Particle Deposition in a Cast of Human Oral Airways

Oral and nasal airways are entryways to the respiratory tract. Most people breathe through the nasal airway during rest or light exercise, then switch to oral/nasal breathing during heavy exercise or work. Resistance through the oral airways is much lower than through the nasal airways, so fewer aerosol particles are deposited in the oral airways. Aerosol drugs are usually delivered by inhalation to the lung via the oral route for that reason. Oral deposition data from humans are limited, and those available show great intersubject variability. The purpose of this study was to investigate the effects of particle size and breathing rate on the deposition pattern in a human oral airway cast with a defined geometry. The airway replica included the oral cavity, pharynx, larynx, trachea, and 3 generations of bronchi. The oral portion of the cast was molded from a dental impression of the oral cavity in a human volunteer, while the other airway portions of the cast were made from a cadaver. Nine different sizes of polystyrene latex fluorescent particles in the size range of 0.93-30 mu m were used in the study. Regional deposition was measured at a constant inspiratory flow rate of 15, 30, and 60 L min^-1. Deposition in the oral airway appeared to increase with an increasing flow rate and particle diameter. Deposition at the highest flow rate of 60 L min^-1 was close to 90% for particles >20 mu m. Particles> about 10 mu m deposited mainly in the oral cavity. Deposition efficiency has been found to be a unique function of the Stokes number, suggesting that impaction is the dominant deposition mecha nism. Oral deposition can be approximated by a theoretical deposition model of inertial impaction in a 180 degrees curved tube, assuming perfect mixing in a turbulent flow. Our model suggests that the minimum dimension near the larynx and the average cross-sectional area are important parameters for oral airway deposition; however, additional data from the oral airway replica are needed to ascertain whether these are indeed the critical dimensions. Information from the present study will add to our knowledge of the deposition mechanism, the correlation of particle deposition with airway geometry, and eventually the best way to deliver aerosol drugs.     

Deposition of micrometer-sized aerosol particles in neonatal nasal airway replicas

The nasal aerosol filtration properties of infants 0–3 months old have been quantified through in vitro measurements. Computed tomography (CT) scan data was obtained of seven individuals with ages of 5–79 days. Nasal airway replicas based on these images were manufactured using rapid prototyping. Deposition in the replicas was measured using an electrical low pressure impactor (ELPI) to measure the concentration of aerosol particles in the inertial regime. Comparing the difference in concentration when sampling through the model versus sampling through a blank line gave the deposition fraction. Deposition was measured for particles with aerodynamic diameters between 0.53 and 5.54 μm. Nonlinear least squares curve fitting was performed to collapse intersubject variability and represent the data with a single curve. To achieve satisfactory intersubject variability collapse, a non-dimensional pressure drop, the Euler number (Eu), was required in addition to the Reynolds number (Re) and the particle Stokes number (Stk) where the dimensionless parameters are evaluated with a length scale, D, defined as the airway volume divided by the airway surface area. The equation describing the deposition fraction, η, is η = 1- (14590 / (14590 + Stk^1.2201Re^1.7742Eu^1.5772))^0.3687. An analysis of the expected intersubject variability in in vivo deposition was also performed, yielding a method for predicting variance in neonatal nasal airway deposition.

Copyright © 2018 American Association for Aerosol Research     

Deposition of Ultrafine Aerosols in a Human Oral Cast

This paper reports experimental measurements of the total deposition of ultrafine aerosols in a human oral airway cast. A clear polyester resin cast of the upper airways of a normal human adult, including the nasal airways, oral cavity, tongue, nasopharynx, and larynx, was made from a postmortem solid cast. Measured pressure drop in the oral airway was slightly lower than in the nasal airway. The measured oral flow resistance was similar to the values reported for human volunteers breathing through the mouth at rest and for spontaneously opening of the mouth. Aerosol deposition data in the cast for monodisperse NaCl aerosols between 0.2 and 0.005 μm in diameter deposited in the cast were obtained for inspiratory and expiratory flow rates of 4, 20, and 40 L/min. Deposition efficiency increased with decreasing particle size and flow rate indicating that turbulent diffusion was the dominant mechanism for deposition. Higher deposition efficiency was observed for inspiratory flow in the oral airway than for expiratory flow. Oral deposition and nasal deposition for inspiratory flow were similar, but oral deposition was lower for expiratory flow. Deposition efficiency can be expressed as a function of the flow rate and diffusion coefficient of the particle.     

Deposition of Ultrafine Aerosols and Thoron Progeny in Replicas of Nasal Airways of Young Children

The deposition efficiencies of ultrafine aerosols and thoron progeny were measured in youth nasal replicas. Clear polyester-resin casts of the upper airways of 1.5-yr-old (Cast G), 2.5-yr-old (Cast H), and 4-yr-old (Cast I) children were used. These casts were constructed from series of coronal magnetic resonance images of healthy children. The casts extended from the nostril tip to the junction of the nasopharynx and pharynx. These casts were similar in construction to those used in previous studies (Swift et al. 1992; Cheng et al. 1993). Total deposition was measured for monodisperse NaCl or Ag aerosols between 0.0046 and 0.20 (Jim in diameter at inspiratory and expiratory flow rates of 3, 7, and 16 L min^?1 (covering a near-normal range of breathing rates for children of different ages). Deposition efficiency decreased with increasing particle size and flow rate, indicating that diffusion was the main deposition mechanism. Deposition efficiency also decreased with increasing age at a given flow rate and particle size. At 16 L min^?1, the inspiratory deposition efficiencies in Cast G were 33% and 6% for 0.008- and 0.03-μm particles, respectively. Nasal deposition of thoron progeny with a mean diameter of 0.0013 μm was substantially higher (80%-93%) than those of the ultrafine aerosol particles, but still had a similar flow dependence. Both the aerosol and thoron progeny data were used to establish a theoretical equation relating deposition efficiency to the diffusion coefficient (D in cm² s^?1) and flow rate (Q in L min^?1) based on a turbulent diffusion process. Data from all casts can be expressed in a single equation previously developed from an adult nasal cast: E = 1 - exp(-aD ^0.5 Q ^?0.125). We further demonstrated that the effect of age, including changes to nasal airway size and breathing flow rate, on nasal deposition can be expressed in the parameter “a” of the fitted equation. Based on this information and information on minute volumes for different age groups, we predicted nasal deposition in age groups ranging from 1.5- to 20-yr-old at resting breathing rates. Our results showed that the nasal deposition increases with decreasing age for a given particle size between 0.001 to 0.2 μm. This information will be useful in deriving future population-wide models of respiratory tract dosimetry.     

Deposition of Inhaled Ultrafine Aerosols in Replicas of Nasal Airways of Infants

Experimentally measured deposition of ultrafine particles, ranging from 13–100 nm in diameter, in nasal airway replicas of ten infants aged 3–18 months is presented. The replicas included the face, nostrils, and nasal airways including the upper trachea. A differential mobility analyzer (DMA) and a condensation particle counter (CPC) were used to quantify the nasal deposition by comparing the number of polydisperse sodium chloride particles, generated by evaporation from a Collison atomizer, at the inlet and outlet of the replicas. Particles were individually classified in size by DMA and subsequently were counted one size bin at a time by CPC upstream and downstream of each replica. Since in vivo data is not available for infants to compare to, we validated our experimental procedure instead by comparing deposition in nasal airway replicas of six adults with in vivo measurements reported in literature. In the infant replicas, tidal inhalation was simulated at two physiologically compatible flow rates and the effect of flow rate on deposition was found to be small. Deposition obtained at constant flow rates is lower than with tidal breathing, indicating the importance of unsteadiness, in contrast to similar data in adults where unsteadiness is known to be unimportant. An empirical equation, containing geometrical features of the nasal airways in the form of related non-dimensional dynamical parameters (Reynolds, Schmidt, and Womersley numbers), was best fitted to the infant data. This equation may be useful for a priori prediction of nasal deposition and intersubject variability during exposure of infants to ultrafine aerosols.     

Deposition of Fiber in the Human Nasal Airway

Inhalation is the main route for aerosol entering the human body. Many occupational lung diseases are associated with exposure to fiber aerosol in the workplace. However, very few studies to date have been conducted for investigating fiber deposition in the human airway. As a result, there is a notable lack of information on the nature of the fiber deposition pattern in the human respiratory tract. With this in mind, this research consisted of a large number of experimental works to investigate the effects of fiber dimension on the deposition pattern for a human nasal airway. Carbon fibers with uniform diameter (3.66 μm) and polydispersed length were adopted as the test material. Deposition studies were conducted by delivering aerosolized carbon fibers into a nasal airway replica (encompassing the nasal airway regions from vestibule to nasopharynx) at constant inspiratory flow rates of 7.5, 15, 30, and 43.5 l/min. Fibers deposited in each nasal airway region were washed out and the length distribution was determined by microscopic measurement. The results showed that impaction is the dominant deposition mechanism. Most of the fibers with high inertia deposited in the anterior region of the nasal airway (vestibule and nasal valve). In contrast, fibers with low inertia were found to pass through the entire nasal airway easily and collected on the filter at the outlet. Comparing the deposition results between fibers and spherical particles, our data showed that the deposition efficiencies of fibers are significantly lower than that of spherical particles, which implies that the inhaled fibers could pass through the entire nasal airway comparatively easier than spherical particles. Thus, relatively more fibers would be able to enter the lower respiratory tract.     

Particle Deposition in a Cast of Human Tracheobronchial Airways

Abstract

Regional particle deposition efficiency and deposition patterns were studied experimentally in a human airway replica made from an adult cadaver. The replica includes the oral cavity, pharynx, larynx, trachea, and four generations of bronchi. This study reports deposition results in the tracheobronchial (TB) region. Nine different sizes of monodispersed, polystyrene latex fluorescent particles in the size range of 0.93–30 μm were delivered into the lung cast with the flow rates of 15, 30, and 60 l min^{? 1}. Deposition in the TB region appeared to increase with the increasing flow rate and particle size. Comparison of deposition data obtained from physical casts showed agreement with results obtained from realistic airway replicas that included the larynx. Deposition data obtained from idealized airway models or replicas showed lower deposition efficiency. We also compared experimental data with theoretical models based on a simplified bend and bifurcation model. A deposition equation derived from these models was used in a lung dosimetry model for inhaled particles, and we demonstrated that there was general agreement with theoretical models. However, the agreement was not consistent over the large range of Stokes number. The deposition efficiency was found as a function of the Stokes number, bifurcation angle, and the diameters of parent and daughter tubes. An empirical model was developed for the particle deposition efficiency in the TB region based on the experimental data. This model, combined with the oral deposition model developed previously, can be used to predict the particle deposition for inertial effects with improved accuracy.     

In-Vivo Measurements of Micrometer-Sized Particle Deposition in the Nasal Cavities of Taiwanese Adults

It has been observed that Asians and Caucasians possess considerably different craniofacial features, which may affect the anatomical structure of the upper respiratory tract and, consequently, the characteristics of particle deposition. Most deposition studies on the human respiratory tract were primarily based on a limited number of Caucasian subjects. Therefore, data of the particle deposition efficiency in the upper respiratory tract of Asians are needed to supplement the understanding of the deposition characteristics in the human respiratory tract. This study measured the nasal deposition efficiency of particles ranging from 0.5 to 20 μm in five Taiwanese male and four Taiwanese female adults under different inspiratory flow rates. The measured deposition efficiency showed a very large intersubject variability in the inertial parameters, ranging between 10³ to 5 × 10⁴ μm² cm³/s, and the deposition efficiency of the subjects with similar values of the minimum nasal cross-sectional area approaches to each other. This study showed that Taiwanese adults have lower nasal deposition efficiency than Caucasians, and that the differences in the nostril shape, inclination of nostrils, and nasal hair density between the two ethnic groups are likely the causes. In addition, this study suggested that up to 15% of overestimation in the nasal deposition efficiency for larger particles may occur if the inhalation efficiency is not considered. An empirical equation adopting inspiratory flow rate and the minimum nasal cross-sectional area was developed to predict the nasal particle deposition in the upper airway of Taiwanese adults.

Copyright 2012 American Association for Aerosol Research     

Experiments on Particle Deposition in the Human Upper Respiratory System

ABSTRACT

In this study, the deposition of particles (0.3 μm to 2.5 μm in diameter) within a silicone rubber model of the human upper respiratory system was studied. The domain of the respiratory tract under investigation begins at the entrance (nostrils and mouth) and continues through to the second generation of the tracheobronchial airways (main bronchi). The particle deposition efficiency of the sample respiratory system was computed by measuring particle concentration at the inlet and outlet of the model. The regional deposition patterns of fluorescent particles (0.3 μm to 0.7 μm in diameter) was examined by measuring the fluorescent intensity with a fluorescence spectrophotometer. For simulated oral inhalation, the deposition efficiency of the oral cavity (0.9%-5.4%) is approximately the same as that of the oropharynx-trachea region (0.8%-4.8%). During simulated nasal inhalation, the deposition efficiency of the nasal region (20%-43.6%) is greater than the values of the nasopharynx-trachea region (2.8%-8.2%). The nasopharynx-trachea region exhibits a higher deposition efficiency than that of the oropharynx-trachea region. Deposition during the simultaneous oral and nasal inhalation is mostly affected by particle size. Flow rate through the model has less effect on deposition for particle diameter less than 1 μm. When particle diameter is greater than 1 μm deposition efficiencies are weakly and inversely related to the flow rate.     

Deposition of Ultrafine Particles in Human Tracheobronchial Airways of Adults and Children

Inhalation exposure to ultrafine particles, including radon progeny and other combustion aerosols, has been implicated in potential health risks of ambient and indoor environments. These particles deposit in the respiratory tract mainly by diffusion. The purpose of this study was to determine the deposition pattern of nanometer-sized particles in the human tracheobronchial (TB) airways of children and young adults. The deposition was determined for 1.75, 10, and 40 nm ²¹²Pb particles at flow rates corresponding to respiratory minute volumes at rest and during moderate exercise. The 1.75 nm particles were unattached clusters, whereas the 10 and 40 nm particles were silver particles with attached ²¹²Pb clusters. Replicate casts of the upper TB airways of 3, 16, and 23 year old humans were used, including the larynx, trachea, and bronchial airways down to generations 5-8. Deposition in each generation and total deposition were measured by counting the ²¹²Pb gamma photopeak in a NaI (Tl) detector. The effects of airway geometry, particle size, and flow rate on deposition efficiency were studied. The deposition of the 1.75 nm particle, corresponding to unattached indoor radon progeny, was substantially higher than that of the 10 and 40 nm particles. The dependence of particle deposition on the flow rate was relatively weak, and deposition efficiencies were only slightly higher at the lower flow rates. The deposition models for diffusion from parabolic flow underestimated aerosol deposition, whereas the diffusion deposition predicted for plug flow overestimated the TB deposition. The deposition models resulting from this study can be used for developing lung deposition models and in the risk assessment of radon progeny and ultrafine ambient particles.     

Theoretical analysis of particle deposition in human lungs considering stochastic variations of airway morphology

Particle deposition in human lungs was investigated theoretically considering a stochastic variation of airway morphology using a Monte Carlo method. In computing the total and regional deposition each airway generation was divided into infinitesimal volume segments and each volume segment was allowed to pass through randomly selected airway branches of which morphology (e.g., airway dimensions and branching angle) was varied randomly. Deposition values obtained by the Monte Carlo method were compared with those obtained by the traditional deterministic method. It was found that the Monte Carlo method predicted deposition values generally comparable to those predicted by deterministic method for sub-micron size particles. However, for micron size particles the Monte Carlo method provided greater deposition values in the proximal airway regions where deposition occurs mainly by inertial impaction. The difference could be attributed to the non-linear relationship between deposition efficiency and airway dimensions in the inertial deposition regime. The results suggest that a Monte Carlo method may be a useful tool for evaluating deposition of inhaled particles in the lungs with a wide variation of airway dimensions.     

In vitro deposition measurement of inhaled micrometer-sized particles in extrathoracic airways of children and adolescents during nose breathing

An in vitro study was conducted with the goal of developing empirical correlations to predict the deposition of particles with an aerodynamic diameter of 0.5–5.3 μm in nasal airways of children with ages 4–14 years. CT images of nasal airways of thirteen healthy subjects and one with congested nasal airways were used for fabricating the replicas by rapid prototyping. Replicas included nasal airways to the level of the upper trachea as well as the face. Four physiological breathing patterns (sinusoidal waves) of children were simulated by a pulmonary waveform generator. Using an Electrical Low Pressure Impactor (ELPI) we measured deposition of sunflower oil particles generated by a Collison atomizer. Moreover, using the same setup, particle deposition in five adult replicas fabricated using MRI images was measured for direct comparison with the child replicas and in vivo data available for adults. Deposition increased by increasing particle size and flow rate, indicating impaction as the dominant deposition mechanism. Existing correlations for adults were unable to reduce the scatter in the deposition data for children. A correlation was developed for prediction of deposition including the relevant non-dimensional numbers (Stokes and Reynolds numbers) that were calculated considering the dimensions of the airways. The corrected correlations should be useful for exposure estimation of children and for efficient pediatric drug delivery using face masks.     

Mechanisms of aerosol deposition in a nasal model

Total and regional aerosol deposition were investigated in a model of a normal human nasal airway. Contributions of fluid turbulence and particle inertia were evaluated using monodisperse aerosols. At fixed turbulent flow conditions, deposition percentage increased with particle size greater than 1 μm, suggesting that turbulent inertial deposition is a primary mechanism.

With same size aerosol, deposition increased with increasing fluid turbulence but its contribution was less with larger size aerosol. Turbulent diffusion was the dominant transport mechanism for particles less than 1 μm, where deposition decreased with particle size. Two major deposition sites were visualized with radio-aerosol in the anterior region of the nasal airway. One is close to the ostium internum where turbulent eddies are well developed, and the other is the anterior region of the middle turbinate where direction of airflow changes from upward to horizontal.     

Experimental measurements and computational modeling of aerosol deposition in the Carleton-Civic standardized human nasal cavity

Aerosol deposition in the novel, “Carleton-Civic” standardized geometry of the human nasal cavity was studied both numerically and experimentally. Inhalation flow rates varied from 30 to 90 L/min in the experiments, and aerosol droplets had diameters ranging from 1.71 to 9.14 μm (impaction parameters ranging from 123.3 to 2527.6 μm L/min). For the numerical simulations, both the RANS/EIM (Reynolds averaged Navier–Stokes equations for the gas phase and eddy-interaction random walk models for the particulate phase) and large eddy simulations were used. The mechanism of aerosol deposition in the standardized nasal cavity was dominated by inertial impaction. Deposition data from the standardized nasal cavity transected cited in vitro data based on individual subjects. The data also correlated very well with cited in vivo measurements but generally showed less aerosol deposition for a given value of the impaction parameter. Regional deposition characteristics within the nasal passages were also investigated both experimentally and numerically and new trends of regional deposition versus impaction parameter are discussed. These trends provide new insight into the general deposition behaviour of various sized aerosols within the human nasal cavity.     

Characterization of Submicrometer Aerosol Deposition in Extrathoracic Airways during Nasal Exhalation

Submicrometer and especially fine aerosols that enter the respiratory tract are largely exhaled. However, the deposition of these aerosols under expiratory conditions is not well characterized. In this study, expiratory deposition patterns of both ultrafine (<100 nm) and fine (100–1000 nm) respiratory aerosols were numerically modeled in a realistic nasal-laryngeal airway geometry. Particle sizes ranging from 1 through 1000 nm and exhalation flow rates from 4 through 45 L/min were considered. Under these conditions, turbulence only appeared significant in the laryngeal and pharyngeal regions, whereas the nasal passages were primarily in the laminar regime. Exhaled particles were simulated with both a continuous-phase drift flux velocity correction (DF-VC) model and a discrete Lagrangian tracking approach. For the deposition of ultrafine particles, both models provided a good match to existing experimental values, and simulation results corroborated an existing in vivo–based diffusion parameter (i.e., D ^0.5 Q ^?0.28). For fine particles, inertia-based deposition was found to have a greater dependence on the Reynolds number than on the Stokes number (i.e., St^0.1 _kRe^0.9), indicating that secondary flows may significantly influence aerosol deposition in the nasal-laryngeal geometry. A new correlation was proposed for deposition in the extrathoracic airways that is applicable for both ultrafine and fine aerosols over a broad range of nasal exhalation conditions. Results of this study indicate that physical realism of the airway model is crucial in determining particle behavior and fate and that the laryngeal and pharyngeal regions should be retained in future studies of expiratory deposition in the nasal region.     

Particle deposition in the guinea pig respiratory tract

Equations relating particle size of aerosols to deposition by impaction, diffusion and sedimentation are applied to a previously established model of the guinea pig lung using a tidal volume of 4.44 cm³ and a respiratory rate of 60 breath min⁻¹. These calculated deposition values are combined with measured values of nasal deposition to give an estimate of the particle deposition characteristics of the guinea pig respiratory tract. The nasopharyngeal-tracheobronchial (NP-TB) region removes 99% of unit density spherical particle 10 μm or more in diameter. Deposition in this region reaches a minimum of 10% at a particle diameter of 0.8 μm. For particles less than 0.8 μm, deposition increases because of diffusion. Deposition in the pulmonary region is about 17% for particle diameters from 0.08 to 4 μm. For typical polydisperse aerosols with mass median diameters above 1 μm, a greater fraction of the mass than of the count is deposited in the NP-TB region, while a smaller fraction of the mass than of the count is deposited in the pulmonary region. Aerosol clouds with mass median diameters less than 0.1 μm deposit a greater fraction of the count than of the mass in the NP-TB region and a smaller fraction of the count than of the mass in the pulmonary region.     

Aerosol deposition in 3D models of the upper airways and trachea of rhesus macaques

Abstract

Little is known about aerosol deposition in macaques, variability in deposition between animals, or how deposition in macaques and humans compare. This is despite the use of macaques in assessments of toxic aerosols that are often translated to estimates of human exposure. We used three dimensional (3D) physical models of the upper airways and trachea (UAT) of Rhesus macaques to begin to fill in this information gap. Models of the UAT of five, living rhesus macaques were produced from CT scans, using 3D printing technology. Models were exposed to a polydisperse aerosol containing 0.54 to 9.65 micron particles, during constant flowrates of 2, 4, and 6 liters per min. Percent deposition in UAT models was quantified using an Aerodynamic Particle Sizer and was compared to in vivo upper airway deposition in ten, adult human subjects. Deposition in the UAT models increased as Stokes number increased. Deposition also varied significantly between models, but intermodel variability was reduced when plotted as a function of Stokes number. Using Stokes number, deposition in four of the five UAT models overlapped with each other and also overlapped with human upper airway deposition. These models could be used to explore the relationship between factors that affect toxic aerosol deposition in the UAT in vitro and pathology following toxic aerosol exposure in Rhesus macaques in vivo. Results from those experiments could also be applicable to humans because of deposition similarities.

Copyright © 2020 American Association for Aerosol Research     

Implementation of Charged Particles Deposition in Stochastic Lung Model and Calculation of Enhanced Deposition

The experimental studies using hollow lung cast of human tracheobronchial (TB) tree and in-vivo experiments have demonstrated enhanced charged deposition in the lung. The present study was carried out to implement charge particle deposition into the stochastic human lung model and to estimate enhanced deposition for various charged particles at the airway generation level. Enhanced deposition calculations of charged particles are performed by implementing two different efficiency equations derived for the TB and alveolar (Al) region. Deposition fractions of inhaled charged particles are computed by the stochastic airway generation model IDEAL (Inhalation, Deposition and Exhalation of Aerosols in the Lung) for various breathing conditions and particle sizes. Enhanced deposition of charged particles in the Al region is found to be up to five times higher than in the TB region. Enhanced deposition in the TB region is higher under sitting breathing condition than under light exercise breathing condition. The introduction of pause time, during inhalation, increases the probability of increased enhanced deposition up to a certain breath-hold time limit. The calculated enhancement factors (EF) reveals that more than two times higher deposition can be achieved in the lung by the introduction of charged particles during inhalation. By introducing the charged particles during inhalation and by optimizing the flow rate, tidal volume, and particle size, the targeted deposition in the lung is improved for the best therapeutic aerosols utilization. In addition, the unnecessarily high deposition of toxic particles in the sensitive lung regions can be avoided.

Copyright 2012 American Association for Aerosol Research     

Simulation of airflow and aerosol deposition in the nasal cavity of a 5-year-old child

As a human grows from birth to adulthood, both airway anatomy and breathing conditions vary that alter the deposition rate and pattern of inhaled aerosols. However, deposition studies have typically focused on adult subjects, results of which may not be readily extrapolated to children. Furthermore, because of greater ventilation rate per body weight, children receive a greater dose than adults and therefore are more susceptible to respiratory risks. This study is to evaluate the transport and deposition of respiratory aerosols in a nasal-laryngeal airway model based on MRI head images of a 5-year-old boy. Differences between this child and adults in nasal physiology and aerosol filtering efficiency will be emphasized. A validated low Reynolds number (LRN) k?ω turbulence model was employed to simulate laminar, transitional, and fully turbulent flow regimes within the nasal airways. Particle trajectories and deposition in the spectrum of 0.5–32 μm were evaluated using a well-tested Lagrangian tracking approach for inhalation flow rates ranging from sedentary (3 L/min) to heavily active (30 L/min) conditions. Simulation results of the inhalation pressure drop and particle deposition rate provided a reasonable match with existing experimental results in nasal airway casts of children. Much higher breathing resistance was observed in the 5-year-old child compared to adults. Furthermore, deposition patterns were sensitive to inhalation flow rate under low activity conditions. An empirical correlation of child nasal filtering efficiency was proposed for micrometer particles based on a wide range of test conditions. Results of this study demonstrate that significant child–adult difference exists in inhaled aerosol depositions, which should be taken into account for risk assessment of airborne toxicants on infants and children.     

A Model of Deposition of Hygroscopic Particles in the Human Lung

Many aerosols in the environment are hygroscopic and grow in size once inhaled into the humid respiratory tract. The deposited amount and the distribution of the deposited particles among airways differ from insoluble particles of the same initial diameter. As particles grow in size, diffusive behavior tends to diminish while impaction and sedimentation effects increase. A multiple-path model for deposition of hygroscopic particles in the respiratory tract was developed for symmetric and asymmetric lung geometries by implementing particle size change in a model of insoluble particle deposition in lungs. Particle growth by molecular diffusion of water vapor to the particle surface was formulated. The growth model included temperature depression, solute, Kelvin, and Fuchs effects. Particle growth during travel time in each lung airway was computed. Average loss efficiency per airway was calculated by incorporating contributions from particles of various sizes acquired in that airway. A mass balance on the number of particles that entered, exited, deposited, or remained suspended was performed per airway to obtain regional and local deposition fractions of particles in the lung. The deposition fractions calculated for salt particles showed a drop for submicrometer particles in the tracheobronchial region and a significant increase in deposition for micrometer particles or larger. Consequently, very few fine and coarse salt particles reached the alveolar region to be available for deposition. Overall, lung deposition of ultrafine particles decreased for salt particles. Deposition for fine and coarse salt particles in the lung was larger than that of insoluble particles of the same initial particle size.