1H Nuclear Magnetic Resonance Spectroscopic Analysis for Determination of Glucuronic and Iduronic Acids in Dermatan Sulfate, Heparin, and Heparan Sulfate

2001 ◽  
Vol 297 (1) ◽  
pp. 42-51 ◽  
Author(s):  
Masahiro Sudo ◽  
Kenji Sato ◽  
Amornrut Chaidedgumjorn ◽  
Hidenao Toyoda ◽  
Toshihiko Toida ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Heparan Sulfate ◽  
Spectroscopic Analysis ◽  
Dermatan Sulfate ◽  
1H Nuclear Magnetic Resonance ◽  
Magnetic Resonance Spectroscopic Analysis ◽  
Nuclear Magnetic

Determination of Ephedrine, Pseudoephedrine, and Norephedrine in Mixtures (Bulk and Dosage Forms) by Proton Nuclear Magnetic Resonance Spectroscopy

1995 ◽  
Vol 78 (4) ◽  
pp. 946-953 ◽  
Author(s):  
George M Hanna
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Spectroscopic Method ◽  
Internal Standard ◽  
Dosage Forms ◽  
Proton Nuclear Magnetic Resonance ◽  
Resonance Spectroscopy ◽  
1H Nuclear Magnetic Resonance ◽  
Nuclear Magnetic

Abstract A simple, specific, and accurate 1H nuclear magnetic resonance (NMR) spectroscopic method has been developed for quantitative determination of the Ephedra alkaloids (−)-ephedrine, (+)-pseudoephedrine, and (±)-norephedrine, either singly or in mixtures with each other. Determination of individual alkaloids was carried out in D2O solution, with acetamide as internal standard. Although calculations were based on integrals for the C–CH3 protons, those for the N–CH3 and –CH–O– protons may also be useful, depending on the compound. Determination of diastereomeric cross-contamination of ephedrine and pseudoephedrine—or of the concentrations of these alkaloids in the presence or absence of (±)-norephedrine—was feasible by using the integrals for the –CH–O– protons after addition of a trace of DCI. Mean recoveries for ephedrine and pseudoephedrine from their respective synthetic mixtures with the internal standard (acet- amide) were ≥99.9 ± 0.6% (n = 10) and 99.6 ± 0.8% (n = 10) of the amount added. Recovery for pseudoephedrine from diastereomeric mixtures with ephedrine was >99.4 ± 0.7% (n = 10) of the amount added, with as little as 1.92% still being measurable. Mean recovery of (±)-norephedrine from mixtures with ephedrine and pseudoephedrine was >99.7 ± 2.5% (n = 4) of the amount added, with about 1% still being measurable. Application of the proposed NMR spectroscopic method to commercial dosage forms, including ephedrine sulfate injections and pseudoephedrine hydrochloride tablets, yielded assay results ranging from 97.8 to 100.2% (mean, 99.2%) and from 98.7 to 100.5% (mean, 99.7%) of declared, respectively.

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