Hugonis Grotii de jure belli ac pacis libri tres : cum annotatis auctoris, nec non J. F. Gronovii notis, & J. Barbeyracii animadversionibus, commentariis insuper locupletissimis Henr. l.b. de Cocceii ... sub titulo Grotii illustrati antea editis, nunc ad calcem cujusque capitis adjectis : insertis quoque observationibus Samuelis l.b. de Cocceii ... : adduntur tandem ipsius Grotii Dissertatio de mari libero, ac Libellus singularis de aequitate, indulgentia et facilitate.

Vols. 2 and 4 have at end Bibliopolae monitum = Avis du libraire, about pricing in various European currencies in 1751 and 1752.

Christopheri Heinrici Loeberi historia ecclesiastica quae ephoriam Orlamundanam in Ducatu Altenburgensi describit, potentissimorum ac serenissimorum Saxoniae electorum ac Ducum studium propagandae veritatis divinae à temporibus reformationis refert, ipsam Reformationem per B. Lutherum factam, & quae tum temporis in his terris acta sunt, recenset, multa insuper notatu dignissima, de Carolstadio praesertim, & Flacio, qui Orlamundae docuerunt aliquando, aut innotuerunt, de libris symbolicis libro interim &c. annectit, memoriam tandem omnium ministrorum qui post pulsas papales tenebras in huius ephoriae ecclesiis verbum Dei docuerunt & adhuc docent, conservat; eorumpue nomina multis memorabilibus distinguit.

Title on two leaves.

Welding engineer.

Vols. 25, no. 10-v. 44, Oct. 1940-49 include Welding engineer data sheet.

Athanasii Kircheri ... Mundi subterranei : Tomus IIus in V. libros digestus, quibus Mundi Subterranei fructus exponuntur, et quidquid tandem rarum, insolitum, et portentosum in foecundo Naturae utero continetur, ante oculos ponitur curiosi Lectoris.

Mode of access: Internet.

The Sporting repository : containing horse racing, hunting, coursing, shooting, archery, trotting and tandem matches, cocking pedestrianism, pugilism, anecdotes on sporting subjects, interspersed with essays, tales, and a great variety of miscellaneous articles.

"This edition is limited to 500 copies".

Welding metallurgy; iron and steel,

Includes "Suggested reading."

The oxy-acetylene handbook : a manual on oxy-acetylene welding and cutting procedures.

Includes index.

The Welding encyclopedia.

"Compiled and edited by": 1921-24, L.B. Mackenzie, H.S. Card; 1926-32, H.S. Card; 1938-41, "re-edited by" Stuart Plumley; 1943- "completely revised and re-edited by" T.B. Jefferson.

Electric arc welding /

Includes index.

Procedure handbook of arc welding design and practice.

Mode of access: Internet.

How to repair and build farm equipment with arc welding.

Mode of access: Internet.

Platinum(II) olefin hydroarylation catalysts: tuning selectivity for the anti-Markovnikov product Tandem catalytic ester hydrogenation and deoxygenation of polyethylene terephthalate

Thesis (Master's)--University of Washington, 2016-06

The measurement of nicotine in human plasma by high-performance liquid chromatography-electrospray-tandem mass spectrometry

The authors describe a reverse-phase high-performance liquid chromatography-electrospray-tandem mass spectrometry method for the measurement of nicotine in human plasma. Samples (500 muL) with added deuterium-labeled d(3)-nicotine as an internal standard (IS) were treated with a 2-step process of ether extraction (6 mL) followed by back-extraction into 0.1% formic acid (50 muL). Chromatography was performed on a phenyl Novapak column with a mobile phase consisting of 50% 10 mM ammonium fortriate (pH 3.3) and acetonitrile (50:50, vol/vol). A flow rate of 0.2 mL/min resulted in a total analysis time of 5 minutes per sample. Mass spectrometric detection was by selected reactant monitoring (nicotine m/z 163.2 --> 130.2; IS m/z 166.2 --> 87.2). The assay was linear from 0.5 to 100 mug/L (r > 0.993, n = 9). The accuracy and imprecision of the method for quality control sampleswere 87.5% to 113% and < 10.2%, respectively. Interday accuracy and imprecision at the limit of quantification (0.5 mug/L) was 113% and 7.2% (n = 4). The process efficiency for nicotine in plasma was > 75%. The method described has good process efficiency, stabilized nicotine, avoided concentration steps, and most importantly minimized potential contamination. Further, we have established that water-based standards and controls are interchangeable with plasma-based samples. This method was used successfully to measure the pharmacokinetic profiles of subjects involved in the development of an aerosol inhalation drug delivery system.

Simultaneous determination of morphine, oxycodone, morphine-3-glucuronide, and noroxycodone concentrations in rat serum by high performance liquid chromatography-electrospray ionization-tandem mass spectrometry

An assay using high performance liquid chromatography (HPLC)-electrospray ionization-tandem mass spectrometry (ESI-MS-MS) was developed for simultaneously determining concentrations of morphine, oxycodone, morphine-3-glucuronide, and noroxycodone, in 50 mul samples of rat serum. Deuterated (d(3)) analogues of each compound were used as internal standards. Samples were treated with acetonitrile to precipitate plasma proteins: acetonitrile was removed from the supernatant by centrifugal evaporation before analysis. Limits of quantitation (ng/ml) and their between-day accuracy and precision (%deviation and %CV) were-morphine, 3.8 (4.3% and 7.6%); morphine-3-glucuronide, 5.0 (4.5% and 2.9%); oxycodone, 4.5 (0.4% and 9.3%); noroxycodone, 5.0 (8.5% and 4.6%). (C) 2004 Elsevier B.V. All rights reserved.

Matrix effects: The Achilles heel of quantitative high-performance liquid chromatography-electrospray-tandem mass spectrometry

High-performance liquid chromatography coupled by an electrospray ion source to a tandem mass spectrometer (HPLC-EST-MS/ MS) is the current analytical method of choice for quantitation of analytes in biological matrices. With HPLC-ESI-MS/MS having the characteristics of high selectivity, sensitivity, and throughput, this technology is being increasingly used in the clinical laboratory. An important issue to be addressed in method development, validation, and routine use of HPLC-ESI-MS/MS is matrix effects. Matrix effects are the alteration of ionization efficiency by the presence of coeluting substances. These effects are unseen in the chromatograrn but have deleterious impact on methods accuracy and sensitivity. The two common ways to assess matrix effects are either by the postextraction addition method or the postcolumn infusion method. To remove or minimize matrix effects, modification to the sample extraction methodology and improved chromatographic separation must be performed. These two parameters are linked together and form the basis of developing a successful and robust quantitative HPLC-EST-MS/MS method. Due to the heterogenous nature of the population being studied, the variability of a method must be assessed in samples taken from a variety of subjects. In this paper, the major aspects of matrix effects are discussed with an approach to address matrix effects during method validation proposed. (c) 2004 The Canadian Society of Clinical Chemists. All rights reserved.