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Volumn 1215, Issue 1-2, 2008, Pages 100-106

Simple high-performance liquid chromatography-fluorescence detection method for plasma, kidney and liver of rat as a tool for toxicology studies

Author keywords

HPLC; Kidney; Liver; Mycotoxin; Ochratoxin A; Plasma; Rat; Toxicokinetic; Validation

Indexed keywords

ACETONITRILE; ANIMALS; BODY FLUIDS; CHROMATOGRAPHIC ANALYSIS; CHROMATOGRAPHY; DISCRIMINANT ANALYSIS; DISSOLUTION; ETHANOL; FLUORESCENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; LIGHT EMISSION; LIQUID CHROMATOGRAPHY; LIVER; LUMINESCENCE; METHANOL; PLASMA STABILITY; PLASMAS; POLYMORPHISM; SODIUM; TOXIC MATERIALS;

EID: 56949108305     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chroma.2008.10.119     Document Type: Article
Times cited : (19)

References (43)
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  • 19
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  • 22
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    • ICH Harmonised Tripartite Guideline, Q2(R1): Validation of Analytical Procedures: Text and Methodology, International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Geneva, November 2005.
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    • ICH Harmonised Tripartite Guideline, S3A: Note for Guidance on Toxicokinetics: The Assessment of Systemic Exposure in Toxicity Studies, International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Geneva, October 1994.
    • ICH Harmonised Tripartite Guideline, S3A: Note for Guidance on Toxicokinetics: The Assessment of Systemic Exposure in Toxicity Studies, International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Geneva, October 1994.
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    • Committee for medicinal products for human use (CHMP), EMEA/CPMP/SWP/1094/04: Guideline on the evaluation of control samples in nonclinical safety studies: checking for contamination with the test substance, European Medicines Agency (EMEA), London, 2005.
    • Committee for medicinal products for human use (CHMP), EMEA/CPMP/SWP/1094/04: Guideline on the evaluation of control samples in nonclinical safety studies: checking for contamination with the test substance, European Medicines Agency (EMEA), London, 2005.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.