ANALYTIC METHOD;
ARTICLE;
CONDUCTOMETRY;
DRUG DEGRADATION;
DRUG DETERMINATION;
DRUG IMPURITY;
DRUG STABILITY;
ENVIRONMENTAL TEMPERATURE;
FLOW RATE;
HUMIDITY;
HYDROLYSIS;
ION PAIR CHROMATOGRAPHY;
LINEAR SYSTEM;
OXIDATIVE STRESS;
PARTICLE SIZE;
PHOTOLYSIS;
PRIORITY JOURNAL;
PROCESS DEVELOPMENT;
PROCESS OPTIMIZATION;
REPRODUCIBILITY;
SENSITIVITY AND SPECIFICITY;
THERMOSTABILITY;
VALIDATION PROCESS;
CHROMATOGRAPHY, ION EXCHANGE;
CHROMATOGRAPHY, REVERSE-PHASE;
DIPHOSPHONATES;
DRUG CONTAMINATION;
DRUG STABILITY;
HUMANS;
HUMIDITY;
HYDROLYSIS;
PHOTOLYSIS;
REPRODUCIBILITY OF RESULTS;
SENSITIVITY AND SPECIFICITY;
TEMPERATURE;
Effects of treatment with ibandronate on bone mass, architecture, biomechanical propertites, and bone concentration of ibandronate in ovariectomized aged rats
Bauss F., Lalla S., Endele R., Hothorn L.A. Effects of treatment with ibandronate on bone mass, architecture, biomechanical propertites, and bone concentration of ibandronate in ovariectomized aged rats. J. Rheumatol. 2002, 29:2200-2208.
Anion-exchange separation and determination of bisphosphonates and related analytes by post-column indirect fluorescence detection
Lovdahl M.J., Pietrzyk D.J. Anion-exchange separation and determination of bisphosphonates and related analytes by post-column indirect fluorescence detection. J. Chromatogr. A 2000, 868:141-142.
Validation of a capillary electrophoresis method for the analysis of ibandronate related impurities
Rodriguez J.A.B., Desimone M.F., Iglesias S.L., Giorgieri S.A., Diaz L.E. Validation of a capillary electrophoresis method for the analysis of ibandronate related impurities. J. Pharm. Biomed. Anal. 2007, 44:305-308.
Determination of Ibandronate and its degradation products by ion-pair RP LC with evaporative light-scattering detection
Jiang Y., Xie Z. Determination of Ibandronate and its degradation products by ion-pair RP LC with evaporative light-scattering detection. Chromatographia 2005, 62:257-261.
Determination of bisphosphonate active pharmaceutical ingredients in pharmaceuticals and biological material: a review of analytical methods
Zacharis C.K., Tzanavaras P.D. Determination of bisphosphonate active pharmaceutical ingredients in pharmaceuticals and biological material: a review of analytical methods. J. Pharm. Biomed. Anal. 2008, 48:483-496.
International Conference on Harmonization of technical requirements for registration of pharmaceuticals for human use, ICH harmonized tripartite guideline, Validation of analytical procedures: text and methodology Q2(R1), step 4
International Conference on Harmonization of technical requirements for registration of pharmaceuticals for human use, ICH harmonized tripartite guideline, Validation of analytical procedures: text and methodology Q2(R1), step 4 2005.
(2005)
9
78149498189
International Conference on Harmonization of technical requirements for registration of pharmaceuticals for human use, ICH harmonized tripartite guideline, Stability testing of new drug substances and products Q1A(R2), step 4
International Conference on Harmonization of technical requirements for registration of pharmaceuticals for human use, ICH harmonized tripartite guideline, Stability testing of new drug substances and products Q1A(R2), step 4 2003.
(2003)
* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.