Coagulant & Anticoagulants

Total Page:16

File Type:pdf, Size:1020Kb

Coagulant & Anticoagulants Coagulant & Anticoagulants Dr. Saurabh C. Khadse COAGULANTS • Several pathologic and toxicologic conditions can result in excessive bleeding from inadequate coagulation • Depending on the severity of the hemorrhagic condition, several blood coagulants are therapeutically used. • Vitamin K is effective in the treatment hemorrhagic condition • Vitamin K1 (phytonadione) is most often used therapeutically. • Vitamin K1 is safe for use in infants, pregnant womens • Phytonadione is more lipid soluble, has a faster onset than vitamin K3 (menadione) or vitamin K4 (menadiol sodium diphosphate) 10/4/2020 Saurabh Khadse 2 • Only advantage of vitamins K3 and K4 over vitamin K1 is that they dont require presence of bile for absorption • Vit K3 & K4 because are absorbed via a passive process directly from the intestine 10/4/2020 Saurabh Khadse 3 Role of Vitamin K in coagulation • Vitamin K helps to regulate the process of blood coagulation by helping in the formation of some coagulation factors • Without vitamin K, our bodies would be unable to control clot formation. • Vitamin K is required to produce coagulation factors II, VII, IX, and X 10/4/2020 Saurabh Khadse 4 Role of Vitamin K in activation of coagulation factors 10/4/2020 Saurabh Khadse 5 Scheme of blood coagulation and fibrinolysis.( vitamin K–dependent factor; †, inhibition 10/4/2020 Saurabh Khadse 6 by heparin and antithrombin III.) Examples of coagulants O O CH3 CH3 H3C O O Menadione Acetomenadione 2-methylnaphthalene-1,4-dione 2-methylnaphthalene-1,4-diyl diacetate Acetomenadione is also known as davitamon-K or Acetomenaphthone 10/4/2020 Saurabh Khadse 7 MOA of Menadione • Menadione acts as a vitamin K analogue • Which acts as a cofactor in the synthesis of Factor II, VII, IX, X in the liver. • The Vitamin K analogue is needed in the step of gamma carboxylation of these factors to activate them • which makes them capable of binding Ca ++ ions to phospholipid surfaces which is essential for the coagulation cascade. 10/4/2020 Saurabh Khadse 8 Anticoagulants and antiplatelet drugs • Venous thromboembolism (VTE) is a complicating condition responsible for high morbidity and mortality worldwide • Thrombotic disorders involves the major vasculature, heart, brain, and lungs • In the heart, a thrombotic condition may be involved in the disease state of acute myocardial infarction, valvular heart disease, unstable angina, and atrial fi brillation • as surgical procedures, such angioplasty and prosthetic heart valve replacement. • Thrombosis in lungs result in pulmonary embolism (PE). • In such cases two different classes of antithrombotic agents are used namely anticoagulants and antiplatelet drugs 10/4/2020 Saurabh Khadse 9 ORAL ANTICOAGULANTS • There are two different chemical classes of orally active anticoagulants Coumarin derivatives : Warfarin 1,3-indandiones : Anisindione 3-(α- acetonylbenzyl)-4-hydroxycoumarin 2-(p-methoxyphenyl)-1,3-indandione sodium10/4/2020 salt Saurabh Khadse 10 MOA of anti-coagulants • Activation (carboxylation) of coagulation factors requires reduced form of vitamin K • The warfarin like anticoagulants (i.e., vitamin K antagonists) exert their anticoagulant activity through the inhibition of vitamin K quinone reductase enzyme. • inhibition of vitamin K quinone reductase inhibits activation of the four coagulation factors • Therefore, warfarin like compounds acts as vitamin K antagonists 10/4/2020 Saurabh Khadse 11 MOA of warfarin like compounds 10/4/2020 Saurabh Khadse 12 SAR of warfarin like compounds in vivo formation of cyclic hemiketal conformer Coumarin derivatives with 3,4-substitution •Substitution of the lactone ring, specifically in positions 3 and 4 is important •The acidity of the proton on the 4-hydroxy group allows formation of water- soluble sodium salts • in vivo formation of cyclic hemiketal conformers is important for activity 10/4/2020 Saurabh Khadse 13 Platelet aggregation inhibitor • Antiplatelet drugs work by inhibiting platelet activation via a number of different mechanisms • The antiplatelet drugs are mainly used in patients with coronarydiseases • These drugs also are effective in combination with moderate- intensity anticoagulants for patients with atrial fibrillation. Clopidogrel is an antiplatelet agent, or blood thinner 10/4/2020 belonging to chemicalSaurabh class Khadse- thienopyridine 14 Platelet aggregation • Pathological formation of clots within the circulatory system creates serious clinical situation • Platelets bind to collagen in the vessel wall and trigger other platelets to adhere to them • Calcium binding to the platelet membrane cause adhesiveness • ADP released by the first few adhering cells further stimulates aggregation process. 10/4/2020 Saurabh Khadse 15 Inhibition of platelet aggregation • While, increased levels of cAMP inhibit platelet aggregation • cAMP activates specific dependent kinases, which form protein- phosphate complexes that chelate calcium ions. • The reduced levels of calcium inhibit aggregation • Inhibitors of platelet aggregation can increase cAMP levels by either stimulating adenylate cyclase or inhibiting phosphodiesterase 10/4/2020 Saurabh Khadse 16 Role of adenosine 3,5-cyclic monophosphate (cAMP) in inhibition of platelet aggregation ADP binds to platelet P2Y Purinergic Receptor & promotes platelet aggregation • Purinergic receptors P2Y1 and P2Y12 in platelet are activated by ADP • P2Y1 and P2Y12 are G protein-coupled purinergic receptors • Initial binding of ADP to the P2Y1 induces platelet shape changes, causes intracellular calcium mobilization, and initiates aggregation • Subsequent binding of ADP to the P2Y12 leads to sustained platelet aggregation by inhibiting adenylate cyclase and, thereby, decreasing cellular cAMP levels 10/4/2020 Saurabh Khadse 17 MOA of Clopidogrel • The antithrombotic drugs ticlopidine and clopidogrel are irreversible antagonists of P2Y12 purinergic receptor • Antagonism of P2Y12 receptor increases cellular cAMP levels • Increased cAMP levels initiates chelation of calcium ions • The reduced levels of calcium inhibits aggregation Clopidogrel 10/4/2020 Saurabh Khadse 18 10/4/2020 Saurabh Khadse 19 synthesis of warfarin 10/4/2020 Saurabh Khadse 20.
Recommended publications
  • Perioperative Management of Patients Treated with Antithrombotics in Oral Surgery
    SFCO/Perioperative management of patients treated with antithrombotic agents in oral surgery/Rationale/July 2015 SOCIÉTÉ FRANÇAISE DE CHIRURGIE ORALE [FRENCH SOCIETY OF ORAL SURGERY] IN COLLABORATION WITH THE SOCIÉTÉ FRANÇAISE DE CARDIOLOGIE [FRENCH SOCIETY OF CARDIOLOGY] AND THE PERIOPERATIVE HEMOSTASIS INTEREST GROUP Space Perioperative management of patients treated with antithrombotics in oral surgery. RATIONALE July 2015 P a g e 1 | 107 SFCO/Perioperative management of patients treated with antithrombotic agents in oral surgery/Rationale/July 2015 Abbreviations ACS Acute coronary syndrome(s) ADP Adenosine diphosphate Afib Atrial Fibrillation AHT Arterial hypertension Anaes Agence nationale d’accréditation et d’évaluation en santé [National Agency for Accreditation and Health Care Evaluation] APA Antiplatelet agent(s) aPTT Activated partial thromboplastin time ASA Aspirin BDMP Blood derived medicinal products BMI Body mass index BT Bleeding Time cAMP Cyclic adenosine monophosphate COX-1 Cyclooxygenase 1 CVA Cerebral vascular accident DIC Disseminated intravascular coagulation DOA Direct oral anticoagulant(s) DVT Deep vein thrombosis GEHT Study Group on Hemostasis and Thrombosis (groupe d’étude sur l’hémostase et la thrombose) GIHP Hemostasis and Thrombosis Interest Group (groupe d’intérêt sur l’hémostase et la thrombose) HAS Haute autorité de santé [French Authority for Health] HIT Heparin-induced thrombocytopenia IANB Inferior alveolar nerve block INR International normalized ratio IV Intravenous LMWH Low-molecular-weight heparin(s)
    [Show full text]
  • Malaysian STATISTICS on MEDICINE 2005
    Malaysian STATISTICS ON MEDICINE 2005 Edited by: Sameerah S.A.R Sarojini S. With contributions from Goh A, Faridah A, Rosminah MD, Radzi H, Azuana R, Letchuman R, Muruga V, Zanariah H, Oiyammal C, Sim KH, Fong AYY, Tamil Selvan M, Basariah N, Hooi LS, Zaki Morad, Fadilah O, Lim V.K.E., Tan KK, Biswal BM, Lim YS, Lim GCC, Mohammad Anwar H.A, Ahmad Sabri O, Mary SC, Marzida M, Benjamin Chan TM, Suarn Singh, Zoriah A, Noor Ratna N , Abdul Razak M, Norzila Z, Shamsinah H A publication of the Pharmaceutical Services Division and the Clinical Research Centre Ministry of Health Malaysia Malaysian Statistics On Medicine 22005005 Edited by: Sameerah S.A.R Sarojini S. With contributions from Goh A, Faridah A, Rosminah MD, Radzi H, Azuana R, Letchuman R, Muruga V, Zanariah H, Oiyammal C, Sim KH, Fong AYY, Tamil Selvan M, Basariah N, Hooi LS, Zaki Morad, Fadilah O, Lim V.K.E., Tan KK, Biswal BM, Lim YS, Lim GCC, Mohammad Anwar H.A, Ahmad Sabri O, Mary SC, Marzida M, Benjamin Chan TM, Suarn Singh, Zoriah A, Noor Ratna N , Abdul Razak M, Norzila Z, Shamsinah H A publication of the Pharmaceutical Services Division and the Clinical Research Centre Ministry of Health Malaysia Malaysian Statistics On Medicine 2005 April 2007 © Ministry of Health Malaysia Published by: The National Medicines Use Survey Pharmaceutical Services Division Lot 36, Jalan Universiti 46350 Petaling Jaya Selangor, Malaysia Tel. : (603) 4043 9300 Fax : (603) 4043 9400 e-mail : [email protected] Web site : http://www.crc.gov.my/nmus This report is copyrighted.
    [Show full text]
  • Neuraxial Blockade and Anticoagulants
    Soli Deo Gloria NEURAXIAL BLOCKADE AND ANTICOAGULANTS Developing Countries Regional Anesthesia Lecture Series Lecture 4 Daniel D. Moos CRNA, Ed.D. U.S.A. [email protected] Disclaimer Every effort was made to ensure that material and information contained in this presentation are correct and up-to-date. The author can not accept liability/responsibility from errors that may occur from the use of this information. It is up to each clinician to ensure that they provide safe anesthetic care to their patients. INTRODUCTION Benefits of Neuraxial Blockade Decreased nausea and vomiting Decreased blood loss Decreased incidence of graft occlusion Improved mobility after major knee surgery Superior postoperative pain control Less alteration to the cardiopulmonary status of the patient The need for formalized guidance for anticoagulated patient: Advances in pharmacology Desire to prevent thromboembolism Formulation of thromboembolism prophylaxis Use of regional anesthesia ASRA Guidelines 1998 the first Consensus Conference on Neuraxial Anesthesia and Analgesia was held. 2002 the second Consensus Conference was held. The result: formalized guidelines to assist the anesthesia provider in decision making. THROMBOPROPHYLAXIS Medications for total joint thromboprophylaxis Unfractionated heparin Low molecular weight heparin (ardeparin sodium or Normoflo®, dalteparin sodium or Fragmin®, danaparoid sodium or Orgaran®, enoxaprin sodium or Lovenox® and tinzaprin or Innohep®). Warfarin sodium Medications for general surgery thromboprophylaxis
    [Show full text]
  • Glycoprotein Iib/Iiia Inhibitors During Percutaneous Coronary Interventions
    REVIEW Glycoprotein IIb/IIIa inhibitors during percutaneous coronary interventions Intravenous glycoprotein IIb/IIIa inhibitors are widely used during percutaneous coronary interventions (PCIs). There are three commercially available pharmacological agents: abciximab, eptifibatide and tirofiban. This article presents the evidence indicating their use in connection with PCI, and focuses on the differences between the three regimens, as well as on their use in special clinical conditions. The documentation for their use in high-risk PCI (in other words, for acute coronary syndromes and complex coronary anatomy), and in primary PCI for ST-elevation myocardial infarction will be scrutinized, as well as the use of intracoronary administration. Furthermore, the role of glycoprotein IIb/IIIa inhibitors as opposed to, or in combination with, thienopyridines and thrombin inhibitors will be analyzed, as will their use in diabetics, in patients with renal insufficiency and when performing PCI in vein grafts. Finally, the possible effects of glycoprotein IIb/IIIa inhibitors on restenosis and inflammation, as well as dosing and bleeding issues will be discussed. †1 KEYWORDS: abciximab n eptifibatide n glycoprotein IIb/IIIa inhibitor n myocardial Michael Koutouzis infarction n percutaneous coronary intervention n tirofiban & Lars Grip1 1Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden Percutaneous coronary intervention, to be developed and brought forward for clini- †Author for correspondence: coronary thrombosis & development cal use [6,7]. Abciximab has a high molecular Tel.: +46 313 427 565 Fax: +46 3182 0062 of glycoprotein IIb/IIIa inhibitors weight of more than 47,000 Da, a high affinity [email protected] Percutaneous coronary intervention (PCI) was to the GP IIb/IIIa receptor and a relatively short introduced as balloon dilatation by Grüntzig in plasma half-life (20–30 min).
    [Show full text]
  • Advances in Interventional Cardiology New Directions In
    Advances in Interventional Cardiology New Directions in Antiplatelet Therapy Jose´ Luis Ferreiro, MD; Dominick J. Angiolillo, MD, PhD therosclerosis is a chronic inflammatory process that is A2 (TXA2) from arachidonic acid through selective acetylation Aknown to be the underlying cause of coronary artery of a serine residue at position 529 (Ser529). TXA2 causes disease (CAD).1 In addition to being the first step of primary changes in platelet shape and enhances recruitment and aggre- hemostasis, platelets play a pivotal role in the thrombotic gation of platelets through its binding to thromboxane and process that follows rupture, fissure, or erosion of an athero- prostaglandin endoperoxide (TP) receptors. Therefore, aspirin sclerotic plaque.2 Because atherothrombotic events are essen- decreases platelet activation and aggregation processes mediated tially platelet-driven processes, this underscores the impor- by TP receptor pathways.7 tance of antiplatelet agents, which represent the cornerstone Although the optimal dose of aspirin has been the subject of treatment, particularly in the settings of patients with acute of debate, the efficacy of low-dose aspirin is supported by the coronary syndromes (ACS) and undergoing percutaneous results of numerous studies.8–10 In these investigations, a coronary intervention (PCI). dose-dependent risk for bleeding, particularly upper gastro- Currently, there are 3 different classes of antiplatelet drugs that are approved for clinical use and recommended per intestinal bleeding, with no increase in
    [Show full text]
  • Antiplatelet Therapy in Diabetes: Efficacy and Limitations of Current
    Bench to Clinic Symposia EDITORIAL REVIEW Antiplatelet Therapy in Diabetes: Efficacy and Limitations of Current Treatment Strategies and Future Directions DOMINICK J. ANGIOLILLO, MD, PHD of low-dose aspirin (75–162 mg/day) as a primary prevention strategy in patients with type 1 or type 2 diabetes at increased Ͼ ardiovascular disease is the leading patients undergoing percutaneous coro- cardiovascular risk, including those 40 cause of morbidity and mortality in nary interventions (PCI) (4). However, years of age or who have additional risk C patients with diabetes (1). The con- these agents are available only for paren- factors (family history of cardiovascular comitant presence of multiple classical teral use and have a short duration of ac- disease, hypertension, smoking, dyslipi- cardiovascular risk factors in diabetic tion, which impedes their use for long- demia, or albuminuria) (8). However, subjects contributes to enhanced athero- term protection. The need for alternative aspirin therapy should not be recom- thrombotic risk (2). However, other risk antiplatelet treatment strategies led to the mended for patients aged Ͻ21 years be- factors may be important such as abnor- evaluation of effects obtained from a com- cause this may increase the risk of Reye’s mal platelet function (3). Platelets, in fact, bination of oral antiplatelet agents inhib- syndrome. The role of aspirin in diabetic play a key role in atherogenesis, and its iting other platelet-activating pathways. patients aged Ͻ30 years remains unclear thrombotic complications and measures, Ticlopidine is a first-generation thienopy- because it has not been investigated. which lead to blockade of one or multiple ridine, which irreversibly blocks the Several clinical trials have evaluated the efficacy of aspirin in diabetic patients pathways modulating platelet activation platelet ADP P2Y12 receptor (6).
    [Show full text]
  • Updated Guideline of Glycoprotein Iib/Iiia Inhibitor for Acute Coronary Syndrome
    Updated Guideline of Glycoprotein IIb/IIIa Inhibitor for Acute Coronary Syndrome Young-Hak Kim, MD, PhD Heart Institute, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea 1 Disclosure Information Honorarium from Handok Corp Clinical Classification of ACS Acute Coronary Syndrome Hx EKG No ST Elevation ST Elevation Cardiac Biomarker Final Unstable Non- Dx STEMI Angina STEMI 3 Platelet Activation Epinephrine Collagen ADP Thrombin AA Thienopyridines Aspirin Platelet TxA2 GP IIb/IIIa Platelet GPIIb/IIIa inhibitors Membrane Fibrinogen Target Sites of Antiplatelet Therapy Disruption of Shear Stress, Prostaglandins Endothelium Binding of Agonists: Direct GPlb/vWF Platelet l Thrombin Antithrombins Antagonists, Adhesion Dipyridamole Serotonin l Serotonin Antagonists Platelet Activation Clopidogrel l ADP Ticlopidine Aspirin, Platelet TxS Inhibitors Release TXA Receptor l TXA 2 2 Antagonists l Others GPllb/llla Platelet GP = Glycoprotein Antagonists Aggregation vWF = von Willebrand factor TxS = Thromboxane synthase TXA2 = Thromboxane A2 Schafer AI. Am J Med. 1996;101:202. Parenteral GP IIb/IIIa inhibitors Antibody • abciximab (ReoProâ, Centocor/Lilly) Cyclic peptide • eptifibatide (INTEGRILIN®, COR/Key) Nonpeptide • tirofiban HCI (Aggrastatâ, Merck) GP IIb/IIIa Receptor Antagonists Abciximab Tirofiban Eptifibatide (ReoPro®) (Aggrastat®) (Integrilin®) Fab portion of Pharma chimeric monoclonal Synthetic non-peptide Cyclic heptapeptide antibody Half-life 30 minutes 1.8 hours 2.5 hours Renal Adj. No Yes Yes Dosage 0.25 mcg/kg
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2016/0324897 A1 INGBER Et Al
    US 20160324897A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2016/0324897 A1 INGBER et al. (43) Pub. Date: Nov. 10, 2016 (54) PLATELET DECOYS AND USE THEREOF Related U.S. Application Data (60) Provisional application No. 61/928,458, filed on Jan. (71) Applicant: PRESIDENT AND FELLOWS OF 17, 2014, provisional application No. 61/938,329, HARVARD COLLEGE, Cambridge, filed on Feb. 11, 2014. MA (US) Publication Classification (72) Inventors: Donald E. INGBER, Boston, MA (US); Anne-Laure PAPA, Boston, MA (51) Int. Cl. (US) A 6LX 35/9 (2006.01) CI2N 5/078 (2006.01) (52) U.S. Cl. (73) Assignee: PRESIDENT AND FELLOWS OF CPC ............. A61K 35/19 (2013.01); C12N5/0644 HARVARD COLLEGE, Cambridge, (2013.01) MA (US) (57) ABSTRACT (21) Appl. No.: 15/111.999 The invention provides platelet decoys and mimics that can bind to platelet receptor substrate but do not undergo platelet (22) PCT Filed: Jan. 16, 2015 activation. The invention also provides methods of using the platelet decoys for treating, preventing or inhibiting a dis (86) PCT No.: PCT/US 15/11805 ease or disorder in Subject when platelet activation, aggre S 371 (c)(1), gation and/or adhesion contributes to the pathology or (2) Date: Jul. 15, 2016 symptomology of the disease. Patent Application Publication Nov. 10, 2016 Sheet 1 of 13 US 2016/0324897 A1 """ FC a C E -aos FIG. I.A. A. 1828 15. s ar st s: -- as X A. i "f '" C ... C. E. P.C..re- -...-FC CSF--...-kee. FIG. IC FIG.
    [Show full text]
  • Curriculum Vitae
    Duxin Sun, Ph.D. CV 03042021 Department of Pharmaceutical Sciences University of Michigan College of Pharmacy North Campus Research Complex Building 520 Duxin Sun, Ph.D. 1600 Huron Parkway, Ann Arbor, MI 48109 Tel: 734-615-8740 (Office); 734-615-8851 (Lab) Charles R. Walgreen, Jr. Professor Email: [email protected] of Pharmacy (With Tenure) http://pharmacy.umich.edu/people/duxins Education 1998-2002 Ph.D. in Pharmaceutical Sciences Department of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, Michigan 1994-1998 Visiting Scholar in Molecular Pharmacology Department of Pharmacology, University of Pennsylvania (Philadelphia, PA) and Vanderbilt University (Nashville, TN) 1989-1992 Master of Pharmacology School of Pharmacy, Second Military Medical University, Shanghai, China 1982-1986 Bachelor of Pharmacy School of Pharmacy, Second Military Medical University, Shanghai, China Appointments 2021- Charles R. Walgreen, Jr. Professor of Pharmacy Department of Pharmaceutical Sciences, College of Pharmacy, The University of Michigan, Ann Arbor, MI 48109 2017-2021 J.G. Searle Endowed Professor Department of Pharmaceutical Sciences, College of Pharmacy, The University of Michigan, Ann Arbor, MI 48109 2014-2017 William I. Higuchi Collegiate Professor Department of Pharmaceutical Sciences, College of Pharmacy, The University of Michigan, Ann Arbor, MI 48109 2013- Professor Department of Pharmaceutical Sciences, College of Pharmacy, The University of Michigan, Ann Arbor, MI 48109 Director of Pharmacokinetics Core, College
    [Show full text]
  • BARMER GEK Arzneimittelreport 2013
    Gerd Glaeske Christel Schicktanz mit Beiträgen von Christian Bachmann, Stanislava Dicheva, Anna Hinrichs, Falk Hoffmann, Guido Schmiemann, Jana Schulze und Roland Windt unter Mitarbeit von Michaela Dollhopf, Angela Fritsch, Friederike Höfel, Tim Jacobs, Claudia Kretschmer und Daniela Stahn BARMER GEK Arzneimittelreport 2013 Auswertungsergebnisse der BARMER GEK Arzneimitteldaten aus den Jahren 2011 bis 2012 Juni 2013 1 Bibliografische Information der Deutschen Bibliothek Die Deutsche Bibliothek verzeichnet diese Publikation in der deutschen Nationalbibliografie; detaillierte bibliografische Daten sind im Internet unter http://dnb.ddb.de abrufbar. Schriftenreihe zur Gesundheitsanalyse, Band 20 BARMER GEK Arzneimittelreport 2013 Herausgeber: BARMER GEK Postfach 110704 10837 Berlin Fachliche Betreuung: BARMER GEK Kompetenzzentrum Medizin und Versorgungsforschung (1100) Gottlieb-Daimler-Straße 19 73529 Schwäbisch Gmünd [email protected] Autoren: Gerd Glaeske, Christel Schicktanz Universität Bremen, Zentrum für Sozialpolitik (ZeS), Abteilung für Gesundheitsökonomie, Gesundheitspolitik und Versorgungsforschung [email protected] Verlag: Asgard Verlagsservice GmbH, Schützenstraße 4, 53721 Siegburg ISBN: 978-3-943-74485-9 Das Werk einschließlich aller seiner Teile ist urheberrechtlich geschützt. Jede Verwertung außerhalb der engen Grenzen des Urheberrechtsgesetzes ist ohne Zustimmung des Herausgebers unzulässig und strafbar. Das gilt insbesondere für Vervielfältigungen, Übersetzungen, Mikroverfilmung und die Einspeicherung
    [Show full text]
  • Computer-Aided Design of Novel Antithrombotic Agents
    UNIVERSITÉ DE STRASBOURG en cotutelle avec INSTITUT BOGATSKY DE CHIMIE PHYSIQUE, ODESSA, UKRAINE ÉCOLE DOCTORALE DES SCIENCES CHIMIQUE UMR 7140 Unistra/CNRS THÈSE présentée par Tetiana KHRISTOVA soutenue le 15 novembre 2013 pour obtenir le grade de Docteur de l’Université de Strasbourg Discipline: Chimie Spécialité: Chemoinformatique Computer-aided design of novel antithrombotic agents Directeurs de thèse: M.VARNEK Alexandre Professeur, Université de Strasbourg M. KUZMIN Victor Professeur, Institut Bogatsky de Chimie Physique, Odessa, Ukraine Rapporteurs: M. VILLOUTREIX Bruno Docteur, Université Paris-Diderot M. TETKO Igor Docteur, Institut of Structural Biology, Helmholtz Zentrum München, Neuherberg, Allemagne Examinateurs: M. STOTE Roland Docteur, Université de Strasbourg M. LANGER Thierry Professeur, Prestwick Chemical, Strasbourg Ms Tetiana Khristova was a member of the European Doctoral College of the University of Strasbourg during the preparation of her PhD, from 2010 to 2013, class name Jane Goodall. She has benefited from specific financial supports offered by the College and, along with her mainstream research, has followed a special course on topics of general European interests presented by international experts. This PhD research project has been led with the collaboration of two universities: the A.V.Bogatsky Physico-Chemical Institute, Ukraine and the University of Strasbourg, France. 2 Acknowledgment I would like to thanks French Embassy in Ukraine for the PhD fellowship. As well I want to express my gratitude to my supervisors Professor Alexandre Varnek and Professor Victor Kuz‟min for the opportunity to participate in this exciting French-Ukrainian project. Without their guidance and persistent help this PhD thesis would not have been possible. Then I would like to express my gratitude to Dr.
    [Show full text]
  • Anticoagulants: Newer Ones, Mechanisms, and Perioperative Updates
    Anticoagulants: Newer Ones, Mechanisms, and Perioperative Updates a, b Julie A. Gayle, MD *, Alan D. Kaye, MD, PhD , c d Adam M. Kaye, PharmD , Rinoo Shah, MD KEYWORDS New anticoagulants Anesthetic concerns Herbal medications Perioperative anticoagulation The ongoing research and development of new anticoagulant/antiplatelet drugs deserves special attention in the evaluation and management of patients presenting for surgery. As part of the development of the ideal anticoagulant, the newer drugs aim to provide safe, effective, and predictable anticoagulant activity with ease of use (ie, oral administration or minimal number of daily injections) and no need for moni- toring.1 Anesthesiologists must be familiar with the newly developed anticoagulants because their use in the perioperative setting will likely increase. Mechanisms of action of these newer anticoagulants warrant consideration as do the risks and benefits of discontinuation or reversal of the drugs before surgery.2 Of equal importance are the recommendations by the American Society of Regional Anesthesia and Pain Medi- cine (ASRA) pertaining to regional anesthesia in patients receiving these new anticoagulants. The use of herbal medications and certain vitamin supplements has dramatically increased in recent years. Some of these alternative medicines enhance the effects of anticoagulant drugs. Therefore, it is important to elicit a history of use to avoid exag- gerated effects, specifically bleeding.3 a Department of Anesthesiology, Louisiana State University Health Sciences Center, New Orleans, LA, USA b Departments of Anesthesiology and Pharmacology, Louisiana State University School of Medicine, 1542 Tulane Avenue, Room 656, New Orleans, LA, USA c Department of Pharmacy Practice, Thomas J. Long School of Pharmacy and Health Sciences, University of the Pacific, Stockton, CA, USA d Department of Anesthesiology, Guthrie Clinic-Big Flats, Horseheads, NY, USA * Corresponding author.
    [Show full text]