Micellization of the diblock copolymer poly(ethylene oxide)-b-polybutadiene, PEO(132)-PB(89), where the subscripts denote the number of monomers in each block, has been studied in solution in deuterated methanol and in deuterated cyclohexane, in order to compare the micellar assembly in deuterated solvents to that in protonated solvents. The methods used were dynamic light scattering and small angle neutron scattering. In CD(3)OD, PEO(132)-PB(89) forms only spherical micelles that change little in size or shape over the temperature range 21-68°C. In CH(3)OH, PEO(132)-PB(89) forms coexisting cylindrical and spherical structures over the entire temperature range. Thus cylindrical micelles form in CH(3)OH, but do not form in CD(3)OD. In C(6)D(12), the copolymer forms flexible, cylindrical micelles at lower temperatures; above about 40°C, spherical micelles and free copolymers appear and coexist with the cylindrical micelles. The behavior in C(6)H(12) is the same as in C(6)D(12), except that no free copolymers are observed in C(6)H(12). The stronger hydrogen bonding in deuterated methanol as compared to protonated methanol is assumed to be the source of the difference in assembly.
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http://dx.doi.org/10.1016/j.jcis.2012.06.091 | DOI Listing |
J Pharm Biomed Anal
December 2024
Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa. Electronic address:
For the effective treatment of tuberculosis with first-line anti-tubercular drugs, drug concentrations need to be measured at the site of infection to determine drug exposure. To enable the measurement of the anti-tuberculosis drugs isoniazid and pyrazinamide in the nervous system of patients with tuberculous meningitis, an analytical method was developed and validated for the quantification of these drugs in human cerebrospinal fluid. Samples were prepared by solid phase extraction using Strata-X polymeric extraction plates.
View Article and Find Full Text PDFACS Phys Chem Au
November 2024
Department of General, Inorganic and Theoretical Chemistry, University of Innsbruck, Innrain 80, Innsbruck 6020, Austria.
Unraveling methanol's infrared spectrum has challenged spectroscopists for a century, with numerous loose ends still to be explored. We engage in this exploration based on experiments of isolating single methanol molecules in solid argon and neon matrices. We report infrared spectra of methanol in its natural isotopic composition and with partial and full deuteration.
View Article and Find Full Text PDFMetabolites
November 2024
Department of Chemistry, University of Oxford, Oxford OX1 3TA, UK.
: Metabolic profiling of tissue samples via liquid-state nuclear magnetic resonance (NMR) requires the extraction of polar metabolites in a suitable deuterated solvent. Such methods often prioritise metabolite recovery over protein removal due to the relatively low sensitivity of NMR metabolomics and the routine use of methods able to supress residual protein signals. However, residual protein may impact metabolite integrity and the metabolite stability after NMR sample preparation is often overlooked.
View Article and Find Full Text PDFDrug Test Anal
August 2024
Key Laboratory of Drug Monitoring and Control, Drug Intelligence and Forensic Center, Ministry of Public Security, Beijing, China.
The effective implementation of drug precursor legislation has driven the innovation and design of new alternative substances. The application of 1,3-dicarbonyl precursors as alternative precursors for the synthesis of 1-phenyl-2-propanone (P2P) and 3,4-methylenedioxyphenyl-2-propanone (MDP2P) has created new challenges to legal control. Their 1,3-dicarbonyl structure allows the precursors to exist as an equilibrium mixture of the tautomeric diketo and keto-enolic forms during the nuclear magnetic resonance (NMR) analysis.
View Article and Find Full Text PDFMolecules
July 2024
Dipartimento di Chimica "G. Ciamician" Università di Bologna, Via Selmi 2, I-40126 Bologna, Italy.
The rotational spectra of the 1:1 complex formed by acrolein and methanol and its deuterated isotopologues have been analyzed. Two stable conformations in which two hydrogen bonds between the two moieties are formed were detected. The rotational lines show a hyperfine structure due to the methyl group internal rotation in the complex and the barriers hindering the motion were determined as 2.
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