.87% of the variation, where maximum loadings were from apigenin, trailed by gallic acid, rutin, and catechol.

Evaluation of thiamine and riboflavin in different varieties of rice grown in Kurigram district, Bangladesh

ContextRice is indeed a staple food in many parts of the world, including Bangladesh. This research aimed to evaluate the two essential vitamin levels in different processed rice sunned, parboiled, cooked sunned, cooked parboiled, and washed cooked rice. ObjectiveThe study focused on analyzing the thiamine (vitamin B1) and riboflavin (vitamin B2) contents in 10 different varieties of paddy samples grown in the Kurigram district of Bangladesh. MethodsA high performance liquid chromatographic (HPLC) technique assembled with fluorescence detector was employed for these analyses. Two calibration curves were generated to analyze vitamin B1 and B2 (for thiamine the regression coefficient, r2 = 0.9992 and riboflavin r2 = 0.9989). The study demonstrated a recovery rate of 96.88 % for vitamin B1 and 104.24 % for vitamin B2. Overall, these findings provide valuable insights into the vitamin B1 and B2 contents across different rice samples. Results and conclusionThe results showed that the parboiled samples had the highest thiamine content, ranging from 342.50 ± 0.3 to 673.0 ± 7.5 μg/100 g, compared to the sunned samples, which had a range of 209.5 ± 0.3 to 337.4 ± 4.3 μg/100 g. Conversely, the sunned samples had the highest riboflavin content, ranging from 26.4 ± 0.2 to 59.6 ± 0.3 μg/100 g, while the parboiled samples had a range of 3.0 ± 0.1 to 26.6 ± 0.01 μg/100 g. Additionally, it was observed that the steaming process increased the thiamine content and reduced the riboflavin content in parboiled rice samples but decreased both the thiamine and riboflavin in sunned rice samples. Another study showed a gradual decrease in the levels of both vitamins B1 and B2 in sunned, cooked sunned and washed cooked sunned rice samples. SignificanceThese findings provide valuable insights into the impact of processing methods, such as parboiling and steaming, on the thiamine and riboflavin contents in rice. The results suggest that parboiled rice may be a preferable choice for individuals seeking higher thiamine content in their diet, while sunned rice may contain higher levels of riboflavin. The results shed light on the nutritional profiles of different rice varieties and highlight the potential impact of processing techniques on the vitamin content of rice.

Assessment of miligram(Mg) content of some notable analgesics used by residents of Maiduguri Metropolis: evidence from high performance liquid chromatographic technique

Diclofenac sodium and paracetamol are Over the counter (OTC) medications used as analgesic and antipyretic agents to relieve pains, fever and headaches. The aim of this work was determine the mg content of paracetamol and diclofenac sodium in selected samples across the Maiduguri metropolis using High Performance liquid chromatography (HPLC) method. For paracetamol samples an intersil ODS-3V column (150 mm × 4.6 mm; 5 μm pore size) was used at the temperature of 35oC the mobile phase was methanol: water (20:80) using isocratic elution at the flow rate of 2 mL/min, injection volume of 10 μL and a diode array detector. For diclofenac sodium samples, the chromatographic conditions were the same except the mobile phase which was methanol: water (63:37), flow rate of 0.8 mL min, injection volume of 20 μL and column temperature was set at 30 oC. A total of 45 samples were analysed; which comprised of paracetamol tablet, paracetamol syrup and diclofenac sodium tablet which were randomly selected from three different sources; hospital pharmacy, community pharmacy and drug patent stores. The percentage mg content for paracetamol tablets ranged from 48 to 83 % while that of the paracetamol syrups ranged from 72 to 120 % and finally diclofenac sodium tablets ranged from 73 to 174 %. Adopting the United State Pharmacopoeia (USP) as reference for assessment tool, it was observed that all the paracetamol tablet samples failed, 4 out of 15 paracetamol syrup samples failed, and 11 out of 15 diclofenac sodium tablet samples failed. There was statistical significance (p< 0.05) between class of drug and percentage mg content but there was no significance (p< 0.05) between source of drug and percentage constituent. HPLC technique was used successfully for quantitative determination of paracetamol and diclofenac sodium dosage forms.

Antibacterial and Antioxidant Activities of Flavonoids, Phenolic and Flavonoid Glycosides from Gouania longispicata Leaves

The leaves of Gouania longispicata Engl. (GLE) have been traditionally used to treat more than forty ailments in Uganda, including stomachache, lung and skin cancers, syphilis, toothache, and allergies. In this study, pure compounds were isolated from the methanolic extract of GLE leaves and their structures elucidated using ultraviolet visible spectroscopy, liquid chromatography–tandem mass spectrometry, high performance liquid chromatography, and 1D and 2D NMR techniques. The antibacterial and antioxidant activities of the compounds were assessed using the broth dilution and DPPH assays, respectively. Two known flavonoid glycosides (kaempferol-3-O-α-rhamnopyranoside and rutin), a phenolic glycoside (4,6-dihydroxy-3-methylacetophenone-2-O-β-D-glucopyranoside), and flavonoids (kaempferol and quercetin) were characterized. This is the first time that the kaempferol derivative, the acetophenone as well as free forms of quercetin, kaempferol, and rutin, are being reported in GLE and the Gouania genus. The compounds exhibited antibacterial activity against Streptococcus pneumoniae and Escherichia coli with minimum inhibitory concentrations between 16 µg/mL and 125 µg/mL. The radical scavenging activities recorded half-minimum inhibitory concentrations (IC50) ranging from 18.6 ± 1.30 µg/mL to 28.1 ± 0.09 µg/mL. The IC50 of kaempferol and quercetin were not significantly different from that of ascorbic acid (p > 0.05), highlighting their potential as natural antioxidant agents. These results lend credence to the use of GLE leaves in herbal treatment of microbial infections and oxidative stress-mediated ailments.

Antidiabetic, antihyperlipidemic effects and quantification of bioactive compounds by HPLC from Crassula ovata leaves extracts on streptozotocin induced diabetic Wistar rats

Background: Crassula ovata have been recommended in ethno medicines for the treatment of diabetes. In this research the scientific claim is studied and validated. Objective: Objective of the current study has been focused to assess the traditional use of Crassula ovata to heal diabetes, hyperlipidemia and to check the presence of constituents responsible for these actions. Methods: The approved plant's ethanol, acetone, and chloroform extracts were prepared by maceration. For in vivo activity, the model of streptozotocin induced diabetes mellitus in rats was chosen, wherein antidiabetic parameters such as body weight, urine volume, blood glucose level, and lipid profile parameters were evaluated. Quantification of bioactive compounds was done by a high-performance liquid chromatographic technique using diode-array detection. Results: The ethanolic extract noticeably depleted increased blood glucose levels and has positive effects on altered lipid profile after administering a dose of 200 mg/kg orally compared with oral hypoglycemic drug metformin. HPLC analysis of ethanolic extract identified several secondary metabolites in Crassula ovata, including Gallic acid, Rutin, Luteolin, Caffeic acid, Catechin, Kaempferol and Quercetin. These compounds have been reported for their potential antidiabetic effects. The analytical data on the chemical composition supported its traditional use in diabetes management. Conclusion: From the results, it can be concluded that, Crassula ovata ethanolic extract can be ideal for the treatment of diabetes and hyperlipidemia. Further studies are required to locate the active pharmaceutical ingredient for the said actions.

HPLC analysis and antibacterial activity of methanolic extract of Centella asiatica (L.) urban

ObjectivesIncreasingly resistant antibiotics and new bacteria have fueled the demand for herbal remedies. Our current study aimed to find out whether the methanolic extract from Centella asiatica aerial parts contained asiatic acid and madecassoside, as well as their antibacterial properties. MethodsA high-performance liquid chromatography (HPLC) technique was used to measure asiatic acid and madecassoside. We assessed the antibacterial activity of both compounds and crude aerial methanolic extract using the agar-well diffusion method. ResultsAs identified through HPLC analysis, madecassoside was found to be 1.89 % and asiatic acid to be 0.35 %. C. asiatica had strong inhibitory activity against E. coli (MIC of 6.25 mg ml-1 and ZOI of 9 mm) and S. aureus (MIC of 3.12 mg ml-1 and ZOI of 8 mm). The ZOI for S. typhimurium, P. vulgaris, and B. subtilis was 7, 6, and 10 mm, respectively, and the MIC was 12.5 mg ml-1. Comparing asiatic acid to madecassoside, it has a potent antibacterial effect. ConclusionsThe methanolic crude extract and measured compounds of C. asiatica exhibit strong antibacterial activity, especially against S. typhimurium and E. coli. The asiatic acid and madecassoside identified by HPLC analysis could potentially be associated with this activity. These compounds exhibit antimicrobial activity can be found and employed as low-resistance, multi-target antibacterial drugs to treat a range of bacterial and fungal infections that have become resistant to existing antibiotics.

Effect of ozone, hydrogen peroxide, and chlorine solution in reduction of chlorpyrifos and cypermethrin residues from cauliflower

The extensive utilization of chlorpyrifos and cypermethrin in agriculture raises concerns regarding the accumulation of pesticide residues in human food, posing a threat to human health. This study aimed to investigate the effect of ozonation on cauliflower to decrease the level of pesticides. Cypermethrin and organophosphate chlorpyrifos were applied to cauliflower at specific doses. High-performance liquid chromatographic techniques were employed to detect pesticide residues in cauliflower. The effects of common oxidizers (hydrogen peroxide, chlorine, and ozone) on the reduction of pesticide residues were investigated. Solutions of hydrogen peroxide (10 and 100 ppm), chlorine (10 and 100 ppm), and ozone (10 and 100 ppm) were prepared, and the cauliflower sample was immersed for 20 min. The immersion in 10 ppm hydrogen peroxide solution reduced chlorpyrifos and cypermethrin by 68 and 65%, respectively. Meanwhile, at 100 ppm hydrogen peroxide solution, the reduction rates of chlorpyrifos and cypermethrin residues were 72 and 75%, respectively. Immersion in ozone solution at 10 ppm concentration reduced chlorpyrifos and cypermethrin by 58 and 57%, respectively. At 100 ppm ozone, chlorpyrifos was reduced up to 64%, and cypermethrin reduction was 74%. Chlorine immersion at 10 ppm reduced chlorpyrifos residues by 68% and cypermethrin residues by 81%, while a 100 ppm chlorine solution reduced chlorpyrifos residues by 100% and cypermethrin residues by 84%. From these results, it was concluded that chlorine was the most effective of all the cleaning solutions to remove pesticides from vegetables.

Clinical Risk Assessment and Comparison of Bias between Laboratory Methods for Estimation of HbA1c for Glycated Hemoglobin in Hyperglycemic Patients.

Hemoglobin A1c (HbA1c), also known as glycated hemoglobin, is a blood test used to evaluate and track a patient's blood sugar levels over the previous 2-3 months. We have compared the analytical performance of the D10 hemoglobin (HPLC) testing system to that of the immunoturbidimetric technique, which is a light-scattering immunoassay. To assess the clinical risk assessment between two methods (Compare the two Immunoturbidometric methods (AU680) vs. HPLC method (D10)) in hyperglycemic patients and assess the acceptability of the respective methods in the Clinical biochemistry laboratory. The charge of the globins in Hb was used as the basis for the HPLC method used to measure HbA1c. HPLC detects and quantifies even the tiniest Hb fractions and the full spectrum of Hb variants. HbA1c was measured using the immunoturbidimetric (AU 680 Beckmann coulter analyzer) and high-performance liquid chromatography (HPLC) techniques. Experiments also made use of immunoturbidimetric techniques (using an AU 680 Beckmann coulter analyzer equipment). There is no statistically significant difference in HbA1c readings between male and female patients, as measured by either the Immunoturbidimetric or HPLC techniques. The immunoturbidimetric and high-performance liquid chromatography techniques for estimating HbA1c yielded identical results. From the results of this study, we may deduce that both techniques are valid for estimating HbA1c. As a result, it may be suggested that both approaches can be used to estimate HbA1c in diabetic individuals.

HPLC analysis of costunolide from Costus speciosus (Koen ex. Retz.) Sm. plants of Chhattisgarh region

Costus speciosus (Koen ex. Retz.) Sm. is a medicinal plant known for its therapeutic properties, prominently attributed to its bioactive constituents like costunolide, diosgenin, eremanthin etc. This study presents a detailed investigation on the quantitative analysis of costunolide in Costus speciosus plants collected from different geographical regions of Chhattisgarh, employing High-Performance Liquid Chromatography (HPLC) technique. The research methodology involved the crude extraction of metabolites from the rhizome using methanol as solvent followed by HPLC analysis. The results revealed significant variations in the content of costunolide among the collected samples, possibly influenced by environmental factors and genetic variability. Moreover, phytochemical characterization of Costus speciosus extracts was conducted to complement the quantitative analysis. This study contributes to the understanding of the phytochemical profile of Costus speciosus plants in the Chhattisgarh region. The findings help to get the elite plant with significant concentration and hold implications for the standardization and quality control of herbal medicines derived from Costus speciosus, facilitating their utilization in pharmaceutical and therapeutic applications.

Quality by Design Approach for the Development and Validation of a Robust RP-HPLC Method for the Estimation of Aloe-Emodin

Introduction/Objective: The current study examines the methodical Quality by Design (QbD) that facilitated the creation of an easy-to-use, quick, affordable, and stability-indicating reversed- phase high-performance liquid chromatography (RP-HPLC) technique for the efficient analysis of aloe-emodin. Methods: The chromatographic conditions were optimized with the Design Expert software 11.0 version, i.e., flow rate, buffer concentration, and column temperature. Results: The results of the linearity graph show R2 = 0.9988. The LOQ was 0.07949 μg/mL and the LOD was 0.02623 μg/mL. According to ICH rules, the technique validation parameters were within the allowed range. Utilizing the Design Expert 11.0 version, the Box–Behnken design experimental design explains the relationships between flow rate, buffer concentration, and column temperature at three distinct levels. The responses were monitored: the retention time (Rt), tailing factor (Tf), and number of theoretical plates (NTPs). Conclusion: The suggested approach was appropriate for quantitative determination and may be used in clinical pharmacokinetic investigations, biopharmaceutics, accredited testing laboratories, and quality control departments in enterprises.

Evaluating larvicidal, ovicidal and growth inhibiting activity of five medicinal plant extracts on Culex pipiens (Diptera: Culicidae), the West Nile virus vector

Mosquitoes, one of the deadliest animals on the planet, cause millions of fatalities each year by transmitting several human illnesses. Synthetic pesticides were previously used to prevent the spread of diseases by mosquitoes, which was effective in protecting humans but caused serious human health problems, environmental damage, and developed mosquito pesticide resistance. This research focuses on exploring new, more effective, safer, and environmentally friendly compounds to improve mosquito vector management. Phytochemicals are possible biological agents for controlling pests and many are target-specific, rapidly biodegradable, and eco-friendly. The potential of extracts of Lantana camara, Melia azedarach, Nerium oleander, Ricinus communis, and Withania somnifera against 3rd instar Culex pipiens (Common house mosquito) larvae was evaluated. Methanol extracts had more toxic effects against Cx. pipiens larvae (95–100%, 24 h post-treatment) than aqueous extracts (63–91%, 24 h post-treatment). The methanol extracts of Nerium oleander (LC50 = 158.92 ppm) and Ricinus communis (LC50 = 175.04 ppm) were very effective at killing mosquito larvae, 24 h after treatment. N. oleander (LC50 = 373.29 ppm) showed high efficacy in aqueous plant extracts. Among the different extracts of the five plants screened, the methanol extract of R. communis recorded the highest ovicidal activity of 5% at 800 ppm concentration. Total developmental duration and growth index were highly affected by R. communis and M. azedarach methanol extracts. In field tests it was clear that plant extracts decreased mosquito larval density, especially when mixed with mosquito Bti briquette, with stability up to seven days for N. oleander. GC–MS results showed that the methanol extract had a higher number of chemical compounds, particularly with more terpene compounds. A high-performance liquid chromatography (HPLC) technique was used to detect the existence of non-volatile polyphenols and flavonoids. All five methanol extracts showed high concentrations of active ingredients such as gallic acid, chlorogenic acid (more than 100 μg/ml) and the rosmarinic acid was also found in all the five extracts in addition to 17 active polyphenols and flavonoids presented at moderate to low concentrations. Molecular modeling of 18 active ingredients detected by the HPLC were performed to the vicinity of one of the fatty acid binding proteins of lm-FABP (PDB code: 2FLJ). Rutin, Caffeic acid, coumaric acid and rosmarinic acid which presented densely in R. communis and N. oleander showed multiple and stable intermolecular hydrogen bonding and π–π stacking interactions. The inhibition ability of the fatty acid binding protein, FABP4, was evaluated with remarkable receptor inhibition evident, especially with R. communis and N. oleander having inhibitory concentrations of IC50 = 0.425 and 0.599 µg/mL, respectively. The active phytochemical compounds in the plants suggest promising larvicidal and ovicidal activity, and have potential as a safe and effective alternative to synthetic insecticides.

Climatic effects on aflatoxin contamination of maize

Aflatoxins are frequent contaminants of maize especially in the face of climate change with deleterious health and socio-economic impacts. South Africa is ranked 9th maize exporter globally; hence, insights need to be gained in terms of the maize value chain in South Africa with respect to aflatoxin contamination to evaluate consumers’ exposure. High-performance liquid chromatography (HPLC) technique was used in this study to quantify aflatoxins in South African commercial maize. One thousand and twenty-eight (1028) maize samples were collected across six distinct agro-climatic regions over five harvest seasons (2017 – 2021). A total of 205 samples (19.94 %) were found to be contaminated with aflatoxins, with mean total aflatoxin concentration of 64.17 ppb amongst the contaminated samples, which is above the SA regulatory limit of 20 ppb for animal consumption. The year 2018 recorded the highest mean total aflatoxin value while North-West agro-climatic region had the highest mean total aflatoxin value. Drastic reduction in average rainfall significantly influence aflatoxin contamination of South African maize.

Development of Uv-visible and Hplc Analytical Methods for Quantitative Analysis of Antiulcer Drugs in Dosage Forms

Precise measurement of active pharmaceutical ingredients (APIs) in dosage forms is crucial in the pharmaceutical business to guarantee the quality, effectiveness, and safety of the product. This research is focused on creating and confirming analytical techniques for accurately measuring the amount of antiulcer medicines in different types of medication. The measurement of antiulcer medicines in their respective formulations was carried out using two analytical techniques: UV-Visible spectroscopy and High-Performance Liquid Chromatography (HPLC). UV-Visible spectroscopy is a straightforward and cost-effective method that allows for quick examination. It is particularly useful for regular quality control applications. HPLC, in contrast, offers exceptional sensitivity, specificity, and precision, facilitating the isolation and measurement of many constituents in complex matrices. The technique development procedure included optimizing experimental parameters, including solvent systems, detection wavelengths, column types, mobile phase composition, and flow rates. The reliability and robustness of the suggested procedures were ensured by validation studies done in accordance with ICH recommendations. The adequacy of the procedures for their intended purpose was assessed by evaluating parameters such as linearity, precision, accuracy, specificity, and robustness. The UV-Visible and HPLC techniques that were developed showed exceptional linearity over the examined concentration range, with correlation values (R²) above 0.99. The precision experiments showed low relative standard deviations (RSDs), suggesting excellent repeatability and moderate accuracy. The accuracy checks demonstrated that the recovery values were within acceptable ranges, therefore verifying the dependability of the methodologies used for quantitative analysis.

Detection of trace levels of selected allergic chemicals in commercial hair dyes in local market of Jeddah, Saudi Arabia

Hair dyes are now commonly used in Saudi Arabia, and other nations across the world, to cover up grey hairs and/or to modify the natural color of the hair. The principal ingredients of hair dyes are aromatic amines and phenols and which most likely cause allergic reactions, irritated skin, and even cancer in certain cases. Thus, the current study reports the separation and subsequent identification of four chemical constituents namely p-Phenylenediamine (PPD), 3-aminophenol (3AP), resorcinol (RES), and 2-methylresorcinol (2MRS) in 26 commercial hair dyes that represent ten famous brands available in the local market of Jeddah city, Saudi Arabia. High-performance liquid chromatography (HPLC) technique was successfully employed to identify the four chemical compounds using methanol-aqueous solution (10:90 v/v) containing diethanolamine (0.05 %) and ammonium acetate (0.02 M) at pH 5.2 as a proper mobile phase. The column was 150 × 4.6 mm ID and 5 µm Eclipse Plus C18 column and the retention times were 1.26, 3.16, 4.99 and 6.01 min for PPD, 3AP, RES, and 2MRS, respectively. The four standards PPD, 3AP, RES, and 2MRS at 254 nm displayed excellent linear calibration plots in the concentration range 5–100 µg/mL with acceptable correlation coefficients (R2) of 0.9964, 0.9980, 0.9952 and 0.9961, respectively. The low limits of detection (LOD) and quantification (LOQ) based on the standard deviation of the response and the slopes of the plots were found to be equal 7.17, 5.39, 8.33, and 7.47 µg/mL and 23.91, 17.97, 27.75, 24.89 µg/mL for PPD, 3AP, RES, and 2MRS, respectively.

A highly sensitive of electrochemical biosensor based on new aptamer sequence for 17α-ethinylestradiol detection in water

The remarkable features of aptamer as biological agent in detecting various compound with high binding affinity could be useful in monitoring of 17α-ethinylestradiol (EE2). EE2 is considered as an endocrine disrupting compound due its ecotoxicity and has widespread in the aquatic ecosystem due to improper disposal. Hence, there is a pressing requirement for sensitive and selective detection of EE2. In this study, we developed a new electrochemical biosensor based on modified DNA aptamers and gold nanoparticles/poly(n-butyl acrylate-co-N-acryloxysuccinimide) microspheres (Au/P(nBA-NAS)). The DNA aptamers was truncated from a 76-mer sequence to 39-mer sequences via computational method, has showed improved binding affinity and stability for EE2. The biosensor was fabricated by attaching the aptamers to the Au/P(NBA-NAS) microspheres, which is provided a large surface area and enhanced electron transfer for the immobilization and signal amplification of the aptamers. The detection principle of the [Fe(CN)6]−3/−4 redox probe in differential pulse voltammetry (DPV) measurement by the presence of aptamer-EE2 complexes on the electrode surface. The biosensor exhibited a linear relationship between the current decrease and the EE2 concentration in the range of 1 × 10−6 M to 1 × 10−12 M, with a detection limit of 1.7 × 10−13 M. The biosensor exhibited excellent selectivity, repeatability, and recovery for detecting EE2 in real samples, with results that closely matched those obtained using the high-performance liquid chromatography (HPLC) technique. This study provided a promising alternative for developing aptamer-based sensors for onsite environmental monitoring.

Avocado seed extract encapsulated in zein nanoparticles as a functional ingredient

Nano-delivery of natural compounds has gained increasing attention in the food and pharmaceutical ingredients industry. Avocado seed was extracted by a total lipid extraction and the presence of two acetogenin compounds was confirmed by the high-performance liquid chromatography (LC-MS) technique. Then, the avocado seed extract (Avo) was encapsulated into zein nanoparticles by liquid-liquid dispersion and the formation of zein nanoparticles loaded with avocado seed extract (Avo-ZNPs) was confirmed by FTIR analysis. The Avo-ZNPs with various Avo contents showed an average size ranging from 166.9 ± 14.1 to 305.2 ± 16.2 nm with 0.19–0.26 of polydispersity index (PDI), and a surface charge range was −59.5 ± 8.1 to −32.9 ± 0.4 mV, as measured by dynamic light scattering (DLS). The entrapment efficiency (EE) values were up to 82 % and the highest loading capacity (LoC) was 14.8 %. The Avo-ZNPs were found to have significantly higher antioxidant potency compared to the control, as measured by DPPH and FRAP assays. Moreover, the zein nanoparticles were also biocompatible with the acute myeloid leukemia (AML) cell lines, and encapsulated avocado extract induced leukemia cell death. Thus, zein nanoparticles could be a promising delivery system for natural avocado seed extract to be used in the medical and food industries.