Environmental Health Criteria 206 Methyl Tertiary-Butyl Ether -J

Total Page:16

File Type:pdf, Size:1020Kb

Environmental Health Criteria 206 Methyl Tertiary-Butyl Ether -J INTERNATIONAL PROGRAMME ON CHEMICAL SAFETY Environmental Health Criteria 206 Methyl tertiary-Butyl Ether -J. l \r LNTER-ORGAN1ZATON PROGRAMME FOR THE SOUND MANAGEMENT OF CHEMICALS I JiVJ A cooperative agreement among UNEP, ILO, FAO, WHO, UNIDO, UNITAR and OECD THE ENVIRONMENTAL HEALTH CRITERIA SERIES Acetaldehyde (No. 167, 1995) Chiorofluorocarbons, partially halogenated Acetonitrile (No. 154, 1993) (ethane derivatives) (No. 139, 1992) Acrolein (No. 127, 1991) (methane derivatives) (No. 126, 1991) Acrylamide (No. 49, 1985) Chloroform (No. 163, 1994) Acrylic acid (No. 191, 1997) Chlorophenols (No. 93, 1989) Acrylonitrile (No. 28, 1983) Chlorothalonil (No. 183, 1996) Aged population, principles for evaluating Chromium (No. 61, 1988) the effects of chemicals (No. 144, 1992) Chrysotile asbestos (No. 203, 1998) Aldicarb (No. 121, 1991) Copper (No. 200, 1998) Aldrin and dieldrin (No. 91, 1989) Cresols (No. 168, 1995) Allethrins (No. 87, 1989) Cyhalothrin (No. 99, 1990) Aluminium (No. 194, 1997) Cypermethrin (No. 82, 1989) Amitrole (No. 158, 1994) Cypermethrin, alpha- (No. 142, 1992) Ammonia (No. 54, 1986) DOT and its derivatives (No. 9, 1979) Anticoagulant rodenticides (No. 175, 1995) DOT and its derivatives - Arsenic (No. 18, 1981) environmental aspects (No, 83, 1989) Asbestos and other natural mineral fibres Deltamethrjn (No. 97, 1990) (No. 53, 1986) Demeton-S-methyl (No. 197, 1997) Barium (No. 107, 1990) Diaminotoluenes (No. 74, 1987) Benomyl (No. 148, 1993) Diazinon (No. 198, 1997) Benzene (No. 150, 1993) 1,2-Dibromoethane (No. 177, 1996) Beryllium (No. 106, 1990) Oi-n-butyl phthalate (No. 189, 1997) Biomarkers and risk assessment: concepts 1 ,2-Dichloroethane and principles (No. 155, 1993) (No. 62, 1987, 1St edition) Blotoxins, aquatic (marine and freshwater) (No. 176, 1995, 2nd edition) (No. 37, 1984) 2,4-Dichlorophenoxyacetic acid Boron (No. 204, 1998) (2,4-D) (No. 29, 1984) Brominated diphenylethers (No. 162, 1994) 2,4-Dichlorophenoxyacetic acid - Butanols - four isomers (No. 65, 1987) environmental aspects (No. 84, 1989) Cadmium (No. 134, 1992) 1 ,3-Dichloropropene, 1 ,2-dichloropropane Cadmium - environmental aspects and mixtures (No. 146, 1993) (No. 135, 1992) Dichlorvos (No. 79, 1988) Camphechlor (No. 45, 1984) Diesel fuel and exhaust emissions Carbamate pesticides: a general (No. 171, 1996) introduction (No. 64, 1986) Diethyihexyl phthalate (No. 131, 1992) Carbaryl (No. 153, 1994) Diflubenzuron (No. 184, 1996) Carbendazim (No. 149, 1993) Dimethoate (No. 90, 1989) Carbon disulfide (No. 10, 1979) Dimethylformamide (No. 114, 1991) Carbon monoxide (No. 13, 1979) Oimethyl sulfate (No. 48, 1985) Carcinogens, summary report on the Diseases of suspected chemical evaluation of short-term in vitro tests etiology and their prevention, (No. 47, 1985) principles of studies on (No. 72, 1987) Carcinogens, summary report on the Dithiocarbamate pesticides, evaluation of short-term in vivo tests ethylenethiourea, and propylenethiourea: (No. 109, 1990) a general introduction (No. 78, 1988) Chlordane (No. 34, 1984) Electromagnetic fields (No. 137, 1992) Chiordimeform (No. 199, 1997) Endosulfan (No. 40, 1984) Chiordecone (No. 43, 1984) Endrin (No. 130, 1992) Chiorendic acid and anhydride Environmental epidemiology, guidelines on (No. 185, 1996) studies in (No. 27, 1983) Chlorinated paraffins (No. 181, 1996) Epichlorohydrin (No. 33, 1984) Chlorine and hydrogen chloride Ethylbenzene (No. 186, 1996 (No. 21,1982) Ethylene oxide (No. 55, 1985) Chloroalkyl ethers, selected (No. 201, 1998) Extremely low frequency (ELF) fields Chlorobenzenes other than (No. 36, 1984) hexachlorobenzene(No. 128, 1991) Fenitrothion (No. 133, 1992) Chlorofluorocarbons, fully halogenated Fenvalerate (No. 95, 1990) (No. 113, 1990) continued at end of book This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the United Nations Environment Programme, the International Labour Organisation, or the World Health Organization. Environmental Health Criteria 206 METHYL TERTJARY-BUTYL ETHER First draft prepared by Dr M. Giliner, National Chemicals Inspectorate, Solna, Sweden, with contributions from Ms A.S. Nihlén, Institute for Working Life, Solna, Sweden Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organisation, and the World Health Organization, and produced within the framework of the Inter-Organization Programme for the Sound Management of Chemicals. World Health Organization Geneva, 1998 The International Programme on Chemical Safety (WCS), estabirshed in 1980, is a joint venture of the United Nations Environment Programme (UNEP), the International Labour Organisation (ILO), and the World l-Iealth Organization (WHO). The overall objectives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environncnt from exposure to chemicals, through international peer review processes, as a prerequisite for the promotion olchemical safety, and to provide technical assistance in strengthening national capacities for the sound management of chemicals. The inter-Organization Programme for the Sound Management of Chemicals (IOMC) was established in 1995 by UNEP, ELO, the Food and Agriculture Organization of the United Nations. WHO, the United Nations Industrial Development Organization, the United Nations Institute for Training and Research, and the Organisation for Economic Co-operation and Development (Participating Organizations), following recommendations made by the 1992 UN Conference on Environment and Development to strengthen cooperation and increase coordination in the field of chemical safety. The purpose of the IOMC is to promote coordination of the policies and activities pursued by the Participating Organizations, jointly or separately, to achieve the sound management of chemicals in relation to human health and the environment. WHO Library Cataloguing in Publication Data Methyl tertiary-hutyl ether, (Enyiromnental health criteria 206) l.Methyl ethers 2.Environmental exposure 3.Occupational exposure l.International Programme on Chemical Safety 11.Series JSBN 924 157206 X (NLM Classification: QD 305.E7) ISSN 0250-863X The World Health Organization welcomes requests for permission to reproduce or translate its publications, in part or in bill. Applications and enquiries should be addressed to the Office of Publications, World health Organization, Geneva, Switzerland, which will he glad to provide the latest information on any changes made to the text, plans for new editions, and reprints and translations already available. CWorld Health Organization 1998 Publications of the World Health Organization enjoy copyright protection in accordance with the provisions of Protocol 2 of the Universal Copyright Convention. All rights reserved. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the World Health Organization concerning the legal Status of any country, territory, city, or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The mention of specific companies or of certain manufacturers' products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. PR1NTED IN FINLAND 08/1 2223 - VAMMALA - 5000 CONTENTS ENVIRONMENTAL HEALTH CRITERIA FOR METHYL TERTIARY-BUTYL ETHER PREAMBLE ix ABBREVIATIONS xviii SUMMARY 1.1 Identity, physical and chemical properties, analytical methods 1.2 Sources of human and environmental exposure 1.3 Environmental transport, distribution and transformation 2 1.4 Environmental levels and human exposure 2 1.5 Kinetics and metabolism 5 1.6 Effects on laboratory animals and in vitro systems 5 1.7 Effects on humans 7 1.8 Effects on other organisms in the laboratory and field S 1.9 Evaluation of human health risks and effects on the environment 8 IDENTITY, PHYSICAL AND CHEMICAL PROPERTIES, ANALYTICAL METHODS 10 2.1 Identity 10 2.2 Physical and chemical properties 11 2.3 Conversion factors 11 2.4 Analytical methods ii 2.4.1 Procedures 11 2.4.1.1 Air 11 2.4.1.2 Soil, water and sediment 15 2.4.1.3 Gasoline 16 2.4.14 Biological samples 17 rm EHC 206: Methyl tertiary-Bury! Ether SOURCES OF E-ITJMAN AND ENVIRONMENTAL EXPOSURE 19 3.1 Natural occurrence 19 3.2 Anthropogenic sources 19 3.2.1 Production levels and processes 19 3.2.2 Uses 20 32.3 Sources and releases to the environment 22 3.2.3.1 industrial releases 22 3.2.3.2 Storage tank release 22 3.2.3.3 Engine emissions from on-road and off-road vehicles and recreational boats 23 3.3 Other pertinent information 24 ENVIRONMENTAL BEHAVIOUR AND FATE 26 4.1 Transport and distribution between media 26 4.1.1 Air 26 4.1.2 Water 26 4.1.3 Soil 29 4.1.4 Multimedia 29 4.2 Bioconcentration 29 4.3 Biodegradation and transformation 30 4.3.1 Aerobic conditions 30 4.12 Anaerobic conditions 33 4.4 Abiotic degradation 35 4.4.1 Air 35 4.4.1.1 Photolysis 35 4.4.1 .2 Hydrolysis 35 4.4.1.3 Photooxidation 35 4.4.2 Natural waters 37 4.4.3 MTBE half-life ranges in environmental Compartments 37 4.5 Ozone-forming potential 37 4.6 Remediation 38 iv 5. ENVIRONMENTAL LEVELS AND HUMAN EXPOSURE 39 5.1 Environmental levels 39 5.1.1 Exposure 39 5.1.1A Levels in ambient air and
Recommended publications
  • Cyproterone Art. 31
    Приложение I Списък на лекарствените продукти и форми 1 Държава членка Притежател на Наименование на INN/Активно Фармацевтична Начин на (ЕИП) разрешението за продукта вещество + форма приложение употреба Количество на активното вещество (в дозова единица) Австрия Bayer Austria Gmbh Androcur Depot Cyproterone Acetate Инжекционен Интрамускулно 300mg/3ml разтвор приложение Австрия Bayer Austria Gmbh Climen Cyproterone Acetate 1mg Обвита таблетка Перорално таблетка, Estradiol приложение Valerate 2mg таблетка| Estradiol Valerate 2mg таблетка Австрия Bayer Austria Gmbh Climen 28-Tage Cyproterone Acetate 1mg Обвита таблетка Перорално таблетка, Estradiol приложение Valerate 2mg таблетка| Estradiol Valerate 2mg таблетка Австрия Bayer Austria Gmbh Diane Mite Cyproterone Acetate 2mg Обвита таблетка Перорално таблетка, Ethinylestradiol приложение 35μg таблетка Австрия Bayer Austria Gmbh Minerva Cyproterone Acetate 2mg Обвита таблетка Перорално таблетка, Ethinylestradiol приложение 0,035mg таблетка Австрия Bayer Austria Gmbh Andro-Diane Cyproterone Acetate Таблетка Перорално 10mg таблетка приложение Австрия Bayer Austria Gmbh Androcur Cyproterone Acetate Таблетка Перорално 100mg таблетка приложение Австрия Bayer Austria Gmbh Androcur Cyproterone Acetate Таблетка Перорално 50mg таблетка приложение Австрия Gynial Gmbh Alisma Cyproterone Acetate 2mg Филмирана таблетка Перорално таблетка, Ethinylestradiol приложение 35μg таблетка 2 Държава членка Притежател на Наименование на INN/Активно Фармацевтична Начин на (ЕИП) разрешението за продукта вещество +
    [Show full text]
  • Aldosterone Enhances Renal Calcium Reabsorption by Two Types of Channels
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Kidney International, Vol. 66 (2004), pp. 242–250 Aldosterone enhances renal calcium reabsorption by two types of channels MARIE LECLERC,MICHELE` G. BRUNETTE, and DENIS COUCHOUREL Maisonneuve-Rosemont Hospital and University of Montreal, Canada Aldosterone enhances renal calcium reabsorption by two types transepithelial potential difference in the late segments of channels. of the nephron, reflecting a stimulation of the amiloride- Background. Aldosterone has been known for many years + + sensitive Na transport by the apical membranes. to increase sodium (Na ) reabsorption by the distal nephron. The present in vitro experiments investigated the effect of the In contrast to the abundant literature dealing with the + hormone on calcium (Ca2 ) transport by the luminal membrane antinatriuretic effect of aldosterone, data concerning its + of the rabbit nephron, independent of any systemic influence. action on Ca2 transport are relatively scarce. Clearance Methods. Proximal and distal tubules were incubated with studies showed either an increase in calciuria [2] or an + either aldosterone or the carrier. The luminal membranes of absence of significant change of Ca2 excretion [3, 4] af- these tubules were purified, vesiculated, and 45Ca uptake by these vesicles was subsequently measured. ter aldosterone administration. In a randomized study in Results. Treatment of the distal tubules with 10−8 mol/L al- male volunteers, Van Hamersvelt et al [5] compared the + + dosterone enhanced both 0.1 and 0.5 mmol/L Ca2 transport. effect of the Ca2 channel blocker felodipine, alone or The hormone action was abolished by tyrosine kinase inhibitors.
    [Show full text]
  • The Comparative Effects of Three Toxic Substances on Bluegill Behavior Mary Gerard Henry Iowa State University
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital Repository @ Iowa State University Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1984 The comparative effects of three toxic substances on bluegill behavior Mary Gerard Henry Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Ecology and Evolutionary Biology Commons, and the Environmental Sciences Commons Recommended Citation Henry, Mary Gerard, "The ompc arative effects of three toxic substances on bluegill behavior " (1984). Retrospective Theses and Dissertations. 8996. https://lib.dr.iastate.edu/rtd/8996 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This reproduction was made from a copy of a document sent to us for microfilming. While the most advanced technology has been used to photograph and reproduce this document, the quality of the reproduction is heavily dependent upon the quality of the material submitted. The following explanation of techniques is provided to help clarify markings or notations which may appear on this reproduction. 1.The sign or "target" for pages apparently lacking from the document photographed is "Missing Page(s)". If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages.
    [Show full text]
  • Chemical-Specific Parameters Supporting Table May 2016 Analyte
    Regional Screening Level (RSL) Chemical-specific Parameters Supporting Table May 2016 Contaminant Molecular Weight Volatility Parameters Melting Point Density Diffusivity in Air and Water Partition Coefficients Water Solubility Tapwater Dermal Parameters H` (atm- Density Dia Diw Dia and Diw Kd Kd Koc log Kow S B τevent t* Kp 3 3 2 2 Analyte CAS No. MW MW Ref (unitless) m /mole) H` and HLC Ref VP VP Ref MP MP Ref (g/cm ) Density Ref (cm /s) (cm /s) Ref (L/kg) Ref (L/kg) Koc Ref (unitless) log Kow Ref (mg/L) S Ref (unitless) (hr/event) (hr) (cm/hr) K Ref Acephate 30560-19-1 1.8E+02 PHYSPRO 2.0E-11 5.0E-13 EPI 1.7E-06 PHYSPROP 8.8E+01 PHYSPROP 1.4E+00 CRC89 3.7E-02 8.0E-06 WATER9 1.0E+01 EPI -8.5E-01 PHYSPRO 8.2E+05 PHYSPROP 2.1E-04 1.1E+00 2.7E+00 4.0E-05 EPI Acetaldehyde 75-07-0 4.4E+01 PHYSPRO 2.7E-03 6.7E-05 PHYSPROP 9.0E+02 PHYSPROP -1.2E+02 PHYSPROP 7.8E-01 CRC89 1.3E-01 1.4E-05 WATER9 1.0E+00 EPI -3.4E-01 PHYSPRO 1.0E+06 PHYSPROP 1.3E-03 1.9E-01 4.5E-01 5.3E-04 EPI Acetochlor 34256-82-1 2.7E+02 PHYSPRO 9.1E-07 2.2E-08 PHYSPROP 2.8E-05 PHYSPROP 1.1E+01 PubChem 1.1E+00 PubChem 2.2E-02 5.6E-06 WATER9 3.0E+02 EPI 3.0E+00 PHYSPRO 2.2E+02 PHYSPROP 3.1E-02 3.4E+00 8.2E+00 5.0E-03 EPI Acetone 67-64-1 5.8E+01 PHYSPRO 1.4E-03 3.5E-05 PHYSPROP 2.3E+02 PHYSPROP -9.5E+01 PHYSPROP 7.8E-01 CRC89 1.1E-01 1.2E-05 WATER9 2.4E+00 EPI -2.4E-01 PHYSPRO 1.0E+06 PHYSPROP 1.5E-03 2.2E-01 5.3E-01 5.1E-04 EPI Acetone Cyanohydrin 75-86-5 8.5E+01 PHYSPRO 8.1E-08 2.0E-09 PHYSPROP 3.4E-01 PHYSPROP -1.9E+01 PHYSPROP 9.3E-01 CRC89 8.6E-02 1.0E-05 WATER9 1.0E+00
    [Show full text]
  • PESTICIDES Criteria for a Recommended Standard
    CRITERIA FOR A RECOMMENDED STANDARD OCCUPATIONAL EXPOSURE DURING THE MANUFACTURE AND FORMULATION OF PESTICIDES criteria for a recommended standard... OCCUPATIONAL EXPOSURE DURING THE MANUFACTURE AND FORMULATION OF PESTICIDES * U.S. DEPARTMENT OF HEALTH, EDUCATION, AND WELFARE Public Health Service Center for Disease Control National Institute for Occupational Safety and Health July 1978 For sale by the Superintendent of Documents, U.S. Government Printing Office, Washington, D.C. 20402 DISCLAIMER Mention of company names or products does not constitute endorsement by the National Institute for Occupational Safety and Health. DHEW (NIOSH) Publication No. 78-174 PREFACE The Occupational Safety and Health Act of 1970 emphasizes the need for standards to protect the health and provide for the safety of workers occupationally exposed to an ever-increasing number of potential hazards. The National Institute for Occupational Safety and Health (NIOSH) has implemented a formal system of research, with priorities determined on the basis of specified indices, to provide relevant data from which valid criteria for effective standards can be derived. Recommended standards for occupational exposure, which are the result of this work, are based on the effects of exposure on health. The Secretary of Labor will weigh these recommendations along with other considerations, such as feasibility and means of implementation, in developing regulatory standards. Successive reports will be presented as research and epideiriologic studies are completed and as sampling and analytical methods are developed. Criteria and standards will be reviewed periodically to ensure continuing protection of workers. The contributions to this document on pesticide manufacturing and formulating industries by NIOSH staff members, the review consultants, the reviewer selected by the American Conference of Governmental Industrial Hygienists (ACGIH), other Federal agencies, and by Robert B.
    [Show full text]
  • TOXICOLOGICAL PROFILE for METHYL Tert-BUTYL ETHER
    TOXICOLOGICAL PROFILE FOR METHYL tert-BUTYL ETHER U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Agency for Toxic Substances and Disease Registry August 1996 METHYL tert-BUTYL ETHER ii DISCLAIMER The use of company or product name(s) is for identification only and does not imply endorsement by the Agency for Toxic Substances and Disease Registry. METHYL tert-BUTYL ETHER iii UPDATE STATEMENT Toxicological profiles are revised and republished as necessary, but no less than once every three years. For information regarding the update status of previously released profiles, contact ATSDR at: Agency for Toxic Substances and Disease Registry Division of Toxicology/Toxicology Information Branch 1600 Clifton Road NE, E-29 Atlanta, Georgia 30333 vi *Legislative Background The toxicological profiles are developed in response to the Superfund Amendments and Reauthorization Act (SARA) of 1986 (Public Law 99-499) which amended the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA or Superfund). This public law directed ATSDR to prepare toxicological profiles for hazardous substances most commonly found at facilities on the CERCLA National Priorities List and that pose the most significant potential threat to human health, as determined by ATSDR and the EPA. The availability of the revised priority list of 275 hazardous substances was announced in the Federal Register on April 29, 1996 (61 FR 18744). For prior versions of the list of substances, see Federal Register notices dated April 17, 1987 (52 FR 12866); October 20, 1988 (53 FR 41280); October 26, 1989 (54 FR 43619); October 17, 1990 (55 FR 42067); October 17, 199l (56 FR 52166); October 28, 1992 (57 FR 48801); and February 28, 1994 (59 FR 9486).
    [Show full text]
  • The Effect of Dosing Regimen on Outcomes of Vitamin D Supplementation Trials a Study of Current Literature
    Faculty of Medicine The effect of dosing regimen on outcomes of vitamin D supplementation trials A study of current literature — Anette Uhlving Larsen Master thesis in Medicine (MED-3950) June 2019 Supervisor: Professor Rolf Jorde, Institute of Clinical Medicine Abstract Results from observational studies have indicated associations between vitamin D and extra- skeletal outcomes, including respiratory tract infections (RTI) and all-cause mortality. However, available trial-data have shown inconsistent results. The main objective of this thesis was to investigate whether a beneficial effect of daily supplementation of vitamin D on RTI and all-cause mortality could have been masked by the use of less frequent supplementation intervals. This thesis included data from double-blinded, randomized controlled trials (RCTs) published in the last 10 years. Eligible trials were identified through screening of the reference lists of systematic reviews of meta-analyses (MAs), and of reference lists of MAs on the selected outcomes included in these reviews. Also, additional searches were performed to ensure that also recently published RCTs, not identified in a previous step of the search strategy, were considered for inclusion. The search strategy was designed to promote selection of trials of adequate methodological quality. To be included the record had to be written in English and report results of a double-blinded placebo-controlled RCT with vitamin D supplementation in a human population. Studies including pregnant women or assessing the effect of prenatal supplementation were not included, nor were studies including populations with chronic kidney disease and/or other diseases known to affect the conversion of active metabolites of vitamin D.
    [Show full text]
  • Focus on China TOP ARTICLES SUPPLEMENT
    Powered by Focus on China TOP ARTICLES SUPPLEMENT CONTENTS RESEARCH ARTICLE: Simultaneous determination of hyzetimibe and its main active metabolite in plasma by LC–MS/MS and its application in PK study Bioanalysis Vol. 7 Issue 15 RESEARCH ARTICLE: Highly specific and sensitive immunoassay for the measurement of prostaglandin E2 in biological fluids Bioanalysis Vol. 7 Issue 19 REVIEW: Derivatization methods for LC–MS analysis of endogenous compounds Bioanalysis Vol. 7 Issue 19 METHODOLOGY: Development of an Excel-based laboratory information management system for improving workflow efficiencies in early ADME screening Bioanalysis Vol. 8 Issue 2 Research Article For reprint orders, please contact [email protected] 7 Research Article 2015/07/30 Simultaneous determination of hyzetimibe and its main active metabolite in plasma by LC–MS/MS and its application in PK study Bioanalysis Background: Hyzetimibe is a new compound belonging to a novel class of selective Jinliang Chen1, Honggang cholesterol absorption inhibitors. A simple, highly sensitive LC–MS/MS method has Lou1, Bo Jiang1, Rong Shao1, been developed for the quantification of hyzetimibe and its main active metabolite, Zourong Ruan1 ,1 hyzetimibe-glucuronide, in human plasma. Results: Analytical samples were prepared & Jian’an Wang* 1Center of Clinical Pharmacology, using a protein precipitation method coupled with a concentration process. The the Second Affiliated Hospital of linearity of this method was established for concentrations in the ranges of 0.05–50 Zhejiang University School of Medicine, and 0.5–500 ng/ml for hyzetimibe and hyzetimibe-glucuronide, respectively. The Hangzhou, Zhejiang, China accuracy and precision of the method varied from 97.9 to 105% and 2.6 to 7.4%, *Author for correspondence: respectively.
    [Show full text]
  • G Protein-Coupled Estrogen Receptor in Cancer and Stromal Cells: Functions and Novel Therapeutic Perspectives
    cells Review G Protein-Coupled Estrogen Receptor in Cancer and Stromal Cells: Functions and Novel Therapeutic Perspectives Richard A. Pepermans 1, Geetanjali Sharma 1,2 and Eric R. Prossnitz 1,2,3,* 1 Division of Molecular Medicine, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA; [email protected] (R.A.P.); [email protected] (G.S.) 2 Center of Biomedical Research Excellence in Autophagy, Inflammation and Metabolism, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA 3 University of New Mexico Comprehensive Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA * Correspondence: [email protected]; Tel.: +1-505-272-5647 Abstract: Estrogen is involved in numerous physiological and pathophysiological systems. Its role in driving estrogen receptor-expressing breast cancers is well established, but it also has important roles in a number of other cancers, acting both on tumor cells directly as well as in the function of multiple cells of the tumor microenvironment, including fibroblasts, immune cells, and adipocytes, which can greatly impact carcinogenesis. One of its receptors, the G protein-coupled estrogen receptor (GPER), has gained much interest over the last decade in both health and disease. Increasing evidence shows that GPER contributes to clinically observed endocrine therapy resistance in breast cancer while also playing a complex role in a number of other cancers. Recent discoveries regarding the targeting of GPER in combination with immune checkpoint inhibition, particularly in melanoma, have led to the initiation of the first Phase I clinical trial for the GPER-selective agonist G-1.
    [Show full text]
  • 2019 Complete Drug List (Formulary)
    20191 COMPLETE DRUG LIST (FORMULARY) Prescription drug list information UnitedHealthcare® Group Medicare Advantage Important Notes: This document has information about the drugs covered by this plan. For more up-to-date information or if you have any questions, please call Customer Service at: Toll-free 1-800-457-8506, TTY 711 8 a.m. - 8 p.m. local time, Monday - Friday www.UHCRetiree.com Formulary ID Number 00019090, Version 9 Y0066_180629_042324 Last updated October 1, 2018 TABLE2 11 OF CONTENTS What is a drug list?......................................................................................................................................3 Note to existing members.......................................................................................................................... 3 How do I use the drug list?.........................................................................................................................4 What are generic drugs?............................................................................................................................ 4 Drug payment stage and drug tiers...........................................................................................................5 Getting Extra Help.......................................................................................................................................5 Are there any rules or limits on my drug coverage?................................................................................ 6 What if my drug is not
    [Show full text]
  • Diethylstilbestrol Activates Catsper and Disturbs Progesterone Actions in Human Spermatozoa
    Human Reproduction, Vol.32, No.2 pp. 290–298, 2017 Advanced Access publication on December 28, 2016 doi:10.1093/humrep/dew332 ORIGINAL ARTICLE Andrology Diethylstilbestrol activates CatSper and disturbs progesterone actions in human spermatozoa † † Qian-xing Zou1, , Zhen Peng1, , Qing Zhao1, Hou-yang Chen2, Yi-min Cheng1, Qing Liu1, Yuan-qiao He1, Shi-qi Weng1, Hua-feng Wang1, Tao Wang1, Li-ping Zheng1, and Tao Luo1,* 1Institute of Life Science and School of Life Science, Nanchang University, Nanchang, Jiangxi 330031, PR China 2Reproductive Medical Center, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, Jiangxi 330006, PR China *Correspondence address. Institute of Life Science and School of Life Science, Nanchang University, Nanchang, Jiangxi 330031, PR China. E-mail: [email protected] Submitted on June 24, 2016; resubmitted on November 24, 2016; accepted on December 16, 2016 STUDY QUESTION: Is diethylstilbestrol (DES), a prototypical endocrine-disrupting chemical (EDC), able to induce physiological changes in human spermatozoa and affect progesterone actions? + SUMMARY ANSWER: DES promoted Ca2 flux into human spermatozoa by activating the cation channel of sperm (CatSper) and sup- + pressed progesterone-induced Ca2 signaling, tyrosine phosphorylation and sperm functions. WHAT IS KNOWN ALREADY: DES significantly impairs the male reproductive system both in fetal and postnatal exposure. Although various EDCs affect human spermatozoa in a non-genomic manner, the effect of DES on human spermatozoa remains unknown. STUDY DESIGN, SIZE, DURATION: Sperm samples from normozoospermic donors were exposed in vitro to a range of DES concen- trations with or without progesterone at 37°C in a 5% CO2 incubator to mimic the putative exposure to this toxicant in seminal plasma and the female reproductive tract fluids.
    [Show full text]
  • Clinical Practice Guidelines for Managing Dyslipidemias in Kidney
    American Journal of Transplantation 2004; 4 (Suppl. 7): 13–53 Copyright # Blackwell Munksgaard 2004 Blackwell Munksgaard Clinical practice guidelines for managing dyslipidemias in kidney transplant patients: a report from the Managing Dyslipidemias in Chronic Kidney Disease Work Group of the National Kidney Foundation Kidney Disease Outcomes Quality Initiative National Kidney Foundation kidney transplant patients. These guidelines are divided WorkGroupMembers:B.Kasiske,F.G.Cosio, into four sections. The first section (Introduction) pro- J.Beto,K.Bolton,B.M.Chavers,R.GrimmJr., vides the rationale for the guidelines, and describes the target population, scope, intended users, and methods. A. Levin, B. Masri, R. Parekh, C. Wanner, The second section presents guidelines on the assess- D.C. Wheeler and P.W.F. Wilson ment of dyslipidemias (guidelines 1–3), while the third section offers guidelines for the treatment of dyslipid- Correspondence: Karen Glowacki, National Kidney emias (guidelines 4–5). The key guideline statements Foundation 30 E. 33rd Street, 11th Fl. New York, are supported mainly by data from studies in the general NY 10016, USA; email: [email protected] population, but there is an urgent need for additional studies in CKD and in transplant patients. Therefore, the last section outlines recommendations for research. ABSTRACT The incidence of cardiovascular disease (CVD) is very high in patients with chronic kidney (CKD) disease and in kidney transplant recipients. Indeed, available evi- INTRODUCTION dence for these patients suggests that the 10-year cumulative risk of coronary heart disease is at least The rationale for these guidelines 20%, or roughly equivalent to the risk seen in patients These guidelines are the result of an ongoing effort by the with previous CVD.
    [Show full text]