The use of 19F in Medicine in Poland and in the World

Fluorine is a chemical element belonging to the group of halogens. Due to its many properties, it has been used in various fields of medicine, mainly in dentistry, pharmacology, oncology, and radiology. It is an element that occurs naturally in the environment with a very high chemical activity. In addition, it has a high affinity for calcium or magnesium [1], which may have a large impact on the body's functioning when a higher dose of fluoride is taken. Moreover, fluorine is an element that has toxic effects, not only on living organisms but also on the environment. Fluoride-based preparations are widely used in several areas of medicine. This paper presents the use of fluoride in its various branches of medicine.

Versatility of Photosensitizers in Dye-Sensitized Solar Cells (DSSCs)

Because of their scientific relevance in the field of energy conversion, dye-sensitized solar cells (DSSCs) have become a focus of major studies in the last two decades. At present, DSSC is generally either sensitized with inorganic dyes, metal-free organic dyes, or natural dyes. These dyes have emerged as potential alternatives to costly and scarce Ru-based dyes because of being economical, simple attainability, ease of preparation, and environmental friendliness. The majority of alternatives to Ru-based dyes have so far proved to be inferior to Ru-based dyes due to their fragility, narrow absorption bands, and unfavorable dye aggregation. The present review focuses on recent research about sensitizers comprising inorganic dyes, metal-free organic dyes, and natural dyes for DSSCs. Following the introduction, Section 2 describes the DSSC operation, including the essential operational principles and basic components of a DSSC. Section 3 introduces various photosensitizers used in DSSC, and Section 4 states the conclusion and outlook on the field of DSSC research. It also describes and summarizes related sensitizers and their efficiency.

Microwave-Assisted Synthesis of Lactose Acetates with Antimicrobial, Cytotoxic, and Antiviral Properties

The task of this study was to perform the "green" synthesis of lactose octaacetate through microwave irradiation and to establish their biological activities. Lactose ester was prepared after microwave-assisted esterification of lactose with acetic anhydride (yield 85-90 %). Lactose octaacetate was characterized by a high degree of acetylation (DS 3.2-3.7). The lactose esters' structure was elucidated by infrared spectroscopy and nuclear magnetic resonance spectroscopy. Lactose octaacetate showed better antifungal activities than antibacterial activities. It possessed slight to moderate antifungal activities against Aspergillus niger ATCC 1015, Penicillium sp., Rhizopus sp., Fusarium moniliforme ATCC 38932. Lactose acetates demonstrated low cytotoxicity against three cell lines: Madin-Darby bovine kidney (MDBK) cells, human epithelial type 2 (HEp-2), and Madin-Darby canine kidney (MDCK) cells. This is the first report for antiviral activity of lactose acetates against herpes simplex virus type 1 (HSV-1), influenza virus A/Panama/2007/99/H3N2 - (IAV/H3N2), PV-1 and Coxsackievirus B1. It was found that this compound showed activity with SI = 2.4 only against PV-1, but against HSV-1, IAV/H3N2, and Coxsackievirus B1 was inactive. The current study demonstrated the applications of lactose acetates as antimicrobial and antiviral substances in food, pharmaceutical, agricultural and cosmetic preparations.

Virtual Screening in Pharmacokinetics, Bioactivity, and Toxicity of the Amburana cearensis Secondary Metabolites

Bioprospecting has contributed to the work of pharmaceutical chemists in the development and commercial disposal of new drugs. Currently, the pharmaceutical industry has emphasized drugs produced from bioactive compounds extracted from natural sources, based on popular medicine discussed in the literature, such as secondary metabolites isolated from the stem bark and seeds of the Amburana cearensis, rich in coumarin derivatives, flavonoids, and phenolic acids and is popularly used in the treatment of respiratory diseases and with anti-inflammatory and antioxidant bioactivity. This review is a study of the structure/activity and structure/property (SAR/SPA) relationship with the physicochemical properties calculated by the algorithms of the MarvinSketch software for the secondary metabolites of A. cearensis, as well as their correlation with in silico test values the SwissADME and admetSAR 2.0 servers and in vitro and in vivo models of the dataset from the PreADMET, GUSAR Online and PASS Online servers. The results showed that substances derived from coumarin, flavonoids, and phenolic acids have attributes of good permeability and low efflux, which favor their oral bioavailability, since phenolic heterosides, amburoside analogs, and biflavonoids are effective in local action as subcutaneous application, constituting promising antimicrobial, anti-inflammatory and antioxidant therapeutic actions in their proper administration routes.

Effects of Extraction Technique and Solvent on Phytochemicals, Antioxidant, and Antimicrobial Activities of Cultivated and Wild Rosemary (Rosmarinus officinalis L.) from Taounate Region (Northern Morocco)

This work was set up to investigate the effects of domestication, solvent, and extraction technique on extracts yield, total phenolics content (TPC), flavonoids content (TFC), antimicrobial (minimal inhibitory concentration, MIC), and antioxidant (IC50) activities in rosemary aerial parts at flowering stage. Although solvent was the main variability source in our data, all tested factors significantly impacted yield, TPC, TFC, MIC, and IC50. These results were confirmed via principal component analysis, which separated solvents, extraction techniques, and rosemary types on the first three components accounting for more than 99% of data variability. Better values of yield (4.17 ± 0.30 –21.58 ± 0.93% DM ), TPC (12.48 ± 1.17–34.72 ± 1.65 mg GAE/g DM), TFC (6.51 ± 1.79–25.02 ± 1.53 mg QE/g DM), MIC (8.17 ± 1.04–24.20 ± 0.98 μg/mL), and IC50 (50.02 ± 0.08–390.00 ± 1.00 µg/mL) were obtained in the case of wild rosemary with Soxhlet extraction especially when combined with more polar solvents (ethanol and methanol). It could be concluded that domestication had negative effects on rosemary phytochemicals and associated antimicrobial and antioxidant activities. Rosemary extracts could serve as important ingredients as food preservatives, antimicrobial agents, and nutraceuticals.

Disruption of Glycolysis, TCA Cycle, Respiratory Chain, Calcium and Iron Homeostasis in Doxorubicin Induced Cardiomyopathy-An In-silico Approach

Doxorubicin is a well-known anthracycline antibiotic that is frequently used to treat a variety of malignancies. However, its clinical use is limited due to its adverse consequences, most notably cardiomyopathy. In the present work, we evaluated the molecular mechanisms behind the impairment of cardiac energetics in doxorubicin-induced cardiomyopathy. According to molecular docking, the interaction of doxorubicin with phosphofructokinase (PKF) and α-enolase is likely to negatively affect glycolysis. The interaction between doxorubicin with HMOX1 results in the accumulation of free iron. The free iron contributes to the heme-driven toxicity and the oxidizing environment that results in reactive oxygen species (ROS) production resulting from cell death. Additionally, the interaction of doxorubicin with HMOX1 impairs the availability of iron required for the Krebs cycle and ETC function. The interaction between doxorubicin and PINK1 results in a reduced membrane potential, which results in calcium accumulation. On the other hand, a lack of iron and calcium in the mitochondrial matrix results in ATP depletion, impairing the Krebs cycle activity. At the same time, the primary cause of doxorubicin-induced cardiomyopathy is cardiac energy metabolism. Thus, our work shows that doxorubicin impairs the activity of PFK, α-enolase, HMOX1, and PINK1, resulting in ATP production failure. As a result of changes in the heart energy metabolism, this ultimately leads to dilated cardiomyopathy caused by doxorubicin. Understanding the critical function of cardiac energy metabolism in doxorubicin-induced cardiomyopathy is critical for overcoming the obstacles that effectively limit the clinical effectiveness of this life-saving anti-cancer treatment.

Chemotherapeutic Evaluation of Ethanol Extract of Chromolaena odorata on Biochemical Aberrations Associated with Experimentally-induced Benign Prostatic Hyperplasia in Male Rats

The sudden rise in benign prostatic hyperplasia (BPH) cases, severe side effects, and the high cost of conventional methods have necessitated the intensive search for alternative BPH management strategies. This study investigated the restorative effects of ethanol leaf extract of Chromolaena odorata (EECO) on testosterone-induced BPH in male albino rats. Thirty male albino rats with a weight range of 150-210 g were randomly distributed into six groups of five rats each. Group 1 was normal rats and not induced. Groups 2-6 were induced via daily subcutaneous injection of testosterone propionate (3 mg/kg) for 28 days. After induction, group 2 received vehicle (carboxyl methylcellulose), group 3 received finasteride (1 mg/kg), while groups 4-6 received 100, 200, and 400 mg/kg of EECO, respectively, for 21 days orally. Prostate and biochemical parameters were determined using standard methods. Treatments with EECO decreased the concentrations of prostate-sensitive antigen, dihydrotestosterone, testosterone, malondialdehyde, cholesterol, low-density cholesterol, and liver enzyme activities compared with BPH-control. Furthermore, there was increased superoxide dismutase, and catalase activities in extract treated groups compared with BPH- control. The findings from this study showed that EECO inhibited testosterone-induced BPH anomalies, making it promising phytotherapy for the management of BPH in males.

Azo-dye Antibacterial with Nanotube-[SiO2(OH)2]9 System for Drug Delivery Investigation

Azo dye, [SiO2(OH)2]9 molecular ring, and single-walled carbon nanotubes (4,4) SWCNT were considered like an axle, a wheel, and stoppers, respectively. The combination of the azo dye on the [SiO2(OH)2]9 molecular ring with (4,4) SWCNTs may be thought of as a non-covalent system in UV light-isomer- machine. A new molecular motor system that runs like a hinge motion is demonstrated like light-powered molecular hinges. A new molecular motor system that acts as a hinge motion has been demonstrated and introduced as light-moving molecular hinges. By emitting various ultraviolet, visible lights, the [SiO2 (OH)2]9 molecular ring in the system can be reversed with the various dumb-bell size on one side attached halogens and fixing it on the other side of the (4,4) SWCNTs surface, a variety of systems in a wide variety of ultraviolet sensors can be designated to a better model of molecular machines and can be used for drug delivery of some antibiotics that are difficult to administer by straight injection. Molecular machines containing a wide variety of ultraviolet sensors have been designed with the combination of azo derivatives formed by replacing different halogens with hydrogen in the azo dye on the [SiO2(OH)2]9 molecular ring to the (4,4) SWCNTs surface.

β Cyclodextrin Nanocomplexes with Biologically Active Peptides from Hydrolysed Bovine Whey and Colostrum

β Cyclodextrin nanocomplexes with extensive whey and colostrum hydrolysates possessing acceptable flavor properties serve as potential sources of bioactive peptides. In this study, comparative characterization of dairy protein hydrolysates and their complexes with β cyclodextrin is presented. Antioxidant activity of studied samples was estimated by fluorometric method, the formation of clathrates with cyclic oligosaccharide was determined using thermogravimetric analysis. A significant decrease in bitterness of peptides included in cyclic oligosaccharides was established compared with samples of dairy hydrolysates. 2.1/1.3 fold increase in the antioxidant potential of β cyclodextrin clathrates with whey/colostrum hydrolysates was recorded versus unbound peptide fractions. According to toxicological tests on Tetrahymena pyriformis, the samples of whey hydrolysate and the resulting nanocomplex were referred to as non-toxic and slightly hazardous compounds, respectively. The dynamics of body weight gain and the relative weight coefficient of internal organs revealed no differences compared to the control group of Rattus norvegicus. The data on differentiation of blood cells, their death, and cytogenetic disorders demonstrated that a sample of cyclic oligosaccharides with whey peptides is non-toxic at the maximum dosages allowable for administration. β Cyclodextrin complexing with dairy peptides resulted in enhanced radical-reducing activity and improved flavor properties, making the clathrates promising and safe ingredients of special nutrition formulas.

In-Silico Investigation on Chloroquine Derivatives: A Potential Anti-COVID-19 Main Protease

SARS-CoV-2 (Covid 19) continues to be a great threat to lives globally as it causes illnesses such as the common cold, severe acute respiratory syndrome and spreads easily among people. In this work, thirteen molecular compounds were studied via quantum chemical calculations, molecular docking, and dynamic simulation, and ADMET (absorption, distribution, metabolism, excretion, and toxicity). The obtained descriptors (Log P, HBA, HBD, and molecular weight) showed that the studied compounds have the ability to act as a drug. Thus, it was detected that all the studied selected compounds possess a better tendency to inhibit main coronavirus protease; however, compound C1 has a higher tendency to inhibit main coronavirus protease than the other compounds, including the standard (Chloroquine). ADMET properties of compound C1 proved that the predicted ADMET level was better than the ADMET properties of the referenced drug.