Disinfectants and Antiseptics Introduction And
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Airgid - Instructions for Use Im3 Airgid Is a Gelatin Collagen Sponge of Hemostatic Action to Which 5 % Colloidal Silver Is Added
Airgid - Instructions for Use iM3 Airgid is a gelatin collagen sponge of hemostatic action to which 5 % colloidal silver is added. It facilitates optimum wound treatment when applied to a surgical cavity and can be cut to the required size to fit smaller wound cavities. The evenly porous foam structure absorbs its own weight in blood several times over, promotes thrombocyte aggregation due to the large surface and fills the wound cavity. The plug thus formed has a constant volume, fits snugly and stabilises blood coagulum. This prevents the formation of fissures and secondary cavities which, without iM3 Airgid, could form by contraction of the blood coagulum and trigger infection due to the invasion of contaminated saliva. Does not block the callus formation. iM3 Airgid remains in the wound and completely absorbed within 3-4 weeks. The addition of colloidal silver has an antimicrobial effect and does not develop any body resistance. Unlike other potential antimicrobial additives, colloidal silver cannot be washed away from the sponge so that its insolubility produces a long-lasting depot effect. Gamma-ray sterilisation process finalizes the manufacturing cycle of the product. Composition: One iM3 Airgid Small Animal (10 × 10 × 10 mm) contains: Hardened gelatine Ph. Eur. 13.85 mg. Colloid silver Ph. Eur. 0.73 mg. One iM3 Airgid Equine (20 × 20 × 20 mm) contains: Hardened gelatine Ph. Eur. 110.8 mg. Colloid silver Ph. Eur. 5.8 mg. Indications: • Socket extraction as part of one or two-stage implant placement. • The general treatment of alveoli and wound cavities, e.g. after cystostomies, apical amputations, maxillary sinus perforations, following surgical removal of tumours or retained teeth. -
)&F1y3x PHARMACEUTICAL APPENDIX to THE
)&f1y3X PHARMACEUTICAL APPENDIX TO THE HARMONIZED TARIFF SCHEDULE )&f1y3X PHARMACEUTICAL APPENDIX TO THE TARIFF SCHEDULE 3 Table 1. This table enumerates products described by International Non-proprietary Names (INN) which shall be entered free of duty under general note 13 to the tariff schedule. The Chemical Abstracts Service (CAS) registry numbers also set forth in this table are included to assist in the identification of the products concerned. For purposes of the tariff schedule, any references to a product enumerated in this table includes such product by whatever name known. Product CAS No. Product CAS No. ABAMECTIN 65195-55-3 ACTODIGIN 36983-69-4 ABANOQUIL 90402-40-7 ADAFENOXATE 82168-26-1 ABCIXIMAB 143653-53-6 ADAMEXINE 54785-02-3 ABECARNIL 111841-85-1 ADAPALENE 106685-40-9 ABITESARTAN 137882-98-5 ADAPROLOL 101479-70-3 ABLUKAST 96566-25-5 ADATANSERIN 127266-56-2 ABUNIDAZOLE 91017-58-2 ADEFOVIR 106941-25-7 ACADESINE 2627-69-2 ADELMIDROL 1675-66-7 ACAMPROSATE 77337-76-9 ADEMETIONINE 17176-17-9 ACAPRAZINE 55485-20-6 ADENOSINE PHOSPHATE 61-19-8 ACARBOSE 56180-94-0 ADIBENDAN 100510-33-6 ACEBROCHOL 514-50-1 ADICILLIN 525-94-0 ACEBURIC ACID 26976-72-7 ADIMOLOL 78459-19-5 ACEBUTOLOL 37517-30-9 ADINAZOLAM 37115-32-5 ACECAINIDE 32795-44-1 ADIPHENINE 64-95-9 ACECARBROMAL 77-66-7 ADIPIODONE 606-17-7 ACECLIDINE 827-61-2 ADITEREN 56066-19-4 ACECLOFENAC 89796-99-6 ADITOPRIM 56066-63-8 ACEDAPSONE 77-46-3 ADOSOPINE 88124-26-9 ACEDIASULFONE SODIUM 127-60-6 ADOZELESIN 110314-48-2 ACEDOBEN 556-08-1 ADRAFINIL 63547-13-7 ACEFLURANOL 80595-73-9 ADRENALONE -
NINDS Custom Collection II
ACACETIN ACEBUTOLOL HYDROCHLORIDE ACECLIDINE HYDROCHLORIDE ACEMETACIN ACETAMINOPHEN ACETAMINOSALOL ACETANILIDE ACETARSOL ACETAZOLAMIDE ACETOHYDROXAMIC ACID ACETRIAZOIC ACID ACETYL TYROSINE ETHYL ESTER ACETYLCARNITINE ACETYLCHOLINE ACETYLCYSTEINE ACETYLGLUCOSAMINE ACETYLGLUTAMIC ACID ACETYL-L-LEUCINE ACETYLPHENYLALANINE ACETYLSEROTONIN ACETYLTRYPTOPHAN ACEXAMIC ACID ACIVICIN ACLACINOMYCIN A1 ACONITINE ACRIFLAVINIUM HYDROCHLORIDE ACRISORCIN ACTINONIN ACYCLOVIR ADENOSINE PHOSPHATE ADENOSINE ADRENALINE BITARTRATE AESCULIN AJMALINE AKLAVINE HYDROCHLORIDE ALANYL-dl-LEUCINE ALANYL-dl-PHENYLALANINE ALAPROCLATE ALBENDAZOLE ALBUTEROL ALEXIDINE HYDROCHLORIDE ALLANTOIN ALLOPURINOL ALMOTRIPTAN ALOIN ALPRENOLOL ALTRETAMINE ALVERINE CITRATE AMANTADINE HYDROCHLORIDE AMBROXOL HYDROCHLORIDE AMCINONIDE AMIKACIN SULFATE AMILORIDE HYDROCHLORIDE 3-AMINOBENZAMIDE gamma-AMINOBUTYRIC ACID AMINOCAPROIC ACID N- (2-AMINOETHYL)-4-CHLOROBENZAMIDE (RO-16-6491) AMINOGLUTETHIMIDE AMINOHIPPURIC ACID AMINOHYDROXYBUTYRIC ACID AMINOLEVULINIC ACID HYDROCHLORIDE AMINOPHENAZONE 3-AMINOPROPANESULPHONIC ACID AMINOPYRIDINE 9-AMINO-1,2,3,4-TETRAHYDROACRIDINE HYDROCHLORIDE AMINOTHIAZOLE AMIODARONE HYDROCHLORIDE AMIPRILOSE AMITRIPTYLINE HYDROCHLORIDE AMLODIPINE BESYLATE AMODIAQUINE DIHYDROCHLORIDE AMOXEPINE AMOXICILLIN AMPICILLIN SODIUM AMPROLIUM AMRINONE AMYGDALIN ANABASAMINE HYDROCHLORIDE ANABASINE HYDROCHLORIDE ANCITABINE HYDROCHLORIDE ANDROSTERONE SODIUM SULFATE ANIRACETAM ANISINDIONE ANISODAMINE ANISOMYCIN ANTAZOLINE PHOSPHATE ANTHRALIN ANTIMYCIN A (A1 shown) ANTIPYRINE APHYLLIC -
A Screening-Based Approach to Circumvent Tumor Microenvironment
JBXXXX10.1177/1087057113501081Journal of Biomolecular ScreeningSingh et al. 501081research-article2013 Original Research Journal of Biomolecular Screening 2014, Vol 19(1) 158 –167 A Screening-Based Approach to © 2013 Society for Laboratory Automation and Screening DOI: 10.1177/1087057113501081 Circumvent Tumor Microenvironment- jbx.sagepub.com Driven Intrinsic Resistance to BCR-ABL+ Inhibitors in Ph+ Acute Lymphoblastic Leukemia Harpreet Singh1,2, Anang A. Shelat3, Amandeep Singh4, Nidal Boulos1, Richard T. Williams1,2*, and R. Kiplin Guy2,3 Abstract Signaling by the BCR-ABL fusion kinase drives Philadelphia chromosome–positive acute lymphoblastic leukemia (Ph+ ALL) and chronic myelogenous leukemia (CML). Despite their clinical activity in many patients with CML, the BCR-ABL kinase inhibitors (BCR-ABL-KIs) imatinib, dasatinib, and nilotinib provide only transient leukemia reduction in patients with Ph+ ALL. While host-derived growth factors in the leukemia microenvironment have been invoked to explain this drug resistance, their relative contribution remains uncertain. Using genetically defined murine Ph+ ALL cells, we identified interleukin 7 (IL-7) as the dominant host factor that attenuates response to BCR-ABL-KIs. To identify potential combination drugs that could overcome this IL-7–dependent BCR-ABL-KI–resistant phenotype, we screened a small-molecule library including Food and Drug Administration–approved drugs. Among the validated hits, the well-tolerated antimalarial drug dihydroartemisinin (DHA) displayed potent activity in vitro and modest in vivo monotherapy activity against engineered murine BCR-ABL-KI–resistant Ph+ ALL. Strikingly, cotreatment with DHA and dasatinib in vivo strongly reduced primary leukemia burden and improved long-term survival in a murine model that faithfully captures the BCR-ABL-KI–resistant phenotype of human Ph+ ALL. -
In Vitro Efficacy of Bacterial Cellulose Dressings Chemisorbed with Antiseptics Against Biofilm Formed by Pathogens Isolated from Chronic Wounds
Supplementary Materials In Vitro Efficacy of Bacterial Cellulose Dressings Chemisorbed with Antiseptics Against Biofilm Formed by Pathogens Isolated from Chronic Wounds Karolina Dydak 1, Adam Junka 1,*, Agata Dydak 2, Malwina Brożyna 1, Justyna Paleczny 1, Karol Fijalkowski 3, Grzegorz Kubielas 4, Olga Aniołek 5 and Marzenna Bartoszewicz 1 1 Department of Pharmaceutical Microbiology and Parasitology, Medical University of Wroclaw, 50-556 Wroclaw, Poland; [email protected] (K.D.); [email protected] (M.B.); [email protected] (J.P.); [email protected] (M.B.) 2 Faculty of Biological Sciences, University of Wroclaw, 51-148 Wroclaw, Poland; [email protected] 3 Department of Microbiology and Biotechnology, Faculty of Biotechnology and Animal Husbandry, West Pomeranian University of Technology, Szczecin, Piastow 45, 70-311 Szczecin, Poland; [email protected] 4 Faculty of Health Sciences, Wroclaw Medical University, 50-996 Wroclaw, Poland; [email protected] 5 Faculty of Medicine, Lazarski University, 02-662 Warsaw, Poland; [email protected] * Correspondence: [email protected]; Tel.: +48-889229341 Citation: Dydak, K.; Junka, A.; Dydak, A.; Brożyna, M.; Paleczny, J.; Abstract: Local administration of antiseptics is required to prevent and fight against biofilm-based Fijalkowski, K.; Kubielas, G.; infections of chronic wounds. One of the methods used for delivering antiseptics to infected wounds Aniołek, O.; Bartoszewicz, M. In is the application -
Bleach) in Health-Care Facilities
CLINICAL MICROBIOLOGY REVIEWS, Oct. 1997, p. 597–610 Vol. 10, No. 4 0893-8512/97/$04.0010 Copyright © 1997, American Society for Microbiology Uses of Inorganic Hypochlorite (Bleach) in Health-Care Facilities WILLIAM A. RUTALA* AND DAVID J. WEBER Division of Infectious Diseases, University of North Carolina School of Medicine, and Department of Hospital Epidemiology, University of North Carolina Hospitals, Chapel Hill, North Carolina 27599-7030 INTRODUCTION .......................................................................................................................................................597 HISTORY.....................................................................................................................................................................597 DEFINITIONS ............................................................................................................................................................598 DISEASE TRANSMISSION IN HEALTH-CARE FACILITIES ..........................................................................598 CHARACTERISTICS OF THE IDEAL DISINFECTANT....................................................................................599 CHLORINE COMPOUNDS WITH ANTIMICROBIAL ACTIVITY ...................................................................599 Available Agents......................................................................................................................................................599 Mechanism of Action..............................................................................................................................................600 -
Ethacridine Lactate Monohydrate
Ethacridine Lactate Monohydrate sc-205315 Material Safety Data Sheet Hazard Alert Code Key: EXTREME HIGH MODERATE LOW Section 1 - CHEMICAL PRODUCT AND COMPANY IDENTIFICATION PRODUCT NAME Ethacridine Lactate Monohydrate STATEMENT OF HAZARDOUS NATURE CONSIDERED A HAZARDOUS SUBSTANCE ACCORDING TO OSHA 29 CFR 1910.1200. NFPA FLAMMABILITY1 HEALTH2 HAZARD INSTABILITY0 SUPPLIER Santa Cruz Biotechnology, Inc. 2145 Delaware Avenue Santa Cruz, California 95060 800.457.3801 or 831.457.3800 EMERGENCY: ChemWatch Within the US & Canada: 877-715-9305 Outside the US & Canada: +800 2436 2255 (1-800-CHEMCALL) or call +613 9573 3112 SYNONYMS C15-H15-N3-O.C3H6O3, "lactic acid, compd. with 6.9-diamino-2-ethoxyacridine (1:1)", "6, 9-acridinediamine, 2-ethoxy-, 2-hydroxypropanoate (1:1)", "acridine, 6, 9-diamino-2-ethoxy-, compd. with lactic acid (1:1)", "acridine, 6, 9-diamino-2-ethoxy-, monolactate", "2, 5-diamino-7-ethoxyacridine lactate", "6, 9-diamino-2-ethoxyacridine lactate", "6, 9-diamino-2-oxyethylacridine lactate", "2-ethoxy-6, 9-diaminoacridine lactate", "2-ethoxy-6, 9-diaminoacridinium lactate", Acrinol, Acrolactine, Ethodin, Flavitrol, Metifex, Rimaon, Rivanol, Rivinol, Vucine, "antiseptic/ disinfectant" Section 2 - HAZARDS IDENTIFICATION CHEMWATCH HAZARD RATINGS Min Max Flammability: 1 Toxicity: 2 Body Contact: 2 Min/Nil=0 Low=1 Reactivity: 1 Moderate=2 High=3 Chronic: 2 Extreme=4 CANADIAN WHMIS SYMBOLS 1 of 7 EMERGENCY OVERVIEW RISK May cause SENSITISATION by skin contact. Irritating to eyes, respiratory system and skin. Toxic to aquatic organisms. POTENTIAL HEALTH EFFECTS ACUTE HEALTH EFFECTS SWALLOWED ! Accidental ingestion of the material may be damaging to the health of the individual. ! Acridines may cause nausea, vomiting, and digestive tract irritation. -
Application of Rotating Magnetic Fields Increase the Activity of Antimicrobials Against Wound Biofilm Pathogens
www.nature.com/scientificreports OPEN Application of Rotating Magnetic Fields Increase the Activity of Antimicrobials Against Wound Received: 6 June 2017 Accepted: 16 November 2017 Bioflm Pathogens Published: xx xx xxxx A. F. Junka1, R. Rakoczy2, P. Szymczyk3, M. Bartoszewicz1, P. P. Sedghizadeh4 & K. Fijałkowski 5 Infective complications are a major factor contributing to wound chronicity and can be associated with signifcant morbidity or mortality. Wound bacteria are protected in bioflm communities and are highly resistant to immune system components and to antimicrobials used in wound therapy. There is an urgent medical need to more efectively eradicate wound bioflm pathogens. In the present work, we tested the impact of such commonly used antibiotics and antiseptics as gentamycin, ciprofoxacin, octenidine, chlorhexidine, polihexanidine, and ethacridine lactate delivered to Staphylococcus aureus and Pseudomonas aeruginosa bioflms in the presence of rotating magnetic felds (RMFs) of 10–50 Hz frequency and produced by a customized RMF generator. Fifty percent greater reduction in bioflm growth and biomass was observed after exposure to RMF as compared to bioflms not exposed to RMF. Our results suggest that RMF as an adjunct to antiseptic wound care can signifcantly improve antibioflm activity, which has important translational potential for clinical applications. Wounds, especially chronic ones and protracted with infective complications, become an increasing burden for patients and healthcare systems and lead to signifcant deterioration of life or, if untreated appropriately, to death1. Te infective complication of wound ulcerations of virtually each etiology: venous, arterial, diabetic, neoplastic, bedsores, or of burn origin impedes or stops the process of wound healing and is responsible for persistence or chronicity of a wound. -
New Spectrophotometric Methods for Estimation of Ethacridine Lactate in Pharmaceutical Formulations
Available online a t www.pelagiaresearchlibrary.com Pelagia Research Library Der Chemica Sinica, 2011, 2 (1): 15-20 ISSN: 0976-8505 CODEN (USA) CSHIA5 New spectrophotometric methods for estimation of Ethacridine lactate in pharmaceutical formulations 1* 1 1 Aziz Unnisa , B. Hemalatha , N. V. Chenchu Lakshmi and D. Srinivasulu 2 1K.V.S.R Siddhartha College of Pharmaceutical Sciences, Vijayawada, A. P., India 2Andhra University, Vishakapatnam, A. P., India ______________________________________________________________________________ ABSTRACT Ethacridine lactate is an antiseptic in solutions of 0.1%; it is also used as an agent for second trimester abortion. Upto 150ml of 0.1% solution is instilled extra amniotically using a foley catheter. Three simple and sensitive spectrophotometric methods (Method A, Method B and Method C) were developed for the estimation of Ethacridine lactate in pharmaceutical formulations. These methods are based on the oxidative coupling of Eathacridine Lactate with 2,2’-bipyridyl, Bathophenanthroline and 2,4,6-tripyridyl- s-triazine in the presence of Fe(III) to form coloured chromophores which can be estimated at absorption maximums of 450nm, 600 and 540 respectively.. Method A, Method B and Method C obey the beers law in the concentration range of 5-25 µg/ml, 4-24 µg/ml and 6-26µg/ml respectively. The methods were validated for use in routine quality control of Ethacridine lactate in pharmaceutical formulations. Interference studies were conducted and it was found that the common excipients usually present in dosage forms do not interfere in the proposed methods. The optical characteristics, regression analysis data and precision of the methods were calculated. The accuracy of the methods was evaluated by estimating the amount of Ethacridine Lactate in previously analyzed samples to which known amounts of Ethacridine Lactate was spiked. -
Ehealth DSI [Ehdsi V2.2.2-OR] Ehealth DSI – Master Value Set
MTC eHealth DSI [eHDSI v2.2.2-OR] eHealth DSI – Master Value Set Catalogue Responsible : eHDSI Solution Provider PublishDate : Wed Nov 08 16:16:10 CET 2017 © eHealth DSI eHDSI Solution Provider v2.2.2-OR Wed Nov 08 16:16:10 CET 2017 Page 1 of 490 MTC Table of Contents epSOSActiveIngredient 4 epSOSAdministrativeGender 148 epSOSAdverseEventType 149 epSOSAllergenNoDrugs 150 epSOSBloodGroup 155 epSOSBloodPressure 156 epSOSCodeNoMedication 157 epSOSCodeProb 158 epSOSConfidentiality 159 epSOSCountry 160 epSOSDisplayLabel 167 epSOSDocumentCode 170 epSOSDoseForm 171 epSOSHealthcareProfessionalRoles 184 epSOSIllnessesandDisorders 186 epSOSLanguage 448 epSOSMedicalDevices 458 epSOSNullFavor 461 epSOSPackage 462 © eHealth DSI eHDSI Solution Provider v2.2.2-OR Wed Nov 08 16:16:10 CET 2017 Page 2 of 490 MTC epSOSPersonalRelationship 464 epSOSPregnancyInformation 466 epSOSProcedures 467 epSOSReactionAllergy 470 epSOSResolutionOutcome 472 epSOSRoleClass 473 epSOSRouteofAdministration 474 epSOSSections 477 epSOSSeverity 478 epSOSSocialHistory 479 epSOSStatusCode 480 epSOSSubstitutionCode 481 epSOSTelecomAddress 482 epSOSTimingEvent 483 epSOSUnits 484 epSOSUnknownInformation 487 epSOSVaccine 488 © eHealth DSI eHDSI Solution Provider v2.2.2-OR Wed Nov 08 16:16:10 CET 2017 Page 3 of 490 MTC epSOSActiveIngredient epSOSActiveIngredient Value Set ID 1.3.6.1.4.1.12559.11.10.1.3.1.42.24 TRANSLATIONS Code System ID Code System Version Concept Code Description (FSN) 2.16.840.1.113883.6.73 2017-01 A ALIMENTARY TRACT AND METABOLISM 2.16.840.1.113883.6.73 2017-01 -
In Vitro Evaluation of Polihexanide, Octenidine and Naclo/Hclo-Based Antiseptics Against Biofilm Formed by Wound Pathogens
membranes Article In Vitro Evaluation of Polihexanide, Octenidine and NaClO/HClO-Based Antiseptics against Biofilm Formed by Wound Pathogens Grzegorz Krasowski 1, Adam Junka 2,3,* , Justyna Paleczny 2, Joanna Czajkowska 3, Elzbieta˙ Makomaska-Szaroszyk 4, Grzegorz Chodaczek 5, Michał Majkowski 5, Paweł Migdał 6, Karol Fijałkowski 7 , Beata Kowalska-Krochmal 2 and Marzenna Bartoszewicz 2 1 Nutrikon, KCZ Surgical Ward, 47-300 Krapkowice, Poland; [email protected] 2 Department of Pharmaceutical Microbiology and Parasitology, Faculty of Pharmacy, Wrocław Medical University, 50-556 Wrocław, Poland; [email protected] (J.P.); [email protected] (B.K.-K.); [email protected] (M.B.) 3 Laboratory of Microbiology, Łukasiewicz Research Network—PORT Polish Center for Technology Development, 54-066 Wrocław, Poland; [email protected] 4 Faculty of Medicine, Lazarski University, 02-662 Warszawa, Poland; [email protected] 5 Bioimaging Laboratory, Łukasiewicz Research Network—PORT Polish Center for Technology Development, 54-066 Wrocław, Poland; [email protected] (G.C.); [email protected] (M.M.) 6 Department of Environment Hygiene and Animal Welfare, Wroclaw University of Environmental and Life Sciences, 51-630 Wrocław, Poland; [email protected] 7 Department of Microbiology and Biotechnology, Faculty of Biotechnology and Animal Husbandry, West Pomeranian University of Technology, 70-311 Szczecin, Poland; karol.fi[email protected] * Correspondence: [email protected]; Tel.: +48-71-784-06-75 Citation: Krasowski, G.; Junka, A.; Paleczny, J.; Czajkowska, J.; Makomaska-Szaroszyk, E.; Abstract: Chronic wounds complicated with biofilm formed by pathogens remain one of the most Chodaczek, G.; Majkowski, M.; significant challenges of contemporary medicine. -
IV. CONTENTS of the 10Th EDITION
EUROPEAN PHARMACOPOEIA 10.0 Contents of the 10th Edition IV. CONTENTS OF THE 10th EDITION The 10th Editionconsistsofnewtextsaswellasallcurrenttextsfromthe9th Edition, some of which have been revised or corrected. Lists of the monographs and general chapters that, for the 10th Edition, are new, revised or corrected, or have had their titles or chapter numbers changed, are given below. Theversiondate(forexample01/2020foratextthatisneworrevisedforthe10th Edition), completed by ‘corrected X.X’ if a corrected version of the text has subsequently been published in Supplement X.X, and the reference number (4 digits for monographs and 5 digits for general chapters) are specified above the title of each monograph and general chapter. The version date, completed by ‘corrected X.X’ if appropriate, makes it possible to identify the successive versions of texts in different editions. ThevolumeinwhichthecurrentversionwasfirstpublishedisstatedintheKnowledgedatabaseontheEDQMwebsite. As of the 10th Edition, all revised or corrected parts of a text are indicated by vertical lines in the margin and horizontal lines in themarginindicatewherepartsofatexthavebeendeleted.Linesinthemarginthatwerepresentinrevisedorcorrectedtexts in the previous edition are deleted with each new edition. Corrected texts are to be taken into account as soon as possible and not later than the end of the month following the month of publication of the volume. New and revised texts are to be taken into account not later than the implementation date. A barcode is included at the start of each text, providing a link to further information on the text (e.g. the Knowledge database) for smartphones and tablets with a camera and a barcode reader app. In addition to corrections made to individual texts, the following decisions and systematic modifications have been made to the texts of the European Pharmacopoeia for the 10th Edition.