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Volumn 93, Issue 2, 2008, Pages 353-360

DSC and physico-chemical properties of a substituted pyridoquinoline and its interaction study with excipients

Author keywords

BG 637; DSC; Excipients; Interactions; Physico chemical properties; Stability

Indexed keywords

ARSENIC COMPOUNDS; CHEMICAL PROPERTIES; CHEMOTHERAPY; CHROMATOGRAPHIC ANALYSIS; DEPOSITS; DIFFERENTIAL SCANNING CALORIMETRY; DIGITAL CAMERAS; DRUG DELIVERY; DRUG DOSAGE; FOURIER TRANSFORM INFRARED SPECTROSCOPY; FOURIER TRANSFORMS; GAS CHROMATOGRAPHY; HEALTH; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INFRARED SPECTROSCOPY; LASER INTERFEROMETRY; LIGHT METALS; MAGNESIUM; MAGNETIC FIELDS; MAGNETIC RESONANCE; MASS SPECTROMETRY; MELTING POINT; MIXTURES; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RESONANCE; SODIUM; SPECTROMETERS; SPECTROMETRY; SUGARS; THEOREM PROVING;

EID: 48249149971     PISSN: 13886150     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10973-008-9062-7     Document Type: Article
Times cited : (29)

References (29)
  • 6
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    • Stability Testing of New Drug Substances and Products, ICH Q1A(R2). The European Agency for the Evaluation of Medicinal Products (CPMP/ICH/2736/99)
    • ICH Harmonised Tripartite Guideline, Stability Testing of New Drug Substances and Products, ICH Q1A(R2). The European Agency for the Evaluation of Medicinal Products (CPMP/ICH/2736/99), 2003.
    • (2003) ICH Harmonised Tripartite Guideline
  • 16
    • 48249109330 scopus 로고    scopus 로고
    • Council of Europe, Strasbourg
    • th Ed., Council of Europe, Strasbourg 2008.
    • (2008) th Ed.
  • 20
    • 10044239677 scopus 로고    scopus 로고
    • Impurities: Residual Solvents, ICH Q3C(R3). The European Agency for the Evaluation of Medicinal Products (CPMP/ICH/283/95)
    • ICH Harmonised Tripartite Guideline, Impurities: Residual Solvents, ICH Q3C(R3). The European Agency for the Evaluation of Medicinal Products (CPMP/ICH/283/95), 1997.
    • (1997) ICH Harmonised Tripartite Guideline
  • 27
    • 48249116583 scopus 로고    scopus 로고
    • Pharmaceutical Development, ICH Q8. The European Agency for the Evaluation of Medicinal Products (CPMP/ICH/167068/04)
    • ICH Harmonised Tripartite Guideline, Pharmaceutical Development, ICH Q8. The European Agency for the Evaluation of Medicinal Products (CPMP/ICH/167068/04), 2005.
    • (2005) ICH Harmonised Tripartite Guideline


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.