2004 Doping Control Annual Report
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Synthesis, Physicochemical Characterization and Study of the Antimicrobial Activity of Chlorobutanol H
World Academy of Science, Engineering and Technology International Journal of Pharmacological and Pharmaceutical Sciences Vol:12, No:3, 2018 Synthesis, Physicochemical Characterization and Study of the Antimicrobial Activity of Chlorobutanol H. Nadia, G. Bahdja, S. Thili Malha, Y. Zahoua, D. Taoufik, B. Mourad, M. Marzouk, F. Z. Hadjadj Aoul, L. R. Mekacher I. INTRODUCTION Abstract—Introduction and objectives: Chlorobutanol is a raw XCIPIENTS play a vital role in the design, manufacture material, mainly used as an antiseptic and antimicrobial preservative and preservation of drugs. The addition of an in injectable and ophthalmic preparations. The main objective of our E study was the synthesis and evaluation of the antimicrobial activity of antimicrobial agents is of great interest in the case where the chlorobutanol hemihydrates. Material and methods: Chlorobutanol pharmaceutical preparations do not have adequate was synthesized according to the nucleophilic addition reaction of antimicrobial properties, (especially aqueous preparations), to chloroform to acetone, identified by an infrared absorption using prevent proliferation or limit microbial contamination [1], [2]. Spectrum One FTIR spectrometer, melting point, Scanning electron Chlorobutanol is a trihalogen alcohol with bacteriostatic and microscopy and colorimetric reactions. The dosage of Carvedilol fungistatic activity. The main objective of our work was to active substance was carried out by assaying the degradation products of chlorobutanol in a basic solution. The chlorobutanol obtained was obtain chlorobutanol hemihydrate by chemical synthesis, its subjected to bacteriological tests in order to study its antimicrobial purification and characterization as well as the study of its activity. The antibacterial activity was evaluated against strains such antimicrobial activity. as Escherichia coli (ATCC 25 922), Staphylococcus aureus (ATCC 25 923) and Pseudomonas aeroginosa (ATCC = American type II. -
)&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 -
CAS No.) Screening Justification Is Public Comment Now Open? CAS No
EGLE Air Quality Division (AQD) Air Toxics Screening Level Justifications (Numerically by CAS No.) Screening Justification Is Public Comment Now Open? CAS No. Chemical Name Level & Responses Info E-Mail AQD Deadline None ad acid View View Not Open for Public Comment None amyl acetate (mixture) View View Not Open for Public Comment None atlox 848 View View Not Open for Public Comment None biosam tp-1.5 View View Not Open for Public Comment None calcium chloride View View Not Open for Public Comment None epoxy resin solution View View Not Open for Public Comment None heptamethyl-1-vinyl-1,7-dichlorotetrasilazane View View Not Open for Public Comment None n-butylglucamine View View Not Open for Public Comment None n-chloro-2,6-difluorobenzamide View View Not Open for Public Comment None trichloroethylene View View Not Open for Public Comment None triethylammonium suleptanate View View Not Open for Public Comment 50-00-0 formaldehyde View View Not Open for Public Comment 50-03-3 hydrocortisone acetate View View Not Open for Public Comment 50-21-5 lactic acid View View Not Open for Public Comment 50-28-2 estradiol View View Not Open for Public Comment 50-29-3 ddt View View Not Open for Public Comment 50-32-8 benzo(a)pyrene View View Not Open for Public Comment 51-28-5 2,4-dinitrophenol View View Not Open for Public Comment 53-36-1 methyl predisolone acetate View View Not Open for Public Comment 53-70-3 dibenz(a,h)anthracene View View Not Open for Public Comment 56-23-5 carbon tetrachloride View View Not Open for Public Comment 56-49-5 3-methylcholanthrene View View Not Open for Public Comment 56-55-3 benz(a)anthracene View View Not Open for Public Comment 56-81-5 glycerol View View Not Open for Public Comment 57-11-4 stearic acid View View Not Open for Public Comment Revised Monday, September 27, 2021 Page 1 of 51 EGLE Air Quality Division (AQD) Air Toxics Screening Level Justifications (Numerically by CAS No.) Screening Justification Is Public Comment Now Open? CAS No. -
Guide to Extractables in Effluents from Ultipor® N66 and Posidyne® Filter
Validation Guide USTR 2521 Guide to Extractables in Effluents from Pall Ultipor ® N66 and Posidyne ® Filter Cartridges Contents 1. Introduction ........................................................................................................................3 2. Design and Manufacture of Pall N66 Pharmaceutical-rated (P-rated) Filters ................3 3. Principles of Extraction and the Non-Volatile Residue Test ............................................3 3.1 Factors Limiting Extraction ............................................................................................3 3.2 Defining Solvent Strength ..............................................................................................4 3.3 Materials of Construction of Ultipor N66 and Posidyne Filter Cartridges ........................5 3.4 Extractable Substances in Polymers Used in Pall Ultipor N66 and Posidyne Filter Cartridges ....................................................................................................5 4. Total Non-volatile Residues Extracted from Ultipor N66 and Posidyne Filters ..............6 4.1 Introduction ....................................................................................................................6 4.2 Summary of Method ......................................................................................................6 4.3 Results ..........................................................................................................................6 4.4 Conclusions ..................................................................................................................6 -
United States Patent Office Patented Aug
2,760,990 United States Patent Office Patented Aug. 28, 1956 acid. If an acid group other than acetate is desired, mercury acetate and higher boiling carboxylic acid may 2,760,990 be intimately mixed together and the mixture is taken VNY TRANSETHERFICATION up with the starting vinyl ether. At this point the 5 mixture may be heated with stripping off of acetic acid. Warren H. Watanabe, Philadelphia, Pa., and Lawrence The reacting alcohol is then added and the mixture heated. E. Conlon, Moorestown, N.J., assignors to Rohm & Alternatively mercury acetate, carboxylic acid, vinyl Haas Company, Philadelphia, Pa., a corporation of ether, and alcohol are mixed and heated. Acetic acid Delaware may now be distilled off. The preparation of catalyst in No Drawing. Application August 15, 1952, O these ways, gives a highly active material, effective even Serial No. 304,648 at elevated temperatures. Another method of forming transetherifying catalysts 9 Claims. (C.260-614) is to mix together a common mercury salt of a strong acid, such as mercuric sulfate, and an alkali metal salt This invention concerns a process for preparing vinyl 5 of a desired carboxylic acid. Thus mercuric sulfate may ethers by transetherifying other vinyl ethers with alcohols be mixed with sodium oleate, or sodium benzoate, or in the presenec of soluble mercury salts of weak acids. It sodium ethylbutyrate. Such mixtures simulate the mer also deals with novel vinyl ethers, cury salts of weak acids, although they still give consid It has been proposed that volatile vinyl alkyl ethers erable acetal formation. in which the alkyl group is primary be reacted with pri 20 When alcohols are used which are acid sensitive, or mary or secondary monohydric alcohols: consisting of which are unstable to acid, or which decompose to give. -
Papaverine Hydrochloride Injection, Solution American Regent, Inc
PAPAVERINE HYDROCHLORIDE- papaverine hydrochloride injection, solution American Regent, Inc. Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here. ---------- PAPAVERINE HYDROCHLORIDE INJECTION, USP Rx Only This product is to be used by or under the direction of a physician. Each vial contains a sufficient amount to permit withdrawal and administration of the volume specified on the label. DESCRIPTION Papaverine Hydrochloride, USP, is the hydrochloride of an alkaloid obtained from opium or prepared synthetically. It belongs to the benzylisoquinoline group of alkaloids. It does not contain a phenanthrene group as do morphine and codeine. Papaverine Hydrochloride, USP, is 6,7-dimethoxy-1- veratrylisoquinoline hydrochloride and contains, on the dried basis, not less than 98.5% of C20H21NO4•HCI. The molecular weight is 375.85. The structural formula is as shown. Papaverine Hydrochloride occurs as white crystals or white crystalline powder. One gram dissolves in about 30 mL of water and in 120 mL of alcohol. It is soluble in chloroform and practically insoluble in ether. Papaverine Hydrochloride Injection, USP, is a clear, colorless to pale-yellow solution. Papaverine Hydrochloride, for parenteral administration, is a smooth-muscle relaxant that is available in vials containing 30 mg/mL. Each vial also contains edetate disodium 0.005%. The 10 mL vials also contain chlorobutanol 0.5% as a preservative. pH may be adjusted with sodium citrate and/or citric acid. CLINICAL PHARMACOLOGY The most characteristic effect of papaverine is relaxation of the tonus of all smooth muscle, especially when it has been spasmodically contracted. -
Fast Facts Core Curriculum Wounds and Oral Care
Fast Facts Core Curriculum Wounds and Oral Care #37 Pruritus . .2-3 #40 Pressure Ulcer Management: Staging and Prevention . 4-5 #41 Pressure Ulcers: Debridement and Dressings . .6-7 #46 Malignant Wounds . 8-9 #121 Oral Mucositis: Diagnosis and Assessment . .10-11 #130 Oral Mucositis: Prevention and Treatment . 12-13 #147 Oropharyngeal Candidiasis . 14-15 #182 Xerostomia . 16-17 #218 Managing Wound Odor . 18-20 #249 Topical Nonsteroidal Anti-Inflammatory Drugs . 21-22 #250 Tracheostomy Care . .23-25 #281 Care of the Post-Laryngectomy Stoma . .26-28 1 #327 Topical Treatments for Acute and Chronic Wound Pain . .29-31 2 ! FAST FACTS AND CONCEPTS #37 PRURITUS Charles von Gunten MD and Frank Ferris MD Background Pruritus (itching) is a common and often distressing symptom near the end of life. The itch sensation may arise from stimulation of the skin itch receptor via unmyelinated C fibers, or itch may arise as a central phenomenon without skin involvement (e.g. opioid induced pruritus). Although histamine causes pruritus, many patients with pruritis show no signs of histamine release. Besides histamine, serotonin, prostaglandins, kinins, proteases and physical stimuli have all been implicated as mediators of pruritus. Common Causes • Dermatological (dryness, wetness, irritation, eczema, psoriasis) • Metabolic (hepatic failure, renal failure, hypothyroidism) • Hematologic (iron deficiency, polycythemia, thrombocytosis, leukemia, lymphoma) • Drugs (opioids, aspirin, drug reactions) • Infectious (scabies, lice, candida) • Allergy (urticaria, contact dermatitis, drug reactions) • Psychogenic Management Management of pruritus involves eliminating the cause when possible. Symptomatic strategies include: • Moisturizers: Dryness (xerosis) is very common and may exacerbate other causes. The mainstay of treatment is skin hydration. -
EUROPEAN PHARMACOPOEIA 10.0 Index 1. General Notices
EUROPEAN PHARMACOPOEIA 10.0 Index 1. General notices......................................................................... 3 2.2.66. Detection and measurement of radioactivity........... 119 2.1. Apparatus ............................................................................. 15 2.2.7. Optical rotation................................................................ 26 2.1.1. Droppers ........................................................................... 15 2.2.8. Viscosity ............................................................................ 27 2.1.2. Comparative table of porosity of sintered-glass filters.. 15 2.2.9. Capillary viscometer method ......................................... 27 2.1.3. Ultraviolet ray lamps for analytical purposes............... 15 2.3. Identification...................................................................... 129 2.1.4. Sieves ................................................................................. 16 2.3.1. Identification reactions of ions and functional 2.1.5. Tubes for comparative tests ............................................ 17 groups ...................................................................................... 129 2.1.6. Gas detector tubes............................................................ 17 2.3.2. Identification of fatty oils by thin-layer 2.2. Physical and physico-chemical methods.......................... 21 chromatography...................................................................... 132 2.2.1. Clarity and degree of opalescence of -
Safety Data Sheet - Version 5.0 Preparation Date 5/8/2017 Latest Revision Date (If Revised) 2/24/2021 SDS Expiry Date 2/23/2024
Safety Data Sheet - Version 5.0 Preparation Date 5/8/2017 Latest Revision Date (If Revised) 2/24/2021 SDS Expiry Date 2/23/2024 1. IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND OF THE COMPANY/UNDERTAKING 1.1 Product Identifier Chemical Name Chlorbutanol Hemihydrate Catalogue # C364795 1.2 Relevant Identified Uses of the Substance or Mixture and Uses Advised Against Product Uses To be used only for scientific research and development. Not for use in humans or animals. 1.3 Details of the Supplier of the Safety Data Sheet Company Toronto Research Chemicals 2 Brisbane Road Toronto, ON M3J 2J8 CANADA Telephone +14166659696 FAX +14166654439 Email [email protected] 1.4 Emergency Telephone Number Emergency# +1(416) 665-9696 between 0800-1700 (GMT-5) 2. HAZARDS IDENTIFICATION 2.1/2.2 Classification of the Substance or Mixture and Label Elements GHS Hazards Classification (According to EU Regulation 1272/2008 and US OSHA 1910.1200) Acute Toxicity, Oral (Category 4) GHS Hazards Identification (According to EU Regulation 1272/2008 and US OSHA 1910.1200) Signal Word Warning GHS Hazard Statements H302 Harmful if swallowed. GHS Precautionary Statements P264 Wash hands thoroughly after handling. P270 Do no eat, drink or smoke when using this product. P301/P312 IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell. P330 Rinse mouth. 2.3 Unclassified Hazards/Hazards Not Otherwise Classified No data available. 3. COMPOSITION/INFORMATION ON INGREDIENTS 3.1 Substances Molecular Formula: C4H7Cl3O•0.5[H2O] Molecular Weight: 177.46 [Anhydrous] -
Pharmaceutical Compoundingand Dispensing, Second
Pharmaceutical Compounding and Dispensing Pharmaceutical Compounding and Dispensing SECOND EDITION John F Marriott BSc, PhD, MRPharmS, FHEA Professor of Clinical Pharmacy Aston University School of Pharmacy, UK Keith A Wilson BSc, PhD, FRPharmS Head of School Aston University School of Pharmacy, UK Christopher A Langley BSc, PhD, MRPharmS, MRSC, FHEA Senior Lecturer in Pharmacy Practice Aston University School of Pharmacy, UK Dawn Belcher BPharm, MRPharmS, FHEA Teaching Fellow, Pharmacy Practice Aston University School of Pharmacy, UK Published by the Pharmaceutical Press 1 Lambeth High Street, London SE1 7JN, UK 1559 St Paul Avenue, Gurnee, IL 60031, USA Ó Pharmaceutical Press 2010 is a trade mark of Pharmaceutical Press Pharmaceutical Press is the publishing division of the Royal Pharmaceutical Society of Great Britain First edition published 2006 Second edition published 2010 Typeset by Thomson Digital, Noida, India Printed in Great Britain by TJ International, Padstow, Cornwall ISBN 978 0 85369 912 5 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, without the prior written permission of the copyright holder. The publisher makes no representation, express or implied, with regard to the accuracy of the information contained in this book and cannot accept any legal responsibility or liability for any errors or omissions that may be made. The right of John F Marriott, Keith A Wilson, Christopher A Langley and Dawn Belcher to be identified as the author of this work has been asserted by them in accordance with the Copyright, Designs and Patents Act, 1988. -
(12) Patent Application Publication (10) Pub. No.: US 2013/02254.12 A1 Sardari Lodriche Et Al
US 20130225412A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2013/02254.12 A1 Sardari Lodriche et al. (43) Pub. Date: Aug. 29, 2013 (54) SILICON NANOCARRIER FOR DELIVERY A613 L/702 (2006.01) OF DRUG, PESTICIDES AND HERBICIDES, A6IP3 L/10 (2006.01) AND FOR WASTE WATER TREATMENT A6IP3/04 (2006.01) A6IP35/00 (2006.01) (76) Inventors: Soroush Sardari Lodriche, Tehran (IR): AOIP3/00 (2006.01) Saeed Soltani, Tehran (IR); Roghieh AOIPI3/00 (2006.01) Mirzazadeh, Tehran (IR) BOI 20/22 (2006.01) AOIN 25/08 (2006.01) (21) Appl. No.: 13/406,538 (52) U.S. Cl. USPC ........... 504/322:504/358:504/326; 514/394; (22) Filed: Feb. 28, 2012 514/383: 514/177: 514/274: 514/254.07; 514/110: 514/197; 514/165; 514/253.08: Publication Classification 514/21.1: 514/31; 514/343; 514/61; 424/400; 252/18O (51) Int. Cl. A6 IK9/00 (2006.01) (57) ABSTRACT AOIN37/22 (2006.01) The various embodiments herein provide a nano silicon car AOIN33/06 (2006.01) rier as a drug delivery mechanism. The nano silicon carrier AOIN 43/32 (2006.01) comprises a diatom frustules loaded with a drug molecule to AOIN 43/653 (2006.01) be released at the target site. The diatom frustules are of A 6LX3/57 (2006.01) Hannaea arcus and Navicula inflexia species of diatom. The A6 IK3I/53 (2006.01) pore size of the diatom frustules is 1 to 100 nm. The diatom A6 IK3I/496 (2006.01) frustules are comb-like in structure. -
Mar. Biol. Ass. India, 1965, 8 (1): 28-56 EFFECTS OF
/. Mar. biol. Ass. India, 1965, 8 (1): 28-56 EFFECTS OF ANAESTHETICS ON THE BEHAVIOUR OF MULLET FINGERLINGS AND THE SCOPE OF USING THESE IN DIFFERENT FISHERY PROCEDURES-!* By V. S. DURVE** AND S. K. DHARMA RAJA Central Marine Fisheries Research Institute, Mandapam Camp INTRODUCTION THE use of anaesthetics in fishery work, mainly in the transport of live-fish and also in handling fish for tagging, fin-clipping, weighing and stripping has been recognised by fishery workers everywhere. In live-fish transport, anaesthetics are useful in lowering the metabolic activity of fish, which facilitates the transport of more fish in a given quantity of water for a longer time. It has also been proved that anaes thetics make the otherwise time consuming work of tagging and fin-clipping much easier and also lower the mortality of the fish due to handling. Considerable effort has gone into a search for a proper anaesthetic and its different concentrations to give varying degrees of anaesthesia useful for works from tagging to transport of live-fish. Several methods have been used to produce anaesthesia. Abramowitz (1937), Parker (1937, 1939), Abramowitz et al. (1940) Osborn (1938, 1941) immersed fishes in crushed ice or ice water. Haskell (1940) employed electric shock to produce a paralysis lasting about two minutes. It is doubtful whether the anaesthesia induced by these methods is similar to that induced by chemicals. The disadvantages of such methods have been discussed by Pickford and Atz (1957). Chemicals used to anaesthetize fishes include Ether, Urethane, Chlorobutanol, MS-222 SANDOZ, Sodium Amytal and Chloral Hydrate, besides 8 to 9 others.