Development and validation of a sensitive LC-MS/MS method for the determination of adefovir in human serum and urine

Journal of Pharmaceutical and Biomedical Analysis

Volumn 42, Issue 3, 2006, Pages 372-378

  Sun, Deqing ^a   Wang, Haisheng ^a   Wang, Benjie ^b   Guo, Ruichen ^b  

^a SHANDONG UNIVERSITY   (China)

^b SHANDONG UNIVERSITY   (China)

Author keywords

Adefovir; Human; LC MS MS; Pharmacokinetics

Indexed keywords

ADEFOVIR; FORMIC ACID; ION; METHANOL; WATER;

ACCURACY; ADULT; ANALYTIC METHOD; ARTICLE; CALIBRATION; CLINICAL TRIAL; COLUMN CHROMATOGRAPHY; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CORRELATION COEFFICIENT; CROSSOVER PROCEDURE; DRUG BLOOD LEVEL; DRUG DETERMINATION; DRUG STABILITY; DRUG URINE LEVEL; ELUTION; FLOW RATE; HUMAN; LIQUID CHROMATOGRAPHY; MALE; MASS SPECTROMETRY; NORMAL HUMAN; PARTICLE SIZE; PRECURSOR; PRIORITY JOURNAL; RANDOMIZED CONTROLLED TRIAL; REACTION ANALYSIS; SERUM; STANDARD; STORAGE TEMPERATURE; TANDEM MASS SPECTROMETRY; URINE; VALIDATION STUDY;

ADENINE; ADULT; CALIBRATION; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DRUG STABILITY; HUMANS; MALE; MASS SPECTROMETRY; PHOSPHONIC ACIDS; SENSITIVITY AND SPECIFICITY;

EID: 33748199122     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2006.04.019     Document Type: Article

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