ARTICLE;
CONTROLLED STUDY;
DRUG DETERMINATION;
DRUG FORMULATION;
DRUG IMPURITY;
DRUG ISOLATION;
DRUG STABILITY;
DRUG STRUCTURE;
INFRARED SPECTROSCOPY;
MASS SPECTROMETRY;
MECHANICAL STRESS;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PRIORITY JOURNAL;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
CHEMISTRY, PHARMACEUTICAL;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CHROMATOGRAPHY, LIQUID;
DIPYRIDAMOLE;
DRUG CONTAMINATION;
TANDEM MASS SPECTROMETRY;
Efficacy and safety of a novel synergistic drug candidate, CRx-102, in hand osteoarthritis
Kvien T.K., Fjeld E., Slatkowsky-Christensen B., Nichols M., Zhang Y., Proven A., et al. Efficacy and safety of a novel synergistic drug candidate, CRx-102, in hand osteoarthritis. Ann. Rheum. Dis. 2008, 67:942-948.
Purine metabolism and clinical status of patients with rheumatoid arthritis treated with Dipyridamole
Forrest C.M., Stone T.W., Mackay G.M., Oxford L., Stoy N., Harman G., et al. Purine metabolism and clinical status of patients with rheumatoid arthritis treated with Dipyridamole. Nucleosides Nucleotides Nucleic Acids 2006, 25:1287-1290.
Development and validation of a stability-indicating HPLC method for the determination of degradation products in Dipyridamole injection
Zhang J., Miller R.B., Jacobus R. Development and validation of a stability-indicating HPLC method for the determination of degradation products in Dipyridamole injection. Chromatographia 1997, 44:247-252.
Rapid and simultaneous determination of aspirin and Dipyridamole in pharmaceutical formulations by reversed-phase high performance liquid chromatography (RP-HPLC) method
Prakash K., Kalakuntla Rama Rao, Reddy Sama Jayapal Rapid and simultaneous determination of aspirin and Dipyridamole in pharmaceutical formulations by reversed-phase high performance liquid chromatography (RP-HPLC) method. Afr. J. Pharm. Pharacol. 2011, 5:244-251.
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, ICH Q3A (R2), Impurities in New Drug substances 2006, 1-15.
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, ICH Q3B (R2), Impurities in New Drug Products 2006, 1-16.
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human use, ICH Q1A (R2) Stability Testing of New Drug Substances and Products 2003, 1-24.