On the isolation of immunostimulatory active acemannan from Aloe barbadensis

Acemannan from Aloe barbadensis was obtained with four processes: 1) size exclusion chromatography (SEC) using Sepharose CL-4B matrix followed by ethanolic precipitation; 2) SEC, ultrafiltration using hollow-fiber cartridges (30 kDa or 0.1 µm) and ethanolic precipitation; 3) SEC, precipitation with...

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Main Authors: Mabel Alonso, Yanet Támbara, Matilde López, Julio C Aguilar, Orestes Mayo, Enrique Prieto, José Cremata, Gerrit Gerwig, Hans Kamerling, Eugenio Hardy
Format: Article
Language:English
Published: Elfos Scientiae
Series:Biotecnología Aplicada
Subjects:
Online Access:http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S1027-28522012000200004&lng=en&tlng=en
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author Mabel Alonso
Yanet Támbara
Matilde López
Julio C Aguilar
Orestes Mayo
Enrique Prieto
José Cremata
Gerrit Gerwig
Hans Kamerling
Eugenio Hardy
author_facet Mabel Alonso
Yanet Támbara
Matilde López
Julio C Aguilar
Orestes Mayo
Enrique Prieto
José Cremata
Gerrit Gerwig
Hans Kamerling
Eugenio Hardy
author_sort Mabel Alonso
collection DOAJ
description Acemannan from Aloe barbadensis was obtained with four processes: 1) size exclusion chromatography (SEC) using Sepharose CL-4B matrix followed by ethanolic precipitation; 2) SEC, ultrafiltration using hollow-fiber cartridges (30 kDa or 0.1 µm) and ethanolic precipitation; 3) SEC, precipitation with cetyltrimethylammonium bromide (CTAB) and ethanolic precipitation; and 4) direct precipitation with CTAB and ethanolic precipitation. The detergent CTAB was effective to concentrate chromatographic eluates (process 3) and allowed the direct isolation and purification of acemannan from crude ethanolic extracts (process 4), without recurring to SEC. Process 4 also decreases operation time (9 days vs. 15 days in process 3), and costs regarding raw materials. Both processes generate materials devoid of detectable levels of anthraquinones and contaminating DNA, and proteins below 5% of dry weight. This material was essentially made of mannose; 97% obtained in processes 1-3 and 75% in process 4, with a molecular mass ranging from 2000 to 5000 Mr according to G5000 PW SEC. Acemannan in dry form was sterilized at the optimal 10 kGy ?-radiation dose, and retained both its physical-chemical properties and adjuvanticity for HBsAg co-delivered by the nasal route in mice. The mixture of acemannan-1% benzyl alcohol (w/v) does not affect the adjuvanticity. The total carbohydrates content, SEC-HPLC, pH, microbial limit and organoleptic characteristics of the irradiated polysaccharide suspended in phosphate buffer remained stable at -20 ºC for at least 6 months of storage. These results may be useful for designing processes for producing pharmaceutical quality acemannan to be used in vaccine clinical studies.
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spelling doaj.art-e418529691764295aa4b1c537feb79c52022-12-22T01:12:02ZengElfos ScientiaeBiotecnología Aplicada1027-285229287101S1027-28522012000200004On the isolation of immunostimulatory active acemannan from Aloe barbadensisMabel Alonso0Yanet Támbara1Matilde López2Julio C Aguilar3Orestes Mayo4Enrique Prieto5José Cremata6Gerrit Gerwig7Hans Kamerling8Eugenio Hardy9International Centre for Genetic Engineering and BiotechnologyInternational Centre for Genetic Engineering and BiotechnologyInternational Centre for Genetic Engineering and BiotechnologyInternational Centre for Genetic Engineering and BiotechnologyNational Center for Biopreparations, BioCenCenter for Applied Studies on the Development of Nuclear EnergyInternational Centre for Genetic Engineering and BiotechnologyUtrecht UniversityUtrecht UniversityInternational Centre for Genetic Engineering and BiotechnologyAcemannan from Aloe barbadensis was obtained with four processes: 1) size exclusion chromatography (SEC) using Sepharose CL-4B matrix followed by ethanolic precipitation; 2) SEC, ultrafiltration using hollow-fiber cartridges (30 kDa or 0.1 µm) and ethanolic precipitation; 3) SEC, precipitation with cetyltrimethylammonium bromide (CTAB) and ethanolic precipitation; and 4) direct precipitation with CTAB and ethanolic precipitation. The detergent CTAB was effective to concentrate chromatographic eluates (process 3) and allowed the direct isolation and purification of acemannan from crude ethanolic extracts (process 4), without recurring to SEC. Process 4 also decreases operation time (9 days vs. 15 days in process 3), and costs regarding raw materials. Both processes generate materials devoid of detectable levels of anthraquinones and contaminating DNA, and proteins below 5% of dry weight. This material was essentially made of mannose; 97% obtained in processes 1-3 and 75% in process 4, with a molecular mass ranging from 2000 to 5000 Mr according to G5000 PW SEC. Acemannan in dry form was sterilized at the optimal 10 kGy ?-radiation dose, and retained both its physical-chemical properties and adjuvanticity for HBsAg co-delivered by the nasal route in mice. The mixture of acemannan-1% benzyl alcohol (w/v) does not affect the adjuvanticity. The total carbohydrates content, SEC-HPLC, pH, microbial limit and organoleptic characteristics of the irradiated polysaccharide suspended in phosphate buffer remained stable at -20 ºC for at least 6 months of storage. These results may be useful for designing processes for producing pharmaceutical quality acemannan to be used in vaccine clinical studies.http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S1027-28522012000200004&lng=en&tlng=enacemannancetyltrimethylammonium bromidealoe verahbsagpurification
spellingShingle Mabel Alonso
Yanet Támbara
Matilde López
Julio C Aguilar
Orestes Mayo
Enrique Prieto
José Cremata
Gerrit Gerwig
Hans Kamerling
Eugenio Hardy
On the isolation of immunostimulatory active acemannan from Aloe barbadensis
Biotecnología Aplicada
acemannan
cetyltrimethylammonium bromide
aloe vera
hbsag
purification
title On the isolation of immunostimulatory active acemannan from Aloe barbadensis
title_full On the isolation of immunostimulatory active acemannan from Aloe barbadensis
title_fullStr On the isolation of immunostimulatory active acemannan from Aloe barbadensis
title_full_unstemmed On the isolation of immunostimulatory active acemannan from Aloe barbadensis
title_short On the isolation of immunostimulatory active acemannan from Aloe barbadensis
title_sort on the isolation of immunostimulatory active acemannan from aloe barbadensis
topic acemannan
cetyltrimethylammonium bromide
aloe vera
hbsag
purification
url http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S1027-28522012000200004&lng=en&tlng=en
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