Liquid Chromatography 2013
DOI: 10.1016/b978-0-12-415807-8.00009-2
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Size-Exclusion Chromatography

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Cited by 18 publications
(11 citation statements)
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“…The peaks were observed at elusion times 60 min, 130 min and 245 min, which refer to high, intermediate and low molecular weight bands, respectively. According to Brookes et al [91] and Striegel [92], the retention time of the molecules in the chromatography column is inversely proportional to their molecular weights. Hence, the largest molecules are eluted at the lowest elution times, which is called an "inverse-sieving" mechanism.…”
Section: Chromatographic Separation Of Prepolymerized Aluminium Coagumentioning
confidence: 99%
“…The peaks were observed at elusion times 60 min, 130 min and 245 min, which refer to high, intermediate and low molecular weight bands, respectively. According to Brookes et al [91] and Striegel [92], the retention time of the molecules in the chromatography column is inversely proportional to their molecular weights. Hence, the largest molecules are eluted at the lowest elution times, which is called an "inverse-sieving" mechanism.…”
Section: Chromatographic Separation Of Prepolymerized Aluminium Coagumentioning
confidence: 99%
“…This phenom enon enables the separation of a broad range of sizes, but results in poor selectivity 88 . In size exclusion chromatography (SEC) columns, packed with porous material, size fractionation results from the fast est elution of bigger particles and delayed elution of particles of size smaller than or equal to that of the pores 89 . The resolving power of chromatographic separation can be compromised by the interaction of nanoparticles with the stationary phase or with the species present in the mobile phase.…”
Section: Detection and Quantification Of Enps At Low Concentrationsmentioning
confidence: 99%
“…This is essential in the field of venomics, as toxins are often large proteins that may or may not exist in complexes with other proteins [48,49]. This technique can also be achieved using HPLC to perform a high-resolution fractionation of molecules based on their molecular weight [47]. However, depending on the separation technology used to achieve SEC, it is not a particularly high-resolution chromatographic technique and has a limited dynamic range for protein separation.…”
Section: Separation Techniquesmentioning
confidence: 99%
“…SEC is a chromatographic method in which hydrophilic molecules (proteins or other solutes) are separated based on their size or molecular weight, either through molecular-weight sieves or through gel-filtration chromatography [ 47 ]. It has proven to be very useful in separating proteins, due to the technique’s ability to separate native proteins (undigested) or protein complexes.…”
Section: Techniques In Venomicsmentioning
confidence: 99%
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