Asthma Search Strategies Appendix F

Total Page:16

File Type:pdf, Size:1020Kb

Asthma Search Strategies Appendix F National Clinical Guidelines Centre Draft Asthma Search strategies appendix F Clinical guideline Appendix F 19 November 2014 Draft for consultation Commissioned by the National Institute for Health and Care Excellence Asthma Contents Disclaimer Healthcare professionals are expected to take NICE clinical guidelines fully into account when exercising their clinical judgement. However, the guidance does not override the responsibility of healthcare professionals to make decisions appropriate to the circumstances of each patient, in consultation with the patient and/or their guardian or carer. Copyright National Clinical Guideline Centre, 2014. Funding National Institute for Health and Care Excellence National Clinical Guideline Centre, 2014. Asthma Contents Contents Appendix F: Literature search strategies ................................ ................................ ........................ 5 National Clinical Guideline Centre, 2014. 4 <ClickAsthma this field on the first page and insert document title / header text> Literature search strategies Appendix F: Literature search strategies Contents Introduction Search methodology Section F.1 Population terms F.1.1 Standard population search strategy This population was used for all search questions unless stated Section F.2 Study filter terms F.2.1 Systematic reviews (SR) F.2.2 Randomised controlled trials (RCT) F.2.3 Observational studies (OBS) F.2.4 Diagnostic test accuracy studies (DIAG1) F.2.5 Diagnostic studies (DIAG2) F.2.6 Prognostic studies (PROG) F.2.7 Validation studies (VAL) F.2.8 Health economic studies (HE) F.2.9 Quality of life studies (QoL) F.2.10 Excluded study designs and publication types Section F.3 Searches for specific questions with intervention (and population where different from A.1) Diagnosing asthma F.3.1 Signs and symptoms F.3.2 Personal/family history of atopic disorders F.3.3 Symptoms in response to exercise F.3.4 Symptoms after drugs F.3.5 Occupational asthma F.3.6 Spirometry/flow volume loop measures F.3.7 Bronchodilator response F.3.8 Peak expiratory flow F.3.9 Skin prick test F.3.10 IgE F.3.11 FeNO F.3.12 Peripheral blood eosinophil count F.3.13 Bronchial challenge test: histamine, methacholine, mannitol F.3.14 Bronchial challenge test: exercise Monitoring asthma control F.3.15 Questionnaires F.3.16 Lung function tests F.3.17 FeNO (monitoring) F.3.18 Peripheral blood eosinophil count (monitoring) National<Click this Clinical field on Guideline the first Centre,page and 2014. insert footer text if required> 5 Asthma Literature search strategies F.3.19 Airway hyper-reactivity measures F.3.20 Adherence to treatment F.3.21 Inhaler technique F.3.22 Tele-healthcare Section F.4 Health economics searches F.4.1 Health economic reviews F.4.2 Quality of life reviews Section F.5 References Search strategies used for the asthma guideline are outlined below and were run in accordance with the methodology in the NICE guidelines manual 2012.{National Institute for Health and Clinical Excellence, 2012 NICE2012 /id} All searches were run up to 2 October 2014 unless otherwise stated. Any studies added to the databases after this date (even those published prior to this date) were not included unless specifically stated in the text. We do not routinely search for electronic, ahead of print or “online early” publications . Where possible searches were limited to retrieve material published in English. Table 1: Database date parameters Database Dates searched Medline 1946—1 October 2014 Embase 1980 – 1 October 2014 (week 39) The Cochrane Library Cochrane Reviews to 2014 Issue 10 of 12 CENTRAL to 2014 Issue 9 of 12 DARE, HTA and NHSEED to 2014 Issue 3 of 4 Searches for the clinical reviews were run in Medline (OVID), Embase (OVID) and the Cochrane Library (Wiley). Searches for intervention and diagnostic studies were usually constructed using a PICO format where population (P) terms were combined with Intervention (I) and sometimes Comparison (C) terms. An intervention can be a drug, a procedure or a diagnostic test. Outcomes (O) are rarely used in search strategies for interventions. Search filters were also added to the search where appropriate. Searches for prognostic studies were usually constructed combining population terms with prognostic variable terms and sometimes outcomes. Search filters were added to the search where appropriate. Searches for the health economic reviews were run in Medline (OVID), Embase (OVID), the NHS Economic Evaluations Database (NHS EED), the Health Technology Assessment (HTA) database and the Health Economic Evaluation Database (HEED). Searches in NHS EED and HEED were constructed using population terms only. For Medline and Embase an economic filter (instead of a study type filter) was added to the same clinical search strategy. F.1 Population search strategies F.1.1 Standard population This population was used in all clinical questions except F.3.5 occupational asthma. Medline and Embase search terms National Clinical Guideline Centre, 2014. 6 Asthma Literature search strategies 1. exp asthma/ 2. asthma*.ti. 3. or/1-2 Cochrane search terms #1. MeSH descriptor: [Asthma] explode all trees #2. asthma*:ti #3. {or #1-#2} F.2 Study filter search terms F.2.1 Systematic review (SR) search terms Medline search terms 1. meta-analysis/ 2. meta-analysis as topic/ 3. (meta analy* or metanaly* or metaanaly*).ti,ab. 4. ((systematic* or evidence*) adj2 (review* or overview*)).ti,ab. 5. (reference list* or bibliograph* or hand search* or manual search* or relevant journals).ab. 6. (search strategy or search criteria or systematic search or study selection or data extraction).ab. 7. (search* adj4 literature).ab. 8. (medline or pubmed or cochrane or embase or psychlit or psyclit or psychinfo or psycinfo or cinahl or science citation index or bids or cancerlit).ab. 9. cochrane.jw. 10. ((multiple treatment* or indirect or mixed) adj2 comparison*).ti,ab. 11. or/1-10 Embase search terms 1. systematic review/ 2. meta-analysis/ 3. (meta analy* or metanaly* or metaanaly*).ti,ab. 4. ((systematic or evidence) adj2 (review* or overview*)).ti,ab. 5. (reference list* or bibliograph* or hand search* or manual search* or relevant journals).ab. 6. (search strategy or search criteria or systematic search or study selection or data extraction).ab. 7. (search* adj4 literature).ab. 8. (medline or pubmed or cochrane or embase or psychlit or psyclit or psychinfo or psycinfo or cinahl or science citation index or bids or cancerlit).ab. 9. cochrane.jw. 10. ((multiple treatment* or indirect or mixed) adj2 comparison*).ti,ab. 11. or/1-10 F.2.2 Randomised controlled trials (RCTs) search terms Medline search terms 1. randomized controlled trial.pt. 2. controlled clinical trial.pt. 3. randomi#ed.ab. 4. placebo.ab. National Clinical Guideline Centre, 2014. 7 Asthma Literature search strategies 5. randomly.ab. 6. clinical trials as topic.sh. 7. trial.ti. 8. or/1-7 Embase search terms 1. random*.ti,ab. 2. factorial*.ti,ab. 3. (crossover* or cross over*).ti,ab. 4. ((doubl* or singl*) adj blind*).ti,ab. 5. (assign* or allocat* or volunteer* or placebo*).ti,ab. 6. crossover procedure/ 7. double blind procedure/ 8. single blind procedure/ 9. randomized controlled trial/ 10. or/1-9 F.2.3 Observational studies (OBS) search terms Medline search terms 1. epidemiologic studies/ 2. exp case control studies/ 3. exp cohort studies/ 4. cross-sectional studies/ 5. case control.ti,ab. 6. (cohort adj (study or studies or analys*)).ti,ab. 7. ((follow up or observational or uncontrolled or non randomi#ed or nonrandomi#ed or epidemiologic*) adj (study or studies)).ti,ab. 8. ((longitudinal or retrospective or prospective or cross sectional) and (study or studies or review or analys* or cohort*)).ti,ab. 9. or/1-8 Embase search terms 1. clinical study/ 2. exp case control study/ 3. family study/ 4. longitudinal study/ 5. retrospective study/ 6. prospective study/ 7. cross-sectional study/ 8. cohort analysis/ 9. follow-up/ 10. cohort*.ti,ab. 11. 9 and 10 12. case control.ti,ab. 13. (cohort adj (study or studies or analys*)).ti,ab. 14. ((follow up or observational or uncontrolled or non randomi#ed or nonrandomi#ed or National Clinical Guideline Centre, 2014. 8 Asthma Literature search strategies epidemiologic*) adj (study or studies)).ti,ab. 15. ((longitudinal or retrospective or prospective or cross sectional) and (study or studies or review or analys* or cohort*)).ti,ab. 16. or/1-8,11-15 Cochrane search terms #1. case control:ti,ab,kw #2. (cohort near/2 (study or studies or analys*)):ti,ab,kw #3. ((follow up or observational or uncontrolled or non randomi?ed or nonrandomi?ed or epidemiologic*) near/2 (study or studies)):ti,ab,kw #4. ((longitudinal or retrospective or prospective or cross sectional) and (study or studies or review or analys* or cohort*)):ti,ab,kw #5. {or #1-#4} F.2.4 Diagnostic test accuracy studies (DIAG1) search terms Medline search terms 1. exp "sensitivity and specificity"/ 2. (sensitivity or specificity).ti,ab. 3. ((pre test or pretest or post test) adj probability).ti,ab. 4. (predictive value* or PPV or NPV).ti,ab. 5. likelihood ratio*.ti,ab. 6. likelihood function/ 7. (ROC curve* or AUC).ti,ab. 8. (diagnos* adj2 (performance* or accurac* or utilit* or value* or efficien* or effectiveness)).ti,ab. 9. gold standard.ab. 10. or/1-9 Embase search terms 1. exp "sensitivity and specificity"/ 2. (sensitivity or specificity).ti,ab. 3. ((pre test or pretest or post test) adj probability).ti,ab. 4. (predictive value* or PPV or NPV).ti,ab. 5. likelihood ratio*.ti,ab. 6. (ROC curve* or AUC).ti,ab. 7. (diagnos* adj2 (performance* or accurac* or utilit* or value* or efficien* or effectiveness)).ti,ab. 8. diagnostic accuracy/ 9. diagnostic test accuracy study/ 10. gold standard.ab. 11. or/1-10 Cochrane search terms #1.
Recommended publications
  • Nitrate Prodrugs Able to Release Nitric Oxide in a Controlled and Selective
    Europäisches Patentamt *EP001336602A1* (19) European Patent Office Office européen des brevets (11) EP 1 336 602 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.7: C07C 205/00, A61K 31/00 20.08.2003 Bulletin 2003/34 (21) Application number: 02425075.5 (22) Date of filing: 13.02.2002 (84) Designated Contracting States: (71) Applicant: Scaramuzzino, Giovanni AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU 20052 Monza (Milano) (IT) MC NL PT SE TR Designated Extension States: (72) Inventor: Scaramuzzino, Giovanni AL LT LV MK RO SI 20052 Monza (Milano) (IT) (54) Nitrate prodrugs able to release nitric oxide in a controlled and selective way and their use for prevention and treatment of inflammatory, ischemic and proliferative diseases (57) New pharmaceutical compounds of general effects and for this reason they are useful for the prep- formula (I): F-(X)q where q is an integer from 1 to 5, pref- aration of medicines for prevention and treatment of in- erably 1; -F is chosen among drugs described in the text, flammatory, ischemic, degenerative and proliferative -X is chosen among 4 groups -M, -T, -V and -Y as de- diseases of musculoskeletal, tegumental, respiratory, scribed in the text. gastrointestinal, genito-urinary and central nervous sys- The compounds of general formula (I) are nitrate tems. prodrugs which can release nitric oxide in vivo in a con- trolled and selective way and without hypotensive side EP 1 336 602 A1 Printed by Jouve, 75001 PARIS (FR) EP 1 336 602 A1 Description [0001] The present invention relates to new nitrate prodrugs which can release nitric oxide in vivo in a controlled and selective way and without the side effects typical of nitrate vasodilators drugs.
    [Show full text]
  • Enzyme Mediated Inflammation: Epidemiology and Therapeutic Implications Parteek Prasher*
    Available online www.jocpr.com Journal of Chemical and Pharmaceutical Research, 2016, 8(9):89-100 ISSN : 0975-7384 Review Article CODEN(USA) : JCPRC5 Enzyme Mediated Inflammation: Epidemiology and Therapeutic implications Parteek Prasher* Assistant Professor of Chemistry, University of Petroleum and Energy Study, Energy acres, Uttrakhand, India ___________________________________________________________________________________ ABSTRACT The identification of various enzymes participating in the arachidonic acid metabolism and recognition of inflammatory metabolites led to systematic studies for the development of anti-inflammatory drugs. Starting with the stimulatory role of phospholipases to release arachidonic acid from phospholipids, over-expression of cyclooxygenase-2 (COX-2) and lipoxygenase (LOX) enzymes cause more than normal production of the respective metabolites. Excessive production of prostaglandins and leukotrienes leads to the manifestation of acute to chronic inflammation in humans. The consequent ailments are expressed in the form of asthma, atherosclerosis, irritable bowel syndrome, arthritis and cancer. Targeting the induced isoform of cyclooxygenase viz. cyclooxygenase-2 (COX-2) and 5-LOX enzyme has opened new aspects for capping the enzyme mediated inflammation. A number of such aspects have been discussed in this comprehensive review. Keywords: COX; Cyclooxygenase; LOX; Lipoxygenase; Arachidonic acid ___________________________________________________________________________________ INTRODUCTION According to a recent survey of the World Health Organization (WHO), cancer causes around 13% of the total deaths worldwide and if it continues rising, it is estimated to cause 13.1 million deaths in 2030 [1]. Moreover, the reason for about 15% of the total cancer deaths has been reported [2] to be associated with chronic inflammation. Hence, an obvious way out to minimize cancer deaths is to put control over the inflammatory conditions.
    [Show full text]
  • Toiminta Unita on Ulla La Mungukurti |
    TOIMINTAUNITA USON 20180071390A1ULLA LA MUNGUKURTI | ( 19) United States (12 ) Patent Application Publication (10 ) Pub. No. : US 2018/ 0071390 A1 PATEL et al. (43 ) Pub . Date : Mar . 15 , 2018 ( 54 ) COMPOSITIONS OF PHARMACEUTICAL A61K 9 / 06 (2006 .01 ) ACTIVES CONTAINING DIETHYLENE A61K 9 /00 (2006 .01 ) GLYCOL MONOETHYL ETHER OR OTHER A61K 31 /573 ( 2006 .01 ) ALKYL DERIVATIVES A61K 31/ 565 ( 2006 .01 ) A61K 31/ 4439 ( 2006 . 01 ) ( 71 ) Applicant : THEMIS MEDICARE LIMITED , A61K 31 / 167 ( 2006 . 01 ) Mumbai (IN ) A61K 31 / 57 (2006 . 01) (52 ) U . S . CI. (72 ) Inventors : Dinesh Shantilal PATEL , Mumbai CPC .. .. .. A61K 47 / 10 ( 2013 . 01 ) ; A61K 9 /4858 ( IN ) ; Sachin Dinesh PATEL , Mumbai ( 2013 .01 ) ; A61K 9 /08 ( 2013 .01 ) ; A61K 9 / 06 ( IN ) ; Shashikant Prabhudas ( 2013 .01 ) ; A61K 9 / 0014 ( 2013 .01 ) ; A61K KURANI, Mumbai ( IN ) ; Madhavlal 31/ 573 ( 2013 .01 ) ; A61K 31 /57 ( 2013 .01 ) ; Govindlal PATEL , Mumbai ( IN ) A61K 31/ 565 ( 2013 .01 ) ; A61K 31 /4439 (73 ) Assignee : THEMIS MEDICARE LIMITED , ( 2013 .01 ) ; A61K 31/ 167 ( 2013 .01 ) ; A61K Mumbai (IN ) 9 /0048 ( 2013 .01 ) ; A61K 9 /0019 (2013 .01 ) ( 57 ) ABSTRACT (21 ) Appl. No .: 15 / 801, 390 The present invention relates to pharmaceutical composi tions of various pharmaceutical actives, especially lyophilic ( 22 ) Filed : Nov . 2 , 2017 and hydrophilic actives containing Diethylene glycol mono ethyl ether or other alkyl derivatives thereof as a primary Related U . S . Application Data vehicle and /or to pharmaceutical compositions utilizing (62 ) Division of application No. 14 /242 , 973 , filed on Apr. Diethylene glycol monoethyl ether or other alkyl derivatives 2 , 2014 , now Pat. No. 9 , 827 ,315 .
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2014/0296.191 A1 PATEL Et Al
    US 20140296.191A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2014/0296.191 A1 PATEL et al. (43) Pub. Date: Oct. 2, 2014 (54) COMPOSITIONS OF PHARMACEUTICAL (52) U.S. Cl. ACTIVES CONTAINING DETHYLENE CPC ............... A61K 47/10 (2013.01); A61 K9/0019 GLYCOL MONOETHYLETHER OR OTHER (2013.01); A61 K9/0048 (2013.01); A61 K ALKYL DERVATIVES 45/06 (2013.01) USPC ........... 514/167: 514/177; 514/178: 514/450; (71) Applicant: THEMIS MEDICARE LIMITED, 514/334: 514/226.5: 514/449; 514/338; Mumbai (IN) 514/256; 514/570; 514/179; 514/174: 514/533; (72) Inventors: Dinesh Shantilal PATEL, Mumbai (IN); 514/629; 514/619 Sachin Dinesh PATEL, Mumbai (IN); Shashikant Prabhudas KURANI, Mumbai (IN); Madhavlal Govindlal (57) ABSTRACT PATEL, Mumbai (IN) (73) Assignee: THEMIS MEDICARE LIMITED, The present invention relates to pharmaceutical compositions Mumbai (IN) of various pharmaceutical actives, especially lyophilic and hydrophilic actives containing Diethylene glycol monoethyl (21) Appl. No.: 14/242,973 ether or other alkyl derivatives thereofas a primary vehicle and/or to pharmaceutical compositions utilizing Diethylene (22) Filed: Apr. 2, 2014 glycol monoethyl ether or other alkyl derivatives thereofas a primary vehicle or as a solvent system in preparation of Such (30) Foreign Application Priority Data pharmaceutical compositions. The pharmaceutical composi Apr. 2, 2013 (IN) ......................... 1287/MUMA2013 tions of the present invention are safe, non-toxic, exhibits enhanced physical stability compared to conventional formu Publication Classification lations containing such pharmaceutical actives and are Suit able for use as injectables for intravenous and intramuscular (51) Int. Cl. administration, as well as for use as a preformed solution/ A647/ (2006.01) liquid for filling in and preparation of capsules, tablets, nasal A6 IK 45/06 (2006.01) sprays, gargles, dermal applications, gels, topicals, liquid oral A6 IK9/00 (2006.01) dosage forms and other dosage forms.
    [Show full text]
  • The Use of Stems in the Selection of International Nonproprietary Names (INN) for Pharmaceutical Substances
    WHO/PSM/QSM/2006.3 The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances 2006 Programme on International Nonproprietary Names (INN) Quality Assurance and Safety: Medicines Medicines Policy and Standards The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances FORMER DOCUMENT NUMBER: WHO/PHARM S/NOM 15 © World Health Organization 2006 All rights reserved. Publications of the World Health Organization can be obtained from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be addressed to WHO Press, at the above address (fax: +41 22 791 4806; e-mail: [email protected]). 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 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. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. 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.
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 7,795,310 B2 Lee Et Al
    US00779531 OB2 (12) United States Patent (10) Patent No.: US 7,795,310 B2 Lee et al. (45) Date of Patent: Sep. 14, 2010 (54) METHODS AND REAGENTS FOR THE WO WO 2005/025673 3, 2005 TREATMENT OF METABOLIC DISORDERS OTHER PUBLICATIONS (75) Inventors: Margaret S. Lee, Middleton, MA (US); Tenenbaum et al., “Peroxisome Proliferator-Activated Receptor Grant R. Zimmermann, Somerville, Ligand Bezafibrate for Prevention of Type 2 Diabetes Mellitus in MA (US); Alyce L. Finelli, Patients With Coronary Artery Disease'. Circulation, 2004, pp. 2197 Framingham, MA (US); Daniel Grau, 22O2.* Shen et al., “Effect of gemfibrozil treatment in sulfonylurea-treated Cambridge, MA (US); Curtis Keith, patients with noninsulin-dependent diabetes mellitus'. The Journal Boston, MA (US); M. James Nichols, of Clinical Endocrinology & Metabolism, vol. 73, pp. 503-510, Boston, MA (US) 1991 (see enclosed abstract).* International Search Report from PCT/US2005/023030, mailed Dec. (73) Assignee: CombinatoRx, Inc., Cambridge, MA 1, 2005. (US) Lin et al., “Effect of Experimental Diabetes on Elimination Kinetics of Diflunisal in Rats.” Drug Metab. Dispos. 17:147-152 (1989). (*) Notice: Subject to any disclaimer, the term of this Abstract only. patent is extended or adjusted under 35 Neogi et al., “Synthesis and Structure-Activity Relationship Studies U.S.C. 154(b) by 0 days. of Cinnamic Acid-Based Novel Thiazolidinedione Antihyperglycemic Agents.” Bioorg. Med. Chem. 11:4059-4067 (21) Appl. No.: 11/171,566 (2003). Vessby et al., “Effects of Bezafibrate on the Serum Lipoprotein Lipid and Apollipoprotein Composition, Lipoprotein Triglyceride Removal (22) Filed: Jun. 30, 2005 Capacity and the Fatty Acid Composition of the Plasma Lipid Esters.” Atherosclerosis 37:257-269 (1980).
    [Show full text]
  • Nonsteroidal Anti-Inflammatory Drugs for Dysmenorrhoea (Review)
    Cochrane Database of Systematic Reviews Nonsteroidal anti-inflammatory drugs for dysmenorrhoea (Review) Marjoribanks J, Ayeleke RO, Farquhar C, Proctor M Marjoribanks J, Ayeleke RO, Farquhar C, Proctor M. Nonsteroidal anti-inflammatory drugs for dysmenorrhoea. Cochrane Database of Systematic Reviews 2015, Issue 7. Art. No.: CD001751. DOI: 10.1002/14651858.CD001751.pub3. www.cochranelibrary.com Nonsteroidal anti-inflammatory drugs for dysmenorrhoea (Review) Copyright © 2015 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd. TABLE OF CONTENTS HEADER....................................... 1 ABSTRACT ...................................... 1 PLAINLANGUAGESUMMARY . 2 SUMMARY OF FINDINGS FOR THE MAIN COMPARISON . ..... 4 BACKGROUND .................................... 5 OBJECTIVES ..................................... 6 METHODS ...................................... 6 Figure1. ..................................... 8 Figure2. ..................................... 10 Figure3. ..................................... 12 RESULTS....................................... 14 Figure4. ..................................... 16 Figure5. ..................................... 18 Figure6. ..................................... 24 ADDITIONALSUMMARYOFFINDINGS . 25 DISCUSSION ..................................... 26 AUTHORS’CONCLUSIONS . 27 ACKNOWLEDGEMENTS . 27 REFERENCES ..................................... 28 CHARACTERISTICSOFSTUDIES . 40 DATAANDANALYSES. 130 Analysis 1.1. Comparison 1 NSAIDs vs placebo, Outcome 1 Pain relief dichotomous data. 136
    [Show full text]
  • Cyclooxygenase
    COX Cyclooxygenase Cyclooxygenase (COX), officially known as prostaglandin-endoperoxide synthase (PTGS), is an enzyme that is responsible for formation of important biological mediators called prostanoids, including prostaglandins, prostacyclin and thromboxane. Pharmacological inhibition of COX can provide relief from the symptoms of inflammation and pain. Drugs, like Aspirin, that inhibit cyclooxygenase activity have been available to the public for about 100 years. Two cyclooxygenase isoforms have been identified and are referred to as COX-1 and COX-2. Under many circumstances the COX-1 enzyme is produced constitutively (i.e., gastric mucosa) whereas COX-2 is inducible (i.e., sites of inflammation). Non-steroidal anti-inflammatory drugs (NSAID), such as aspirin and ibuprofen, exert their effects through inhibition of COX. The main COX inhibitors are the non-steroidal anti-inflammatory drugs (NSAIDs). www.MedChemExpress.com 1 COX Inhibitors, Antagonists, Activators & Modulators (+)-Catechin hydrate (-)-Catechin Cat. No.: HY-N0355 ((-)-Cianidanol; (-)-Catechuic acid) Cat. No.: HY-N0898A (+)-Catechin hydrate inhibits cyclooxygenase-1 (-)-Catechin, isolated from green tea, is an (COX-1) with an IC50 of 1.4 μM. isomer of Catechin having a trans 2S,3R configuration at the chiral center. Catechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM. Purity: 99.59% Purity: 98.78% Clinical Data: Phase 4 Clinical Data: No Development Reported Size: 100 mg Size: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg (-)-Catechin gallate (-)-Epicatechin ((-)-Catechin 3-gallate; (-)-Catechin 3-O-gallate) Cat. No.: HY-N0356 ((-)-Epicatechol; Epicatechin; epi-Catechin) Cat. No.: HY-N0001 (-)-Catechin gallate is a minor constituent in (-)-Epicatechin inhibits cyclooxygenase-1 (COX-1) green tea catechins.
    [Show full text]
  • Stembook 2018.Pdf
    The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances FORMER DOCUMENT NUMBER: WHO/PHARM S/NOM 15 WHO/EMP/RHT/TSN/2018.1 © World Health Organization 2018 Some rights reserved. This work is available under the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 IGO licence (CC BY-NC-SA 3.0 IGO; https://creativecommons.org/licenses/by-nc-sa/3.0/igo). Under the terms of this licence, you may copy, redistribute and adapt the work for non-commercial purposes, provided the work is appropriately cited, as indicated below. In any use of this work, there should be no suggestion that WHO endorses any specific organization, products or services. The use of the WHO logo is not permitted. If you adapt the work, then you must license your work under the same or equivalent Creative Commons licence. If you create a translation of this work, you should add the following disclaimer along with the suggested citation: “This translation was not created by the World Health Organization (WHO). WHO is not responsible for the content or accuracy of this translation. The original English edition shall be the binding and authentic edition”. Any mediation relating to disputes arising under the licence shall be conducted in accordance with the mediation rules of the World Intellectual Property Organization. Suggested citation. The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances. Geneva: World Health Organization; 2018 (WHO/EMP/RHT/TSN/2018.1). Licence: CC BY-NC-SA 3.0 IGO. Cataloguing-in-Publication (CIP) data.
    [Show full text]
  • Novel Composition for Treating Metabolic Syndrome
    (19) & (11) EP 2 494 967 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 05.09.2012 Bulletin 2012/36 A61K 31/155 (2006.01) A61K 31/60 (2006.01) A61K 45/06 (2006.01) A61K 31/4045 (2006.01) (21) Application number: 12170283.1 (22) Date of filing: 16.01.2008 (84) Designated Contracting States: (72) Inventor: Chen, Chien-Hung AT BE BG CH CY CZ DE DK EE ES FI FR GB GR Forest Hills, NY New York 11375 (US) HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR (74) Representative: Coehn, Markus Fish & Richardson P.C. (30) Priority: 16.01.2007 US 885212 P Mies-van-der-Rohe-Strasse 8 80807 München (DE) (62) Document number(s) of the earlier application(s) in accordance with Art. 76 EPC: Remarks: 08727718.2 / 2 118 279 This application was filed on 31-05-2012 as a divisional application to the application mentioned (71) Applicant: IPINTL, LLC under INID code 62. Flushing, NY 11354 (US) (54) Novel composition for treating metabolic syndrome (57) The invention relates to a composition that in- kinase (AMPK) activator; a second agent that possesses cludes a first agent selected from the group consisting anti-inflammatory activity; and a third agent that possess- of an oxidative phosphorylation inhibitor, an ionophore, es serotonin activity. and an adenosine 5’-monophosphate-activated Protein EP 2 494 967 A1 Printed by Jouve, 75001 PARIS (FR) 1 EP 2 494 967 A1 2 Description serotonin (e.g., serotonin sulfate, a serotonin creatinine sulfate complex, or serotonin hydrochloride) and a sero- CROSS-REFERENCE TO RELATED APPLICATION tonin re-uptake inhibitor.
    [Show full text]
  • Can Nsaids Contribute to Alzheimer's Disease?
    SCIENCE AND MEDICINE A NALYSIS Can NSAIDs contribute to Alzheimer’s disease? everal years ago it was dis- inhibitors were coming under S covered that some NSAIDs fire for increasing the risk of ad- lower the levels of amyloid β verse cardiovascular events.3 peptide (Aβ). This peptide is a key component of neuritic plaques, which, along with neu- Mimicking Alzheimer’s disease rofibrillary tangles and cerebral In a recent study, Kukar and atrophy, are a pathologic hall- colleagues tested over 300 mark of Alzheimer’s disease. compounds, including COX-2 Not all NSAIDs produce this selective NSAIDs, NSAID de- result, however, and new re- rivatives and several novel com- search reveals that some cy- pounds, with the goal of finding clooxygenase-2 (COX-2) in- drugs that had little effect on cy- hibitors actually increase the clooxygenase but decreased the production of Aβ, an effect production of Aβ42.1 They ex- comparable to that of muta- posed cultured H4 neuroglioma tions thought to cause Alzhei- cells to various drugs and mea- 1 mer’s disease. sured production of Aβ. Photo.com There are several forms of Their results were surprising. Aβ; the one with 42 amino acids Although they discovered that used in the study have the same (Aβ42) is the insoluble form one NSAID, R-flurbiprofen, effects in the human brain as found in neuritic plaques. The lacked cyclooxygenase activity they did in the mouse model deposition of Aβ42 is thought to and reduced Aβ42 levels, many used in the study. If they do, it is play an important role in the of the COX-2 inhibitors, in- conceivable that they may have cascade of events leading to the cluding tilmacoxib and valde- an impact on the pathology of formation of neurofibrillary tan- coxib, increased the production Alzheimer’s disease, which gles and the eventual degenera- of Aβ42.
    [Show full text]
  • Customs Tariff - Schedule
    CUSTOMS TARIFF - SCHEDULE 99 - i Chapter 99 SPECIAL CLASSIFICATION PROVISIONS - COMMERCIAL Notes. 1. The provisions of this Chapter are not subject to the rule of specificity in General Interpretative Rule 3 (a). 2. Goods which may be classified under the provisions of Chapter 99, if also eligible for classification under the provisions of Chapter 98, shall be classified in Chapter 98. 3. Goods may be classified under a tariff item in this Chapter and be entitled to the Most-Favoured-Nation Tariff or a preferential tariff rate of customs duty under this Chapter that applies to those goods according to the tariff treatment applicable to their country of origin only after classification under a tariff item in Chapters 1 to 97 has been determined and the conditions of any Chapter 99 provision and any applicable regulations or orders in relation thereto have been met. 4. The words and expressions used in this Chapter have the same meaning as in Chapters 1 to 97. Issued January 1, 2020 99 - 1 CUSTOMS TARIFF - SCHEDULE Tariff Unit of MFN Applicable SS Description of Goods Item Meas. Tariff Preferential Tariffs 9901.00.00 Articles and materials for use in the manufacture or repair of the Free CCCT, LDCT, GPT, following to be employed in commercial fishing or the commercial UST, MXT, CIAT, CT, harvesting of marine plants: CRT, IT, NT, SLT, PT, COLT, JT, PAT, HNT, Artificial bait; KRT, CEUT, UAT, CPTPT: Free Carapace measures; Cordage, fishing lines (including marlines), rope and twine, of a circumference not exceeding 38 mm; Devices for keeping nets open; Fish hooks; Fishing nets and netting; Jiggers; Line floats; Lobster traps; Lures; Marker buoys of any material excluding wood; Net floats; Scallop drag nets; Spat collectors and collector holders; Swivels.
    [Show full text]