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Surprising Antibacterial Activity and Selectivity of Hydrophilic Polyphosphoniums Featuring Sugar and Hydroxy Substituents
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Tyler J. Cuthbert Benjamin Hisey Tristan D. Harrison Dr. John F. Trant Prof. Elizabeth R. Gillies Prof. Paul J. Ragogna 《Angewandte Chemie (International ed. in English)》2018,57(39):12707-12710
There is currently an urgent need for the development of new antibacterial agents to combat the spread of antibiotic‐resistant bacteria. We explored the synthesis and antibacterial activities of novel, sugar‐functionalized phosphonium polymers. While these compounds exhibited antibacterial activity, we unexpectedly found that the control polymer poly(tris(hydroxypropyl)vinylbenzylphosphonium chloride) showed very high activity against both Gram‐negative Escherichia coli and Gram‐positive Staphylococcus aureus and very low haemolytic activity against red blood cells. These results challenge the conventional wisdom in the field that lipophilic alkyl substituents are required for high antibacterial activity and opens prospects for new classes of antibacterial polymers. 相似文献
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Janusz Sarapuk Krzysztof Bielecki Halina Kleszczyska Anna Dziamska Stanisaw Przestalski 《应用有机金属化学》2001,15(1):56-60
The influence of trialkylleads on haemolysis of red blood cells (RBCs), growth of Spirodela oligorrhiza and stability of planar lipid membranes (PLMs) at different pH of solution has been studied. The results obtained show that the efficiency of trialkylleads (methyl‐, ethyl‐, propyl‐ and butyl‐lead chlorides) in modifying the physiological and mechanical properties of the objects studied depended both on pH of solution and hydrophobicity of the compounds. Namely, it was found that this efficiency increased with pH of solution. The most significant increase was observed in PLM experiments. Also, the hydrophobicity of trialkylleads influenced the properties mentioned. The more hydrophobic a compound the greater was its haemolytic toxicity. The same applies to the physiological toxicity of the compounds, whose measure was 50% inhibition of plant growth. Generally, the sequence of modifying possibilities of the compounds studied at any pH of the solution was the following:
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Stanisaw Przestalski Halina Kleszczyska Zenon Trela Zofia Spiak Maria Zamarajeva Natalia Glazyrina Andrea Gagelgans 《应用有机金属化学》2000,14(8):432-437
We have studied the effect of triphenyl‐lead chloride on the lipid phase of erythrocyte membranes, on lipid monomolecular layers and Na+/K+‐ATPase of the microsomal fraction of rat brain. It was found that the haemolytic effect induced by this compound occurs when its concentration exceeds 30 µM . The minimal lead concentration inducing measurable effects in monomolecular lecithin layers is about 1 µM . Inhibition of Na+/K+‐ATPase activity begins at a concentration exceeding 0.5 µM . Maximum inhibition is observed at around 40 µM —a concentration at which haemolysis also occurs. It can thus be thought that at very low lead concentrations the main (or exclusive) role in modifying membrane function is played by direct interaction between lead and the sulphydryl groups of ATPase, whereas at higher concentrations two effects seem to overlap: direct interaction between lead and enzymic proteins via their sulphydryl groups and as indirect influence on the proteins via changes in the organization of the lipid phase of the membrane. Copyright © 2000 John Wiley & Sons, Ltd. 相似文献
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Dr. Lior Sepunaru Stanislav V. Sokolov Jennifer Holter Dr. Neil P. Young Prof. Dr. Richard G. Compton 《Angewandte Chemie (International ed. in English)》2016,55(33):9768-9771
We demonstrate that the concentration of a red blood cell solution under physiological conditions can be determined by electrochemical voltammetry. The magnitude of the oxygen reduction currents produced at an edge‐plane pyrolytic graphite electrode was diagnosed analytically at concentrations suitable for a point‐of‐care test device. The currents could be further enhanced when the solution of red blood cells was exposed to hydrogen peroxide. We show that the enhanced signal can be used to detect red blood cells at a single entity level. The method presented relies on the catalytic activity of red blood cells towards hydrogen peroxide and on surface‐induced haemolysis. Each single cell activity is expressed as current spikes decaying within a few seconds back to the background current. The frequency of such current spikes is proportional to the concentration of cells in solution. 相似文献
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The toxicity of many amphiphilic compounds may result from their effect on the lipid phase of biological membranes. Upon incorporation such compounds may change the properties of membranes in general and in particular alter the organization of membrane lipids. These changes should affect, among other things, the mechanical properties of membranes. We selected two amphiphilic compounds, diphenyltin dichloride (Ph2SnCl2) and triphenyltin chloride (Ph3SnCl), which are known to be located at different regions of the lipid bilayer and to be toxic. As a model biological membrane the erythrocyte plasma membrane was used. Analysis of the haemolysis kinetics showed differences between the effect of the compound studied on mechanical properties at so‐called non‐lytic concentrations. Diphenyltin dichloride showed a limited effect on erythrocyte haemolysis, whereas triphenyltin chloride affected all the parameters measured (extent of initial haemolysis, extent of final haemolysis and membrane mechanical strength). We correlated these effects with the location of the investigated compounds in liposomes. The presented data show that triphenyltin chloride reduces the erythrocyte plasma membrane mechanical strength and increases the extent of haemolysis under osmotic stress conditions. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
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Vladimir M. Gun’ko Natalia P. Galagan Irina V. Grytsenko Vladimir I. Zarko Olena I. Oranska Vyacheslav L. Osaulenko Viktor M. Bogatyrev Vladimir V. Turov 《Central European Journal of Chemistry》2007,5(4):951-969
Interaction of red blood cells (RBCs) with unmodified and partially (50%) silylated fumed silica A-300 (nanosilica)was studied
by microscopic, XRD and thermally stimulated depolarisation current (TSDC) methods. Nanosilica at a low concentration C
A-300 < 0.01 wt.% in buffered aqueous suspension is characterised by a weak haemolytic effect on RBCs. However, at C
A-300 = 1 wt% all RBCs transform into shadow corpuscles because of 100% haemolysis. Partial (one-half) hydrophobization of nanosilica
leads to reduction of the haemolytic effect in comparison with unmodified silica at the same concentrations. A certain portion
of the TSDC spectra of the buffered suspensions with RBC/A-300 is independent of the amounts of silica. However, significant
portions of the low-and high-temperature TSDC bands have a lower intensity at C
A-300 = 1 wt% than that for RBCs alone or RBC/A-300 at C
A-300 = 0.01 wt.% because of structural changes in RBCs. Results of microscopic and XRD investigations and calculations using the
TSDC-and NMR-cryoporometry suggest that the intracellular structures in RBCs (both organic and aqueous components) depend
on nanosilica concentration in the suspension.
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The influence of tri‐ and di‐alkyltins (TATs and DATs) as well as di‐ and triphenyltin compounds (DPhTs and TPhTs) on haemolysis of red blood cells (RBCs) and stability of planar lipid membranes (PLMs) has been studied. The results obtained show that the efficiency of TATs (trimethyl‐, triethyl‐, tri‐n‐propyl‐ and tributyl‐tin chlorides) in destroying PLMs did not differ greatly when the compounds were studied in solutions of physiological pH (phosphate buffer, pH 7.4). A decrease in pH to 5.0 caused small changes in the efficiency of the three largest TAT molecules and a significant decrease in the efficiency of trimethyltin chloride. Both haemolytic and PLM experiments showed that the most active TAT was tri‐n‐propyltin chloride. The destructive action of DAT (dimethyl‐ and dibutyltin) and DPhT dichlorides was somewhat more differentiated. Dimethyltin dichloride (DMT) interaction with model membranes was a little weaker than that of DPhT and dibutyltin dichlorides and all these compounds influenced the model membranes to a lesser extent than TATs or TPhT. To bring about comparable haemolysis effects the dichlorides had to be used at much greater concentrations than the chlorides. The haemolytic properties of the dichlorides, especially of that of DMT, significantly increased in solution at pH 5.0. TPhT chloride interacted with model membranes similarly to TAT chlorides. Also, no great difference in efficiency of this compound was found for the two buffer solutions used. Copyright © 2000 John Wiley & Sons, Ltd. 相似文献
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Natsima Viriyaadhammaa Aroonchai Saiai Waranya Neimkhum Wariya Nirachonkul Wantida Chaiyana Sawitree Chiampanichayakul Singkome Tima Toyonobu Usuki Suwit Duangmano Songyot Anuchapreeda 《Molecules (Basel, Switzerland)》2020,25(22)
Curcuma comosa belongs to the Zingiberaceae family. In this study, two natural compounds were isolated from C. comosa, and their structures were determined using nuclear magnetic resonance. The isolated compounds were identified as 7-(3,4-dihydroxyphenyl)-5-hydroxy-1-phenyl-(1E)-1-heptene (1) and trans-1,7-diphenyl-5-hydroxy-1-heptene (2). Compound 1 showed the strongest cytotoxicity effect against HL-60 cells, while its antioxidant and anti-inflammatory properties were stronger than those of compound 2. Compound 1 proved to be a potent antioxidant, compared to ascorbic acid. Neither compounds had any effect on red blood cell haemolysis. Furthermore, compound 1 significantly decreased Wilms’ tumour 1 protein expression and cell proliferation in KG-1a cells. Compound 1 decreased the WT1 protein levels in a time- and dose- dependent manner. Compound 1 suppressed cell cycle at the S phase. In conclusion, compound 1 has a promising chemotherapeutic potential against leukaemia. 相似文献
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Francesco Trotta Roberta Cavalli Michele Trotta 《Journal of inclusion phenomena and macrocyclic chemistry》2002,44(1-4):345-346
New alkyl carbonates of -cyclodextrin have been obtained. These derivatives show lower haemolytic effect than the parent -cyclodextrin. The complexation behaviour was tested with three important drugs, namely: progesterone, diazepam and flurbiprofen. DSC analyses were consistent with the inclusion complex formation. 相似文献
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