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Hypochlorous Acid Handling
Hypochlorous Acid Handling 1 Identification of Petitioned Substance 2 Chemical Names: Hypochlorous acid, CAS Numbers: 7790-92-3 3 hypochloric(I) acid, chloranol, 4 hydroxidochlorine 10 Other Codes: European Community 11 Number-22757, IUPAC-Hypochlorous acid 5 Other Name: Hydrogen hypochlorite, 6 Chlorine hydroxide List other codes: PubChem CID 24341 7 Trade Names: Bleach, Sodium hypochlorite, InChI Key: QWPPOHNGKGFGJK- 8 Calcium hypochlorite, Sterilox, hypochlorite, UHFFFAOYSA-N 9 NVC-10 UNII: 712K4CDC10 12 Summary of Petitioned Use 13 A petition has been received from a stakeholder requesting that hypochlorous acid (also referred 14 to as electrolyzed water (EW)) be added to the list of synthetic substances allowed for use in 15 organic production and handling (7 CFR §§ 205.600-606). Specifically, the petition concerns the 16 formation of hypochlorous acid at the anode of an electrolysis apparatus designed for its 17 production from a brine solution. This active ingredient is aqueous hypochlorous acid which acts 18 as an oxidizing agent. The petitioner plans use hypochlorous acid as a sanitizer and antimicrobial 19 agent for the production and handling of organic products. The petition also requests to resolve a 20 difference in interpretation of allowed substances for chlorine materials on the National List of 21 Allowed and Prohibited Substances that contain the active ingredient hypochlorous acid (NOP- 22 PM 14-3 Electrolyzed water). 23 The NOP has issued NOP 5026 “Guidance, the use of Chlorine Materials in Organic Production 24 and Handling.” This guidance document clarifies the use of chlorine materials in organic 25 production and handling to align the National List with the November, 1995 NOSB 26 recommendation on chlorine materials which read: 27 “Allowed for disinfecting and sanitizing food contact surfaces. -
Pathologic Patterns of the Sebaceous Gland* John S
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector PATHOLOGIC PATTERNS OF THE SEBACEOUS GLAND* JOHN S. STRAUSS, M.D.t AND ALBERT M. KLIGMAN, M.D. By studying the way in which a structurecells which subsequently rupture in the fundus reacts to an imposed experimental stress, oneof the gland. Fragments of the thin eosinophilie can often better understand the changes ex-cell wall, which morphologically resemble kera- hibited in spontaneous dlsease. Much has beentin, persist in the sebum; occasionally the entire learned about the potentialities of the eccrinecell walls survive as ghosts. Furthermore, the in- and apocrine sweat units in this fashion (1—12).dividual oil droplets are separated by keratin- Previous study of the response to injury in thelike trabeculae. A dual potentiality is exhibited sebaceous gland has been restricted mainly to theby sebaceous cells in their capacity to produce changes that occur in the sebaceous duct per sefat predominantly and keratin to a minor de- (13). In this study we have followed the reac-gree. Epidermal cells have this bipotentiality tion of the sebaceous gland itself to a variety ofwith keratin as the major product. cutaneous insults and have correlated the findings with those which occur in disease states. MA.TERIALS AND METRODS The scalp and cheek of post-puberal individuals MOBPOLOGY AND FUNCTION OF were selected for study because the glands here TRN SEACEOUS GLAND are among the largest and most numerous. Biopsy 1.Morphology: The glands of the glabrous skinspecimens were obtained before the experimental are not free but are associated with hair follicles,stresses as well as at varying intervals afterwards. -
Study Guide Medical Terminology by Thea Liza Batan About the Author
Study Guide Medical Terminology By Thea Liza Batan About the Author Thea Liza Batan earned a Master of Science in Nursing Administration in 2007 from Xavier University in Cincinnati, Ohio. She has worked as a staff nurse, nurse instructor, and level department head. She currently works as a simulation coordinator and a free- lance writer specializing in nursing and healthcare. All terms mentioned in this text that are known to be trademarks or service marks have been appropriately capitalized. Use of a term in this text shouldn’t be regarded as affecting the validity of any trademark or service mark. Copyright © 2017 by Penn Foster, Inc. All rights reserved. No part of the material protected by this copyright may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without permission in writing from the copyright owner. Requests for permission to make copies of any part of the work should be mailed to Copyright Permissions, Penn Foster, 925 Oak Street, Scranton, Pennsylvania 18515. Printed in the United States of America CONTENTS INSTRUCTIONS 1 READING ASSIGNMENTS 3 LESSON 1: THE FUNDAMENTALS OF MEDICAL TERMINOLOGY 5 LESSON 2: DIAGNOSIS, INTERVENTION, AND HUMAN BODY TERMS 28 LESSON 3: MUSCULOSKELETAL, CIRCULATORY, AND RESPIRATORY SYSTEM TERMS 44 LESSON 4: DIGESTIVE, URINARY, AND REPRODUCTIVE SYSTEM TERMS 69 LESSON 5: INTEGUMENTARY, NERVOUS, AND ENDOCRINE S YSTEM TERMS 96 SELF-CHECK ANSWERS 134 © PENN FOSTER, INC. 2017 MEDICAL TERMINOLOGY PAGE III Contents INSTRUCTIONS INTRODUCTION Welcome to your course on medical terminology. You’re taking this course because you’re most likely interested in pursuing a health and science career, which entails proficiencyincommunicatingwithhealthcareprofessionalssuchasphysicians,nurses, or dentists. -
CHAPTER 4 the Integumentary System
CHAPTER 4 The Integumentary System LEARNING OBJECTIVES Upon completion of this chapter, you should be able to: • Name the two layers of the skin. • Name the accessory structures of the integumentary system. • Build and pronounce medical terms of the integumentary system. • Name the disorders and treatments relating to the integumentary system. • Name the major classifi cations of pharmacologic agents used to treat skin disorders. • Analyze and defi ne the new terms introduced in this chapter. • Interpret abbreviations associated with the integumentary system. 53 54 PART TWO • BODY SYSTEMS Introduction The largest organ of the body is the skin. The skin covers the entire body—more than 20 square feet on average—and weighs about 24 pounds. It is part of the integumentary system, which also includes the accessory structures: hair, nails, and sebaceous (oil) and sudoriferous (sweat) glands. Integumentum is Latin for “covering” or “shelter.” The physician who specializes in the diag- nosis and treatment of skin disorders is called a dermatologist (dermat/o being one of the com- bining forms for skin). Coupling the root dermat/o with the previously learned suffi x -logy gives us the term dermatology , which is the term for the specialty practice that deals with the skin. Word Elements The major word elements that relate to the integumentary system consist of various anatomical components, accessory structures, colors of the skin, and abnormal conditions. The Word Ele- ments table lists many of the roots, their meanings, and examples associated -
Nomina Histologica Veterinaria, First Edition
NOMINA HISTOLOGICA VETERINARIA Submitted by the International Committee on Veterinary Histological Nomenclature (ICVHN) to the World Association of Veterinary Anatomists Published on the website of the World Association of Veterinary Anatomists www.wava-amav.org 2017 CONTENTS Introduction i Principles of term construction in N.H.V. iii Cytologia – Cytology 1 Textus epithelialis – Epithelial tissue 10 Textus connectivus – Connective tissue 13 Sanguis et Lympha – Blood and Lymph 17 Textus muscularis – Muscle tissue 19 Textus nervosus – Nerve tissue 20 Splanchnologia – Viscera 23 Systema digestorium – Digestive system 24 Systema respiratorium – Respiratory system 32 Systema urinarium – Urinary system 35 Organa genitalia masculina – Male genital system 38 Organa genitalia feminina – Female genital system 42 Systema endocrinum – Endocrine system 45 Systema cardiovasculare et lymphaticum [Angiologia] – Cardiovascular and lymphatic system 47 Systema nervosum – Nervous system 52 Receptores sensorii et Organa sensuum – Sensory receptors and Sense organs 58 Integumentum – Integument 64 INTRODUCTION The preparations leading to the publication of the present first edition of the Nomina Histologica Veterinaria has a long history spanning more than 50 years. Under the auspices of the World Association of Veterinary Anatomists (W.A.V.A.), the International Committee on Veterinary Anatomical Nomenclature (I.C.V.A.N.) appointed in Giessen, 1965, a Subcommittee on Histology and Embryology which started a working relation with the Subcommittee on Histology of the former International Anatomical Nomenclature Committee. In Mexico City, 1971, this Subcommittee presented a document entitled Nomina Histologica Veterinaria: A Working Draft as a basis for the continued work of the newly-appointed Subcommittee on Histological Nomenclature. This resulted in the editing of the Nomina Histologica Veterinaria: A Working Draft II (Toulouse, 1974), followed by preparations for publication of a Nomina Histologica Veterinaria. -
Glossary of Hazardous Materials Terms
GLOSSARY OF CHEMICAL HAZARD TERMS ACGIH - The American Conference of Governmental Industrial Hygienists consists of occupational safety and health professionals who recommend occupational exposure limits for many substances. Action Level - An OSHA concentration calculated as an 8-your time-weighted average, which initiates certain required activities such as exposure monitoring and medical surveillance. Acute Health Effect - A severe effect which occurs rapidly after a brief intense exposure to a substance. ANSI - American National Standards Institute is a private group that develops consensus standards. Acute toxicity -Acutely toxic substances cause adverse effects by any of the following exposure methods: 1. Oral or dermal administration of a single dose of a substance. 2. Multiple oral or dermal doses within a 24-hour period 3. An inhalation exposure of 4 hours. Asphyxiant - A chemical (gas or vapor) that can cause death or unconsciousness by suffocation. Aspiration hazard - A liquid or solid chemical that causes severe acute effects if it infiltrates into the trachea and lower respiratory tract. Possible effects include chemical pneumonia, pulmonary injury, or death Autoignition Temperature - The lowest temperature at which a substance will burst into flames without a source of ignition like a spark or flame. The lower the ignition temperature, the more likely the substance is going to be a fire hazard. Boiling Point - The temperature of a liquid at which its vapor pressure is equal to the gas pressure over it. With added energy, all of the liquid could become vapor. Boiling occurs when the liquid's vapor pressure is just higher than the pressure over it. Carcinogen - A substance that causes cancer in humans or, because it has produced cancer in animals, is considered capable of causing cancer in humans. -
Analyzing Binding Data UNIT 7.5 Harvey J
Analyzing Binding Data UNIT 7.5 Harvey J. Motulsky1 and Richard R. Neubig2 1GraphPad Software, La Jolla, California 2University of Michigan, Ann Arbor, Michigan ABSTRACT Measuring the rate and extent of radioligand binding provides information on the number of binding sites, and their afÞnity and accessibility of these binding sites for various drugs. This unit explains how to design and analyze such experiments. Curr. Protoc. Neurosci. 52:7.5.1-7.5.65. C 2010 by John Wiley & Sons, Inc. Keywords: binding r radioligand r radioligand binding r Scatchard plot r r r r r r receptor binding competitive binding curve IC50 Kd Bmax nonlinear regression r curve Þtting r ßuorescence INTRODUCTION A radioligand is a radioactively labeled drug that can associate with a receptor, trans- porter, enzyme, or any protein of interest. The term ligand derives from the Latin word ligo, which means to bind or tie. Measuring the rate and extent of binding provides information on the number, afÞnity, and accessibility of these binding sites for various drugs. While physiological or biochemical measurements of tissue responses to drugs can prove the existence of receptors, only ligand binding studies (or possibly quantitative immunochemical studies) can determine the actual receptor concentration. Radioligand binding experiments are easy to perform, and provide useful data in many Þelds. For example, radioligand binding studies are used to: 1. Study receptor regulation, for example during development, in diseases, or in response to a drug treatment. 2. Discover new drugs by screening for compounds that compete with high afÞnity for radioligand binding to a particular receptor. -
International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification
0031-6997/03/5504-597–606$7.00 PHARMACOLOGICAL REVIEWS Vol. 55, No. 4 Copyright © 2003 by The American Society for Pharmacology and Experimental Therapeutics 30404/1114803 Pharmacol Rev 55:597–606, 2003 Printed in U.S.A International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on Terms and Symbols in Quantitative Pharmacology RICHARD R. NEUBIG, MICHAEL SPEDDING, TERRY KENAKIN, AND ARTHUR CHRISTOPOULOS Department of Pharmacology, University of Michigan, Ann Arbor, Michigan (R.R.N.); Institute de Recherches Internationales Servier, Neuilly sur Seine, France (M.S.); Systems Research, GlaxoSmithKline Research and Development, Research Triangle Park, North Carolina (T.K.); and Department of Pharmacology, University of Melbourne, Parkville, Australia (A.C.) Abstract ............................................................................... 597 I. Introduction............................................................................ 597 II. Working definition of a receptor .......................................................... 598 III. Use of drugs in definition of receptors or of signaling pathways ............................. 598 A. The expression of amount of drug: concentration and dose ............................... 598 1. Concentration..................................................................... 598 2. Dose. ............................................................................ 598 B. General terms used to describe drug action ........................................... -
First Principles and Their Application to Drug Discovery
REVIEWS Drug Discovery Today Volume 17, Numbers 1/2 January 2012 The utilization of the kinetic and thermodynamic signatures of preclinical leads is proving pivotal in their triage and rational optimization towards clinical candidates with maximal in vivo efficacy devoid of adverse events. Reviews KEYNOTE REVIEW Target–drug interactions: first principles and their application to drug discovery 1 1 Sara Nu´n˜ez studied organic Sara Nu´n˜ ez , Jennifer Venhorst and Chris G. Kruse chemistry at the University of Barcelona (Spain) and the Abbott Healthcare Products, 1381 CP Weesp, The Netherlands University of London (UK). She received her Ph.D. in 2003 from the University of Manchester (UK), and thereafter did a In this review, we begin by introducing the basic principles of kinetics postdoc in Biophysics at the and thermodynamics of target–drug binding within the context of Albert Einstein College of Medicine (USA). In 2005, she drug discovery. In addition, we present a meta-analysis of the recent joined Solvay Pharmaceuticals (now Abbott Healthcare) in The Netherlands as a postdoctoral fellow; and in 2008, she literature describing the kinetic and thermodynamic resolution of was promoted to Sr. Computational Medicinal Chemist. At Abbott, she has supported the medicinal chemistry efforts successful clinical candidates with diverse mechanisms of action. for neuroscience drug discovery programs, from target We finish by discussing the best practices in the triage and chemical discovery up to and including clinical proof of principle studies. She has supported more than 15 programs optimization towards clinical candidates with maximal in vivo internationally, and was project manager of the D2-103 Top Institute Pharma innitiative. -
Us: Not Registered; Import Tolerance Established
United States Office of Prevention, Pesticides Environmental Protection and Toxic Substances Agency (7501C) Pesticide Fact Sheet Name of Chemical: Fenpropimorph Reason for Issuance: New Chemical Tolerance Established Date Issued: March 2006 Description of Chemical Generic Name: rel-(2R,6S)-4-[3-[4-(1,1-dimethylethyl)phenyl]-2 methylpropyl]-2,6-dimethylmorpholine Common Name: Fenpropimorph Trade Name: VOLLEY™ 88OL (foreign) Chemical Class: Morpholine Fungicide EPA Chemical Code: 121402 Chemical Abstracts Service (CAS) Number: 67564-91-4 Registration Status: Not Registered; Import Tolerance Established Pesticide Type: Fungicide U.S. Producer: BASF Corporation Agricultural Products Division 26 Davis Drive, P.O. Box 13528 Research Triangle Park, NC 27709 1 Tolerance Established Tolerances were established for fenpropimorph in the 40 CFR §180.616 for imported bananas at 2.0 ppm. Use Pattern and Formulations Fenpropimorph is a systemic morpholine fungicide which controls Sigatoka diseases (Mycosphaerella spp.) in bananas and plantains imported into the U.S. Fenpropimorph provides protectant and eradicant activity by inhibiting ergosterol biosynthesis. The fungicide, known as VOLLEY™ 880L Fungicide, is proposed for registration in Mexico, Guatemala, Belize, El Salvador, Honduras, Columbia, Nicaragua, Costa Rica, and Panama. There are currently no U.S. tolerances established for residues of fenpropimorph in plant or animal commodities and BASF is not proposing any uses for fenpropimorph on bananas grown in the U.S. TABLE 1 Summary of Current Foreign Use Directions for Fenpropimorph on Imported Bananas 1. End-Use Product Applications (EUP) Timing 2 Maximum Single RTI 3 (Days) PHI 4 [Application Rate/Seasonal Rate2 (Days) Sequence] (kg ai/ha) VOLLEY™ 88OL [1] Raceme single rate = 0.44 NA 5 0 formation maximum seasonal rate = Foliar broadcast spray [2] Raceme 12 1.76 applied 4 times per to underside of leaves development season (ground equipment) or [3] Raceme 44 to foliage canopy development (aerial equipment) [4] M ature mats 12 1. -
Protein Conformational Dynamics Dictate the Binding Affinity for a Ligand
ARTICLE Received 26 Dec 2013 | Accepted 24 Mar 2014 | Published 24 Apr 2014 DOI: 10.1038/ncomms4724 Protein conformational dynamics dictate the binding affinity for a ligand Moon-Hyeong Seo1, Jeongbin Park2, Eunkyung Kim1, Sungchul Hohng2,3,4 & Hak-Sung Kim1 Interactions between a protein and a ligand are essential to all biological processes. Binding and dissociation are the two fundamental steps of ligand–protein interactions, and determine the binding affinity. Intrinsic conformational dynamics of proteins have been suggested to play crucial roles in ligand binding and dissociation. Here, we demonstrate how protein dynamics dictate the binding and dissociation of a ligand through a single-molecule kinetic analysis for a series of maltose-binding protein mutants that have different intrinsic conformational dynamics and dissociation constants for maltose. Our results provide direct evidence that the ligand dissociation is determined by the intrinsic opening rate of the protein. 1 Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea. 2 Department of Physics and Astronomy, Seoul National University, Seoul 151-747, Korea. 3 Department of Biophysics and Chemical Biology, Seoul National University, Seoul 151-747, Korea. 4 National Center for Creative Research Initiatives, Seoul National University, Seoul 151-747, Korea. Correspondence and requests for materials should be addressed to H.-S.K. (email: [email protected]). NATURE COMMUNICATIONS | 5:3724 | DOI: 10.1038/ncomms4724 | www.nature.com/naturecommunications 1 & 2014 Macmillan Publishers Limited. All rights reserved. ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms4724 ransient interactions between a protein and a ligand are central to all biological processes including signal trans- K34C Tduction, cellular regulation and enzyme catalysis. -
Signalling Lecturenotesb-1
Activation of a receptor ligand inactive, monomeric active, dimeric • When activated by growth factor binding, the growth factor receptor tyrosine kinase phosphorylates the neighboring receptor. As we learned, when growth factor binds to the extracellular domain of the growth factor receptor, it causes the receptor to dimerize, which in turn activates the intracellular kinase domain. The kinase domain of one monomer of growth factor receptor phosphorylates tyrosine side chains in the neighboring monomer, and the phosphorylated tyrosines have different structural properties than their unphosphorylated counterparts. You will see on the next slide that the phosphorylated groups on the intracellular domain of growth factor receptor are “recognized” by other proteins. 1 Assembly of the complex adaptor proteins • The phosphorylated receptor recruits other signaling proteins • The phosphorylated amino acids on the receptor are recognized and bound by proteins called adaptor proteins The phosphorylated receptor recruits other signaling proteins, called adaptor proteins, which bind to the phosphorylated amino acids on the receptor. Different adaptor proteins can recognize phosphorylated tyrosines on different proteins (or on different parts of the same protein) because they also contact amino acids adjacent to the phosphorylated tyrosine. That is, they bind only to particular phosphopeptide sequences. Adaptor proteins are so-called because, as we will see, they bind to other proteins, which transmit the information about the altered state of growth factor receptor (the signal) into the cytoplasm by changing the activity of still other proteins. (Think of adaptors for electronic equipment.) 2 The adaptor proteins recruit regulatory proteins Inactive Ras Active Ras Relay signal to cytoplasm Ras Gef adaptor protein The adaptor protein bound to the phosphorylated tyrosine kinase domain of the growth factor receptor recruits Ras Gef, a regulator of the small GTPase Ras As we just discussed, the adaptor proteins that bind to the phosphorylated receptor recruit other proteins.