Characterization of some commercial poly (styrene-divinylbenzene) copolymers for reversed-phase HPLC1

1987 ◽  
Vol 23 (5) ◽  
pp. 341-349 ◽  
Author(s):  
H. W. Stuurman ◽  
J. Köhler ◽  
S. -O Jansson ◽  
A. Litzén
1988 ◽  
Vol 442 ◽  
pp. 97-103 ◽  
Author(s):  
S. Coppi ◽  
A. Betti ◽  
C. Bighi ◽  
G.P. Cartoni ◽  
F. Coccioli

1981 ◽  
Vol 46 (7) ◽  
pp. 1675-1681 ◽  
Author(s):  
Josef Baldrian ◽  
Božena N. Kolarz ◽  
Henrik Galina

Porosity variations induced by swelling agent exchange were studied in a styrene-divinylbenzene copolymer. Standard methods were used in the characterization of copolymer porosity in the dry state and the results were compared with related structural parameters derived from small angle X-ray scattering (SAXS) measurements as developed for the characterization of two-phase systems. The SAXS method was also used for porosity determination in swollen samples. The differences in the porosity of dry samples were found to be an effect of the drying process, while in the swollen state the sample swells and deswells isotropically.


1998 ◽  
Vol 63 (3) ◽  
pp. 434-440 ◽  
Author(s):  
Irena Hulová ◽  
Jana Barthová ◽  
Helena Ryšlavá ◽  
Václav Kašička

Glycoproteins that have affinity to Concanavalin A were isolated from the acetone-dried pituitaries of common carp (Cyprinus carpio L.). Two fractions of glycoproteins were separated using gel chromatography on Superdex 75HR. The fraction with lower molecular weight (30 000) corresponding to the carp gonadotropin cGtH II was composed of two subunits as determined using SDS-PAGE. This protein fraction was further divided into four components using reversed-phase HPLC. Two fractions were pure α and β subunits of cGtH II as follows from immunodetection and from determination of N-terminal amino acid sequences. The other two were a mixture of α and β subunits as was also revealed by N-terminal analysis. Capillary electrophoresis was also used for characterization of isolated glycoproteins.


The Analyst ◽  
2021 ◽  
Author(s):  
Harald Schoeny ◽  
Evelyn Rampler ◽  
Yasin El Abiead ◽  
Felina Hildebrand ◽  
Olivia Zach ◽  
...  

We propose a fully automated novel workflow for lipidomics based on flow injection- followed by liquid chromatography high resolution mass spectrometry (FI/LC-HRMS). The workflow combined in-depth characterization of the lipidome...


1983 ◽  
Vol 36 (4) ◽  
pp. 272-276 ◽  
Author(s):  
Kozo Hashimoto ◽  
Kazuharu Murakami ◽  
Norihito Ohno ◽  
Jingo Kageyama ◽  
Teruhiko Hattori ◽  
...  

2021 ◽  
Vol 28 (9) ◽  
pp. 11697-11707
Author(s):  
Benjamin Becker ◽  
Christian Kochleus ◽  
Denise Spira ◽  
Christel Möhlenkamp ◽  
Julia Bachtin ◽  
...  

AbstractIn this study, three different passive sampling receiving phases were evaluated, with a main focus on the comparability of established styrene-divinylbenzene reversed phase sulfonated (SDB-RPS) sampling phase from Empore™ (E-RPS) and novel AttractSPE™ (A-RPS). Furthermore, AttractSPE™ hydrophilic-lipophilic balance (HLB) disks were tested. To support sampling phase selection for ongoing monitoring needs, it is important to have information on the characteristics of alternative phases. Three sets of passive samplers (days 1–7, days 8–14, and days 1–14) were exposed to a continuously exchanged mixture of creek and rainwater in a stream channel system under controlled conditions. The system was spiked with nine pesticides in two peak scenarios, with log KOW values ranging from approx. − 1 to 5. Three analytes were continuously spiked at a low concentration. All three sampling phases turned out to be suitable for the chosen analytes, and, in general, uptake rates were similar for all three materials, particularly for SDB-RPS phases. Exceptions concerned bentazon, where E-RPS sampled less than 20% compared with the other phases, and nicosulfuron, where HLB sampled noticeably more than both SDB-RPS phases. All three phases will work for environmental monitoring. They are very similar, but differences indicate one cannot just use literature calibration data and transfer these from one SDB phase to another, though for most compounds, it may work fine. Graphical abstract


2006 ◽  
Vol 52 (2) ◽  
pp. 212-219 ◽  
Author(s):  
David M Bunk ◽  
Michael J Welch

Abstract Background: To address the continuing need for the standardization of clinical human cardiac troponin I (cTnI) assays, NIST, with the assistance of the AACC/IFCC Cardiac Troponin I Standardization Committee, has developed a new certified reference material, Standard Reference Material (SRM) 2921: Human Cardiac Troponin Complex. Methods: The concentration of cTnI in SRM 2921 was determined through a combination of reversed-phase liquid chromatography (LC) with ultraviolet detection and amino acid analysis. Characterization of the intact troponin subunits was accomplished through reversed-phase LC coupled with mass spectrometry. Posttranslational modifications to the cTnI in SRM 2921 were investigated by combining proteolytic digestion with matrix-assisted laser desorption/ionization mass spectrometry. Additionally, reference concentration values for cTnT and cTnC were also determined. Results: The concentration of human cTnI in SRM 2921 is 31.2 (1.4) mg/L (where 1.4 mg/L is the uncertainty at a 95% level of confidence), as certified through a method that provides traceability to the International System of Units (SI). Reference concentration values of the cTnT and cTnC subunits were determined to be 36.9 (3.8) mg/L and 24.2 (1.3) mg/L, respectively. Conclusions: This first cTnI reference material should provide SI traceability to clinical cTnI assays once commutability has been validated, and could assist in the international harmonization of cTnI assays as a tool for understanding the underlying causes of interassay variability.


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