2008
DOI: 10.1002/jps.21223
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Physicochemical, Crystallographic, Thermal, and Spectroscopic Behavior of Crystalline and X-ray Amorphous Ciclesonide

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Cited by 22 publications
(17 citation statements)
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References 33 publications
(34 reference statements)
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“…DSC was found more accurate and sensitive than FT-Raman spectroscopy [56]. Beclomethasone dipropionate clathrate formation with trichloromonofluoromethane for being used in a suspension metered dose inhaler was characterized by XRPD, X-ray photoelectron spectroscopy, scanning electron microscopy and DSC [57].…”
Section: Solid Phase Characterizationmentioning
confidence: 99%
“…DSC was found more accurate and sensitive than FT-Raman spectroscopy [56]. Beclomethasone dipropionate clathrate formation with trichloromonofluoromethane for being used in a suspension metered dose inhaler was characterized by XRPD, X-ray photoelectron spectroscopy, scanning electron microscopy and DSC [57].…”
Section: Solid Phase Characterizationmentioning
confidence: 99%
“…In another case, dissolution of crystalline and amorphous ciclesonide was studied (Feth et al 2008). Crystalline and amorphous ciclesonide exhibit the same saturation solubility (Feth et al 2008). For the crystalline ciclesonide, within the first 60 min of dissolution, the concentration measured (50 mg/L) was significantly lower than its saturation solubility (90.1 ± 2.2 mg/L).…”
Section: Between Amorphous and Crystalline Phasementioning
confidence: 99%
“…Analysis of the remaining sample after the dissolution experiment confirmed that the sample surface had converted to the dihydrate (crystalline form) during dissolution ). In another case, dissolution of crystalline and amorphous ciclesonide was studied (Feth et al 2008). Crystalline and amorphous ciclesonide exhibit the same saturation solubility (Feth et al 2008).…”
Section: Between Amorphous and Crystalline Phasementioning
confidence: 99%
“…The crystal growth dimension, m, is either one, two, or three, corresponding to rod-like (unidimensional), disk-like (bidimensional), or spherulitic (tridimensional) crystal habits, respectively. 25,26) The reaction order, n, is equal to m for instantaneous nucleation or to m+1 for sporadic nucleation. Figure 2 shows the microscopic aspects of phenytoin crystals.…”
Section: Fig 1 Accumulation Curves Of Phenytoin Crystals After Miximentioning
confidence: 99%