A real-time and modular approach for quick detection and mechanism exploration of DPIs with different carrier particle sizes.
第一作者:
Yingtong,Cui
第一单位:
School of Pharmaceutical Science, Jinan University, Guangzhou 510006, China.;School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
作者:
关键词
AE, aerated energyAPIs, active pharmaceutical ingredientsAR, aeration ratioBFE, basic flow EnergyC.OPT, optical concentrationCFD-DEM, computational fluid dynamics-discrete element methodCPS, carrier particle sizeCarrier particle sizeDPIs, dry powder inhalersDry powder inhalerED, emitted doseEDXS, energy-dispersive X-ray spectroscopyFC, centrifugal forceFD, drag forceFF, friction forceFG, gravityFI, interaction forceFP, press-on forceFPD, fine particle doseFPF, fine particle fractionFT4, Freeman Technology 4HPLC, high performance liquid chromatographyHPMC, hydroxypropyl methyl celluloseLAC, lactoseMFV, minimum fluidization velocityMMAD, mass median aerodynamic diameterMOC, micro orifice collectorMPAP, modular process analysis platformMSS, micronized salbutamol sulfateNGI, Next Generation ImpactorO, oxygenPD, pressure dropPDP, pulmonary delivery processPSF, particle size fractionsPulmonary delivery processQuick detectionR, release amountRAUC, total release amountReal-time monitorRmax, maximum of release amountS, stopping distanceSE, specific energySEM, scanning electron microscopeSSA, specific surface areaT, timeTE, total engeryTmax, the time to reach RmaxTt, terminal timeU0, air flow rateV0, velocitydQ3, the volume percentage of particles within certain rangedae, aerodynamic diameter
DOI
10.1016/j.apsb.2021.06.011
PMID
35127397
发布时间
2022-02-08
- 浏览4
Acta pharmaceutica Sinica. B
2022年12卷1期
437-450页
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