Toxicity of DDT, Dieldrin, Malathion and Fenthion to Rhodnius Prolixus in the Laboratory * by IRVING Fox and ILEANA G
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Replacement Therapy, Not Recreational Tonic Testosterone, Widely Used As a Lifestyle Drug, Is a Medicine and Should Be Kept As Such
correspondence Replacement therapy, not recreational tonic Testosterone, widely used as a lifestyle drug, is a medicine and should be kept as such. Sir — We read with great interest the News male tonics and remedies — most harmless, your Feature that there is a need for large- Feature “A dangerous elixir?” (Nature 431, but some as drastic as grafting goat testicles scale, long-term clinical trials to address 500–501; 2004) reporting the zeal with onto humans. Unfortunately, a certain several issues associated with testosterone which testosterone is being requested by amount of quackery is now perceived to be use. For example, testosterone therapy may men who apparently view the hormone as associated with testosterone therapy, and the be beneficial against osteoporosis, heart a ‘natural’ alternative to the drug Viagra. increased prescription of the hormone in disease and Alzheimer’s disease, but the Like Viagra, testosterone replacement recent years does little to dispel this notion. dangers remain obscure. therapy — with emphasis on the word Nonetheless, as your Feature highlights, Until we know more, both prescribing ‘replacement’ — is a solution to a very real hypogonadism is a very real clinical clinicians and the male population need to clinical problem. There is a distinction condition. It is characterized by abnormally be aware that testosterone, like any other between patients whose testosterone has low serum levels of testosterone, in medication, should only be administered declined to abnormally low levels, and conjunction with symptoms such as to patients for whom such therapy is individuals seeking testosterone as a pick- mood disturbance, depression, sexual clinically indicated. me-up. -
(12) Patent Application Publication (10) Pub. No.: US 2006/0110428A1 De Juan Et Al
US 200601 10428A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2006/0110428A1 de Juan et al. (43) Pub. Date: May 25, 2006 (54) METHODS AND DEVICES FOR THE Publication Classification TREATMENT OF OCULAR CONDITIONS (51) Int. Cl. (76) Inventors: Eugene de Juan, LaCanada, CA (US); A6F 2/00 (2006.01) Signe E. Varner, Los Angeles, CA (52) U.S. Cl. .............................................................. 424/427 (US); Laurie R. Lawin, New Brighton, MN (US) (57) ABSTRACT Correspondence Address: Featured is a method for instilling one or more bioactive SCOTT PRIBNOW agents into ocular tissue within an eye of a patient for the Kagan Binder, PLLC treatment of an ocular condition, the method comprising Suite 200 concurrently using at least two of the following bioactive 221 Main Street North agent delivery methods (A)-(C): Stillwater, MN 55082 (US) (A) implanting a Sustained release delivery device com (21) Appl. No.: 11/175,850 prising one or more bioactive agents in a posterior region of the eye so that it delivers the one or more (22) Filed: Jul. 5, 2005 bioactive agents into the vitreous humor of the eye; (B) instilling (e.g., injecting or implanting) one or more Related U.S. Application Data bioactive agents Subretinally; and (60) Provisional application No. 60/585,236, filed on Jul. (C) instilling (e.g., injecting or delivering by ocular ion 2, 2004. Provisional application No. 60/669,701, filed tophoresis) one or more bioactive agents into the Vit on Apr. 8, 2005. reous humor of the eye. Patent Application Publication May 25, 2006 Sheet 1 of 22 US 2006/0110428A1 R 2 2 C.6 Fig. -
Review of the Mammalian Toxicology
REVIEW OF THE MAMMALIAN TOXICOLOGY AND METABOLISM/TOXICOKINETICS OF FENTHION The APVMA Review of Fenthion © Australian Pesticides and Veterinary Medicines Authority 2012 ISBN 978-0-9873591-5-5 (electronic) This document was originally published in 2005 as part of the preliminary review findings report for Part 1 of the fenthion review. It was subsequently updated in 2007, and revised in 2008. Ownership of intellectual property rights in this publication Unless otherwise noted, copyright (and any other intellectual property rights, if any) in this publication is owned by the Australian Pesticides and Veterinary Medicines Authority (APVMA). Creative Commons licence With the exception of the Coat of Arms, this publication is licensed under a Creative Commons Attribution 3.0 Australia Licence. This is a standard form agreement that allows you to copy, distribute, transmit and adapt this publication provided that you attribute the work. A summary of the licence terms is available from www.creativecommons.org/licenses/by/3.0/au/deed.en. The full licence terms are available from www.creativecommons.org/licenses/by/3.0/au/legalcode. The APVMA’s preference is that you attribute this publication (and any approved material sourced from it) using the following wording: Source: Licensed from the Australian Pesticides and Veterinary Medicines Authority (APVMA) under a Creative Commons Attribution 3.0 Australia Licence. This report was prepared for the APVMA by the Department of Health and Aging Office of Chemical Safety. In referencing this document the Department of Health and Aging Office of Chemical Safety should be cited as the author and the Australian Pesticides and Veterinary Medicines Authority as the publisher and copyright owner. -
DDT and Its Derivatives Have Remained in the Environment
International Journal of Molecular Sciences Review A Novel Action of Endocrine-Disrupting Chemicals on Wildlife; DDT and Its Derivatives Have Remained in the Environment Ayami Matsushima Laboratory of Structure-Function Biochemistry, Department of Chemistry, Faculty of Science, Kyushu University, Fukuoka 819-0395, Japan; [email protected]; Tel.: +81-92-802-4159 Received: 20 March 2018; Accepted: 2 May 2018; Published: 5 May 2018 Abstract: Huge numbers of chemicals are released uncontrolled into the environment and some of these chemicals induce unwanted biological effects, both on wildlife and humans. One class of these chemicals are endocrine-disrupting chemicals (EDCs), which are released even though EDCs can affect not only the functions of steroid hormones but also of various signaling molecules, including any ligand-mediated signal transduction pathways. Dichlorodiphenyltrichloroethane (DDT), a pesticide that is already banned, is one of the best-publicized EDCs and its metabolites have been considered to cause adverse effects on wildlife, even though the exact molecular mechanisms of the abnormalities it causes still remain obscure. Recently, an industrial raw material, bisphenol A (BPA), has attracted worldwide attention as an EDC because it induces developmental abnormalities even at low-dose exposures. DDT and BPA derivatives have structural similarities in their chemical features. In this short review, unclear points on the molecular mechanisms of adverse effects of DDT found on alligators are summarized from data in the literature, and recent experimental and molecular research on BPA derivatives is investigated to introduce novel perspectives on BPA derivatives. Especially, a recently developed BPA derivative, bisphenol C (BPC), is structurally similar to a DDT derivative called dichlorodiphenyldichloroethylene (DDE). -
Pesticides Reduce Symbiotic Efficiency of Nitrogen-Fixing Rhizobia and Host Plants
Pesticides reduce symbiotic efficiency of nitrogen-fixing rhizobia and host plants Jennifer E. Fox*†, Jay Gulledge‡, Erika Engelhaupt§, Matthew E. Burow†¶, and John A. McLachlan†ʈ *Center for Ecology and Evolutionary Biology, University of Oregon, 335 Pacific Hall, Eugene, OR 97403; †Center for Bioenvironmental Research, Environmental Endocrinology Laboratory, Tulane University, 1430 Tulane Avenue, New Orleans, LA 70112-2699; ‡Department of Biology, University of Louisville, Louisville, KY 40292 ; §University of Colorado, Boulder, CO 80309; and ¶Department of Medicine and Surgery, Hematology and Medical Oncology Section, Tulane University Medical School, 1430 Tulane Avenue, New Orleans, LA 70112-2699 Edited by Christopher B. Field, Carnegie Institution of Washington, Stanford, CA, and approved May 8, 2007 (received for review January 8, 2007) Unprecedented agricultural intensification and increased crop by plants, in rotation with non-N-fixing crops (8, 15). The yield will be necessary to feed the burgeoning world population, effectiveness of this strategy relies on maximizing symbiotic N whose global food demand is projected to double in the next 50 fixation (SNF) and plant yield to resupply organic and inorganic years. Although grain production has doubled in the past four N and nutrients to the soil. The vast majority of biologically fixed decades, largely because of the widespread use of synthetic N is attributable to symbioses between leguminous plants (soy- nitrogenous fertilizers, pesticides, and irrigation promoted by the bean, alfalfa, etc.) and species of Rhizobium bacteria; replacing ‘‘Green Revolution,’’ this rate of increased agricultural output is this natural fertilizer source with synthetic N fertilizer would cost unsustainable because of declining crop yields and environmental Ϸ$10 billion annually (16, 17). -
Malathion General Fact Sheet
MALATHION GENERAL FACT SHEET What is malathion Malathion is an insecticide in the chemical family known as organophosphates. Products containing malathion are used outdoors to control a wide variety of insects in agricultural settings and around people’s homes. Malathion has also been used in public health mosquito control and fruit fly eradication programs. Malathion may also be found in some special shampoos for treating lice. Malathion was first registered for use in the United States in 1956. What are some products that contain malathion Products containing malathion may be liquids, dusts, wettable powders, or emulsions. There are thousands of products contain- ing malathion registered for use in the United States. Always follow label instructions and take steps to avoid exposure. If any exposures occur, be sure to follow the First Aid instructions on the product label carefully. For additional treatment advice, contact the Poison Control Center at 1-800-222-1222. If you wish to discuss a pesticide problem, please call 1-800-858-7378. How does malathion work Malathion kills insects by preventing their nervous system from working properly. When healthy nerves send signals to each other, a special chemical messenger travels from one nerve to another to continue the message. The nerve signal stops when an enzyme is released into the space between the nerves. Malathion binds to the enzyme and prevents the nerve signal from stopping. This causes the nerves to signal each other without stopping. The constant nerve signals make it so the insects can’t move or breathe normally and they die. People, pets and other animals can be affected the same way as insects if they are exposed to enough malathion. -
US EPA, Pesticide Product Label, ORTHO MALATHION 50 INSECT
23V 73^ f UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, D.C. 20460 Jff***^ OFFICE OF WAV 00 Onit CHEMICAL SAFETY AND MAY 4 0 201] POLLUTION PREVENTION James Wallace The Scotts Company d/b/a The Ortho Group P.O.Box 190 Marysville, OH 43040 Subject: Submission of amended labeling per May 2009 Malathion RED Label Table EPA Reg. No. 239-739 Submissions dated March 5, 2010 Dear Mr. Wallace: The proposed labeling referred to above, submitted in connection with registration under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), is acceptable under FIFRA § 3(c)(5) provided that you submit two copies of your final printed label before you release the product for shipment. Products shipped after 12 months from the date of this amendment or the next printing of the label whichever occurs first, must bear the new revised label. Your release for shipment of the product bearing the amended label constitutes acceptance of these conditions. If these conditions are not complied with, the registration will be subject to cancellation in accordance with FIFRA sec. 6(e). The Basic Confidential Statement of Formula (CSF) dated 2/19/10 is acceptable. All other CSF's including Alternates have been superseded by this new CSF. This has been added to your record. Your product has met and complied with the risk mitigation provisions of the Malathion RED and therefore your product is reregistered pursuant to FIFRA § 4(g)(2)(C). But note, EPA is currently reassessing the cumulative impacts of organophosphates and that review may impact your product once complete. -
Malathion) Lotion, 0.5% Rx Only
NDC 51672-5276-4 Ovide® (malathion) Lotion, 0.5% Rx Only For topical use only. Not for oral or ophthalmic use. DESCRIPTION OVIDE Lotion contains 0.005 g of malathion per mL in a vehicle of isopropyl alcohol (78%), terpineol, dipentene, and pine needle oil. The chemical name of malathion is (±) - [(dimethoxyphosphinothioyl) - thio] butanedioic acid diethyl ester. Malathion has a molecular weight of 330.36, represented by C10H19O6PS2, and has the following chemical structure: CLINICAL PHARMACOLOGY Malathion is an organophosphate agent which acts as a pediculicide by inhibiting cholinesterase activity in vivo. Inadvertent transdermal absorption of malathion has occurred from its agricultural use. In such cases, acute toxicity was manifested by excessive cholinergic activity, i.e., increased sweating, salivary and gastric secretion, gastrointestinal and uterine motility, and bradycardia (see OVERDOSAGE). Because the potential for transdermal absorption of malathion from OVIDE Lotion is not known at this time, strict adherence to the dosing instructions regarding its use in children, method of application, duration of exposure, and frequency of application is required. INDICATIONS AND USAGE OVIDE Lotion is indicated for patients infected with Pediculus humanus capitis (head lice and their ova) of the scalp hair. CONTRAINDICATIONS OVIDE Lotion is contraindicated for neonates and infants because their scalps are more permeable and may have increased absorption of malathion. OVIDE Lotion should also not be used on individuals known to be sensitive to malathion or any of the ingredients in the vehicle. WARNINGS 1. OVIDE Lotion is flammable. The lotion and wet hair should not be exposed to open flames or electric heat sources, including hair dryers and electric curlers. -
Past Use of Chlordane, Dieldrin, And
The Hazard Evaluation and Emergency Response Office (HEER Office) is part of the Hawai‘i Department of Health (HDOH) Environmental Health Administration, whose mission is to protect human health and the environment. The HEER Office provides leadership, support, and partnership in preventing, planning for, responding to, and enforcing environmental laws relating to releases or threats of releases of hazardous substances. Past Use of Chlordane, Dieldrin, and other Organochlorine Pesticides for Termite Control in Hawai‘i: Safe Management Practices around Treated Foundations or during Building Demolition This fact sheet provides building owners, demolition and construction contractors, developers, realtors, and others with an overview of the potential environmental concerns associated with the past use of organochlorine termiticides (pesticides used to control termites) in Hawai‘i. In addition, this fact sheet discusses methods for reducing exposure to organochlorine termiticides during building demolition or around the foundations of treated buildings and identifies resources for further information. What are organochlorine termiticides? Organochlorine termiticides are a group of pesticides that were used for termite control in and around wooden buildings and homes from the mid-1940s to the late 1980s. These organochlorine pesticides included chlordane, aldrin, dieldrin, heptachlor, and dichlorodiphenyltrichloroethane (DDT). They were used primarily by pest control operators in Hawaii’s urban areas, but also by homeowners, the military, the state, and counties to protect buildings against termite damage. In the 1970s and 1980s, the U.S. Environmental Protection Agency (EPA) banned all uses of these organochlorine pesticides except for heptachlor, which can be used today only for control of fire ants in underground power transformers. -
Prenatal Organochlorine Pesticide Exposure and the Disruption of Steroids and Reproductive Hormones in Cord Blood : Title the Hokkaido Study
Prenatal organochlorine pesticide exposure and the disruption of steroids and reproductive hormones in cord blood : Title The Hokkaido study Araki, Atsuko; Miyashita, Chihiro; Mitsui, Takahiko; Goudarzi, Houman; Mizutani, Futoshi; Chisaki, Youichi; Itoh, Author(s) Sachiko; Sasaki, Seiko; Cho, Kazutoshi; Moriya, Kimihiko; Shinohara, Nobuo; Nonomura, Katsuya; Kishi, Reiko Environment international, 110, 1-13 Citation https://doi.org/10.1016/j.envint.2017.10.006 Issue Date 2018-01 Doc URL http://hdl.handle.net/2115/76437 © 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license Rights http://creativecommons.org/licenses/by-nc-nd/4.0/ Rights(URL) http://creativecommons.org/licenses/by-nc-nd/4.0/ Type article (author version) File Information ENVINT_2017_824_(final).pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP 1 2 3 4 5 6 1 Prenatal organochlorine pesticide exposure and the disruption of steroids and 7 8 2 reproductive hormones in cord blood: The Hokkaido Study 9 10 3 Atsuko Arakia, Chihiro Miyashitaa, Takahiko Mitsuib,c, Houman Goudarzia,d, Futoshi 11 12 4 Mizutanie, Youichi Chisakie, Sachiko Itoha, Seiko Sasakif, Kazutoshi Chog, Kimihiko 13 14 5 Moriyah, Nobuo Shinoharah, Katsuya Nonomurah,i, and Reiko Kishia 15 16 6 17 18 7 aCenter for Environmental and Health Sciences, Hokkaido University, Kita 12, Nishi 7, 19 20 8 Sapporo, Hokkaido, Japan 21 22 b 23 9 Department of Urology, Hokkaido University Hospital, Kita 15, Nishi 7, Sapporo, 24 25 10 Hokkaido, Japan 26 -
A General-Purpose Garden Pesticide C
West Virginia Agricultural and Forestry Experiment Davis College of Agriculture, Natural Resources Station Bulletins And Design 1-1-1954 A general-purpose garden pesticide C. K. Dorsey M. E. Gallegly Follow this and additional works at: https://researchrepository.wvu.edu/ wv_agricultural_and_forestry_experiment_station_bulletins Digital Commons Citation Dorsey, C. K. and Gallegly, M. E., "A general-purpose garden pesticide" (1954). West Virginia Agricultural and Forestry Experiment Station Bulletins. 365T. https://researchrepository.wvu.edu/wv_agricultural_and_forestry_experiment_station_bulletins/630 This Bulletin is brought to you for free and open access by the Davis College of Agriculture, Natural Resources And Design at The Research Repository @ WVU. It has been accepted for inclusion in West Virginia Agricultural and Forestry Experiment Station Bulletins by an authorized administrator of The Research Repository @ WVU. For more information, please contact [email protected]. BULLETIN 365T June 1954 WEST VIRGINIA UNIVERSITY AGRICULTURAL EXPERIMENT STATION AUTHORS Authors of A General-Purpose Garden Pesti- cide are C. K. DORSEY, Entomologist and Professor of Entomology, and M. E. GAL- LEGLY, Assistant Plant Pathologist and As- sistant Professor of Plant Pathology. ACKNOWLEDGEMENT The authors are indebted to Kemper L. Callahan for assistance in portions of the studies. West Virginia University Agricultural Experiment Station College of Agriculture, Forestry, and Home Economics H. R. Varney, Director MORGANTOWN A General-Purpose Garden Pesticide C. K. DORSEY and M. E. GALLEGLY IN recent years numerous new insecticides and fungicides have been developed and many have been recommended for use in the home garden. These vary considerably in their effectiveness in the control of different pests. For example, rotenone is effective in controlling the Mexican bean beetle and the potato flea beetle, but is ineffective against the potato leafhopper. -
Chlorpyrifos (Dursban) Ddvp (Dichlorvos) Diazinon Malathion Parathion
CHLORPYRIFOS (DURSBAN) DDVP (DICHLORVOS) DIAZINON MALATHION PARATHION Method no.: 62 Matrix: Air Procedure: Samples are collected by drawing known volumes of air through specially constructed glass sampling tubes, each containing a glass fiber filter and two sections of XAD-2 adsorbent. Samples are desorbed with toluene and analyzed by GC using a flame photometric detector (FPD). Recommended air volume and sampling rate: 480 L at 1.0 L/min except for Malathion 60 L at 1.0 L/min for Malathion Target concentrations: 1.0 mg/m3 (0.111 ppm) for Dichlorvos (PEL) 0.1 mg/m3 (0.008 ppm) for Diazinon (TLV) 0.2 mg/m3 (0.014 ppm) for Chlorpyrifos (TLV) 15.0 mg/m3 (1.11 ppm) for Malathion (PEL) 0.1 mg/m3 (0.008 ppm) for Parathion (PEL) Reliable quantitation limits: 0.0019 mg/m3 (0.21 ppb) for Dichlorvos (based on the RAV) 0.0030 mg/m3 (0.24 ppb) for Diazinon 0.0033 mg/m3 (0.23 ppb) for Chlorpyrifos 0.0303 mg/m3 (2.2 ppb) for Malathion 0.0031 mg/m3 (0.26 ppb) for Parathion Standard errors of estimate at the target concentration: 5.3% for Dichlorvos (Section 4.6.) 5.3% for Diazinon 5.3% for Chlorpyrifos 5.6% for Malathion 5.3% for Parathion Status of method: Evaluated method. This method has been subjected to the established evaluation procedures of the Organic Methods Evaluation Branch. Date: October 1986 Chemist: Donald Burright Organic Methods Evaluation Branch OSHA Analytical Laboratory Salt Lake City, Utah 1 of 27 T-62-FV-01-8610-M 1.