2009
DOI: 10.1002/jps.21501
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Cascade Impactor Practice for a High Dose Dry Powder Inhaler at 90 L/min: NGI Versus Modified 6-Stage and 8-Stage ACI

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Cited by 17 publications
(8 citation statements)
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“…According to the wall shear stress equation, the intensity of the wall shear stress depended on the flow velocity, it meant that the preseparator could reduce the trapped particles to reentrain back into the stream flow. Then, it might decrease the percentage wall loss of the impactor, due to the decreased air velocity and smoothed on the wall shear stress [7]. It was found that particle removal depended on the shear stress even when it was not a linear correlation, for which the particle removal phenomena needs to have a critical wall shear stress [23].…”
Section: Wall Shear Stress On the Collection Plate (Impaction Plate)mentioning
confidence: 99%
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“…According to the wall shear stress equation, the intensity of the wall shear stress depended on the flow velocity, it meant that the preseparator could reduce the trapped particles to reentrain back into the stream flow. Then, it might decrease the percentage wall loss of the impactor, due to the decreased air velocity and smoothed on the wall shear stress [7]. It was found that particle removal depended on the shear stress even when it was not a linear correlation, for which the particle removal phenomena needs to have a critical wall shear stress [23].…”
Section: Wall Shear Stress On the Collection Plate (Impaction Plate)mentioning
confidence: 99%
“…Conventionally, a dry powder inhaler can be used at an airflow rate of from 28.3 to 90 L/min during an aerodynamic sizing experiment. Several studies have used a preseparator containing liquid or solvent to trap the powder that was overloaded before reaching the cascade impactor stage [6,7].…”
Section: Introductionmentioning
confidence: 99%
“…For the test, powders (25 mg) were accurately weighed and loaded into size 3 gelatin capsules, and subsequently placed into a Cyclohaler ® (Pharmachemie BV, Netherlands) DPI device, connected via a mouthpiece adapter to the USP throat. The powders were subsequently aerosolized (35% relative humidity, 20°C) at 60 L/min for 5 seconds [22,23]. Two capsules (equivalent to 100 μg salbutamol sulphate) were used for each test, and each powder was tested in triplicate.…”
Section: In-vitro Powder Aerosolisationmentioning
confidence: 99%
“…Therefore, the availability of different in vitro methods can impede regulatory evaluation. Some studies compared two or three in vitro methods for aerodynamic assessment of DPIs [23,[26][27][28][29][30][31][32][33], but their results were inconclusive. While some of the studies indicated similarities between ACI and NGI results [26,29,31], there were also reports on diverging results obtained by these two methods [28,29].…”
Section: Introductionmentioning
confidence: 99%
“…Some studies compared two or three in vitro methods for aerodynamic assessment of DPIs [23,[26][27][28][29][30][31][32][33], but their results were inconclusive. While some of the studies indicated similarities between ACI and NGI results [26,29,31], there were also reports on diverging results obtained by these two methods [28,29]. In addition, some differences were shown between NGI and MSLI [28], TSI [33] or FSI results [27].…”
Section: Introductionmentioning
confidence: 99%