Selection and Use of Disinfectants in Disease Prevention
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)&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. -
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 -
Tepzz 459659B T
(19) TZZ _T (11) EP 2 459 659 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.: C09D 7/00 (2006.01) C09D 7/14 (2006.01) of the grant of the patent: C09D 5/16 (2006.01) 17.07.2013 Bulletin 2013/29 (86) International application number: (21) Application number: 10737728.5 PCT/US2010/043382 (22) Date of filing: 27.07.2010 (87) International publication number: WO 2011/017097 (10.02.2011 Gazette 2011/06) (54) REMOVABLEANTIMICROBIAL COATING COMPOSITIONS CONTAINING CATIONIC RHEOLOGY AGENT AND METHODS OF USE ABLÖSBARE ANTIMIKROBIELLE BESCHICHTUNGSZUSAMMENSETZUNGEN MIT KATIONISCHEM RHEOLOGISCHEM ADDITIV UND ANWENDUNGSVERFAHREN COMPOSITIONS DE REVÊTEMENT ANTIMICROBIENNES, APTES À ÊTRE RETIRÉES, CONTENANT UN AGENT DE RHÉOLOGIE CATIONIQUE, ET PROCÉDÉS D’UTILISATION (84) Designated Contracting States: (74) Representative: Dannenberger, Oliver Andre et al AL AT BE BG CH CY CZ DE DK EE ES FI FR GB Abitz & Partner GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO Patentanwälte PL PT RO SE SI SK SM TR Postfach 86 01 09 81628 München (DE) (30) Priority: 27.07.2009 US 228707 P 27.07.2009 US 228711 P (56) References cited: 27.07.2009 US 228715 P WO-A2-2007/100653 WO-A2-2007/100654 27.07.2009 US 228723 P 26.07.2010 US 843120 • Akzo Nobel Surface Chemistry: "Thickening with polymers"[Online] 1 January 2010 (2010-01-01), (43) Date of publication of application: XP002609717 Akzo Nobel Technical Information 06.06.2012 Bulletin 2012/23 Retrieved from the Internet: URL:http: //www.akzonobel.com/surface/syste m/images/ (73) Proprietor: E. -
Emergency Water: Home Storage and Emergency Disinfection Guide
City of Clovis Public Utilities Emergency Water: Home Storage and Emergency Disinfection Guide Why should I store water? Our water supply is energy dependent, without electrical power we have a limited ability to pump water to your home. Something as common as an electrical storm or as unpredictable as an earthquake or another natural disaster could affect the power grid or our infrastructure and our ability to provide water. ” Luck favors the prepared.” How much water should I store? The American Red Cross recommends one gallon of water per person per day with a two-week supply for every person in your household. This is based on 2 quarts per person per day for drinking water and food preparation, and another 2 quarts per person per day for other limited uses such as hand washing, teeth brushing and dishwashing. This is a total of 14 gallons per person for 2 weeks. For a family of four, that's 56 gallons of water. How do I start? Start small, keeping a case or two of bottled water is an easy way to start your storage. You can add to this by purchasing larger containers or by following the directions in this guide. It is important that you start now. Effects of going without water Although two thirds of the human body by weight is composed of water, this water is needed for circulation and other bodily processes including respiration and converting food to energy. If you are losing more water than you are taking in, dehydration will occur. A normally active person needs to drink at least 2 quarts (1/2 gallon) of water each day. -
Selection and Use of Disinfectants in Disease Prevention
FACT SHEET 19.46.07 HERD HEALTH Extension Bulletin E-1596, January 1982 COOPERATIVE EXTENSION SERVICE • MICHIGAN STATE UNIVERSITY Selection and Use of Disinfectants in Disease Prevention Authors Reviewers George W. Meyerholz, USDA, Extension Service, David M. Bedell, University of Georgia Washington, D.C. Glenn Elliott, Galivants Ferry, South Carolina Jack M. Gaskin, University of Florida Dennard R. Hill, Seaford, Delaware Wayne Rawson, Milledgeville, Illinois Cleaning and disinfecting is very important in con- 95 percent of the contamination and permits disinfectants trolling the accumulation and spread of disease-causing to more easily penetrate and kill infective organisms. microorganisms. This is especially true in modern swine buildings where continuous use and high concentrations of Choosing a Disinfectant animals may result in a condition referred to as "disease Many factors must be weighed before choosing a buildup." As disease-producing bacteria, viruses, fungi, proper disinfectant for a particular job. For example, a and parasite eggs accumulate in the environment, disease germicide intended for the disinfection of a building should problems can be transmitted to each successive group of work well in the presence of organic matter, be compatible animals raised. Thorough cleaning and disinfecting often with soaps or detergents, be harmless to building materials, provides the only successful solution to breaking the dis- and be relatively non-toxic. A disinfectant suitable for de- ease cycle and controlling the problem. contaminating a building might be too toxic for use in sani- Because organic matter, such as is found in dirt and tizing feed and water utensils. Select the disinfectant to fit manure, inactivates certain disinfectants and protects in- the job. -
Managing Water in the Home: Accelerated Health Gains from Improved Water Supply
WHO/SDE/WSH/02.07 Distr.: Limited English only Managing Water in the Home: Accelerated Health Gains from Improved Water Supply Water, Sanitation and Health Department of Protection of the Human Environment World Health Organization Geneva Ó World Health Organization 2002 The illustration of the cover page is extracted from Rescue Mission: Planet Earth, Ó Peace Child International 1994; used by permission This document is not issued to the general public and all rights are reserved by the World Health Organization. The document may not be reviewed, abstracted, quoted, reproduced or translated, in part or in whole, without the prior written permission of WHO. No part of this document may be stored in a retrieval system or transmitted in any form or by any means – electronic, mechanical or other without the prior written permission of WHO. The views expressed in documents by named authors are solely the responsibility of those authors. (or The authors alone are responsible for the views expressed in this document) WHO/SDE/WSH/02.07 Distr.: Limited English only Managing Water in the Home: Accelerated Health Gains from Improved Water Supply Prepared by: Professor Mark D. Sobsey Department of Environmental Sciences and Engineering School of Public Health University of North Carolina Chapel Hill North Carolina 27599-7400 USA Tel: +1 919 966 7303 Fax: +1 919 966 4711 E-mail: [email protected] TABLE OF CONTENTS Page Foreword .................................................................................................................................................................. -
Chloramine-T [127-65-1] and Metabolite P-Toluenesulfonamide [70-55-3]
Chloramine-T [127-65-1] and Metabolite p-Toluenesulfonamide [70-55-3] Review of Toxicological Literature February 2002 Chloramine-T [127-65-1] and Metabolite p-Toluenesulfonamide [70-55-3] Review of Toxicological Literature Prepared for Scott Masten, Ph.D. National Institute of Environmental Health Sciences P.O. Box 12233 Research Triangle Park, North Carolina 27709 Contract No. N01-ES-65402 Submitted by Karen E. Haneke, M.S. Integrated Laboratory Systems P.O. Box 13501 Research Triangle Park, North Carolina 27709 February 2002 Toxicological Summary for Chloramine-T [127-65-1] and p-Toluenesulfonamide [70-55-3] Feb/02 Executive Summary Nomination Chloramine-T was nominated by a small commercial organization for toxicology studies based on its current status as an Investigational New Animal Drug (INAD) for controlling proliferative gill disease and bacterial gill disease in aquaculture and the need for additional toxicology studies to support it’s safe use. The metabolite p-Toluenesulfonamide (p-TSA) is of importance as the primary residue of chloramine-T in chloramine-T treated fish intended for human consumption. Non-toxicological Information Chloramine-T, as an anti-microbial agent, has had widespread use in a broad range of practices, including medical, dental, veterinary, food processing, and agricultural. As a disinfectant, it is used to disinfect surfaces and instruments. Chloramine-T has a low degree of cytotoxicity and has been used in direct contact with tissues. As such, it is used in the treatment of burns, in whirlpools for the treatment of wounds, and as an oral mouthwash. In agricultural practices, chloramine-T has been approved as a broad spectrum biocide for foot-and-mouth disease, swine vesicular disease, diseases of poultry, and tuberculosis in the United Kingdom, and is used in numerous branches of industry such as intensive farming, slaughterhouses, and kitchens. -
6. Water Treatment 71 6
6. WATER TREATMENT 71 6. Water treatment 6.1 Introduction Water can be contaminated by the following agents: ■ Pathogens – disease-causing organisms that include bacteria, amoebas and viruses, as well as the eggs and larvae of parasitic worms. ■ Harmful chemicals from human activities (industrial wastes, pesticides, fertilizers). ■ Chemicals and minerals from the natural environment, such as arsenic, common salt and fluorides. Some non-harmful contaminants may influence the taste, smell, colour or temperature of water, and make it unacceptable to the community. Water from surface sources is often contaminated by microbes, whereas groundwater is normally safer, but even groundwater can be contaminated by harmful chemicals from human activities or from the natural environment. Rainwater captured by a rooftop har- vesting system or with small catchment dams is relatively safe, provided that the first water is allowed to flow to waste when the rainy season starts. The amount of water to be treated should also be assessed. This can be estimated by assuming that each person will need a minimum of 20–50 litres of water a day for drinking, cooking, laundry and per- sonal hygiene. A community should be consulted when choosing a water-treatment system and should be made aware of the costs associated with the technology. In particular, community members should be made aware of the behavioural and/or cultural changes needed to make the system effective over the long-term and thus be acceptable to them. Communi- ties may also need to be educated about protecting water sources from animal or human contamination, and mobilized. It should be emphasized that all the positive effects of a water-treatment system could be jeopardized if the water is not drawn, stored and trans- ported carefully and hygienically. -
PURIFICATION of WATER on a SMALL SCALE by Major H
J R Army Med Corps: first published as 10.1136/jramc-93-04-03 on 1 October 1949. Downloaded from 187 PURIFICATION OF WATER ON A SMALL SCALE BY Major H. J. ANDERSON Royal Army Medical Oorps THIS rather ,brief title refers mainly to the purification of'water by the individual for his own personal consumption. In these days of extensive public supplies, and national water policies, it is obvious that such a method of purification has certainly very limited uses, and that the problem is therefore confined almost entirely to the Services. As large-scale purification plants have developed due to the increasiIig tendency of the population to gather together in large cities, so, as the speed of travel increases and the range and mobility of activity of our fighting, forces becomes more extensive, must improvements at the individual level continue to be sought. guest. Protected by copyright. , The realization that purification of water, for drinking purposes for any community, was essential, came towards the end oflast century. It is interesting, at the commencement, to see how the supply of water has developed, to trace the knowledge so acquired from the consequent lessening of disease in large communities to its application to smaller groups of mobile forces, and thence to the individual thrown on his own resources, frequently in extremely difficult circumstances. For, as the fear of disease has in the past forced Governments into action, so a Commander in the Field, equally fearing'disease as he realizes it ci:m destroy his forces more effectively th,an any enemy, demands similar protection for his men. -
Redox Potential Measurements for Determining the Disinfecting Power of Chlorinated Water by K
J. Hyg., Camb. (1972), 70, 313 313 Printed in Great Britain Redox potential measurements for determining the disinfecting power of chlorinated water BY K. VICTORIN, K.-G. HELLSTROM AND R. RYLANDER Department of Environmental Hygiene, The National Institute of Public Health and the Institute of Hygiene, Karolinslca Institute, Stockholm, Sweden (Received 18 October 1971) SUMMARY The kill of Escherichia coli within 3 min. was studied in chlorine-demand-free water using sodium hypochlorite, monochloramine, dichloramine, halazone, chloramine T, cyanuric acid + sodium hypochlorite and cyanuric acid + mono- chloramine. The redox potential and the available chlorine were measured. The redox potential was found to be better correlated with the disinfecting property of the water than was the amount of available chlorine. For individual pure chlorine compounds, the measuring of available chlorine showed in general a somewhat better correlation with reduction of the bacteria than the redox potential showed. INTRODUCTION The most important disinfection agent for tap water, swimming-pool water and waste water is chlorine, which usually is added in the form of gaseous chlorine or hypochlorite. The activity of the chlorine compounds is expressed as the amount of pure gaseous chlorine with a corresponding oxidizing power [(chlorine equi- valents). Most waters contain substances which can reduce chlorine (the' chlorine demand' of the water). When ammonium ions are present inorganic chloramines are formed. The relative amounts of monochloramine, dichloramine and nitrogen trichloride depend upon the pH of the water. In addition, chlorine can form organic chlor- amines with nitrogenous organic compounds. These inorganic and organic chlor- amines are called combined residual chlorine.