The in vitro profile of pulmonary deposition of the powders was determined using the Dry Powder Inhaler Andersen Cascade Impactor (ACI-DPI, Apparatus D European Pharmacopoeia, Copley Scientific Limited, Erweka, Germany), consisting of 8 stages (0–7) with rotary impactor plates connected to a flow controller and vacuum pump. Samples of 5FU-MS (30 mg), 5FU-NS (20 mg), and the drug 5FU pure (21 mg) were transferred to hard gelatin capsules (size 3), which were introduced into the single-dose inhaler (Aerolizer®, Novartis, Basel, Switzerland) and perforated twice. This experiment was conducted under controlled inhalation rate of 28.3 L·min−1 for 4 s and a pressure of 4 kPa. After inhalation, the particles retained in each stage were rinsed off with ultrapure water. The concentration of 5FU was quantified by HPLC-UV according to the extraction method described in Section 4.3.2. The Fine Particle Dose (FPD), Fine Particle Fraction (FPF), Respirable Fraction (RF), and Dose Issued (DI) of inhaled powders for pulmonary absorption were determined according to the equations described by Meenach et al. (2013) [46 (link)].
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