Technique validation by liquid chromatography for the determination of acyclovir in plasma

Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences

Volumn 791, Issue 1-2, 2003, Pages 357-363

  Fernández, Marcos ^a   Sepúlveda, Jacqueline ^a   Aránguiz, Teobaldo ^a   Von Plessing, Carlos ^a  

^a UNIVERSITY OF CONCEPCIÓN   (Chile)

Author keywords

Acyclovir; Validation

Indexed keywords

CALIBRATION; EXTRACTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PHASE COMPOSITION; ULTRAVIOLET DETECTORS; WATER;

SOLID-PHASE EXTRACTION;

PLASMAS;

ACETONITRILE; ACICLOVIR; ADENOSINE 5' (N METHYLCARBOXAMIDE); BUFFER; DODECYL SULFATE SODIUM; PHOSPHATE;

ACIDITY; ARTICLE; BIOEQUIVALENCE; CALIBRATION; DRUG BIOAVAILABILITY; DRUG DETERMINATION; DRUG PURIFICATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; MEAN RESIDENCE TIME; PRIORITY JOURNAL; SEPARATION TECHNIQUE; SOLID PHASE EXTRACTION; SPECTRAL SENSITIVITY; ULTRAVIOLET RADIATION; VALIDATION PROCESS;

EID: 0038021380     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1570-0232(03)00252-6     Document Type: Article

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