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Evaluation of enantiomeric purity of magnesium-L-aspartate dihydrate.

Journal of pharmaceutical and biomedical analysis (2014-09-30)
Oliver Wahl, Ulrike Holzgrabe
ABSTRACT

Magnesium supplementation in form of organic magnesium salts is a very popular practice. We examined the enantiomeric purity of "Magnesium aspartate dihydrate" monographed in the European Pharmacopeia. A chiral capillary zone electrophoresis using (2-hydroxypropyl)-β-cyclodextrin coupled to laser induced fluorescence detection and a HPLC-fluorescence method with chiral derivatization using o-phthaldialdehyde and N-acetyl-L-cysteine as an orthogonal method were developed and validated. Two batch samples of this substance and three drug products containing the salt were analyzed by means of both methods. The concentration of the D-enantiomer of aspartic acid ranged from 0.03 to 0.12%. Simulations of the synthesis revealed that the d-aspartic acid content is elevated if the dissolution of L-aspartic acid was performed at acidic pH values.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Hydrochloric acid, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., fuming, ≥37%, APHA: ≤10
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di-Sodium hydrogen phosphate dihydrate, puriss. p.a., reag. Ph. Eur., 98.5-101.0% (calc. to the dried substance)
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Formamide, ReagentPlus®, ≥99.0% (GC)
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Acetic acid, glacial, puriss., 99-100%
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Magnesium hydroxide, reagent grade, 95%
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Hydrogen chloride solution, 1.0 M in diethyl ether
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Sodium bicarbonate, anhydrous, free-flowing, Redi-Dri, ACS reagent, ≥99.7%
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Hydrochloric acid, ACS reagent, 37%
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Acetic acid, glacial, ReagentPlus®, ≥99%
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