Title of article
Purification and analysis of a 5 kDa component of enamel matrix derivative
Author/Authors
Mumulidu، نويسنده , , Alexandra and Hildebrand، نويسنده , , Bergisa and Fabi، نويسنده , , Beata and Hammarstrِm، نويسنده , , Lars and Cochran، نويسنده , , David L. and Dard، نويسنده , , Michel and Lemoult، نويسنده , , Stephanie، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
9
From page
210
To page
218
Abstract
High performance liquid chromatography (HPLC) methods were used to analyse a 5 kDa component purified from enamel matrix derivative (EMD), the active ingredient in Emdogain®, a commercial product for periodontal tissue regeneration. After initial purification by size-exclusion chromatography (SEC) on a 100 cm × 5 cm column (Bio-Gel P-30 Fine, 280 nm), collected fractions were analysed by size-exclusion HPLC (SE HPLC; TSK-Gel Super SW2000, 220 nm). The fractions containing only the 5 kDa component were analysed by reversed-phase high-pressure chromatography (RP HPLC; YMC-Pack ODS-A, 200 nm), revealing four peaks of the 5 kDa component. From 1200 mg of EMD (of which 9% is the 5 kDa component), approximately 65 mg of lyophilised 5 kDa component were obtained, corresponding to a recovery of 60%. The SE HPLC method was mainly suitable for qualitative analysis, whereas the RP HPLC method was appropriate for both qualitative and quantitative analysis.
Keywords
Reversed-phase HPLC , Protein Purification , Qualitative analysis , Quantitative analysis , Method validation , fractionation , Emdogain , Size-exclusion HPLC , Enamel matrix derivative
Journal title
Journal of Chromatography B
Serial Year
2007
Journal title
Journal of Chromatography B
Record number
1465157
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