Muhammad Ishaq Ali Shah

A series of 40 chalcone derivatives was synthesized through Claisen-Schmidt condensation and characterized by FT-IR and NMR spectroscopy. The compounds were evaluated for α-amylase inhibitory and DPPH radical-scavenging activities to identify chalcone-based hits with a dual in vitro profile relevant to postprandial glycemic control. The series displayed a broad range of activities, with α-amylase IC₅₀, values spanning 10.41 ± 1.23-1021.64 ± 2.75 µM and radical-scavenging IC₅₀ , values ranging from 31.34 ± 0.20 to 698.34 ± 14.56 µM. Among the evaluated compounds, 4, 17, 19, 31, 33, and 35 emerged as the most active α-amylase inhibitors, with compound 4 being the most potent member of the series (IC₅₀ = 10.41 ± 1.23 µM), outperforming acarbose (IC₅₀ = 73.12 ± 5.04 µM). Structure-activity relationship analysis indicated that hydroxy- and methoxy-substituted aryl motifs were generally favorable, whereas some heteroaryl replacements and heavily halogenated patterns were less well tolerated. To rationalize the experimental profile, an ensemble docking workflow coupled to Naive Bayes rescoring was applied to human pancreatic α-amylase. The predicted binding modes supported productive occupation of the catalytic groove and suggested a key interaction between compound 4 and Glu233, consistent with its superior inhibitory potency. In silico ADMET profiling of the leading compounds indicated acceptable lipophilicity, solubility, intestinal absorption, and low predicted cardiotoxicity, with compound 4 showing the most balanced overall profile. In summary, these findings identify this chalcone series as a promising starting point for hit-to-lead optimization toward multifunctional radical scavenging and α-amylase inhibitors.

In recent times, environmental pollution has become a pressing issue. Different methods have been developed to detach hazardous materials from H2O bodies. Among these techniques, photo-catalysis has emerged as a low-cost and advanced method. However, finding a potent photocatalyst has been a topic of considerable research. Our study prepared CuO from copper acetate using hydrothermal treatment in an autoclave at 170 ºC for 14 hours. We introduced various quantities of Fe by adding FeSO4 mixture to Cu (CH3COO)2, following the identical method for preparing CuO. The resulting precipitate was cleaned with deionized H2O and dried at 100 °C. The prepared substance was then heated at 450 ºC in a muffle furnace for 60 minutes. We characterized the manufacture of photocatalysts utilizing various techniques such as Ultraviolet (UV), FT-IR, SEM, EDX, and XRD. Our Ultraviolet (UV) spectrum analysis helped us recognize the adsorption spectroscopic analysis of un-doped and doped CuO with various ratios of Fe. FTIR spectroscopic analysis helped us identify functional groups in CuO NPs. Our XRD study showed the monoclinic composition of copper oxide nanoparticles. The SEM picture suggested that NPs exist in a spherical shape. We studied the catalytic activity of synthesized NPs concerning crystal violet (CV) colorant degradation below a direct ray of light irradiation. Our results showed that the degradation productiveness, as compared to CV colorant, was about 93.52% in 180 min. This research is of great importance in the quest for effective and sustainable solutions to environmental problems. The examination of electrical properties highlighted the promising aspects of Fe-doped CuO, particularly at 6% doping. This variant demonstrated superior dielectric parameters, lower tangent loss, semiconductor-like impedance behavior, and enhanced electrical conductivity, emphasizing its potential for applications in electrical and energy storage domains.

In the present work, several new glycoconjugates (8a–e) were generated from glycopyranosyl-α-trichloroacetimidates (sugar-OTCA) as glycosyl donors and dimethyl-l-tartrate as an aglycone acceptor in good to excellent yields. In the synthetic protocol, various monosaccharides were transformed into pentaacetylated derivatives and then into glycopyranosyl-α-trichloroacetimidates. Afterward, the sugar-OTCA was reacted with dimethyl-l-tartrate using Schmidt’s trichloroacetimidate protocol to give the desired products. The newly synthesized glycoconjugates were characterized by FT-IR, ¹H, and ¹³C-NMR spectroscopic analytical methods. All the target compounds (8a–e) were tested in vitro against various strains of bacteria and fungi at different concentrations. The results revealed that the target compounds had encouraging antibacterial and antifungal potential. The antileishmanial activity of the target compounds against Leishmania tropica promastigotes was also investigated. The in vitro results were further supported by the in silico docking study that indicated minimum values of the docking scores and binding energies for the resulting complexes obtained by the favorable interactions between the target compounds (8a–e) and the selected strains of bacteria and fungi. The docking results proposed promising antibacterial and antifungal activities of the target compounds (8a–e) against the selected bacterial and fungal species.

Microplastic pollution has become a global concern, with potential negative impacts on various ecosystems and wildlife species. Among these species, ducks (Anas platyrhynchos) are particularly vulnerable due to their feeding habits and proximity to aquatic environments contaminated with microplastics. The current study was designed to monitor microplastic (MP) pollutants in the freshwater ecosystem of the Panjkora River, Lower Dir, Pakistan. A total of twenty (20) duck samples were brought up for four months and 13 days on the banks of the river, with no food intake outside the river. When they reached an average weight of 2.41 ± 0.53 kg, all samples were sacrificed, dissected, and transported in an ice box to the laboratory for further analysis. After sample preparation, such as digestion with 10% potassium hydroxide (KOH), density separation, filtration, and identification, the MP content was counted. A total of 2033 MP particles were recovered from 20 ducks with a mean value of 44.6 ± 15.8 MPs/crop and 57.05 ± 18.7 MPs/gizzard. MPs detected in surface water were 31.2 ± 15.5 MPs/L. The major shape types of MPs recovered were fragments in crop (67%) and gizzard (58%) samples and fibers in surface water (56%). Other types of particles recovered were fibers, sheets, and foams. The majority of these detected MP particles were in the size range of 300–500 µm (63%) in crops, and 50–150 µm (55%) in gizzards, while in water samples the most detected particles were in the range of 150–300 µm (61%). Chemical characterization by FTIR found six types of polymers. Low-density polyethylene (LDPE) had the greatest polymer detection rate (39.2%), followed by polyvinyl chloride (PVC) (28.3%), high-density polyethylene (HDPE) (22.7%), polystyrene (6.6%), co-polymerized polypropylene (2.5%), and polypropylene homopolymer (0.7%). This study investigated the presence of microplastics in the crops and gizzards of ducks, as well as in river surface water. The results revealed the significant and pervasive occurrence of microplastics in both the avian digestive systems and the surrounding water environment. These findings highlight the potential threat of microplastic pollution to wildlife and ecosystems, emphasizing the need for further research and effective mitigation strategies to address this pressing environmental concern.

Herein, we describe a urea hydrogen peroxide-mediated sustainable protocol for the synthesis of selenylated imidazo[2,1-b]thiazole by using half molar equivalent diorganyl diselenides in ethyl lactate as a greener solvent. The reaction features high yields, easy performance on gram scale, metal-free conditions, as well as applicability to imidazopyridine and imidazopyrimidine.

The issue of microplastic (MP) pollution is one of the most pressing environmental problems faced today and for the future. Plastics are ubiquitous due to their exponential use and mismanagement, resulting in the accumulation of fragments across the world. Hence, the problem of MP pollution is aggravated when these plastic items disintegrate into smaller particles due to different physical, chemical, and environmental factors. The consumption of these MP pollutants by wildlife is a worldwide concern and a potentially crucial risk for all ecosystems. Consequently, MPs have caused a wide variety of problems for both public health and wildlife concerning vital life processes—specifically reproduction, which is critical to species’ survival in an ecosystem. Despite MPs’ detrimental effects on wildlife reproduction, it remains unclear how MPs can affect the hypothalamic–pituitary–gonadal (HPG) axis. This review highlights the significant reproductive toxicity of MPs in wildlife, with potentially devastating consequences for human health. The findings emphasize the urgency of developing effective solutions for mitigating the adverse effects of MP pollution on the reproductive systems of wildlife and preserving the integrity of aquatic and terrestrial habitats.

Microplastics (MPs) are an emerging environmental health concern due to their widespread occurrence in food sources such as fish, meat, chicken, honey, sugar, salt, tea and drinking water, thereby posing possible risks to human health. This study aimed to observe the existence of MPs in the crop and gizzard of the farm chicken, a significant food source in Pakistan. Twenty-four chicken samples were taken from eight poultry farms across Punjab, Pakistan. A total of 1227 MP particles were found from 24 samples (crop and gizzards) originating from the 8 poultry farms. In all, 429 MP particles were found in 24 chicken crops, with a mean of 17.8 ± 12.1 MPs/crop. In contrast, 798 MP particles were found in 24 chicken gizzards, with a mean of 33.25 ± 17.8 MPs/gizzard. Comparatively larger particles, ranging between 300–500 µm, were more abundant (63%) than other considered sizes (300–150 µm [21%] and 150–50 µm [16%]). Additionally, fragments were the dominant type of shape in both sample types (crop [64%] and gizzard [53%]). The predominant colours of particles extracted from gizzards and crops were yellow (32%) and red (32%), respectively. Chemical characterisation of these particles detected four types of polymers: polyvinyl chloride (PVC) at 51.2%, followed by low-density polyethylene (LDPE) at 30.7%, polystyrene (PS) at 13.6% and polypropylene homopolymer (PPH) at 4.5%. In conclusion, we provide evidence for MPs in the gizzards and crops of farmed chickens which may originate from contaminated poultry feed. Only a few studies have been reported globally to assess MPs ingestion in chickens. The current study is the first report from Pakistan. It could be a valuable addition to support MPs literature to establish a relationship between MPs contamination and intake through the food chain.

Dihydropyrazole (1-22) derivatives were synthesized from already synthesized chalcones. The structures of all of the synthesized compounds were confirmed by elemental analysis and various spectroscopic techniques. Furthermore, the synthesized compounds were screened against α amylase as well as investigated for antioxidant activities. The synthesized compounds demonstrate good to excellent antioxidant activities with IC₅₀ values ranging between 30.03 and 913.58 μM. Among the 22 evaluated compounds, 11 compounds exhibit excellent activity relative to the standard ascorbic acid IC₅₀ = 287.30 μM. Interestingly, all of the evaluated compounds show good to excellent α amylase activity with IC₅₀ values lying in the range between 0.5509 and 810.73 μM as compared to the standard acarbose IC₅₀ = 73.12 μM. Among the investigated compounds, five compounds demonstrate better activity compared to the standard. In order to investigate the binding interactions of the evaluated compounds with amylase protein, molecular docking studies were conducted, which show an excellent docking score as compared to the standard. Furthermore, the physiochemical properties, drug likeness, and ADMET were investigated, and it was found that none of the compounds violate Lipiniski's rule of five, which shows that this class of compounds has enough potential to be used as a drug candidate in the near future.

Green synthesis is the most effective and environmentally friendly way to produce nanoparticles. The present research aimed at the biosynthesizing of silver nanoparticles (AgNPs) using Tribulus terrestris seed extract as the reducing and stabilizing agent and investigating their anti-diabetic properties. Fourier transformation infrared (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV-Vis spectroscopy were used to analyze the synthesized silver nanoparticles from Tribulus terrestris (TT-AgNPs). The spectroscopic characterization revealed a surface Plasmon resonance band at 380 nm, which verified the development of TT-AgNPs. The transmittance peaks were observed at 596, 1450, 1631, 2856, 2921, and 3422 cm⁻¹ through the FTIR spectrophotometer. The XRD spectrum showed four distinct diffraction peaks in the 2θ range at 20° to 60°. Intense peaks were at 26.32°, 30.70°, 44.70°, 56.07°, 53.75°, 66.28°, and 75.32°. The SEM analysis revealed that the prepared TT-AgNPs were clustered loosely with a smooth and spherical structure and were of relatively uniform size. The in vitro antidiabetic potential of TT-AgNPs was assessed by using glucose yeast uptake, glucose adsorption, and alpha-amylase assays. TT-AgNPs showed the highest activity (78.45 ± 0.84%) of glucose uptake by yeast at 80 µg/mL. In the glucose adsorption assay, the highest activity of TT-AgNPs was 10.40 ± 0.52% at 30 mM, while in the alpha-amylase assay, TT-AgNPs exhibited the maximum activity of 75.68 ± 0.11% at 100 µg/mL. The results indicate a substantial anti-diabetic effect of the TT-AgNPs. Furthermore, the in vivo antidiabetic study was performed on TT-AgNPs in streptozotocin-induced diabetic mice. After receiving TT-AgNPs treatment for 30 days, the mice were sacrificed for biochemical and histological analyses of pancreatic and liver samples, which demonstrated a good improvement when compared to the control group. Mice treated with TT-AgNPs showed a significant drop in blood sugar levels, showing that the biosynthesized TT-AgNPs have effective anti-diabetic properties.