PMID- 11498805 OWN - NLM STAT- MEDLINE DCOM- 20010927 LR - 20191025 IS - 0895-8378 (Print) IS - 0895-8378 (Linking) VI - 13 IP - 9 DP - 2001 Sep TI - The influence of suspension nebulization or instillation on particle uptake by guinea pig alveolar macrophages. PG - 773-88 AB - Phagocytosis represents a crucial event in the host defense against pathogens. Experimental methods are required that allow a range of particle doses to be delivered. However, it is not clear that these methods result in the same sites of deposition or mechanisms of clearance. The effect of particle administration by nebulization or instillation on the uptake by guinea pig alveolar macrophages (AMs) has been studied. Suspensions of escalating quantities of 1-microm fluorescent polystyrene latex microspheres were delivered by 15 min of nebulization (1.4 x 10(7)-11.1 x 10(7) particles) or instillation (19 x 10(7)-152 x 10(7) particles) into the lungs of guinea pigs. These doses were selected to maximize delivery using each of these methods. Macrophages were collected by alveolar lavage 6 h postadministration. The total number of cells recovered was 3 x 10(6) and the cell viability was >97%, which was measured by trypan blue exclusion. Differential cell counts of lavaged cell suspensions were conducted and results showed no difference for the two methods of administration with various concentrations of latex particles and control samples. The uptake of particles was measured using epifluorescence, confocal microscopy, and flow cytometry. AMs showed a dose-dependent increase in associated particles measured by microscopy and flow cytometry. There was a direct correlation (R(2) =.99) in the phagocytic indices (PIs) measured by flow cytometry and fluorescence microscopy. The PI was 15 times higher after instillation than that obtained after particle nebulization. The percentage of AMs involved in phagocytosis observed after instillation was 55% and after nebulization 23%. The uptake of aerosolized particles by AMs and the number of cells involved in phagocytosis were dependent on the particle dose and the efficiency of aerosol delivery to the lungs. FAU - Suarez, S AU - Suarez S AD - School of Pharmacy, University of North Carolina at Chapel Hill, Beard Hall CB #7360, Chapel Hill, NC 27599, USA. FAU - Kazantseva, M AU - Kazantseva M FAU - Bhat, M AU - Bhat M FAU - Costa, D AU - Costa D FAU - Hickey, A J AU - Hickey AJ LA - eng GR - HL55789/HL/NHLBI NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - England TA - Inhal Toxicol JT - Inhalation toxicology JID - 8910739 RN - 0 (Latex) RN - 0 (Polystyrenes) RN - 0 (Xenobiotics) SB - IM MH - Administration, Inhalation MH - Animals MH - Cell Count MH - Cell Survival MH - Flow Cytometry MH - Guinea Pigs MH - Instillation, Drug MH - Latex MH - Macrophages, Alveolar/cytology/*metabolism MH - Microscopy, Fluorescence MH - Microspheres MH - Nebulizers and Vaporizers MH - Particle Size MH - Polystyrenes/administration & dosage/metabolism/toxicity MH - Xenobiotics/*administration & dosage/metabolism/toxicity EDAT- 2001/08/11 10:00 MHDA- 2001/09/28 10:01 CRDT- 2001/08/11 10:00 PHST- 2001/08/11 10:00 [pubmed] PHST- 2001/09/28 10:01 [medline] PHST- 2001/08/11 10:00 [entrez] AID - 10.1080/08958370120643 [doi] PST - ppublish SO - Inhal Toxicol. 2001 Sep;13(9):773-88. doi: 10.1080/08958370120643.