Search results for "ntimicrobial"

showing 10 items of 708 documents

Photoactivated chlorophyllin-based gelatin films and coatings to prevent microbial contamination of food products

2008

[EN] The aim of this work was to develop antimicrobial photosensitizer-containing edible films and coatings based on gelatin as the polymer matrix. incorporating sodium magnesium chlorophyllin (E-140) and sodium copper chlorophyllin (E-141). Chlorophyllins were incorporated into the gelatin film-forming solution and the inhibiting effect of the cast films was tested against Staphylococcus aureus and Listeria monocytogenes. The results demonstrated that water soluble sodium magnesium chlorophyllin and water soluble sodium copper chlorophyllin reduced the growth of S. aureus and L monocytogenes by 5 log and 4 log respectively. Subsequently, the activity of self-standing films and coatings con…

Staphylococcus aureusfood.ingredientPorphyrinsTECNOLOGIA DE ALIMENTOSSodiumActive packagingColony Count Microbialchemistry.chemical_elementFood ContaminationMicrobial Sensitivity Testsmedicine.disease_causeMicrobiologyGelatinFood safetychemistry.chemical_compoundfoodListeria monocytogenesFood PreservationmedicineHumansFood sciencePhotosensitizing AgentsChlorophyllidesChemistryMagnesiumChlorophyllinFood PackagingGeneral MedicineAntimicrobialListeria monocytogenesAnti-Bacterial AgentsFoodborne pathogensStaphylococcus aureusConsumer Product SafetyFood MicrobiologyFood PreservativesGelatinActive packagingAntimicrobial packagingFood Science
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Antibacterial Activity of Desert Truffles from Saudi Arabia Against Staphylococcus aureus and Pseudomonas aeruginosa

2017

Abstract Medicinal mushrooms represent an unlimited source of polysaccharides with nutritional, antitumoral, antibacterial, and immune-stimulating properties. Traditional studies of epigeous higher Basidiomycetes have recently been joined by studies of hypogeous fungi and, in particular, of so-called desert truffles. With the aim to obtain novel agents against bacteria of clinical importance, we focused on the edible desert truffle mushrooms Tirmania pinoyi, Terfezia claveryi, and Picoa juniperi as sources of new antimicrobial agents. In particular, we investigated the in vitro antibacterial activity of acid-soluble protein extracts (aqueous extracts) of these 3 species against the Gram-pos…

Staphylococcus aureusmedicine.drug_classAntibioticsSaudi ArabiaHuman pathogenMicrobial Sensitivity TestsBiologymedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiology0404 agricultural biotechnologyAscomycotaDrug DiscoverymedicinePharmacologyTrufflePseudomonas aeruginosa04 agricultural and veterinary sciencesAntimicrobialbiology.organism_classification040401 food scienceAnti-Bacterial AgentsStaphylococcus aureusPseudomonas aeruginosaantibacterial activity Basidiomycetes desert truffle human pathogens medicinal mushrooms Picoa juniperi Terfezia claveryi Tirmania pinoyiSettore BIO/03 - Botanica Ambientale E ApplicataAntibacterial activityBacteria
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A Silicone Ventricular Catheter Coated with a Combination of Rifampin and Trimethoprim for the Prevention of Catheter-related Infections

1998

So-called antiinfective catheters which are generated by incorporation of antimicrobial substances into polymers appear to be effectful devices in the prevention of catheter related infections. Such devices mainly act by prevention of bacterial colonization of the catheter surface rather than by inhibition of adherence. In a preceding study, we developed a rifampin-containing silicone catheter for the prevention of ventricular shunt infection. In the present study, this work was continued with a combination of antimicrobials incorporated in silicone ventricular catheters to reduce the risk of rifampin resistance and to expand the antimicrobial spectrum. We found that the drug release kineti…

Staphylococcus aureusmedicine.medical_specialtymedicine.drug_classImmunologyAntibioticsColony Count Microbialmedicine.disease_causeBacterial AdhesionTrimethoprimchemistry.chemical_compoundCatheters IndwellingSiliconemedicineAntibacterial agentbusiness.industryAntimicrobialTrimethoprimAnti-Bacterial AgentsSurgeryCatheterchemistryStaphylococcus aureusRifampinbusinessRifampicinmedicine.drugZentralblatt für Bakteriologie
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4-Diazopyrazole Derivatives as Potential New Antibiofilm Agents

2008

<i>Background:</i> The recognition that chronic infections and infections associated with medical devices are biofilm related has been the impulse for investigating the antibiofilm properties of some diazopyrazoles biologically active as antimicrobials. <i>Methods:</i> The susceptibility of staphylococcal biofilms was determined at concentrations ranging from 25 to 1.5 µg/ml using crystal violet and methylthiazotetrazolium (MTT) staining. In the case of <i>Candida albicans,</i> we first assessed the anti-germ tube formation effect of 4-NO<sub>2</sub> (compound 1c) and then we evaluated its antibiofilm activity at concentrations ranging from 10…

StaphylococcusGerm tubeMicrobiologychemistry.chemical_compoundCandida albicansDrug DiscoveryPharmacology (medical)Crystal violetCandida albicansPharmacologyTube formationAza CompoundsMolecular StructurebiologyStaphylococcus biofilms Candida Albicans biofilms Antibiofilms activity DiazopyrazolesBiofilmBiological activityGeneral Medicinebiology.organism_classificationAntimicrobialSettore CHIM/08 - Chimica FarmaceuticaCorpus albicansInfectious DiseasesOncologychemistryBiofilmsPyrazoles
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Overlap and diversity in antimicrobial peptide databases: Compiling a non-redundant set of sequences

2015

Abstract Motivation: The large variety of antimicrobial peptide (AMP) databases developed to date are characterized by a substantial overlap of data and similarity of sequences. Our goals are to analyze the levels of redundancy for all available AMP databases and use this information to build a new non-redundant sequence database. For this purpose, a new software tool is introduced. Results: A comparative study of 25 AMP databases reveals the overlap and diversity among them and the internal diversity within each database. The overlap analysis shows that only one database (Peptaibol) contains exclusive data, not present in any other, whereas all sequences in the LAMP_Patent database are inc…

Statistics and ProbabilitySimilarity (geometry)Computer scienceSequence analysisAntimicrobial peptidesPeptaibolPeptidecomputer.software_genreProceduresBiochemistrySet (abstract data type)chemistry.chemical_compoundProtein methodsSequence Analysis ProteinRedundancy (engineering)HumansDatabases ProteinMolecular BiologyAntimicrobial cationic peptideschemistry.chemical_classificationSequenceAntimicrobial cationic peptideDatabaseSequence databaseSequence analysisComputer Science ApplicationsAlgorithmComputational MathematicsChemistryProtein databaseComputational Theory and MathematicschemistryData miningNucleic acid databaseDatabases Nucleic AcidcomputerSoftwareAlgorithmsHuman
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<b>ANTIMICROBIAL DITERPENOID ALKALOIDS FROM <i>ERYTHROPHLEUM SUAVEOLENS</i> (GUILL. & PERR.) BRENAN</b>

2005

An investigation of the stem bark of Erythrophleum suaveolens (Guill. & Perr.) Brenan yielded the known amide norcassaide ( 1 ) and a new diterpenoid alkaloid named norerythrosuaveolide ( 2 ) which was characterized as 7β-hydroxy-7-deoxo-6-oxonorcassaide. The structures were established on the basis of one and two-dimensional 1 H and 13 C NMR spectral data. The compounds showed potent antimicrobial activities against bacteria and yeasts. KEY WORDS: Erythrophleum suaveolens (Guill. & Perr.) Brenan, Norcassaide, Diterpenoid alkaloid, Norerythrosuaveolide, Antimicrobial activities, Bacteria, Yeasts Bull. Chem. Soc. Ethiop. 2005, 19(2), 221-226.

Stem barkbiologyTraditional medicineChemistryStereochemistryErythrophleum suaveolensGeneral ChemistryAntimicrobialbiology.organism_classificationSpectral dataTerpenoidBulletin of the Chemical Society of Ethiopia
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N-Heterocyclic choline analogues based on 1,2,3,4-tetrahydro(iso)quinoline scaffold with anticancer and anti-infective dual action

2016

Pharmacological effects of biologically active “small molecules” can be improved by their targeted modification, which affects drug delivery and interaction with tumor cells and microorganisms. We aimed to evaluate anticancer and antimicrobial activity of lipid-like choline derivatives modified via simultaneous introduction of tetrahydro(iso)quinoline based pharmacophore system at nitrogen atom and long chain alkyl substituent at oxygen atom. Target compounds were synthesized under phase-transfer catalysis conditions followed by quaternization, and evaluated for cytotoxicity and NO-generation ability on HT-1080 and MG-22A tumor cell lines and NIH 3T3 normal mouse fibroblasts, and screened f…

StereochemistryAntineoplastic AgentsMicrobial Sensitivity TestsGram-Positive Bacteriamedicine.disease_cause01 natural sciencesDNA gyraseCholineInhibitory Concentration 50Mice03 medical and health scienceschemistry.chemical_compoundDrug Delivery Systems0302 clinical medicineAnti-Infective AgentsCell Line TumorNeoplasmsGram-Negative BacteriamedicineAnimalsHumansCytotoxicityEscherichia coliPharmacologybiology010405 organic chemistryQuinolineFungiBiological activityGeneral MedicineAntimicrobialbiology.organism_classificationProteus mirabilis0104 chemical scienceschemistry030220 oncology & carcinogenesisNIH 3T3 CellsQuinolinesAntibacterial activityPharmacological Reports
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The effects of structural changes on the anti-microbial and anti-proliferative activities of diimidazolium salts

2017

An array of diimidazolium salts has been synthesized and used to investigate their anti-microbial and anti-proliferative activities. In particular, salts based on the 3,30-di-n-alkyl-1,10-(1,n-phenylenedimethylene)- diimidazolium cation and differing in the alkyl chain length on the imidazolium ion, the isomeric substitution on the aromatic spacer and in the anion nature were used. The anti-proliferative activity was evaluated against cervical (HeLa), colon adenocarcinoma (HT-29) and breast (SKBR3) cancer cell lines. In the latter case, also a morphological assessment after treatment with salts was performed. All salts were tested for their hemolytic activity against human erythrocytes. On …

StereochemistryBacillus subtilis010402 general chemistrymedicine.disease_causeSettore BIO/19 - Microbiologia Generale01 natural sciencesCatalysisHeLaMaterials ChemistrymedicineSettore BIO/06 - Anatomia Comparata E CitologiaEscherichia coliAlkylchemistry.chemical_classificationbiology010405 organic chemistryChemistryCationic polymerizationdiimidazolium salts anti-bacterial activity anti-proliferative activityBiological activityGeneral ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationAntimicrobial0104 chemical sciencesSettore BIO/18 - GeneticaSKBR3
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Antimalarial activity of abietane ferruginol analogues possessing a phthalimide group.

2014

The abietane-type diterpenoid (+)-ferruginol, a bioactive compound isolated from New Zealand’s Miro tree (Podocarpus ferruginea), displays relevant pharmacological properties, including antimicrobial, cardioprotective, anti-oxidative, anti-plasmodial, leishmanicidal, anti-ulcerogenic, anti-inflammatory and anticancer. Herein, we demonstrate that ferruginol (1) and some phthalimide containing analogues 2–12 have potential antimalarial activity. The compounds were evaluated against malaria strains 3D7 and K1, and cytotoxicity was measured against a mammalian cell line panel. A promising lead, compound 3, showed potent activity with an EC50 = 86 nM (3D7 strain), 201 nM (K1 strain) and low cyto…

StereochemistryClinical BiochemistryPlasmodium falciparumPharmaceutical SciencePhthalimidesCHO CellsBiochemistryPhthalimidechemistry.chemical_compoundAntimalarialsCricetulusCricetinaeDrug DiscoveryAnimalsHumansCytotoxicityMolecular BiologyAbietaneChemistryPlant ExtractsOrganic ChemistryHep G2 CellsAntimicrobialTerpenoidBioactive compoundFerruginolAbietanesMolecular MedicineDiterpeneBioorganicmedicinal chemistry letters
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Synthesis of new antimicrobial pyrrolo[2,1-a]isoquinolin-3-ones

2012

The attractive structure of the pyrroloisoquinoline moiety, together with its potential antimicrobial activity, encouraged us to prepare six 8-substituted and seven 8,9-disubstituted-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-ones in a few steps with good yields. We applied a convenient methodology via double intramolecular cyclization conducted by a Bischler-Napieralski cyclodehydration-imine reduction sequence, which is widely employed in the synthesis of isoquinoline alkaloids. Therefore, we synthesized three series of these pyrrolo[2,1-a]isoquinolin-3-ones characterized by the substituent at the 8-position or 8,9-positions of the aromatic ring: (a) different side chains are atta…

StereochemistryFungicideClinical BiochemistrySubstituentPharmaceutical ScienceMicrobial Sensitivity TestsRing (chemistry)Gram-Positive BacteriaBiochemistrychemistry.chemical_compoundStructure-Activity RelationshipQUIMICA ORGANICAAnti-Infective AgentsBischler-Napieralski cyclodehydrationGroup (periodic table)Drug DiscoveryGram-Negative BacteriaSide chainStructure–activity relationshipMoietyPyrrolesBactericideIsoquinolineMolecular BiologyChemistryOrganic ChemistryFungiAntimicrobialIsoquinolinesPyrrolo[21-a]isoquinolin-3-onesMolecular Medicine
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