PHYTOCHEMICALS AND HYPOGLYCEMIC PROPERTIES OF METHANOL LEAF EXTRACT OF PHYLLANTHUS AMARUS

Plants and plant products are continuously being explored in medicine against diabetics. In the present study, phytochemical screening and hypoglycemic properties of methanol leaf extract of Phyllanthus amarus against alloxan-induced diabetic rats were conducted. A total of fifteen (15) albino rats were randomly selected into 5 groups of 3 rats per group. Groups 1-3 rats were treated with   250 and 500 mg/kg methanol extract of Phyllanthus amarus and 5 mg/kg of glibenclamide respectively, while groups 4 and 5 served as diabetic and normal controls respectively. All treatments were administered orally, once daily for fifteen days. Results revealed the presence of alkaloids, terpenoids, saponins, glycosides, flavonoids, total phenols and tannins. A significant (P<0.05) and a progressive increase in blood glucose level were observed in diabetic untreated rats throughout the experimental periods. At the end of the treatment period rat treated with 250 & 500 mg/kg, P. amarus had final glucose level of 117.00±5.43 mg/dl & 106.00±4.56 mg/kg. Rats treated with 2.5mg/kg glibenclamide had final glucose level of 117.33±5.43 while the untreated rat had final glucose level of 562.50±15.45 mg/dl. The extract of phyllanthus amarus at 250 and 500 mg/kg also cause a significant improvement in body weight gain of the rat. It is concluded that phyllanthus amarus contains some useful phytochemicals with potential hypoglycemic reputations. Thus, it may be considered as a natural source of the drug for therapeutic purposes

Ligand-based design, synthesis, computational insights, and in vitro studies of novel N-(5-Nitrothiazol-2-yl)-carboxamido derivatives as potent inhibitors of SARS-CoV-2 main protease

The global outbreak of the COVID-19 pandemic provokes scientists to make a prompt development of new effective therapeutic interventions for the battle against SARS-CoV-2. A new series o

A new isoflavone from Lomariopsis guineensis (Underw.) Alston

Aim/background: Lomariopsis guineensis (Underw.) Alston is an epiphytic climbing fern. It is widely distributed in Africa where it is also used in traditional medicine and as food. There are no previous reports of any constituents of the plant, hence this study to isolate any phytoconstituents. Method: The ethyl acetate extract of the leaves was subjected to column chromatography and isolated constituents were characterized using nuclear magnetic resonance and mass spectrometry. Results: Three compounds were isolated and identified as cycloartenol, pheophytin A and a new isoflavone (5, 7-dihydroxy-4′ methoxy-6,8-dimethylisoflavone). Conclusion: Three phytochemicals including a new isoflavone are reported from the plant for the first time

Greenness assessment of chromatographic methods used for analysis of empagliflozin: a comparative study

The analytical chemistry community is attempting to incorporate green chemistry concepts in the development of analytical techniques to redefine analytical methods and dramatically modify the philosophy of analytical technique development. Each greenness assessment method has its own benefits and drawbacks, as well as its own procedures. The results of each greenness assessment method produce numerous deductions regarding the selection of a greenest chromatographic method on which the determination of a greenness assessment tool depends. The current study examined the greenness behavior of 26 reported chromatographic methods in the literature for the evaluation of the medicine empagliflozin using three evaluation methods: the national environmental methods index (NEMI), the eco-scale assessment (ESA), and the green analytical procedure index (GAPI). This comparative study discussed the value of using more than one greenness evaluation methods while evaluating. The findings showed that the NEMI was a less informative and misleading tool. However, the ESA provided reliable numerical assessments out of 100. Despite the GAPI being a complex assessment compared to the others, it provided a fully descriptive three-colored pictogram and a precise assessment. The findings recommended applying more than one greenness assessment tool to evaluate the greenness of methods prior to planning laboratory-based analytical methods to ensure an environment friendly process

Evaluation of bi-lateral co-infections and antibiotic resistance rates among COVID-19 patients

In addition to the pathogenesis of SARS-CoV-2, bacterial co-infection plays an essential role in the incidence and progression of SARS-CoV-2 infections by increasing the severity of infection, as well as increasing disease symptoms, death rate and antimicrobial resistance (AMR). The current study was conducted in a tertiary-care hospital in Lahore, Pakistan, among hospitalized COVID-19 patients to see the prevalence of bacterial co-infections and the AMR rates among different isolated bacteria. Clinical samples for the laboratory diagnosis were collected from 1165 hospitalized COVID-19 patients, of which 423 were found to be positive for various bacterial infections. Most of the isolated bacteria were Gram-negative rods (n = 366), followed by Gram-positive cocci (n = 57). A significant association (p 50% of COVID-19 patients were fever, fatigue, dyspnea and chest pain with a significant association (p < 0.05) in bacterial co-infected patients. The current study results showed a comparatively high prevalence of AMR, which may become a severe health-related issue in the future. Therefore, strict compliance of antibiotic usage and employment of antibiotic stewardship programs at every public or private institutional level are recommended

Detection and quantification of new psychoactive substances (NPSs) within the evolved "legal high" product, NRG-2, using high performance liquid chromatography-amperometric detection (HPLC-AD)

The global increase in the production and abuse of cathinone-derived New Psychoactive Substances (NPSs) has developed the requirement for rapid, selective and sensitive protocols for their separation and detection. Electrochemical sensing of these compounds has been demonstrated to be an effective method for the in-field detection of these substances, either in their pure form or in the presence of common adulterants, however, the technique is limited in its ability to discriminate between structurally related cathinone-derivatives (for example: (±)-4′-methylmethcathinone (4-MMC, 2a) and (±)-4′-methyl-N-ethylmethcathinone (4-MEC, 2b) when they are both present in a mixture. In this paper we demonstrate, for the first time, the combination of HPLC-UV with amperometric detection (HPLC-AD) for the qualitative and quantitative analysis of 4-MMC and 4-MEC using either a commercially available impinging jet (LC-FC-A) or custom-made iCell channel (LC-FC-B) flow-cell system incorporating embedded graphite screen-printed macroelectrodes. The protocol offers a cost-effective, reproducible and reliable sensor platform for the simultaneous HPLC-UV and amperometric detection of the target analytes. The two systems have similar limits of detection, in terms of amperometric detection [LC-FC-A: 14.66 μg mL−1 (2a) and 9.35 μg mL−1 (2b); LC-FC-B: 57.92 μg mL−1 (2a) and 26.91 μg mL−1 (2b)], to the previously reported oxidative electrochemical protocol [39.8 μg mL−1 (2a) and 84.2 μg mL−1 (2b)], for two synthetic cathinones, prevalent on the recreational drugs market. Though not as sensitive as standard HPLC-UV detection, both flow cells show a good agreement, between the quantitative electroanalytical data, thereby making them suitable for the detection and quantification of 4-MMC and 4-MEC, either in their pure form or within complex mixtures. Additionally, the simultaneous HPLC-UV and amperometric detection protocol detailed herein shows a marked improvement and advantage over previously reported electroanalytical methods, which were either unable to selectively discriminate between structurally related synthetic cathinones (e.g. 4-MMC and 4-MEC) or utilised harmful and restrictive materials in their design

An overview of recent developments in the analytical detection of new psychoactive substances (NPSs)

New psychoactive substances (NPSs), sometimes referred to as “legal highs” in more colloquial environments/ the media, are a class of compounds that have been recently made available for abuse (not necessarily recently discovered) which provide similar effects to the traditional well studied illegal drugs but are not always controlled under existing local, regional or international drug legislation. Following an unprecedented increase in the number of NPSs in the last 5 years (with 101 substances discovered for the first time in 2014 alone) its, occasionally fatal, consequences have been extensively reported in the media. Such NPSs are typically marketed as ‘not for human consumption’ and are instead labelled and sold as plant food, bath salts as well as a whole host of other equally nondescript aliases in order to bypass legislative controls. NPSs are a new multi-disciplinary research field with the main emphasis in terms of forensic identification due to their adverse health effects, which can range from minimal to life threatening and even fatalities. In this mini-review we overview this recent emerging research area of NPSs and the analytical approaches reported to provide detection strategies as well as detailing recent reports towards providing point-of-care/in-the-field NPS (“legal high”) sensors

A study of the mechanism of hydrophilic interaction chromatography and its application in the analysis of medical drugs and metabolites

Hydrophilic interaction chromatography (HILIC) has been the subject of a few excellent reviews in recent years and most focused on different factors which impact on the separation of compounds in HILIC mode including column temperature, mobile phase composition, pH, buffer type and concentration. However, there have not been as many studies focusing on the retention mechanism and selectivity in hydrophilic chromatography. In the light of recent development in HILIC stationary phases and their applications, the need to understand the mechanisms that govern the separation in HILIC, which is not purely due to partitioning, and the contribution of stationary surface became a subject of study. This thesis explored the possible mechanisms which might be involved in HILIC chromatography by comparing the retention of test probes on bare silica gel and on a type-C silica hydride phase. In addition, a comprehensive retention and selectivity study of some commercially available hydride-based stationary phases was carried out in the analysis of hydrophobic acids and bases in hydrophilic interaction chromatography (HILIC). The applications of HILIC technique were also addressed in the analysis of plasma and urinary metabolites, impurity profiling and in the separation of 'Legal high' regioisomers. An interest in the HILIC retention mechanism was mainly inspired by the need to understand how to develop the optimal HILIC conditions and the selection of a stationary phase. The retention of a series of positively charged probes on silica gel column was concluded that for this class of compounds both ion-exchange and hydrophilic partitioning were involved in retention. Ion exchange interactions were minimised by increase the ionic strength of the modifier in the mobile phase. The strength of the overall HILIC mechanism was increased with silica gel surface area. The unique properties of silica-hydride phases also assessed and are still not explained in terms of how the retention mechanism of this type of stationary phase is different from the other separation materials used in chromatography. The study confirmed the usefulness of HILIC in many analytical aspects. However, the mixed-interaction mechanisms which operate on different stationary phases for different compounds are still far from understood and more investigation is required.Hydrophilic interaction chromatography (HILIC) has been the subject of a few excellent reviews in recent years and most focused on different factors which impact on the separation of compounds in HILIC mode including column temperature, mobile phase composition, pH, buffer type and concentration. However, there have not been as many studies focusing on the retention mechanism and selectivity in hydrophilic chromatography. In the light of recent development in HILIC stationary phases and their applications, the need to understand the mechanisms that govern the separation in HILIC, which is not purely due to partitioning, and the contribution of stationary surface became a subject of study. This thesis explored the possible mechanisms which might be involved in HILIC chromatography by comparing the retention of test probes on bare silica gel and on a type-C silica hydride phase. In addition, a comprehensive retention and selectivity study of some commercially available hydride-based stationary phases was carried out in the analysis of hydrophobic acids and bases in hydrophilic interaction chromatography (HILIC). The applications of HILIC technique were also addressed in the analysis of plasma and urinary metabolites, impurity profiling and in the separation of 'Legal high' regioisomers. An interest in the HILIC retention mechanism was mainly inspired by the need to understand how to develop the optimal HILIC conditions and the selection of a stationary phase. The retention of a series of positively charged probes on silica gel column was concluded that for this class of compounds both ion-exchange and hydrophilic partitioning were involved in retention. Ion exchange interactions were minimised by increase the ionic strength of the modifier in the mobile phase. The strength of the overall HILIC mechanism was increased with silica gel surface area. The unique properties of silica-hydride phases also assessed and are still not explained in terms of how the retention mechanism of this type of stationary phase is different from the other separation materials used in chromatography. The study confirmed the usefulness of HILIC in many analytical aspects. However, the mixed-interaction mechanisms which operate on different stationary phases for different compounds are still far from understood and more investigation is required