جستجوی مقالات مرتبط با کلیدواژه « Ionic liquid » در نشریات گروه « پزشکی »

Candida albicans cause a problematic condition in immunocompromised patients that could not be treated quickly due to the resistant behavior of microorganisms. This study aimed to investigate the effect of a novel ionic liquid (IL) as a new drug on C. albicans strains.

Seven newly binary ionic liquids mixtures were synthesized, and among them, ([prollinium chlo- ride] [1-methylimidazolium 3-sulfonate] ([pro-HCl][MImS]) was selected and characterized by 1HNMR, 13C NMR, and FT-IR methods. Samples from patients (n=50) with candidiasis were collected and identified through culture media. ERG11 gene overexpression was related to resistance against azole-bearing drugs. The antibiogram, well diffusion assay, MICs, and MFCs tests were operated. PCR and Real-time evaluated the expression of the ERG11 gene, and the rate of cell death was detected using Flow Cytometry.

Our data manifested that this novel IL (Ionic Liquid) can inhibit C. albican's growth, reduce the expression of ERG11 and increase dead cells.

The newly synthesized IL had an inhibiting effect on the growth of the C. albicans strains and may be used as an alternative candidate for novel drug design.

Previous researchers showed the antimicrobial ability of ionic liquids (ILs) on different infec- tive agents. ILs can dissolve organic components, especially DNA molecules. Among synthesized eight binary ILs mixtures, we have chosen ([Met-HCl] [PyS]) IL for determining the antifungal ability of IL against Candida albicans cells.

Well diffusion assay, chrome agar and Germ tube tests were used to detect the Candida samples. PCR, real-time-PCR, and flow cytometry tests were performed to determine the IL's rate of toxic ability.

Well diffusion assay revealed the diameters of the growth inhibition zones were the largest in IL with methionine and Proline amino acids. Minimum inhibitory concentration (MIC) and the Minimum fungicidal concentration (MFC) tests showed that they inhibited the growth of the C. albicans at a range from 250 μg/ml for sensitivity and 400 μg/ml for resis- tance, MIC average of all samples were 341.62 ± 4.153 μg/ml. IL reduced the expression of CDR1 and CDR2 the genes encoded by the major protein of ABC system transporter by 2.1 (P= 0.009) and 1.2 fold (P= 0.693), revealed by PCR and real time-PCR. In the flow cytometry test, there were increasing dead cells after treating with the ([Met-HCl] [PyS]) even in the most resistant strain.

The novel IL was effective against the most clinical and standard C. albicans.

Recently, fungal drug resistance has significantly increased especially in opportunistic fungus like Candida albicans. Accordingly, it is necessary to use more effective drugs with less toxicity and high influences. Among a large of investigations, ionic liquids showed biological influence and antimicrobial activities. The aim of this study was in vitro investigation of antifungal activity of pyridine –based ionic liquid on a standard strain of Candida albicans and evaluate its toxicity on host cells. A standard strain of Candida albicans was re- cultured on Sabouraud Dextrose Agar (SDA) containing chloramphenicol, incubated at 37℃ for 24 h. Antifungal effect of a novel ionic liquid ([Met-Hcl] [Pys] ), was evaluated using inhibitory zone diameter. The minimum inhibitory concentration (MIC) and minimum fungal concentration (MFC) were performed using micro dilution method. In continue MTT test were done to evaluate the toxicity of the liquid on host cells. The ionic liquid showed a good effect to prevent of Candida albicans growth. Inhibitory zone diameter was between 34±1 mm. The MIC evaluation was 708.4 ppm. Also the results of MTT test showed the viability of host cells at the 16 dilution. In conclusion, the results of this study manifested that the novel ionic liquid has a good antifungal activity against Candida albicans standard strain with low toxicity to human cells and probably can use as a good novel drug in treatment of candidiasis. Although the need for more studies is crystal clear.

In this study, arapid and sensitive electrochemical electrode was fabricated to measure the amount of sunset yellow in food samples. This analytical sensor was mediated using a NiO-decorated single-walled carbon nanotubes (NiO-SWCNTs) nanocomposite and N-octylpyridinium hexafluorophosphate ionic liquid (IL). The morphology of the NiO-SWCNTs nanocomposite was investigated by means of X-Ray Diffraction (XRD) and Transmission electron microscopy (TEM) methods. Cyclic Voltammetry (CV) and Square Wave Voltammetry (SWV) techniques were utilized to verify the appropriateness of the suggested sensor. In comparison to the bare carbon paste electrode (CPE), the electrochemical response of modified electrode had a considerable improve. According to the Chronoamperometry and scan rate analyses, diffusion index (D) and transfer coefficient (α) were obtained 1.8×10-5 cm2/s and 0.52, respectively. The outcomes achieved from SWV technique demonstrated a reasonable linear dynamic range (LDR) between 0.09 and 750 µM, and the Limit of Detection (LOD) was obtained 0.05 µM. Eventually, the quantity of sunset yellow in real samples showed a recovery range between 99.2 and 99.86%, confirming the accuracy of the proposed sensor.

Saccharides are considered as abundant, cheap and renewable starting materials for chemicals and fuels. Recently, ionic liquids have been used as green solvents for saccharides. The solubility values of galactose in aqueous ionic liquid solutions are not available. Thus, the main objective of this research was to determine the solubility of galactose in aqueous solutions containing ionic liquids, 1-butyl-3-methyl imidazolium bromide, [BMIm]Br, 1-butyl-3-methylimidazolium chloride [BMIm]Cl and 1-hexyl-3- methyl imidazolium bromide, [HMIm]Br at different mole fractions of ionic liquids at T = (298.15 and 308.15) K.

In this study, the gravimetric method was used to measure the solubility of galactose in aqueous ionic liquids solutions.

The solubility values of galactose in water and aqueous ionic liquid solutions were correlated with the activity coefficient models of Wilson, NRTL, modified NRTL, NRFNRTL, and UNIQUAC.

It was concluded that with increasing the mole fraction of ionic liquids, the solubility values of galactose decrease and in fact all of these ionic liquids show saltingout effect on aqueous galactose solutions and this behavior is stronger in ionic liquid 1- butyl-3-methylimidazolium chloride.

Sustainable development in the bio-treatment of large-scale biomass bulks requires high performance enzymes adapted to extreme conditions. An extracellular keratinolytic extract was obtained from the culture broth of a halotolerant strain of Salicola marasensis. Keratin hydrolyzing activity of the concentrated enzyme extract was observed on a 100 mg of pretreated feather waste. The concentrated enzyme was able to hydrolyze the poultry feathers by 25% after 12 h incubation. The bio-waste material was optimally hydrolyzed at pH 9 and temperature of 40 °C. Among reductants, 1,4-dithiothreitol, L-cysteine, 2-mercaptoethanol, glutathione, and sodium sulfate showed the most remarkable effect on the bio-waste keratinolysis, while the tested surfactants and urea had no significant effect on the keratinolytic activity. Hexane and hexadecane indicated strong effect on keratinase activity and bio-treatment in the presence of 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]) as a hydrophobic ionic liquid resulted in a maximal of 80% extraction yield of soluble proteins from feathers. Considering the stability of the extracellular keratinolytic content in [BMIM][PF6], the observed keratinase activity was noteworthy suggesting that the secreted enzyme may contribute to the bioconversion of feather wastes.

A simple and efficient ionic liquid-based ultrasound-assisted in-situ solvent formation microextraction (IL-UA-ISFME) in combination with high-performance liquid chromatography-ultraviolet detection (HPLC-UV) has been gainfully developed for the trace determination of four phthalate esters (PEs) in environmental water samples. In this method, a hydrophobic ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate) was created by addition of a hydrophilic ionic liquid (1-butyl-3-methylimidazolium tetrafluoroborate) to sample solution constituting an ion-pairing agent (NaPF6). The analytes were extracted inside the ionic liquid phase while the microextraction solvent was dispersed through the sample by utilizing ultrasonic radiation. The sample was then centrifuged and extracting phase retracted into the microsyringe, diluted with acetonitrile, and injected to HPLC. At first, vigorous parameters controlling the performance of the microextraction process were considered and optimized. The limit of detections (LOD, S/N = 3) were in the range of 0.22-0.33 µg L-1 while the RSD% values were below than 6.1% (n = 5). A good linearity (0.996 ≥ r2 ≥ 0.992) and a broad linear over the concentration range from 1.0 to 500 µg L-1 were achieved. At last, the method was applied for the preconcentration and sensitive determination of the PEs in several environmental water samples. The accuracy of the method in the real samples was examined by the relative recovery experiments with results ranging from 90-107%, which approved that intricate matrixes had approximately slight effect on the developed procedure.

Molecular interactions are crucial between the enzyme molecules and the surrounding solution in an enzymatic catalysis. Although aqueous solutions used as conventional enzymatic reaction media, non-aqueous enzymology emerges as a major area of biotechnology research and development. Ionic liquids, as new generation of promising alternatives to traditional organic solvents, possess potential industrial enzymatic applications. Enzymes in ionic liquids present enhanced activity, stability, and selectivity. In addition, the potential of ionic liquids in bio-catalysis is raised by high ability of dissolving a wide variety of substrates and their extensively tunable solvent properties through appropriate modification of the cations and anions. However, despite the bio-friendly nature of ionic liquids for enzymatic reactions, their growing interests increase concerns associated with toxicity and environmental pollution of such compounds. This mini-review presents a brief highlight of the contemporary knowledge of enzymes activity and stability in ionic liquids and the environmental influences regarding the potential risks related to the growing applications of these green solvents.

An amperometric glucose biosensor was developed based on synergistic contributions of PB and a bucky gel (BG) consisting of carbon nanotubes (CNTs) and ionic liquid (IL). The PB nanoparticles were first deposited onto the surface of a BG modified glassy carbon (GC) electrode (BG/GC). Then, the Ni2 ions were electrochemically inserted into the PB lattice to improve its stability in physiological pH. Afterwards, Glucose oxidase (GOx) was immobilized on the BG/GC electrode using a cross-linking method. Amperometric measurements of glucose were performed at −0.05 V vs. Ag/AgCl in 0.05 M phosphate buffer solution at pH 7.4. The glucose biosensor exhibited a sensitivity of 45.03 µA mM−1 cm−2 with a detection limit of 5×10-7 M. The amperometric response was linear in the range of 5×10-7 to 8.3×10−4 M.

Celecoxib is classified as none traditional nonsteroidal anti-inflammatory drugs (NSAIDs). This compound has conventional properties of NSAIDs such as anti-inflammatory, analgesic, and antipyretic activities beside reduced risk of gastrointestinal side effect of traditional NSAIDs such as ibuprofen. This compound gets a second sale rank of NSAIDs market at 2016 in the world and sales more than 17000 kg in Iran during the past 6 month. So, the simple, rapid and green method for synthesis of this compound is important. In the present study, a novel green method was suggested for the synthesis of celecoxib using the ionic liquid.
Celecoxib was provided by the reaction of trifluorineacetone, 4-methylbenzoylchloride, and 4-hydrazine benzene sulfonate amide hydrochloride. The tris-(2-hydroxyethyl) ammonium acetate as ionic liquid was prepared by mixing tris-(2-hydroxyethyl) ammonium and acetic acid, and used as an efficient catalyst. The structure of the synthetic products was confirmed by analytical and spectroscopic methods including 1HNMR, 13CNMR, IR, MS and elemental analysis.
This ionic liquid can play dual roles in the synthesis of celecoxib, as a catalyst to improve electrophilicity of carbonyl group and also as a solvent of reaction. The reaction rate and yield (86%) were improved considerably. Moreover IL showed the same efficiency when used in 4 consecutive reactions.

The anticoagulant racemic warfarin is synthesized by the Michael addition of 4-hydroxycoumarin with benzalacetone in the present of equimolar amounts of imidazolium based ionic liquids [bmim] BF4 and [bmim] Br and other reaction solvents such as H2O, pyridine and ammonia in five different tests. Also synthesis of a derivative of warfarin (2-methyl-4-phenyl pyrano [3, 2-c] chromen-5(4H)-one) under solvent-free condition is reported. In this paper, we show the potential that ionic liquid have for the development of green methods for the formation of the C-C bond by reaction condensations without catalysts and organic solvents. A ¡green method, according to the well-known principles, must reduce or eliminate the use or generation of unsafe substances. The work-up procedures were fairly simple and the products dont require further purification.