Hours Of Incubation Research Articles

In Vitro and Preclinical Systematic Dose-Effect Studies of Auger Electron- and β Particle-Emitting Radionuclides and External Beam Radiation for Cancer Treatment

Despite a rise in clinical use of radiopharmaceutical therapies, the biological effects of radionuclides and their relationship with absorbed radiation dose are poorly understood. Here, we set out to define this relationship for Auger electron emitters [99mTc]TcO4- and [123I]I- and β--particle emitter [188Re]ReO4-. Studies were carried out using genetically modified cells that permitted direct radionuclide comparisons. Triple-negative MDA-MB-231 breast cancer cells expressing the human sodium iodide symporter (hNIS) and green fluorescent protein (GFP; MDA-MB-231.hNIS-GFP) were used. In vitro radiotoxicity of [99mTc]TcO4-, [123I]I-, and [188Re]ReO4- was determined using clonogenic assays. Radionuclide uptake, efflux, and subcellular location were used to calculate nuclear absorbed doses using the Medical Internal Radiation Dose (MIRD) formalism. In vivo studies were performed using female NSG mice bearing orthotopic MDA-MB-231.hNIS-GFP tumors and compared with X-ray-treated (12.6-15 Gy) and untreated cohorts. Absorbed dose per unit activity in tumors and sodium iodide symporter-expressing organs was extrapolated to reference human adult models using OLINDA/EXM. [99mTc]TcO4- and [123I]I- reduced the survival fraction only in hNIS-expressing cells, whereas [188Re]ReO4- reduced survival fraction in hNIS-expressing and parental cells. [123I]I- required 2.4- and 1.5-fold lower decays/cell to achieve 37% survival compared with [99mTc]TcO4- and [188Re]ReO4-, respectively, after 72 hours of incubation. Additionally, [99mTc]TcO4-, [123I]I-, and [188Re]ReO4- had superior cell killing effectiveness in vitro compared with X-rays. In vivo, X-ray led to a greater median survival compared with [188Re]ReO4- and [123I]I- (54 days vs 45 and 43 days, respectively). Unlike the X-ray cohort, no metastases were visualized in the radionuclide-treated cohorts. Extrapolated human absorbed doses of [188Re]ReO4- to a 1 g tumor were 13.8- and 11.2-fold greater than for [123I]I- in female and male models, respectively. This work reports reference dose-effect data using cell and tumor models for [99mTc]TcO4-, [123I]I-, and [188Re]ReO4- for the first time. We further demonstrate the tumor-controlling effects of [123I]I- and [188Re]ReO4- in comparison with external beam radiation therapy.

Lipase and Protease Production Ability of Multi-drug Resistant Bacteria Worsens the Outcomes of Wound Infections.

Surgical site infections are one of the major clinical problems in surgical departments that cost hundreds of millions of dollars to healthcare systems around the world. The study aimed to address the pressing issue of surgical site infections, which pose significant clinical and financial burdens on healthcare systems globally. Recognizing the substantial costs incurred due to these infections, the research has focused on understanding the role of lipase and protease production by multi-drug resistant bacteria isolated from surgical wounds in the development of post-surgical wound infections. For these purposes, 153 pus specimens were collected from patients with severe post-surgical wound infections having prolonged hospital stays. The specimens were inoculated on appropriate culture media. Gram staining and biochemical tests were used for the identification of bacterial growth on suitable culture media after 24 hours of incubation. The isolated pathogens were then applied for lipase and protease, key enzymes that could contribute to wound development, on tributyrin and skimmed milk agar, respectively. Following the CSLI guidelines, the Kirby-Bauer disc diffusion method was used to assess antibiotic susceptibility patterns. The results revealed that a significant proportion of the samples (127 out of 153) showed bacterial growth of Gram-negative (n = 66) and Gram-positive (n = 61) bacteria. In total, isolated 37 subjects were declared MDR due to their resistance to three or more than three antimicrobial agents. The most prevalent bacteria were Staphylococcus aureus (29.13%), followed by S. epidermidis (18.89%), Klebsiella pneumoniae (18.89%), Escherichia coli (14.96%), Pseudomonas aeruginosa (10.23%), and Proteus mirabilis (7.87%). Moreover, a considerable number of these bacteria exhibited lipase and protease activity with 70 bacterial strains as lipase positive on tributyrin agar, whereas 74 bacteria showed protease activity on skimmed milk agar with P. aeruginosa as the highest lipase (69.23%) and protease (76.92%) producer, followed by S. aureus (lipase 62.16% and protease 70.27%). The antimicrobial resistance was evaluated among enzyme producers and non-producers and it was found that the lipase and protease-producing bacteria revealed higher resistance to selected antibiotics than non-producers. Notably, fosfomycin and carbapenem were identified as effective antibiotics against the isolated bacterial strains. However, gram-positive bacteria displayed high resistance to lincomycin and clindamycin, while gram-negative bacteria were more resistant to cefuroxime and gentamicin. In conclusion, the findings suggest that lipases and proteases produced by bacteria could contribute to drug resistance and act as virulence factors in the development of surgical site infections. Understanding the role of these enzymes may inform strategies for preventing and managing post-surgical wound infections more effectively.

Preparation of tantalum-containing coatings on NiTi shape memory alloys with enhanced in vitro cytocompatibility and antibacterial effectiveness

In this work, the magnetron sputtering method is used to deposit tantalum-containing coatings on NiTi shape memory alloys under various sputtering atmospheres including (i) 100% argon, (ii) 16.6% oxygen and 83.4% argon, and (iii) 16.6% nitrogen and 83.4% argon. This research examines how the sputtering atmosphere can impact surface morphology, roughness, wettability, biocompatibility, in vitro cytocompatibility, and antibacterial performance of tantalum-containing coatings. The calculation of nickel ions release by coupled inductively coupled plasma-optical emission spectrometry displayed that none of the coated samples showed any traces of nickel, unlike the bare NiTi substrate. This has led to an improvement in biocompatibility. Topographical measurements demonstrated the formation of a smooth surface under the argon-oxygen atmosphere, whereas the deposited layer in the argon-nitrogen atmosphere exhibited irregular ups and downs. The coatings deposited under the argon-nitrogen atmosphere result in a hydrophobic surface with many hills and valleys which can considerably enhance protein and cellular absorption. Besides, the samples coated under an argon-oxygen atmosphere with a smooth surface exhibited excellent antibacterial efficiency only as early as 6 h of incubation. This is probably due to the formation of amorphous tantalum pentoxide.

Biosynthesis of Silver Nanoparticles using Aspergillus Niger Isolated from Soil and Studying its Antimicrobial Effect Against Some Multidrug-Resistant Bacterial Species and Candida Albican

Objectives: Biosynthesis of silver nanoparticles using the fungus Aspergillus niger, isolated from the soil for the purpose of studying its ability to produce nanoparticles. Methods: Grown in a liquid fermentation medium in glass flasks for ten days. The biosynthesis process was detected by observing the color changes of the filtrate. The properties of silver nanoparticles were determined by UV-measurement. Use SEM to discover the size, shape and distribution of nanoparticles. The chemical groups responsible for the biosynthesis and encapsulation of nanoparticles were detected using FTIR for both the fungal biomass filtrate and the resulting particles, after turning them into powder. Silver nanoparticles produced from mushrooms using the Well-Diffusion-Method showed antibacterial activity against MDR-bacteria for both Gram-positive and Gram-negative Bacteria, which are: (E. coli, K. Pneumonia, S. aureus, and P. aeruginosa), at two concentrations (50, 100). mg/ml) for AgNPs. Results: The biosynthesis was detected by observing the color changes of the filtrate from transparent to light yellow to dark brown. The properties of silver nanoparticles were determined by measurement (UV). Which showed absorbance values at wavelengths (450 nm). The results showed SEM The shape was spherical with dimensions ranging from (17.84-64.03) nanometers. Conclusions: The fungus Aspergillus niger showed the ability to biosynthesise silver nanoparticles after 24 hours of incubation of the fungal filtrate treated with AgNO3.

Screening of Amino Acids as a Safe Energy Source for Isolated Rat Pancreatic Acini.

Amino acids play an essential role in protein synthesis, metabolism, and survival of pancreatic acini. Adequate nutritional support is important for acute pancreatitis treatment. However, high concentrations of arginine and lysine may induce acute pancreatitis. The study aimed to identify the most suitable l -amino acids as safe energy sources for pancreatic acinar cells. Pancreatic acini were isolated from male Wistar rats. Effects of amino acids (0.1-20 mM) on uncoupled respiration of isolated acini were studied with a Clark electrode. Cell death was evaluated with fluorescent microscopy and DNA gel electrophoresis. Among the tested amino acids, glutamate, glutamine, alanine, lysine, and aspartate were able to stimulate the uncoupled respiration rate of isolated pancreatic acini, whereas arginine, histidine, and asparagine were not. Lysine, arginine, and glutamine (20 mM) caused complete loss of plasma membrane integrity of acinar cells after 24 hours of incubation. Glutamine also caused early (2-4 hours) cell swelling and blebbing. Aspartate, asparagine, and glutamate only moderately decreased the number of viable cells, whereas alanine and histidine were not toxic. DNA fragmentation assay and microscopic analysis of nuclei showed no evidence of apoptosis in cells treated with amino acids. Alanine and glutamate are safe and effective energy sources for mitochondria of pancreatic acinar cells.

STUDY OF ANGIOTENSIN-I CONVERTING ENZYME INHIBITORY PEPTIDES DERIVED FROM Ficus pumila var. awkeotsang SEEDS HYDROLYSATE

Hypertension also known as high blood pressure that has associated with multi-metabolic pathways such as the renin-angiotensin-aldosterone system (RAAS). There have been several synthetic ACE inhibitory drugs used clinically as therapeutics for hypertension. However, synthetic drugs showed side effects on human health after long-term use. Therefore, alternative natural ACE inhibitors from food-derived are necessary to develop. The study aimed to examine the activity of angiotensin-I converting enzyme inhibitory peptides derived from Ficus pumila var. awkeotsang seeds hydrolysate and to study the efficiency of enzymatic digestion. This study used four enzymes (trypsin, pepsin, thermolysin, and chymotrypsin) to release bioactive peptides from Ficus pumila var. awkeotsang seeds that could exhibit an antihypertensive effect. The results showed that Ficus pumila var. awkeotsang trypsin hydrolysate has the highest ACEI activity, 90.37%, and the IC50 reached 169±3.5 µg/mL. Then, the hydrolysate produced by trypsin has the highest degree of hydrolysis, 4%, after 8 hours of incubation. Hence, Ficus pumila var. awkeotsang seeds hydrolysate could develop as an alternative natural product that is responsible for ACE-inhibitory activity.

Saline, chlorhexidine, and povidone-iodine alone or in combination with iodine povacrylex are effective antiseptics in chickens (Gallus gallus domesticus).

To evaluate the topical antiseptic activity of saline, chlorhexidine (CHX), and povidone-iodine (PI) scrubs on the skin of chickens with or without the addition of DuraPrep (DP). 7 healthy adult Orpington hens (Gallus gallus domesticus). The right apterium corporale laterale was swabbed for standard aerobic bacterial culture and colony-forming unit (CFU) determination. The apterium was divided into 3 areas and treated with sterile saline, CHX, or PI. Samples were collected by swabbing each area before and after additional treatment with DP. CFU's were counted after 48 hours of incubation. Statistical analysis was performed using a linear mixed model with a continuous outcome. Compared to saline, CHX and PI treatment without DP decreased CFU count by 119 (95% CI, 55 to 183; P < .001) and 123 (95% CI, 58 to 187; P < .001), respectively. The application of DP after CHX and PI further decreased CFU counts by 6 (P = .01) and 9 (P = .01), respectively. DP after saline treatment decreased counts by 128 CFU (95% CI, 63 to 192; P < .001). No significant difference was detected between saline, PI, or CHX after DP application (-1.0 CFU; 95% CI, 63.4 to -65.4; P = .98 for both PI and CHX). CHX or PI provided greater reductions in bacterial CFU than saline, and all combinations with DP provided similar results. No notable cutaneous reactions were detected at any point. This data suggests that a scrub protocol including CHX or PI with DP is acceptable in surgical site preparation of chickens.

Antileukemia Activity of Human Natural Killer Cell-Derived Nanomagic Bullets against Acute Myeloid Leukemia (AML).

Background: Cancer is among the serious health problems of the medical world, for treatment of which severe treatments are used. However, the prognosis of cancer patients is still poor. The application of NK cell-derived exosomes (NK-Exo) is a new method for cancer immunotherapy. These nanoparticles with a size range of 30-120 nm are a small model of mother cells. In this study, the anti-tumor activity of NK-Exo and LAK-Exo (activated NK cell-derived exosome) against acute myeloid leukemia (AML) is investigated in vitro. Materials and Methods: The MACS method was performed for the separation of NK cells from the buffy coats of healthy donors, and an EXOCIBE kit was used for the isolation of NK-Exo. After treating the KG-1 cell line with different doses of NK-Exo, MTT assay, and annexin V-PE were done to evaluate cell proliferation and apoptosis, respectively, and for confirmation of involved proteins, Real-Time PCR and western blotting were performed. Results: Anti-tumor activity of NK-Exo and LAK-Exo was dose- and time-dependent. Their highest activities were observed following 48 hours of incubation with 50 µg/ml exosome (p<0.0001). However, this cytotoxic activity was also seen over a short period of time with low concentrations of NK-Exo (p<0.05) and LAK-Exo (p<0.001).The cytotoxic effect of LAK-Exo on target cells was significantly higher than NK-EXO. The induction of apoptosis by different pathways was time-point dependent. Total apoptosis was 34.56% and 51.6% after 48 hours of tumor cell coculture with 50µg/ml NK-Exo and LAK-Exo, respectively. Significant expression of CASPASE3, P38, and CYTOCHROME C genes was observed in the cells treated with 50 µg/ml NK-Exo and LAK-Exo. Conclusion: Our study confirmed the antileukemia activity of NK-Exo against AML tumor cells in vitro. Therefore, NK-Exo can be considered as a promising and effective treatment for leukemia therapy.

Screening and Optimization of IAA Production by PGPR isolated from Rhizosphere of a Pterocarpus marsupium Roxb. and their Effect on Plant Growth

Indole Acetic Acid (IAA) production is important attribute of PGPR that promote plant growth and development. The rhizosphere is hotspot in the soil that harbors PGPR. The present study was aimed with isolation and screening of IAA producing bacteria from the rhizosphere of Pterocarpus marsupium Roxb. Optimum culture conditions (pH, temperature, incubation period and L-tryptophan concentration for IAA production were studied for selected isolates and their effect on wheat growth and root development was evaluated. Among twenty four IAA producing isolates five isolates (Et1, Rp1, Rp5, Rp6, and Rp9) produced maximum IAA in range of 50-70 μg/mL and was used in optimization studies. Maximum IAA was produced in 96 hours of incubation, at pH 7 and with 0.1mg/mL of L-tryptophan by all five isolates. 30oC is the most suitable temperature for Et1, Rp1, Rp5, Rp9; whereas Rp6 produced nearly same amount of IAA at wide range of temperature 30-35oC (77-84.12 μg/mL) and at pH 7-8 ( 73-74μg/mL). Out of the five isolates, Rp6 exhibits the highest potential, having a maximum IAA of 84.12 μg/mL at 35°C and pH 7. Although tryptophan influences IAA synthesis but at higher concentration of tryptophan inhibits IAA synthesis. To validate the production of IAA, crude extracts were analyzed using thin layer chromatography (TLC). A spot of standard IAA with the same Rf value (0.91) was found to match a specific spot from the crude IAA.

In vitro Evaluation of Botanical Extracts against Mycelial Growth of Alternaria solani

An experiment was conducted at the laboratory of the Department of Plant Pathology, Sam Higginbottom University of Agriculture, Technology and Sciences, Prayagraj, Uttar Pradesh. To test the efficacy of different treatments viz., Neem (Azadirachta indica), Onion (Allium cepa), Garlic (Allium sativum), Castor (Ricinus communis), Amaltas (Cassia fistula), Henna (lawsonia inermis), Madar (Calotropis gigantea) against Alternaria solani under in vitro condition. Botanicals were tested through the poisoned food technique at 5% and 10 % concentrations and 168 hours of incubation. The Minimum radial growth of observed in Neem (Azadirachta indica) seed kernel extract @ 5% (14.8mm) followed by Henna (lawsonia inermis) leaf extract @ 10% (43.36mm), Amaltas (Cassia fistula) leaf extract @ 10% (67.13mm), Castor (Ricinus communis) leaf extract @ 10% (67.6mm), Madar (Calotropis gigantea) leaf extract @ 10% (69.6mm), Onion (Allium cepa) extract @ 10 % (70.8mm), Garlic (Allium sativum) extract @ 10 % (72.2mm) as compared to Control (89.4mm) untreated check.

Exploring the Diverse Biological Properties of Cannabidiol: A Focus on Plant Growth Stimulation.

The aim of the current study was to compare some biological activities of edible oils enriched with 10 % of cannabidiol (CBD samples) from the Slovak market. In addition, hemp, coconut, argan, and pumpkin pure oils were also examined. The study evaluated the fatty acids content, as well as antibacterial, antifungal, antioxidant, cytotoxic, and phytotoxic activities. The CBD samples presented antimicrobial activity against the tested bacterial strains at higher concentrations (10000 and 5000 mg/L) and antifungal activity against Alternaria alternata, Penicillium italicum and Aspergillus flavus. DPPH⋅ and FRAP assays showed greater activity in CBD-supplemented samples compared to pure oils and vitamin E. In cell lines (IPEC-J2 and Caco-2), a reduced cell proliferation and viability were observed after 24 hours of incubation with CBD samples. The oils showed pro-germinative effects. The tested activities were linked to the presence of CBD in the oils.

Shear wave ultrasound elastography for estimating cartilage stiffness: implications for early detection of osteoarthritis

Current osteoarthritis (OA) diagnosis relies on radiographic abnormalities found in later stages of the disease, posing a challenge to the treatment efficacy. Therefore, earlier detection of OA is essential for improving therapeutic outcomes. The aim of this study was to investigate the feasibility of shear wave ultrasound elastography (SWUE) to detect changes in cartilage mechanical properties under OA conditions ex-vivo. Bovine osteochondral units were harvested from femoral condyles and subjected to either trypsin degradation, cartilage surface roughness defect using varying degrees of sandpaper, or subchondral bone degeneration using formic acid (FA) injection. Shear waves were generated using a mechanical shaker, while a high-frequency ultrasound system operating at 18 MHz was employed to detect wave propagation along the samples. The elasticity of cartilage was estimated by the shear wave speed (SWS) through the auto-correlation method. Our results show that the estimated SWS of cartilage after 24, 48, and 72 hours of trypsin incubation significantly decreased by 37%, 43%, and 59%, respectively, compared to the control group. Surface roughness treatment using 150-grit sandpaper significantly decreased the SWS by 35% compared to the control. Samples treated with 7% FA showed a significant increase in SWS by 62%, 89%, and 53% compared to control, 1% FA, and 3% FA, respectively. Our findings demonstrate the feasibility of SWUE to differentiate the elastic properties of cartilage under different OA conditions. This study presents the potential of a noninvasive, nonionizing tool for early detection of OA, representing a significant step toward its clinical implementation.Graphical

Study of the Fenton Oxidative Reaction on a Culture of Human Fibroblast Cells Incubated with Ablated CeO&lt;sub&gt;2&lt;/sub&gt; Particles

Purpose. Study of the bioprotective properties of ablated cerium dioxide nanoparticles in relation to immortalized human fibroblasts under conditions of oxidative stress caused by the Fenton reaction.Methods. Cerium dioxide nanoparticles with pronounced antioxidant properties were obtained using laser ablation. The average maximum sizes of ablated particles of oxidized cerium in non-centrifuged and centrifuged at a speed of 1000 rpm nanodispersed aqueous solutions were revealed using the method of atomic force microscopy. The spectrophotometric method revealed that ablated cerium dioxide nanoparticles exhibit antioxidant properties and prevent the degradation of the methylene blue dye during the Fenton reaction. Cell culture samples were mapped using scanning electron microscopy using an energy-dispersive attachment after their incubation with ablated cerium dioxide nanoparticles. Using MTT analysis, the effect of ablated cerium dioxide nanoparticles on the survival of BJ TERT cell culture in the Fenton reaction was studied. Non-centrifuged and centrifuged at a speed of 1000 rpm nanodispersed solutions of oxidized cerium were used. The antioxidant activity of cerium dioxide nanoparticles after 6- and 24-hour incubation was studied.Results. The average limiting sizes of ablated cerium dioxide nanoparticles have been established, the values of which are (61,95±0,1) nm for a non-centrifuged aqueous solution and (56,59±0,1) nm for an aqueous solution centrifuged at a microcentrifuge speed of 1000 rpm. It was revealed that in the presence of ablated cerium dioxide nanoparticles, the degree of oxidative degradation of methylene blue during the Fenton reaction was significantly reduced. It was found that with an increase in the concentration of ablated cerium dioxide nanoparticles from 20 to 1000 mg/l, their antioxidant effect increased. From the obtained SEM images of cell cultures with ablated cerium dioxide nanoparticles, it follows that the nanoparticles are captured by cells during incubation and can have a significant effect on oxidative processes during the Fenton reaction. Statistical analysis based on the results of the MTT assay showed that 6-hour and 24-hour incubation with ablated cerium dioxide nanoparticles had a pronounced protective effect on the BJ TERT cell line.Conclusion. This work shows that during the Fenton reaction, cerium dioxide nanoparticles prevent the oxidative degradation of the methylene blue dye. When immortalized human fibroblasts are incubated, ablated cerium oxide nanoparticles are taken up by the cells and have a significant protective effect on them in the oxidative reaction. The high antioxidant activity of nanoparticles is determined by the high content of functional defects on the surface of nanoparticles obtained under sharply nonequilibrium conditions of laser ablation.

Effect of commercial probiotics and antibiotics on the growth of Campylobacter isolated from chicken meat in Ho Chi Minh city markets

This study explores the antibiotic susceptibility of Campylobacter, a prominent foodborne pathogen, isolated in Ho Chi Minh city markets and the efficacy of commercial probiotics in inhibiting these bacteria for enhancing food safety and treating Campylobacter infections. Bacteria were isolated from chicken meat in modified coal deoxycholate cefoperazone agar (mCCD), followed by characterization as per standard procedures. Ten isolates with Gram negative, catalase positive and oxidase positive characteristics were collected. Antibiotic susceptibility is ascertained through the determination of the inhibited zone and minimum inhibitory concentration (MIC) of five distinct antibiotics against Campylobacter on Muller Hinton agar plates, culminating in a comprehensive assessment after a 24-hour incubation duration. The antibiotic susceptibility results underscore substantial diversity in Campylobacter isolates among meat samples, thereby accentuating discernible distinctions among the various antibiotic products. The research also evaluated the suitability of 5 commercial probiotic products (re-named as A, B, C, D, and E for fair assessment) by examining their impact on the growth of Campylobacter colonies. The antimicrobial effect of probiotics against Campylobacter is assessed using the agar well diffusion assay and co-culture method. We obtained consistent results from two methods, indicating no variation in Campylobacter species among meat samples but significant variations among probiotic products. The outcomes of this research provide valuable insights into the antimicrobial potential of each probiotic and antibiotic on Campylobacter, informing recommendations for food hygiene practices and underscoring the role of both probiotics and antibiotics in combating Campylobacter infections.

Effects of silver nanoparticle based on ginger extract on Leishmania infantum and Leishmania tropica parasites: in vitro.

Leishmaniais the primary cause of a significant public health problem known as leishmaniasis in Iran. Pentavalent antimonial chemicals are commonly used for the treatment of leishmaniasis. However, these drugs exhibit a number of adverse effects, including drug resistance, lack of specificity, poor responsiveness, toxic effects, inconvenient injections, tissue damage, and high cost. The present study aimed to prepare and evaluate the efficacy of green-synthesized silver nanoparticles (Ag-NPs) againstLeishmania infantumandLeishmania tropicain vitro. The 2, 5-Diphenyl Tetrazolium Bromide (MTT) assay was used to assess the toxicity of Ag-NPs derived from ginger extract on macrophage cells. The apoptotic potential of promastigotes caused by Ag-NPs was evaluated using the flow cytometry method. According to our findings, the proliferation ofL. infantumandL. tropica, promastigotes are significantly decreased by increasing doses of NPs. The most effective doses of nanoparticle were 80 and 40 ppm after 48 and 72 hours of incubation, respectively, while doses of 0.312 and 0.156 ppm after 24 and 48 hours of incubation had the least effect on the growth and activity ofL. infantumandL. tropicapromastigotes. For the promastigotes ofL. infantumandL. tropica, the flow cytometry test revealed that Ag-NPs-induced programmed cell death in promastigotes ofL. infantumandL. tropicademonstrated 67.1% and 41.9% of apoptosis, respectively. The half-maximal inhibitory concentration for NPs againstL. infantumandL. tropicawere 4.54 and 4.22 ppm, respectively, based on the MTT assay. The higher concentrations of NPs (e.g., 80 ppm) led to more lethality of promastigote. In conclusion, Ag-NPs exhibited goodin vitroanti-leishmanial activity againstL. infantumandL. tropicapromastigotes.

In Vitro Antiviral and Anticancer Effects of Tanacetum sinaicum Essential Oil on Human Cervical and Breast Cancer.

Cervical cancer has been linked to human papillomavirus (HPV) types 16 and 18. Essential oils (EOs) are vital natural products of plants with various therapeutic and biological properties. The purpose of this study is to investigate and assess Tanacetum sinaicum essential oil's possible antiviral and anticancer properties, with a focus on its in vitro effects on human cervical cancer and human breast adenocarcinoma cell lines. Tanacetum sinaicum EO was extracted via hydrodistillation (HD) and characterized using gas chromatography-mass spectrometry (GC-MS). MTT assay was used to determine the cell viability of Hela (a human epithelial cervical cancer) and MCF-7 (human breast adenocarcinoma) cell lines. Quantitative real-time polymerase chain reaction (PCR) was utilized to assess the antiviral efficacy of EO against HPV-16 and 18, and anti-metastatic characteristics. The biological activity of EO was assessed using Autophage and Cell genotoxicity via the comet assay. EO is mostly composed of chrysanthenyl acetate, thujone, and verbenol. The cell viability was reduced after 24 hours of incubation at doses from 100 to 400 µg/ml. Concentrations of 800 to 3,200 µg/ml significantly inhibit cell growth. After a 24-hour incubation period, doses ranging from 100 to 400 µg/ml reduced cell viability from 62 to 72%. Concentrations of 800 to 3,200 µg/ml significantly suppress cell growth by over 95%. In MCF7 and HeLa cell lines, EO lowered virus copy numbers in a dose-dependent manner, with higher concentrations of the oil inhibiting virus replication more effectively. EO treatment increased the number of autophagosomes/autolysosomes and acidic vesicular organelles in both cell lines. On the HeLa and MCF7 cell lines, EO demonstrated antiproliferative and antimetastatic effects. The results demonstrated that EO had dose-dependent genotoxic effects on both cancer cell lines, as evidenced by DNA damage. Tanacetum sinaicum EO is a prospective source of natural bioactive compounds that can be employed in pharmaceutical and medicinal applications due to its antiviral, antiproliferative, anti-metastatic and genotoxic properties.

Studying some of the optimal conditionals for the best bacterial isolates from soil and its effects on their growth rates

The current study aimed to use some bacterial isolates from the local soil of Baghdad city by study the effects of temperature, pH and incubation period on the growth rates of isolated bacteria and choose the optimal conditions for their diversity and for understanding bacterial growth and their requirements for survival and proliferation. This information can be applied to obtain their high growth rate for use in various fields such as agriculture, medicine and environmental sciences in the future. And it used to assess the degree of variation in across bacteria species in pH, temperature and incubation period. A number of local bacterial isolates as Enterobacter cloacae, Aeromonas hydrophila, Pantoea spp., Pseudomonas mendocina and Serratia fonticola identified in this study. The growth rate of the bacterial isolates was tested by growing each bacterial isolate in a different range of pH (4, 7 and 10) and under the influence of several temperatures (52, 35 and 50) and within different incubation periods (24, 48 and 72) hours The optimal conditions were determined by measuring the optical density (absorbance) at a wavelength of 600 nm, which represents bacterial growth. The optimal conditions for E. cloacae were determined to be a pH of 10 and a temperature of 35°C after a 72hour incubation period. Similarly, A. hydrophila exhibited optimal growth at a pH of 7 and a temperature of 35°C after a 72hour incubation period. Pantoea spp. demonstrated optimal growth at a pH of 7 and a temperature of 25°C after a 24hour incubation period. P. mendocina displayed optimal growth at a pH of 7 and a temperature of 25°C after a 72hour incubation period. Lastly, S. fonticola exhibited optimal growth at a pH of 7 and a temperature of 50°C after a 72hour incubation period.

In Vitro Immunomodulatory Activity of Sagalanoi Chooranam (Poly Herbal Formulation) in RAW Macrophage Cell Line

Within the realm of Siddha medicine, an ancient and venerable traditional healing system hailing from India, a comprehensive methodology is deployed to combat liver disorders. This approach is characterised by the utilisation of herbal remedies, accentuating the reinstatement of equilibrium in the body's vital life force, known as "Vatham," "Pitham," and "Kapham." The utilisation of cell line studies is crucial in assessing the immunomodulatory properties of herbal medicine, offering invaluable insights into their capacity to influence the immune system and advancing our comprehension of their therapeutic benefits. The primary objective of this investigation was to elucidate the potential immunomodulatory properties of sagalanoi chooranam, a polyherbal Siddha formulation, through the execution of anti-proliferative assays conducted. On the RAW 264.7 macrophage cell line. Various test solutions were precisely prepared, encompassing a spectrum of concentrations (50, 100 and 200 μg/ml). The RAW 264.7 cells were diligently cultured and then carefully subjected to stimulation with lipopolysaccharide (LPS) to initiate cellular activation. Following this activation, the test formulation was introduced at varying concentrations, after which the cells underwent a 24-hour incubation period. The resultant nitrite levels, serving as indicators of immunomodulatory response, were evaluated within the cell lysate. The outcomes unveiled a notable decline in nitrite levels, correlating with the dosage of the test formulation during the incubation with RAW 264.7 cells. The outcomes of the study elucidate a conspicuous decline in nitrite levels in direct correlation with escalating concentrations of the test formulation, contrasting starkly with the control group exclusively subjected to LPS. Furthermore, the investigation meticulously probed the ramifications of the test formulation on cellular viability. The vitality of RAW 264.7 cells exhibited a discernible downward trajectory as the concentration of the test formulation ascended. Noteworthy is the fact that, at the concentration of 200 μg/ml, cellular viability registered at a mere 55.53 ± 3.567%. Collectively, these findings lend credence to the hypothesis that the test formulation possesses a dose-dependent capacity to attenuate both nitrite levels and cellular viability within the RAW 264.7 cell milieu, underscoring its auspicious immunomodulatory attributes. This research expands our insights into the potential immunological ramifications of the test formulation and underscores its plausible utility within the realm of immunomodulation.

Anti-microbial activity of Ocimum sanctum L. gel against black pigmented microbes.

Black pigmented gram negative anaerobes are associated with periodontal disease and tooth loss. Therefore, it is of interest to evaluate the antimicrobial activity of Ocimum Sanctum.L (Tulsi) gel against black pigmented anaerobes. Plaque samples were collected from the subject and kept in anaerobic broth for 4 hours of incubation at 37°C. 50µL concentration of Tulsi gel was added and kept in gas pack system for 3-5 days. Zone of inhibition was measured. Ocimum sanctum L. (Tulsi) exhibits strong antibacterial activity against Black Pigmented bacteroides at 1% and 2%.Tulasi gel was effective at higher concentrations, indicating the possibility of using it as an adjunct to standard periodontal treatment.

Assessment of Microbial Interactions between Potential Lactic Acid Bacteria Starters and Major Microorganisms During in vitro Fermentation in a Medium Similar to Cocoa Pulp in Côte d'Ivoire

However, uncontrolled or random fermentations carried out in the country by farmers producing marketable cocoa beans of variable quality. The problem of variability in the quality of beans has led to significant economic losses in the country estimated at several billion CFA Francs. The objective of this work was to analyze the interactions between potential starter lactic acid bacteria and the major microorganisms selected during cocoa fermentations in Côte d’Ivoire. The work methodology began with the cultivation of yeast, lactic acid bacteria, acetic acid bacteria and Bacillus strains in their respective YPG, MRS, YEPG and BN media for 48 hours at 30°C. Then, the microbial load of each culture was determined and set at 105 cells/mL. The strains were subsequently placed in the similar interaction medium of cocoa pulp (PSM) alone (monoculture) or together (coculture) for the study of microbial interactions. This study took place over 5 days and samples were taken for analyzes after 0, 48 and 120 hours of incubation at 30°C. The interaction was monitored by assessing microbial growth using optical density and Thoma cell counts for monocultures and agar media for cocultures. Additionally, acid production and reduction in sugar intake were also measured over the 5 days. All crops showed good growth. Growth was greater in cocultures with values ​​ranging from 4.12 log (CFU/mL) to 9.21 log (CFU/mL). In addition, the cocktails acidified the environment much more than the monocultures with values ​​oscillating between 0.10 ± 0.00 and 0.21 ± 0.00. Also, the quantity of sugars in the different broths decreased significantly in the cocktails during the first 48 hours, going from 1.08 ± 0.08 to 0.20 ± 0.01. Microbial starters in monocultures and cocultures have shown their ability to adapt to the environment like cocoa pulp. The high microbial growth, sugar consumption, and acidification of the medium in the cocktails reflected a synergistic interaction between the strains during fermentation when they were together. In short, these strains could be used for a starter composition to control fermentation and obtain good quality beans.