DOCSLIB.ORG

1873 JP XVI Infrared Reference Spectra

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
1873 JP XVI Infrared Reference Spectra JP XVI Infrared Reference Spectra 1873 Ibudilast Ibuprofen Ifenprodil Tartrate 1874 Infrared Reference Spectra JP XVI Imidapril Hydrochloride Imipenem Hydrate Indapamide JP XVI Infrared Reference Spectra 1875 Indenolol Hydrochloride Indometacin Iodamide 1876 Infrared Reference Spectra JP XVI Iopamidol Iotalamic Acid Iotroxic Acid JP XVI Infrared Reference Spectra 1877 Ipratropium Bromide Hydrate Ipriflavone Irsogladine Maleate 1878 Infrared Reference Spectra JP XVI Isoflurane L-Isoleucine Isoniazid JP XVI Infrared Reference Spectra 1879 Isosorbide Isoxsuprine Hydrochloride Itraconazole 1880 Infrared Reference Spectra JP XVI Ketamine Hydrochloride Ketoconazole Ketoprofen JP XVI Infrared Reference Spectra 1881 Ketotifen Fumarate Kitasamycin Acetate Kitasamycin Tartrate 1882 Infrared Reference Spectra JP XVI Labetalol Hydrochloride Anhydrous Lactose Lactose Hydrate JP XVI Infrared Reference Spectra 1883 Latamoxef Sodium Lenampicillin Hydrochloride L-Leucine 1884 Infrared Reference Spectra JP XVI Levallorphan Tartrate Levofloxacin Hydrate Lidocaine JP XVI Infrared Reference Spectra 1885 Lincomycin Hydrochloride Hydrate Lisinopril Hydrate Lorazepam 1886 Infrared Reference Spectra JP XVI Losartan Potassium Loxoprofen Sodium Hydrate L-Lysine Acetate JP XVI Infrared Reference Spectra 1887 L-Lysine Hydrochloride Manidipine Hydrochloride D-Mannitol 1888 Infrared Reference Spectra JP XVI Maprotiline Hydrochloride Medazepam Mefloquine Hydrochloride JP XVI Infrared Reference Spectra 1889 Mefruside Menatetrenone Mepitiostane 1890 Infrared Reference Spectra JP XVI Mepivacaine Hydrochloride Mequitazine Mestranol JP XVI Infrared Reference Spectra 1891 Metenolone Acetate Metformin Hydrochloride L-Methionine 1892 Infrared Reference Spectra JP XVI Methotrexate Methyldopa Hydrate dl-Methylephedrine Hydrochloride JP XVI Infrared Reference Spectra 1893 Methyl Parahydroxybenzoate Methylprednisolone Succinate Methyltestosterone 1894 Infrared Reference Spectra JP XVI Meticrane Metildigoxin Metoprolol Tartrate JP XVI Infrared Reference Spectra 1895 Metronidazole Mexiletine Hydrochloride Miconazole 1896 Infrared Reference Spectra JP XVI Midecamycin Midecamycin Acetate Minocycline Hydrochloride JP XVI Infrared Reference Spectra 1897 Mitomycin C Mizoribine Morphine Hydrochloride Hydrate 1898 Infrared Reference Spectra JP XVI Mosapride Citrate Hydrate Nabumetone Nafamostat Mesilate JP XVI Infrared Reference Spectra 1899 Nalidixic Acid Naloxone Hydrochloride Naproxen 1900 Infrared Reference Spectra JP XVI Nateglinide Neostigmine Methylsulfate Nicardipine Hydrochloride JP XVI Infrared Reference Spectra 1901 Nicergoline Niceritrol Nicomol 1902 Infrared Reference Spectra JP XVI Nicorandil Nifedipine Nilvadipine JP XVI Infrared Reference Spectra 1903 Nitrendipine Nizatidine Noradrenaline 1904 Infrared Reference Spectra JP XVI Norfloxacin Norgestrel Nortriptyline Hydrochloride JP XVI Infrared Reference Spectra 1905 Noscapine Ofloxacin Omeprazole 1906 Infrared Reference Spectra JP XVI Oxapium Iodide Oxaprozin Oxethazaine JP XVI Infrared Reference Spectra 1907 Oxprenolol Hydrochloride Oxycodone Hydrochloride Hydrate Oxymetholone 1908 Infrared Reference Spectra JP XVI Ozagrel Sodium Pancuronium Bromide Pemirolast Potassium JP XVI Infrared Reference Spectra 1909 Penbutolol Sulfate Pentobarbital Calcium Pentoxyverine Citrate 1910 Infrared Reference Spectra JP XVI Pethidine Hydrochloride Phenethicillin Potassium Phenobarbital JP XVI Infrared Reference Spectra 1911 L-Phenylalanine Phytonadione Pimozide 1912 Infrared Reference Spectra JP XVI Pindolol Pioglitazone Hydrochloride Pipemidic Acid Hydrate JP XVI Infrared Reference Spectra 1913 Piperacillin Hydrate Piperacillin Sodium Piperazine Adipate 1914 Infrared Reference Spectra JP XVI Piperazine Phosphate Hydrate Pirenoxine Pirenzepine Hydrochloride Hydrate JP XVI Infrared Reference Spectra 1915 Piroxicam Pivmecillinam Hydrochloride Potassium Canrenoate 1916 Infrared Reference Spectra JP XVI Potassium Clavulanate Povidone Pranoprofen JP XVI Infrared Reference Spectra 1917 Pravastatin Sodium Prazepam Prazosin Hydrochloride 1918 Infrared Reference Spectra JP XVI Prednisolone Prednisolone Acetate Prednisolone Sodium Phosphate JP XVI Infrared Reference Spectra 1919 Prednisolone Succinate Probucol Procainamide Hydrochloride 1920 Infrared Reference Spectra JP XVI Procaine Hydrochloride Procarbazine Hydrochloride Procaterol Hydrochloride Hydrate JP XVI Infrared Reference Spectra 1921 Progesterone Proglumide L-Proline 1922 Infrared Reference Spectra JP XVI Promethazine Hydrochloride Propafenone Hydrochloride Propiverine Hydrochloride JP XVI Infrared Reference Spectra 1923 Propranolol Hydrochloride Propyl Parahydroxybenzoate Protirelin 1924 Infrared Reference Spectra JP XVI Purified Sodium Hyaluronate Pyrantel Pamoate Pyrazinamide JP XVI Infrared Reference Spectra 1925 Pyridoxine Hydrochloride Pyrrolnitrin Quinapril Hydrochloride.
Load more

Recommended publications
  • Anabolic Steroid Use Misuse and Addiction
    Anabolic Steroid Use, Misuse And Addiction JASSIN M. JOURIA Dr. Jassin M. Jouria is a medical doctor, professor of academic medicine, and medical author. He graduated from Ross University School of Medicine and has completed his clinical clerkship training in various teaching hospitals throughout New York, including King’s County Hospital Center and Brookdale Medical Center, among others. Dr. Jouria has passed all USMLE medical board exams, and has served as a test prep tutor and instructor for Kaplan. He has developed several medical courses and curricula for a variety of educational institutions. Dr. Jouria has also served on multiple levels in the academic field including faculty member and Department Chair. Dr. Jouria continues to serve as a Subject Matter Expert for several continuing education organizations covering multiple basic medical sciences. He has also developed several continuing medical education courses covering various topics in clinical medicine. Recently, Dr. Jouria has been contracted by the University of Miami/Jackson Memorial Hospital’s Department of Surgery to develop an e-module training series for trauma patient management. Dr. Jouria is currently authoring an academic textbook on Human Anatomy & Physiology. ABSTRACT The synthetic versions of the male hormone testosterone, also known as anabolic steroids, can play an important role in the treatment of health conditions when used as prescribed by a medical clinician. However, misuse of anabolic steroids occurs when these substances are used solely to improve physical appearance or performance. Because there are some potentially serious physical effects of anabolic steroid use, it is important that anabolic steroids are only used as prescribed and always under a medical clinician’s guidance.
    [Show full text]
  • Use of ²-Blockers and Risk of Fractures
    ORIGINAL CONTRIBUTION Use of ␤-Blockers and Risk of Fractures Raymond G. Schlienger, PhD, MPH Context Animal studies suggest that the ␤-blocker propranolol increases bone for- Marius E. Kraenzlin, MD mation, but data on whether use of ␤-blockers (with or without concomitant use of thiazide diuretics) is associated with reduced fracture risk in humans are limited. Susan S. Jick, DSc Objective To determine whether use of ␤-blockers alone or in combination with thia- Christoph R. Meier, PhD, MSc zides is associated with a decreased risk of fracture in adults. Design, Setting, and Participants Case-control analysis using the UK General Prac- TUDIES HAVE SUGGESTED THAT tice Research Database (GPRD). The study included 30601 case patients aged 30 to the sympathetic nervous sys- 79 years with an incident fracture diagnosis between 1993 and 1999 and 120819 con- tem has a catabolic effect on trols, matched to cases on age, sex, calendar time, and general practice attended. bones.1-4 In vitro data show that Main Outcome Measures Odds ratios (ORs) of having a fracture in association Sadrenergic agonists stimulate bone re- with use of ␤-blockers or a combination of ␤-blockers with thiazides. sorption in organ culture of mouse cal- Results The most frequent fractures were of the hand/lower arm (n=12837 [42.0%]) variae.4 Chemical sympathectomy with and of the foot (n=4627 [15.1%]). Compared with patients who did not use either guanethidine, a sympathetic neuro- ␤-blockers or thiazide diuretics, the OR for current use of ␤-blockers only (Ն3 pre- toxic agent, impairs bone resorption by scriptions) was 0.77 (95% confidence interval [CI], 0.72-0.83); for current use of thia- inhibiting preosteoclast differentiation zides only (Ն3 prescriptions), 0.80 (95% CI, 0.74-0.86); and for combined current ␤ and disturbing osteoclast activation in use of -blockers and thiazides, 0.71 (95% CI, 0.64-0.79).
    [Show full text]
  • Supplementary Information
    Supplementary Information Network-based Drug Repurposing for Novel Coronavirus 2019-nCoV Yadi Zhou1,#, Yuan Hou1,#, Jiayu Shen1, Yin Huang1, William Martin1, Feixiong Cheng1-3,* 1Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA 2Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH 44195, USA 3Case Comprehensive Cancer Center, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA #Equal contribution *Correspondence to: Feixiong Cheng, PhD Lerner Research Institute Cleveland Clinic Tel: +1-216-444-7654; Fax: +1-216-636-0009 Email: [email protected] Supplementary Table S1. Genome information of 15 coronaviruses used for phylogenetic analyses. Supplementary Table S2. Protein sequence identities across 5 protein regions in 15 coronaviruses. Supplementary Table S3. HCoV-associated host proteins with references. Supplementary Table S4. Repurposable drugs predicted by network-based approaches. Supplementary Table S5. Network proximity results for 2,938 drugs against pan-human coronavirus (CoV) and individual CoVs. Supplementary Table S6. Network-predicted drug combinations for all the drug pairs from the top 16 high-confidence repurposable drugs. 1 Supplementary Table S1. Genome information of 15 coronaviruses used for phylogenetic analyses. GenBank ID Coronavirus Identity % Host Location discovered MN908947 2019-nCoV[Wuhan-Hu-1] 100 Human China MN938384 2019-nCoV[HKU-SZ-002a] 99.99 Human China MN975262
    [Show full text]
  • Health Reports for Mutual Recognition of Medical Prescriptions: State of Play
    The information and views set out in this report are those of the author(s) and do not necessarily reflect the official opinion of the European Union. Neither the European Union institutions and bodies nor any person acting on their behalf may be held responsible for the use which may be made of the information contained therein. Executive Agency for Health and Consumers Health Reports for Mutual Recognition of Medical Prescriptions: State of Play 24 January 2012 Final Report Health Reports for Mutual Recognition of Medical Prescriptions: State of Play Acknowledgements Matrix Insight Ltd would like to thank everyone who has contributed to this research. We are especially grateful to the following institutions for their support throughout the study: the Pharmaceutical Group of the European Union (PGEU) including their national member associations in Denmark, France, Germany, Greece, the Netherlands, Poland and the United Kingdom; the European Medical Association (EMANET); the Observatoire Social Européen (OSE); and The Netherlands Institute for Health Service Research (NIVEL). For questions about the report, please contact Dr Gabriele Birnberg ([email protected] ). Matrix Insight | 24 January 2012 2 Health Reports for Mutual Recognition of Medical Prescriptions: State of Play Executive Summary This study has been carried out in the context of Directive 2011/24/EU of the European Parliament and of the Council of 9 March 2011 on the application of patients’ rights in cross- border healthcare (CBHC). The CBHC Directive stipulates that the European Commission shall adopt measures to facilitate the recognition of prescriptions issued in another Member State (Article 11). At the time of submission of this report, the European Commission was preparing an impact assessment with regards to these measures, designed to help implement Article 11.
    [Show full text]
  • Comprehensive Screening of Diuretics in Human Urine Using Liquid Chromatography Tandem Mass Spectrometry
    id5246609 pdfMachine by Broadgun Software - a great PDF writer! - a great PDF creator! - http://www.pdfmachine.com http://www.broadgun.com AAnnaallyyttiiccaaISllS N : 0974-7419 Volume 13 Issue 7 CCHHEEAnMM IndIIiSaSnT TJoRuRrnYaYl Full Paper ACAIJ, 13(7) 2013 [270-283] Comprehensive screening of diuretics in human urine using liquid chromatography tandem mass spectrometry Shobha Ahi1, Alka Beotra1*, G.B.K.S.Prasad2 1National Dope Testing Laboratory, Ministry of Youth Affairs and Sports, CGO Complex, Lodhi Road, New Delhi,-110003, (INDIA) 2SOS in Biochemistry, Jiwaji University, Gwalior, (INDIA) E-mail : [email protected] ABSTRACT KEYWORDS Diuretics are drugs that increase the rate of urine flow and sodium excretion Doping, diuretics; to adjust the volume and composition of body fluids. There are several LC-MS/MS; WADA; major categories of this drug class and the compounds vary greatly in Drugs of abuse. structure, physicochemical properties, effects on urinary composition and renal haemodynamics, and site mechanism of action. Diuretics are often abused by athletes to excrete water for rapid weight loss and to mask the presence of other banned substances. Because of their abuse by athletes, ’s (WADA) diuretics have been included in the World Anti-Doping Agency list of prohibited substances. The diuretics are routinely screened by anti- doping laboratories as the use of diuretics is banned both in-competition and out-of-competition. This work provides an improved, fast and selective –tandem mass spectrometric (LC/MS/MS) method liquid chromatography for the screening of 22 diuretics and probenecid in human urine. The samples preparation was performed by liquid-liquid extraction. The limit of detection (LOD) for all substances was between 10-20 ng/ml or better.
    [Show full text]
  • Metabolism of Anabolic Steroids in Man: Synthesis and Use of Reference Substances for Identification of Anabolic Steroid Metabolites
    Anaiytzca Chumca Acta, 275 (1993) 23-48 23 Elsevler hence Publishers B V , Amsterdam Metabolism of anabolic steroids in man: synthesis and use of reference substances for identification of anabolic steroid metabolites Will1 Schanxer and Manfred Domke LkutscheS’rthochschuk Koln, Inrhtut f?u Bwchemre, Carl-L&m-Weg 4 5ooO Cologne 41 (Germuny) (Recewed 20th May 1992) AhStl-& The use of anabohc steroids was banned by the International Olympic Comnuttee for the first tune at the Olympic Games m Montreal m 1976 Since that tie the nususe of anabohc steroxls by athletes has been controlled by analysis of urme extracts by gas chromatography-mass spectrometry @C-MS) The excreted steroids or their metabohtes, or both, are isolated from urme by XAD-2 adsorption, enzymatx hydrolyss of coqlugated excreted metabobtes anth /?-glucuromdase from Es&en&u co& bqmd-bqmd extractlon mth diethyl ether, and courted mto tnmethylsdyl (‘INiS) derwatwes The confirmation of an anabobc stenxd nususe ts based on comparison of the electron nnpact lomzation (EI) mass spectrum and GC retention tie of the isolated steroid and/or its metabohte with the El mass spectrum and GC retention time of authentic reference substances For this purpose excretion studies with the most common anabobc steroids were performed and the mam excreted metabobtes were synthesued for bolasterone, boldenone, 4-chiorodehydromethyltestosterone, clostebol, drostanolone, tluoxymesterone, forme- bolone, me&a&one, mesterolone, metandlenone, methandnol, metenolone, methyltestosterone, nandrolone, norethandrolone,
    [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, UST, following to be employed in commercial fishing or the commercial MT, MUST, 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]
  • Prostaglandin D2 and the Role of the DP1, DP2 and TP Receptors in the Control of Airway Reflex Events
    ERJ Express. Published on October 16, 2014 as doi: 10.1183/09031936.00061614 ORIGINAL ARTICLE IN PRESS | CORRECTED PROOF Prostaglandin D2 and the role of the DP1, DP2 and TP receptors in the control of airway reflex events Sarah A. Maher1, Mark A. Birrell1,2, John J. Adcock1, Michael A. Wortley1, Eric D. Dubuis1, Sara J. Bonvini1, Megan S. Grace1 and Maria G. Belvisi1,2 Affiliations: 1Respiratory Pharmacology, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK. 2MRC and Asthma UK Centre in Allergic Mechanisms of Asthma, Imperial College London, London, UK. Correspondence: Maria G. Belvisi, Imperial College London, Respiratory Pharmacology, NHLI, Sir Alexander Fleming Building, Exhibition Road, London, SW7 2AZ, UK. E-mail: [email protected] ABSTRACT Prostaglandin D2 (PGD2) causes cough and levels are increased in asthma suggesting that it may contribute to symptoms. Although the prostaglandin D2 receptor 2 (DP2) is a target for numerous drug discovery programmes little is known about the actions of PGD2 on sensory nerves and cough. We used human and guinea pig bioassays, in vivo electrophysiology and a guinea pig conscious cough model to assess the effect of prostaglandin D2 receptor (DP1), DP2 and thromboxane receptor antagonism on PGD2 responses. PGD2 caused cough in a conscious guinea pig model and an increase in calcium in airway jugular ganglia. Using pharmacology and receptor-deficient mice we showed that the DP1 receptor mediates sensory nerve activation in mouse, guinea pig and human vagal afferents. In vivo, PGD2 and a DP1 receptor agonist, but not a DP2 receptor agonist, activated single airway C-fibres.
    [Show full text]
  • Megestrol Acetate/Melengestrol Acetate 2115 Adverse Effects and Precautions Megestrol Acetate Is Also Used in the Treatment of Ano- 16
    Megestrol Acetate/Melengestrol Acetate 2115 Adverse Effects and Precautions Megestrol acetate is also used in the treatment of ano- 16. Mwamburi DM, et al. Comparing megestrol acetate therapy with oxandrolone therapy for HIV-related weight loss: similar As for progestogens in general (see Progesterone, rexia and cachexia (see below) in patients with cancer results in 2 months. Clin Infect Dis 2004; 38: 895–902. p.2125). The weight gain that may occur with meges- or AIDS. The usual dose is 400 to 800 mg daily, as tab- 17. Grunfeld C, et al. Oxandrolone in the treatment of HIV-associ- ated weight loss in men: a randomized, double-blind, placebo- trol acetate appears to be associated with an increased lets or oral suspension. A suspension of megestrol ace- controlled study. J Acquir Immune Defic Syndr 2006; 41: appetite and food intake rather than with fluid reten- tate that has an increased bioavailability is also availa- 304–14. tion. Megestrol acetate may have glucocorticoid ef- ble (Megace ES; Par Pharmaceutical, USA) and is Hot flushes. Megestrol has been used to treat hot flushes in fects when given long term. given in a dose of 625 mg in 5 mL daily for anorexia, women with breast cancer (to avoid the potentially tumour-stim- cachexia, or unexplained significant weight loss in pa- ulating effects of an oestrogen—see Malignant Neoplasms, un- Effects on carbohydrate metabolism. Megestrol therapy der Precautions of HRT, p.2075), as well as in men with hot 1-3 4 tients with AIDS. has been associated with hyperglycaemia or diabetes mellitus flushes after orchidectomy or anti-androgen therapy for prostate in AIDS patients being treated for cachexia.
    [Show full text]
  • 4 Supplementary File
    Supplemental Material for High-throughput screening discovers anti-fibrotic properties of Haloperidol by hindering myofibroblast activation Michael Rehman1, Simone Vodret1, Luca Braga2, Corrado Guarnaccia3, Fulvio Celsi4, Giulia Rossetti5, Valentina Martinelli2, Tiziana Battini1, Carlin Long2, Kristina Vukusic1, Tea Kocijan1, Chiara Collesi2,6, Nadja Ring1, Natasa Skoko3, Mauro Giacca2,6, Giannino Del Sal7,8, Marco Confalonieri6, Marcello Raspa9, Alessandro Marcello10, Michael P. Myers11, Sergio Crovella3, Paolo Carloni5, Serena Zacchigna1,6 1Cardiovascular Biology, 2Molecular Medicine, 3Biotechnology Development, 10Molecular Virology, and 11Protein Networks Laboratories, International Centre for Genetic Engineering and Biotechnology (ICGEB), Padriciano, 34149, Trieste, Italy 4Institute for Maternal and Child Health, IRCCS "Burlo Garofolo", Trieste, Italy 5Computational Biomedicine Section, Institute of Advanced Simulation IAS-5 and Institute of Neuroscience and Medicine INM-9, Forschungszentrum Jülich GmbH, 52425, Jülich, Germany 6Department of Medical, Surgical and Health Sciences, University of Trieste, 34149 Trieste, Italy 7National Laboratory CIB, Area Science Park Padriciano, Trieste, 34149, Italy 8Department of Life Sciences, University of Trieste, Trieste, 34127, Italy 9Consiglio Nazionale delle Ricerche (IBCN), CNR-Campus International Development (EMMA- INFRAFRONTIER-IMPC), Rome, Italy This PDF file includes: Supplementary Methods Supplementary References Supplementary Figures with legends 1 – 18 Supplementary Tables with legends 1 – 5 Supplementary Movie legends 1, 2 Supplementary Methods Cell culture Primary murine fibroblasts were isolated from skin, lung, kidney and hearts of adult CD1, C57BL/6 or aSMA-RFP/COLL-EGFP mice (1) by mechanical and enzymatic tissue digestion. Briefly, tissue was chopped in small chunks that were digested using a mixture of enzymes (Miltenyi Biotec, 130- 098-305) for 1 hour at 37°C with mechanical dissociation followed by filtration through a 70 µm cell strainer and centrifugation.
    [Show full text]
  • (200731) Hypromellose Phthalate (220824) Ibudilast
    21222122 Infrared Reference Spectra JP XVII Hypromellose Phthalate (200731) Hypromellose Phthalate (220824) Ibudilast The JP Drugs are to be tested according to the provisions given in the pertinent monographs, General Notices, General Rules for Crude Drugs, General Rules for Preparations, and General Tests for their conformity to the Japanese Pharmacopoeia. (See the General Notices 5.) JP XVII Infrared Reference Spectra 21232123 Ibuprofen Ibuprofen Piconol Ifenprodil Tartrate The JP Drugs are to be tested according to the provisions given in the pertinent monographs, General Notices, General Rules for Crude Drugs, General Rules for Preparations, and General Tests for their conformity to the Japanese Pharmacopoeia. (See the General Notices 5.) 21242124 Infrared Reference Spectra JP XVII Imidapril Hydrochloride Imipenem Hydrate Indapamide The JP Drugs are to be tested according to the provisions given in the pertinent monographs, General Notices, General Rules for Crude Drugs, General Rules for Preparations, and General Tests for their conformity to the Japanese Pharmacopoeia. (See the General Notices 5.) JP XVII Infrared Reference Spectra 21252125 Indenolol Hydrochloride Indometacin Iohexol The JP Drugs are to be tested according to the provisions given in the pertinent monographs, General Notices, General Rules for Crude Drugs, General Rules for Preparations, and General Tests for their conformity to the Japanese Pharmacopoeia. (See the General Notices 5.) 21262126 Infrared Reference Spectra JP XVII Iopamidol Iotalamic Acid Iotroxic Acid The JP Drugs are to be tested according to the provisions given in the pertinent monographs, General Notices, General Rules for Crude Drugs, General Rules for Preparations, and General Tests for their conformity to the Japanese Pharmacopoeia.
    [Show full text]
  • An Ultra Fast and Sensitive Detection of 165 Drugs of Abuse in Human Urine Using Polarity Switching Ultra Performance Liquid Chromatog- Raphy Tandem Mass Spectrometry
    id15306796 pdfMachine by Broadgun Software - a great PDF writer! - a great PDF creator! - http://www.pdfmachine.com http://www.broadgun.com AAnnaallyyttiiccaaIlSlS N : 0974-7419 Volume 15 Issue 8 CCHHEEAMMn InIdIiSSanTT JoRuRrnYaYl Full Paper ACAIJ, 15(8) 2015 [319-338] An ultra fast and sensitive detection of 165 drugs of abuse in human urine using polarity switching ultra performance liquid chromatog- raphy tandem mass spectrometry Sachin Dubey, Shobha Ahi, Alka Beotra*, Tejinder Kaur, Shila Jain National Dope Testing Laboratory, Ministry of Youth Affairs and Sports, CGO Complex, Lodhi Road, New Delhi, 110003, (INDIA) E-mail : [email protected] ABSTRACT KEYWORDS The screening of wide variety of prohibited substances in a time bound Bioanalytical method; manner by adhering to latest World Anti-Doping Agency (WADA) guide- Sports drug testing; lines is a challenging task for doping control laboratories. The revised crite- UPLC-MS/MS; rion of detection limits (WADATD2013MRPL) has further required the doping Polarity switching; laboratories to review their testing procedures. The present work was aimed WADA. at developing a fast, sensitive and robust analytical method based on solid phase cleanup (SPE) and ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) to achieve the required detection lev- els. The method development involved optimization of deconjugation of phase II metabolites, SPE using mixed-mode ion cartridges for extraction of analytes of wider chemistries; and fast polarity switching UPLC-MS/MS detection. The developed method was validated to detect approximately 165 compounds and/or metabolites prohibited by WADA. The eight min- utes runtime allowed testing of approximately 180 samples in 24 hours at the limit of detection (LOD) of 50% below required detection levels.
    [Show full text]