Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration

This paper investigates the membrane purification and fractionation of a mixture containing the homologous series of cyclodextrins CD6 to CD60 obtained by enzymatic conversion of starch. Three commercial polyamide thin film composite NF and UF membranes (HL, GH and GK from GE-Osmonics) were used for...

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Main Authors: Ellouze, Fatma, Ben Amar, Nihel, Mokhtar, Mohd Noriznan, Zimmermann, Wolfgang, Deratani, Andre
Format: Article
Language:English
Published: Elsevier 2011
Online Access:http://psasir.upm.edu.my/id/eprint/22963/1/Fractionation%20of%20homologous%20CD6%20to%20CD60%20cyclodextrin%20mixture%20by%20ultrafiltration%20and%20nanofiltration.pdf
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author Ellouze, Fatma
Ben Amar, Nihel
Mokhtar, Mohd Noriznan
Zimmermann, Wolfgang
Deratani, Andre
author_facet Ellouze, Fatma
Ben Amar, Nihel
Mokhtar, Mohd Noriznan
Zimmermann, Wolfgang
Deratani, Andre
author_sort Ellouze, Fatma
collection UPM
description This paper investigates the membrane purification and fractionation of a mixture containing the homologous series of cyclodextrins CD6 to CD60 obtained by enzymatic conversion of starch. Three commercial polyamide thin film composite NF and UF membranes (HL, GH and GK from GE-Osmonics) were used for this purpose. In a first step, a binary mixture composed of glucose and heptacyclomaltose (β-cyclodextrin, CD7) was filtered to examine the separation performance of the studied membranes. A mathematical model based on mass balance was proposed for the simulation of the discontinuous diafiltration process assuming that the membrane separation performance is based on a sieving mechanism. A three stage diafiltration cascade (in retentate configuration) was then selected to fractionate the CD6–CD60 crude mixture. The experimental composition of the obtained permeate and retentate solutions in the targeted fractions (glucose, CD6–CD8, CD9–CD21, CD22–CD60) fit well with the predicted data indicating that membrane process enables purification and fractionation of the homologous series of large ring CDs. Some discrepancies were however observed implying that other mechanisms such as coupled transport also took place. The most striking effect was the presence of glucose in the GK retentate possibly as a result of the formation of inclusion complexes with the large ring CDs.
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spelling upm.eprints-229632015-12-09T08:21:07Z http://psasir.upm.edu.my/id/eprint/22963/ Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration Ellouze, Fatma Ben Amar, Nihel Mokhtar, Mohd Noriznan Zimmermann, Wolfgang Deratani, Andre This paper investigates the membrane purification and fractionation of a mixture containing the homologous series of cyclodextrins CD6 to CD60 obtained by enzymatic conversion of starch. Three commercial polyamide thin film composite NF and UF membranes (HL, GH and GK from GE-Osmonics) were used for this purpose. In a first step, a binary mixture composed of glucose and heptacyclomaltose (β-cyclodextrin, CD7) was filtered to examine the separation performance of the studied membranes. A mathematical model based on mass balance was proposed for the simulation of the discontinuous diafiltration process assuming that the membrane separation performance is based on a sieving mechanism. A three stage diafiltration cascade (in retentate configuration) was then selected to fractionate the CD6–CD60 crude mixture. The experimental composition of the obtained permeate and retentate solutions in the targeted fractions (glucose, CD6–CD8, CD9–CD21, CD22–CD60) fit well with the predicted data indicating that membrane process enables purification and fractionation of the homologous series of large ring CDs. Some discrepancies were however observed implying that other mechanisms such as coupled transport also took place. The most striking effect was the presence of glucose in the GK retentate possibly as a result of the formation of inclusion complexes with the large ring CDs. Elsevier 2011-05 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/22963/1/Fractionation%20of%20homologous%20CD6%20to%20CD60%20cyclodextrin%20mixture%20by%20ultrafiltration%20and%20nanofiltration.pdf Ellouze, Fatma and Ben Amar, Nihel and Mokhtar, Mohd Noriznan and Zimmermann, Wolfgang and Deratani, Andre (2011) Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration. Journal of Membrane Science, 374 (1-2). pp. 129-137. ISSN 0376-7388; ESSN: 1873-3123 http://www.sciencedirect.com/science/article/pii/S0376738811002018 10.1016/j.memsci.2011.03.025
spellingShingle Ellouze, Fatma
Ben Amar, Nihel
Mokhtar, Mohd Noriznan
Zimmermann, Wolfgang
Deratani, Andre
Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration
title Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration
title_full Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration
title_fullStr Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration
title_full_unstemmed Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration
title_short Fractionation of homologous CD6 to CD60 cyclodextrin mixture by ultrafiltration and nanofiltration
title_sort fractionation of homologous cd6 to cd60 cyclodextrin mixture by ultrafiltration and nanofiltration
url http://psasir.upm.edu.my/id/eprint/22963/1/Fractionation%20of%20homologous%20CD6%20to%20CD60%20cyclodextrin%20mixture%20by%20ultrafiltration%20and%20nanofiltration.pdf
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AT mokhtarmohdnoriznan fractionationofhomologouscd6tocd60cyclodextrinmixturebyultrafiltrationandnanofiltration
AT zimmermannwolfgang fractionationofhomologouscd6tocd60cyclodextrinmixturebyultrafiltrationandnanofiltration
AT derataniandre fractionationofhomologouscd6tocd60cyclodextrinmixturebyultrafiltrationandnanofiltration