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Volumn 1259, Issue , 2012, Pages 111-120

Quantitative high-performance liquid chromatography-tandem mass spectrometry impurity profiling methods for the analysis of parenteral infusion solutions for amino acid supplementation containing l-alanyl-l-glutamine

Author keywords

LC MS MS; Peptides; Stability indicating methods; Stereoisomeric impurities

Indexed keywords

AMINO ACID SUPPLEMENTATION; BIOACTIVE PEPTIDES; CHIRALPAK; EPIMERS; HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY; IMPURITIES IN; IMPURITY PROFILE; IMPURITY PROFILING; ISOBARIC COMPOUNDS; LC-ESI-MS/MS; LC-MS/MS; MULTICOMPONENTS; PHARMACEUTICAL FORMULATION; QUANTITATIVE DATA; SAMPLE SOLUTION; STABILITY INDICATING METHOD; STANDARD ADDITION; STATIONARY PHASE; STRESS TESTING;

EID: 84866328283     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2012.01.020     Document Type: Article
Times cited : (10)

References (24)
  • 2
    • 84872759481 scopus 로고    scopus 로고
    • ICH, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use
    • ICH, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use Impurities in New Drug Substances Q3A(R2) 2006, http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html.
    • (2006) Impurities in New Drug Substances Q3A(R2)
  • 3
    • 84872759544 scopus 로고    scopus 로고
    • ICH, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use
    • ICH, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use Impurities in New Drug Products Q3B(R2) 2006, http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html.
    • (2006) Impurities in New Drug Products Q3B(R2)
  • 14
    • 77955416237 scopus 로고    scopus 로고
    • ICH, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use
    • ICH, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use Validation of Analytical Procedures: Text and Methodology Q2(R1) 2005, http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html.
    • (2005) Validation of Analytical Procedures: Text and Methodology Q2(R1)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.