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[Purification of oleuropein by sephadex LH-20 column].

Jian-Zhang Dang, Xiao-Zhong Nie, Liqin Liang

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Abstract

OBJECTIVE: To purify the oleuropein crude extracts by sephadex LH-20 column chromatograph. METHODS: This experiment used fast protein chromatography system (AKTA FPLC) produced by Amersham, Sweden. The chromatography column (20 mm x 300 mm) was matched with protein purification instrument. Sephadex LH-20 was used in the Fast Protein Liquid Chromatography columns. The mobile phase was 50% ethanol with a flow velocity of 1.0 mL per minute and the detection wavelength was 254 nm. The content of oleuropein was determined by HPLC. RESULTS: The purity of oleuropein was 82.9% after passing the column twice when the sample volume was 2 mL. CONCLUSION: Sephadex LH-20 can be re-used and the regeneration is convenient, it also provides a reference for the production of oleuropein.

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OBJECTIVE: To purify the oleuropein crude extracts by sephadex LH-20 column chromatograph. METHODS: This experiment used fast protein chromatography system (AKTA FPLC) produced by Amersham, Sweden. The chromatography column (20 mm x 300 mm) was matched with protein purification instrument. Sephadex LH-20 was used in the Fast Protein Liquid Chromatography columns. The mobile phase was 50% ethanol with a flow velocity of 1.0 mL per minute and the detection wavelength was 254 nm. The content of oleuropein was determined by HPLC. RESULTS: The purity of oleuropein was 82.9% after passing the column twice when the sample volume was 2 mL. CONCLUSION: Sephadex LH-20 can be re-used and the regeneration is convenient, it also provides a reference for the production of oleuropein.

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Available abstract

OBJECTIVE: To purify the oleuropein crude extracts by sephadex LH-20 column chromatograph. METHODS: This experiment used fast protein chromatography system (AKTA FPLC) produced by Amersham, Sweden. The chromatography column (20 mm x 300 mm) was matched with protein purification instrument. Sephadex LH-20 was used in the Fast Protein Liquid Chromatography columns. The mobile phase was 50% ethanol with a flow velocity of 1.0 mL per minute and the detection wavelength was 254 nm. The content of oleuropein was determined by HPLC. RESULTS: The purity of oleuropein was 82.9% after passing the column twice when the sample volume was 2 mL. CONCLUSION: Sephadex LH-20 can be re-used and the regeneration is convenient, it also provides a reference for the production of oleuropein.

Key concepts: Oleuropein, Chromatography, Chemistry, Sephadex, Chromatography column, High-performance liquid chromatography, Column chromatography, Fast protein liquid chromatography

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