Identification of new aqueous chemical degradation products of isophosphoramide mustard

2001 ◽  
Vol 25 (3-4) ◽  
pp. 669-678 ◽  
Author(s):  
Stéphane Breil ◽  
Robert Martino ◽  
Véronique Gilard ◽  
Myriam Malet-Martino ◽  
Ulf Niemeyer
2007 ◽  
Vol 25 (9) ◽  
pp. 1082-1088 ◽  
Author(s):  
Carol Aghajanian ◽  
Howard A. Burris ◽  
Suzanne Jones ◽  
David R. Spriggs ◽  
Marvin B. Cohen ◽  
...  

Purpose To establish the maximum-tolerated dose (MTD), dose-limiting toxicity (DLT), safety, pharmacokinetics, and pharmacodynamics of ixabepilone when administered as a 1-hour infusion every 3 weeks to patients with advanced solid tumors or relapsed/refractory non-Hodgkin's lymphoma. Dosing schedules of 40 mg/m2 and 50 mg/m2 over 3 hours were also evaluated. Patients and Methods Sixty-one patients were enrolled using an initial accelerated dose-escalation phase followed by a standard dose-escalation phase, with doses of ixabepilone ranging from 7.4 to 65 mg/m2. The pharmacokinetics of ixabepilone and two of its chemical degradation products were evaluated. Plasma pharmacodynamics were evaluated for both 1- and 3-hour infusions using an assay that measures the amount of endogenous tubulin in peripheral-blood mononuclear cells that exists in the polymerized versus the unpolymerized state. Response evaluation was performed every 6 weeks. Results The most common DLTs were neutropenia, stomatitis/pharyngitis, myalgia, and arthralgia. The MTD of ixabepilone as a 1-hour infusion every 3 weeks was established as 50 mg/m2. The maximum plasma concentration and area under the plasma concentration time curve appeared to increase less than proportionally to dose. Durable objective responses were seen in eight patients, including two complete responses. Five of the responders had experienced treatment failure with a taxane. Conclusion The recommended dose of ixabepilone for the initiation of phase II studies on the basis of these results is 50 mg/m2 over 1 hour every 3 weeks. The promising efficacy and tolerability results demonstrated by ixabepilone in this study warrant its continued development.


2013 ◽  
Vol 6 (5) ◽  
pp. 9005-9036
Author(s):  
J. Timkovsky ◽  
P. Gankema ◽  
R. Pierik ◽  
R. Holzinger

Abstract. A system of two dynamic plant chambers and a downstream reaction chamber has been set up to investigate the emission of biogenic volatile organic compounds (BVOC) and possible effects from pollutants such as ozone. The system can be used to compare BVOC emissions from two sets of differently treated plants, or to study the photochemistry of real plant emissions under polluted conditions without exposing the plants to pollutants. The main analytical tool is a proton-transfer-reaction time-of-flight mass spectrometer (PTR-TOF-MS) which allows online monitoring of biogenic emissions and chemical degradation products. The identification of BVOCs and their oxidation products is aided by cryogenic trapping and subsequent in situ gas chromatographic analysis. The data presented in the paper demonstrates the good performance of the setup.


1973 ◽  
Vol 137 (4) ◽  
pp. 943-953 ◽  
Author(s):  
Jan Andersson ◽  
Fritz Melchers ◽  
Chris Galanos ◽  
Otto Lüderitz

Lipopolysaccharides with different structure, isolated from different mutant strains of Escherichia coli and Salmonella bacteria, and chemical degradation products of these lipopolysaccharides have been employed to investigate which part of the lipopolysaccharide molecule exerts mitogenic effects on bone marrow-derived mouse lymphocytes. Within the structure of lipopolysaccharide consisting of lipid A, a core polysaccharide, and the O-polysaccharide antigen, lipid A was found to be the mitogenic part. The mitogenic effect of lipid A, consisting of phosphorylated glucosamine disaccharide units with ester- and amide-linked fatty acids, was lost after alkali treatment, which removes ester-linked fatty acids. Insertion of the lipid A portion of lipopolysaccharides into the lipid bilayer of the plasma membranes of bone marrow-derived lymphocytes is discussed as the initial mitogenic action.


Holzforschung ◽  
2008 ◽  
Vol 62 (6) ◽  
Author(s):  
Gunnar Almkvist ◽  
Ingmar Persson

Abstract Aqueous wood extracts from the historic Swedish warship Vasa have been analyzed by 1H-NMR spectroscopy, ion chromatography, and matrix assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry as part of studies on the chemical degradation related to increased levels of iron and sulfur. The results show that low molecular organic acids have accumulated in the Vasa wood after the 1961 salvage. The increased acidity was found in a context of chemical degradation of the wood polymers and the conservation agent polyethylene glycol (PEG) in iron-rich parts of the timber. Formic, glycolic and oxalic acid are all possible end-products of oxidative degradation of wood polymers, whereas hydrolysis of acetyl groups in xylan may have contributed to increased concentrations of acetic acid. MALDI-TOF spectra of PEG displaced towards low-molecular PEG oligomers, as reported earlier, were accompanied by increased levels of formic acid, indicating oxidative degradation of PEG. PEG with a carboxylic acid end group (PEGC) was observed to a minor degree in the wood. However, analysis of stored conservation treatment solutions showed high concentrations of PEGC yielding significant contributions to the acidity during the 1960s conservation period. PEGC was probably formed as a result of microbial processes during the early conservation regime. Calculations using concentrations and well-established acidity constants show that oxalic and formic acid are the primary contributors to a low pH in the wood. The increased acidity in the interior of the wood was found in the absence of sulfur compounds but in a context of iron. The majority of the sub-samples with significant levels of sulfate in the surface region with a prospective sulfur oxidation, however, showed neither a decreased pH nor significant depolymerization. This indicates that oxidation pathways of organically bound sulfur do not necessarily produce strong acids, and thereby free protons, as the final product. These observations imply opposing effects of iron and reduced sulfur species, with iron acting as a initiator in oxidative reactions of Fenton type, whereas the reduced organic sulfur compounds may act as anti-oxidants.


Holzforschung ◽  
2000 ◽  
Vol 54 (1) ◽  
pp. 39-54 ◽  
Author(s):  
T. I. Eglinton ◽  
M. A. Goñi ◽  
J. J. Boon ◽  
E. R. E. van der Hage ◽  
N. Terashima ◽  
...  

Summary A suite of four samples of xylem tissue from Ginkgo (Ginkgo biloba L.) shoots grown in a medium containing coniferin 13C-labeled at differing side-chain carbon atoms were studied using thermal and chemical degradation methods in combination with molecular-level isotopic analyses. The aims of the study were threefold: (1) to verify conclusions drawn from Nuclear Magnetic Resonance experiments previously performed on the same tissue samples, (2) to investigate degradation mechanisms and (3) to quantify the proportion of labeled material in each sample. Isotopic analysis of specific degradation products revealed the presence of the label exclusively within lignin-derived (phenolic) products and that the label is retained in its original position on the side-chain. These two results clearly indicate that there is no “scrambling” of carbon atoms as a result of thermal or chemical degradation, and thus lend strong support to analytical pyrolysis and chemolysis as viable approaches for structural investigations of the lignin macromolecule. Indeed, the isotopic enrichment of specific degradation products provides new evidence for certain types of linkages within the lignin polymer. The distribution and isotopic composition of the degradation products also strongly suggest an origin from newly-formed lignin as opposed to DHP-type products or unreacted substrate. As such, the data provides added confidence in the selective labeling approach for elucidation of the structure and biosynthesis of lignin. Isotopic mass balance calculations reveal that certain pyrolysis and CuO oxidation products show enhanced labeling which may be indicative of preferential incorporation of their specific precursors into the growing lignin macromolecule or heterogeneous lignin deposition.


1983 ◽  
Vol 61 (2) ◽  
pp. 323-327 ◽  
Author(s):  
John A. Findlay ◽  
Jia-Sen Liu ◽  
Lajos Radics

Full spectral details in support of the earlier proposed structure 1a for the antitumor antibiotic ravidomycin are presented together with an account of chemical degradation products. A complete corroboration of structure is provided by cross correlation of 1H and 13C nmr for ravidomycin and its diacetate 1b.


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