Effect of surfactants or a water soluble polymer on the crystal transition of clarithromycin during a wet granulation process.
暂无分享,去创建一个
S. Itai | Y. Iwao | K. Nozawa | Shuji Noguchi
[1] S. Itai,et al. Suppressed Release of Clarithromycin from Tablets by Crystalline Phase Transition of Metastable Polymorph Form I. , 2015, Journal of pharmaceutical sciences.
[2] Keiko Takiyama,et al. Polymorphic transformation of antibiotic clarithromycin under acidic condition. , 2014, Journal of pharmaceutical sciences.
[3] J. V. D. Streek. Reinterpretation of the monohydrate of clarithromycin from X-ray powder diffraction data as a trihydrate. , 2012 .
[4] S. Itai,et al. Clarithromycin form I determined by synchrotron X-ray powder diffraction. , 2012, Acta crystallographica. Section C, Crystal structure communications.
[5] S. Itai,et al. Stabilization mechanism of clarithromycin tablets under gastric pH conditions. , 2011, Chemical & pharmaceutical bulletin.
[6] J. Atwood,et al. A new strategy of transforming pharmaceutical crystal forms. , 2011, Journal of the American Chemical Society.
[7] S. Wimperis,et al. Solid-state NMR spectroscopy. , 2009, Physical chemistry chemical physics : PCCP.
[8] N. Rodríguez-Hornedo,et al. Surfactant-facilitated crystallization of dihydrate carbamazepine during dissolution of anhydrous polymorph. , 2004, Journal of pharmaceutical sciences.
[9] T. Oguchi,et al. Characterization and quantitation of clarithromycin polymorphs by powder X-ray diffractometry and solid-state NMR spectroscopy. , 2002, Chemical & pharmaceutical bulletin.
[10] Y. Kawashima,et al. Method of evaluation of the bitterness of clarithromycin dry syrup. , 2002, Chemical & pharmaceutical bulletin.
[11] M. Parvez,et al. Clarithromycin hydrochloride 3.5‐hydrate , 2000 .
[12] Y. Sohn,et al. Polymorphism of clarithromycin , 2000, Archives of pharmacal research.
[13] John Magee,et al. The Method of Evaluation , 2000 .
[14] T. Yajima,et al. Optimum spray congealing conditions for masking the bitter taste of clarithromycin in wax matrix. , 1999, Chemical & pharmaceutical bulletin.
[15] Yoshiaki Watanabe,et al. Structure of 6‐O‐methylerythromycin A (clarithromycin) , 1993 .
[16] T. Nagai,et al. Physicochemical properties and stability in the acidic solution of a new macrolide antibiotic, clarithromycin, in comparison with erythromycin. , 1992, Chemical & pharmaceutical bulletin.
[17] Yoshiaki Watanabe,et al. Chemical modification of erythromycins. VI. Structure and antibacterial activity of acid degradation products of 6-O-methylerythromycins A. , 1990, The Journal of antibiotics.