Use and qualification of primary and secondary standards employed in quantitative 1H NMR spectroscopy of pharmaceuticals

Journal of Pharmaceutical and Biomedical Analysis

Volumn 93, Issue , 2014, Pages 111-117

  Rundlöf, Torgny ^a   McEwen, Ian ^a   Johansson, Monika ^a,b   Arvidsson, Torbjörn ^a,b  

^a MEDICAL PRODUCTS AGENCY   (Sweden)

^b UPPSALA UNIVERSITY   (Sweden)

Author keywords

NMR; Qualification; Quantification; Reference substance; Standardization

Indexed keywords

1,4 BIS(TRIMETHYLSILYL)BENZENE; 3 SULFOLENE; 3,4,5 TRICHLOROPYRIDINE; ACETANILIDE; BENZENE DERIVATIVE; MALEIC ACID; PHLOROGLUCINOL TRIMETHYL ETHER; TEREPHTHALIC ACID; TEREPHTHALIC ACID DIMETHYL ESTER; UNCLASSIFIED DRUG; ACETANILIDE DERIVATIVE; DRUG;

ARTICLE; DRUG PURITY; DRUG STABILITY; PRIORITY JOURNAL; PROTOCOL COMPLIANCE; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTITATIVE ANALYSIS; STANDARD; CHEMISTRY; PROCEDURES; REPRODUCIBILITY; STANDARDS; TIME;

ACETANILIDES; DRUG STABILITY; PHARMACEUTICAL PREPARATIONS; PROTON MAGNETIC RESONANCE SPECTROSCOPY; REFERENCE STANDARDS; REPRODUCIBILITY OF RESULTS; TIME FACTORS;

EID: 84900316484     PISSN: 07317085     EISSN: 1873264X     Source Type: Journal    
DOI: 10.1016/j.jpba.2013.09.010     Document Type: Article

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