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Chemistry, An Asian Journal Jul 2022Titanate nanotubes (TNTs) were coated with a cyclic oligosaccharide (carboxymethyl-β-cyclodextrin, CM-β-CD) to obtain a photocatalyst (CM-β-CD-TNT) for efficiently...
Titanate nanotubes (TNTs) were coated with a cyclic oligosaccharide (carboxymethyl-β-cyclodextrin, CM-β-CD) to obtain a photocatalyst (CM-β-CD-TNT) for efficiently activating molecular oxygen and removing the target contaminant. The hydrophobic cavity and the large specific surface area of the photocatalyst provide abundant active sites for activating molecular oxygen. The free radical capture experiment and quenching experiment showed that cyclodextrin could facilitate adsorption and activation of molecular oxygen to produce O . Therefore, compared with the pristine TNT, CM-β-CD-TNT accelerated the oxidation efficiency of paracetamol (APAP) by 3.4 times. Moreover, the ring cleavage reaction induced by CM-β-CD-TNT effectively reduced the acute toxicity of wastewater containing APAP. Furthermore, 100% of bisphenol A (BPA), bisphenol S (BPS), phenol, 2,4-dichlorophen (2,4-DCP), and carbamazepine (CBZ) were degraded by CM-β-CD-TNT after 2.5 h ultraviolet (UV) light irradiation. This strategy provides a new dimension for the advanced treatment of organic wastewater by organic macrocyclic molecule-modified materials.
Topics: Acetaminophen; Nanotubes; Oxygen; Wastewater; beta-Cyclodextrins
PubMed: 35470547
DOI: 10.1002/asia.202200352 -
Pharmaceutical Development and... 2016Chlorophene-loaded nanospheres with various formulation parameters were evaluated. The optimal formulation was found at 0.1% w/v of poloxamer 407, 15 mL of ethyl...
Chlorophene-loaded nanospheres with various formulation parameters were evaluated. The optimal formulation was found at 0.1% w/v of poloxamer 407, 15 mL of ethyl acetate and 20% initial chlorophene loading that provided the suitable size (179 nm), the highest loading content (19.2%), encapsulation efficiency (88.0%) and yield (91.6%). Moreover, encapsulation of chlorophene in nanospheres was able to prolong and sustain drug release over one month. Chlorophene-loaded nanospheres were effective against Staphylococcus aureus (S. aureus) and Candida albicans (C. albicans), the main cause of hospital-acquired infections. Chlorophene-loaded nanospheres were effective against S. aureus (>46 µg/mL) and C. albicans (>184 µg/mL). These nanospheres appeared to have profound effect on the time-dependent hemolytic activity due to gradual release of chlorophene. At the concentration of 46 µg/mL, nearly no HRBC hemolysis in 24 h compared to 80% of hemolysis from free drug. In conclusion, polymeric nanospheres were successfully fabricated to encapsulate chlorophene which can eliminate inherent toxicity of drugs and have potential uses in prolonged release of antimicrobial.
Topics: Anti-Infective Agents; Candida albicans; Chemistry, Pharmaceutical; Delayed-Action Preparations; Dichlorophen; Dose-Response Relationship, Drug; Drug Delivery Systems; Humans; Microbial Sensitivity Tests; Nanospheres; Staphylococcus aureus
PubMed: 25220889
DOI: 10.3109/10837450.2014.959180 -
Chemical Biology & Drug Design Aug 2019The need for new antibacterial agents is increasingly becoming of great importance as bacterial resistance to current drugs is quickly spreading. Enoyl-acyl carrier...
The need for new antibacterial agents is increasingly becoming of great importance as bacterial resistance to current drugs is quickly spreading. Enoyl-acyl carrier protein reductases (FabI) are important enzymes for fatty acid biosynthesis in bacteria and other micro-organisms. In this project, we conducted structure-based virtual screening against the FabI enzyme, and accordingly, 37 compounds were selected for experimental testing. Interestingly, five compounds were able to demonstrate antimicrobial effect with variable inhibition activity against various strains of bacteria and fungi. Minimum inhibitory concentrations of the active compounds were determined and showed to be in low to medium micromolar range. Subsequently, enzyme inhibition assay was carried out for our five antimicrobial hits to confirm their biological target and determine their IC values. Three of these tested compounds exhibited inhibition activity for the FabI enzyme where our best hit MN02 had an IC value of 7.8 μM. Furthermore, MN02 is a small bisphenolic compound that is predicted to have all required features to firmly bind with the target enzyme. To sum up, hits discovered in this work can act as a good starting point for the future development of new and potent antimicrobial agents.
Topics: Anti-Bacterial Agents; Bacteria; Bacterial Proteins; Drug Design; Enoyl-(Acyl-Carrier-Protein) Reductase (NADH); Enzyme Inhibitors
PubMed: 31063658
DOI: 10.1111/cbdd.13536 -
ACS Omega Sep 2020Of the numerous infectious diseases afflicting humans, anthrax disease, caused by , poses a major threat in its virulence and lack of effective treatment. The currently...
Of the numerous infectious diseases afflicting humans, anthrax disease, caused by , poses a major threat in its virulence and lack of effective treatment. The currently lacking standards of care, as well as the lengthy drug approval process, demonstrate the pressing demand for treatment for infections. The present study screened 1586 clinically approved drugs in an attempt to identify repurposable compounds against , a relative strain that shares many physical and genetic characteristics with . Our study yielded five drugs that successfully inhibited growth: dichlorophen, oxiconazole, suloctidil, bithionol, and hexestrol. These drugs exhibited varying levels of efficacy in broad-spectrum experiments against several Gram-positive and Gram-negative bacterial strains, with hexestrol showing the greatest inhibition across all tested strains. Through tests for the efficacy of each drug on , bithionol was the single most potent compound on both solid and liquid media and exhibited even greater eradication of in combination with suloctidil on solid agar. This multifaceted study of approved drugs demonstrates the potential to repurpose these drugs as treatments for anthrax disease in a time-efficient manner to address a global health need.
PubMed: 32905429
DOI: 10.1021/acsomega.0c03207 -
Dalton Transactions (Cambridge, England... Apr 2018Herein, C,N co-doped porous TiO2 hollow sphere visible light photocatalysts were fabricated using biocompatible N-lauroyl-l-glutamic acid as a doped precursor and...
Herein, C,N co-doped porous TiO2 hollow sphere visible light photocatalysts were fabricated using biocompatible N-lauroyl-l-glutamic acid as a doped precursor and soft-template by a mild and facile self-assembly soft-template method, followed by calcination at 550 °C in air. The structure, morphology, and surface elemental composition were characterized in detail by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. The results show that the prepared TiO2 photocatalysts have a porous hollow sphere structure and are co-doped with C and N. The visible-light-driven photocatalytic degradation rates of phenol and 2-chlorophenol are ∼92 and 90%, respectively. The photocatalytic reaction rate constants of phenol and dichlorophen on HPT550 porous TiO2 hollow spheres were about ∼4 and ∼2 times higher than those on P25, respectively. This enhancement is because the C,N co-doped porous TiO2 hollow spheres not only extend the photoresponse to the visible light region as C,N co-doping narrows the bandgap (2.7 eV), but also expose a large number of surface active sites that favor visible-light-driven photocatalysis. Moreover, the porous hollow structure favors multiple reflections of photons in the interior, increasing the utilization ratio of light. It is worth to pay more efforts to the development of visible light photocatalysts and further promote their practical application.
Topics: Carbon; Catalysis; Catalytic Domain; Dichlorophen; Glutamic Acid; Hot Temperature; Light; Nanospheres; Nitrogen; Phenol; Photolysis; Photons; Porosity; Titanium; Water Pollutants, Chemical
PubMed: 29543290
DOI: 10.1039/C8DT00262B -
British Journal of Pharmacology Apr 2016High-throughput screening of compound libraries using genetically encoded fluorescent biosensors has identified several second-generation. low MW inhibitors of the...
BACKGROUND AND PURPOSE
High-throughput screening of compound libraries using genetically encoded fluorescent biosensors has identified several second-generation. low MW inhibitors of the calcium-activated chloride channel anoctamin 1 (CaCC/Ano1). Here we have (i) examined the effects of these Ano1 inhibitors on gastric and intestinal pacemaker activity; (ii) compared the effects of these inhibitors with those of the more classical CaCC inhibitor, 5-nitro-2-(3-phenylpropylalanine) benzoate (NPPB); (ii) examined the mode of action of these compounds on the waveform of pacemaker activity; and (iii) compared differences in the sensitivity between gastric and intestinal pacemaker activity to the Ano1 inhibitors.
EXPERIMENTAL APPROACH
Using intracellular microelectrode recordings of gastric and intestinal muscle preparations from C57BL/6 mice, the dose-dependent effects of Ano1 inhibitors were examined on spontaneous electrical slow waves.
KEY RESULTS
The efficacy of second-generation Ano1 inhibitors on gastric and intestinal pacemaker activity differed significantly. Antral slow waves were more sensitive to these inhibitors than intestinal slow waves. CaCCinh -A01 and benzbromarone were the most potent at inhibiting slow waves in both muscle preparations and more potent than NPPB. Dichlorophene and hexachlorophene were equally potent at inhibiting slow waves. Surprisingly, slow waves were relatively insensitive to T16Ainh -A01 in both preparations.
CONCLUSIONS AND IMPLICATIONS
We have identified several second-generation Ano1 inhibitors, blocking gastric and intestinal pacemaker activity. Different sensitivities to Ano1 inhibitors between stomach and intestine suggest the possibility of different splice variants in these two organs or the involvement of other conductances in the generation and propagation of pacemaker activity in these tissues.
Topics: Animals; Anoctamin-1; Benzbromarone; Chloride Channels; Dichlorophen; Dose-Response Relationship, Drug; Gastrointestinal Tract; Hexachlorophene; High-Throughput Screening Assays; Mice; Mice, Inbred C57BL; Structure-Activity Relationship; Thiophenes
PubMed: 26774021
DOI: 10.1111/bph.13431 -
Talanta Jan 2018In this work, a glassy carbon electrode modified with β-cyclodextrins and multi-walled carbon nanotubes (β-CDs/MWCNTs/GCE) was constructed and applied for the...
In this work, a glassy carbon electrode modified with β-cyclodextrins and multi-walled carbon nanotubes (β-CDs/MWCNTs/GCE) was constructed and applied for the square-wave adsorptive stripping voltammetric (SWAdSV) determination of the pesticide dichlorophen (Dcp). For the first time, this compound was electrochemically investigated. The voltammetric measurements were conducted in phosphate buffer (PBS) at pH 6.5 as a supporting electrolyte, and SWAdSV technique parameters were optimized. A linear calibration curve in the wide concentration range from 5.0 × 10molL to 2.9 × 10molL was obtained. Excellent analytical performance in terms of limit of detection (LOD) of 1.4 × 10molL was achieved. The utility of the proposed method was verified by the quantitative analysis of Dcp in Pilica River water samples with satisfactory results. The characterization of modified electrodes was conducted by means of atomic force microscopy (AFM), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). Moreover, in this work, the dissociation constants (pK) of Dcp using potentiometric pH titration were estimated. The stoichiometry of the Dcp-β-CDs inclusion complex formed in solution was determined by proton nuclear magnetic resonance (H NMR) spectroscopy, and a binding constant (β) was estimated from NMR titration studies.
Topics: Anti-Infective Agents; Dichlorophen; Dielectric Spectroscopy; Electrochemical Techniques; Electrodes; Microscopy, Atomic Force; Nanotubes, Carbon; beta-Cyclodextrins
PubMed: 28917800
DOI: 10.1016/j.talanta.2017.07.084 -
Journal of Colloid and Interface Science Oct 2019Mesoporous NH-MIL-125(Ti)@BiMoO core-shell heterojunctions with surface defects were fabricated through a facile solvothermal method. The mesoporous core-shell structure...
Surface-defect-rich mesoporous NH-MIL-125 (Ti)@BiMoO core-shell heterojunction with improved charge separation and enhanced visible-light-driven photocatalytic performance.
Mesoporous NH-MIL-125(Ti)@BiMoO core-shell heterojunctions with surface defects were fabricated through a facile solvothermal method. The mesoporous core-shell structure with a large relative surface area of 87.7 m g and narrow pore size of 8.2 nm extends the photoresponse to the range of visible light due to the narrow band gap of ∼1.89 eV. The visible-light-driven photocatalytic degradation efficiency of highly toxic dichlorophen and trichlorophenol were 93.28 and 92.19%, respectively, and the corresponding rate constants were approximately 8 and 17 times higher than the rates achieved by pristine NH-MIL-125(Ti). The photocatalytic oxygen production rate was increased to 171.3 µmol g. Recycling for several cycles indicates high stability, which is favorable for practical applications. The excellent photocatalytic performance can be ascribed to the formation of the core-shell heterojunctions and to the surface defects that favor charge separation and visible light absorption; the mesoporous structure offers an adequate number of surface active sites and mass transfer. This novel mesoporous core-shell photocatalyst will have potential applications in the environment, and this strategy offers a new insight into fabrication of other high-performance core-shell structure photocatalysts.
PubMed: 31306944
DOI: 10.1016/j.jcis.2019.07.021 -
Chemosphere Apr 2023Microbes play a dominant role for the transformation of organic contaminants in the environment, while a significant gap exists in understanding the degradation...
Microbes play a dominant role for the transformation of organic contaminants in the environment, while a significant gap exists in understanding the degradation mechanism and the function of different species. Herein, the possible bio-degradation of triclosan in microbial fuel cell was explored, with the investigation of degradation kinetics, microbial community, and possible degradation products. 5 mg/L of triclosan could be degraded within 3 days, and an intermediate degradation product (2,4-dichlorophen) could be further degraded in system. 32 kinds of dominant bacteria (relative intensity >0.5%) were identified in the biofilm, and 10 possible degradation products were identified. By analyzing the possible involved bioreactions (including decarboxylation, dehalogenation, dioxygenation, hydrolysis, hydroxylation, and ring-cleavage) of the dominant bacteria and possible degradation pathway of triclosan based on the identified products, biodegradation mechanism and function of the bacteria involved in the degradation of triclosan was clarified simultaneously. This study provides useful information for further interpreting the degradation mechanism of organic pollutants in mixed flora by combining analysis microbiome community and degradation pathway.
Topics: Triclosan; Bioelectric Energy Sources; Biodegradation, Environmental; Bacteria; Microbiota
PubMed: 36739987
DOI: 10.1016/j.chemosphere.2023.137983 -
Nanoscale Apr 2019Multifunctional metal-organic framework-based composites display great potentials as electrode materials. Herein, highly dispersed Au nanorods were successfully...
Multifunctional metal-organic framework-based composites display great potentials as electrode materials. Herein, highly dispersed Au nanorods were successfully encapsulated inside the zeolitic imidazolate framework ZIF-8 (AuNRs@ZIF-8) by epitaxial growth or nucleus coalescence. The microporous ZIF-8 shell functions as a protective coating to effectively prevent AuNRs from dissolution, aggregation, and migration during the electrochemical testing, while it provides numerous channels for the mass transfer of reactants to the AuNR surface. The as-synthesized AuNRs@ZIF-8 was then encapsulated in graphene oxide (GO) nanosheets to enhance the chemical resistance of the multicore-shell support, which possesses permanent porosity as well as high specific surface area and hydrophilicity. The excellent electrocatalytic performance of the resulting ternary AuNRs@ZIF-8@GO was demonstrated by the highly sensitive sensing of niclosamide, dichlorophen, carbendazim, and diuron, which outperformed the reported electrocatalysts for these four pesticides. This nanocomposite thus holds great promise as a catalyst for electrochemical sensor fabrication due to its abundant multiple active sites, enhanced catalytic activity, and remarkable stability.
PubMed: 30951076
DOI: 10.1039/c9nr01101c