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Review of the Air Quality Criteria Document for Particulate Matter

Review of the Air Quality Criteria Document for Particulate Matter

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<strong>of</strong> particles due to respective changes in local pH. After dissolution or leaching <strong>of</strong> somecomponents from a particle <strong>the</strong>se can be binding <strong>of</strong> solutes (metals) to macromolecules; animportant pathway also is transport via caveolae across <strong>the</strong> epi<strong>the</strong>lium as well as <strong>the</strong>endo<strong>the</strong>lium. The importance <strong>of</strong> differences between epi<strong>the</strong>lial vs. endo<strong>the</strong>lial pore sizes <strong>for</strong>lower molecular weight solutes could also be addressed here.Page 7-38, line 1: Snipes and Clem used 3, 9, and 15 µm particles and found only <strong>the</strong> 3µm to be translocated, did Takahashi really see 5 and 9 µm particles being translocated?Lines 4-6: One has to be very careful when drawing conclusions with respect tolymphatic transport <strong>of</strong> particles based on intratracheal instillation studies: In such studies highdoses are instilled as a bolus leading to local overload which messes up <strong>the</strong> normal clearancesignificantly and easily can result in lymphatic translocation which will not occur under normalconditions. Also <strong>the</strong> statement that particles >5 µm have significant deposition within <strong>the</strong>alveolar region is not correct <strong>for</strong> <strong>the</strong> rat. In <strong>the</strong> context <strong>of</strong> species differences related tolymphatic clearance, studies by Thomas et al. (1971) could be cited here showing differencesbetween rodents and dogs, accumulation <strong>of</strong> particles in local lymph nodes being much greater indogs.Page 7-42, line 29: A most important feature <strong>of</strong> Morrow's hypo<strong>the</strong>sis is that a volumetricoverloading <strong>of</strong> alveolar macrophages occurs which eventually impairs its clearance function.Page 7-43, line 11: I am not sure I understand why <strong>the</strong> slower alveolar macrophagemediatedclearance in humans compared to rats (it is always slower in humans) would cloud <strong>the</strong>overload relevance <strong>for</strong> humans: Humans also live about 25 times longer than rats.Lines 14-15: It is hard to imagine how under normal environmental exposureconditions, overload will occur in compromised lungs. What compromised lungs would that be?Line 26: Although it is generally assumed that intratracheal instillation deliversan "exact" dose to <strong>the</strong> lung, this does not mean that this dose is really found <strong>the</strong>re shortly after<strong>the</strong> instillation because some <strong>of</strong> <strong>the</strong> material is rapidly cleared out by <strong>the</strong> following exhalations.The amount <strong>of</strong> this loss depends highly on <strong>the</strong> instilled volume as well as <strong>the</strong> instillationtechnique, i.e., synchronizing with respiration or not.Page 7-44, line 9: It is not clear what is said here, <strong>the</strong> amount that is deposited in <strong>the</strong>lower airways by instillation can be adjusted, it is not due to by-passing <strong>the</strong> nose. Probably whatis meant is that <strong>the</strong> distribution <strong>of</strong> material is different between <strong>the</strong> two techniques.Page 7-45, line 11: It is unclear what is meant by percentage retention <strong>of</strong> particles: Isthat <strong>the</strong> intercept <strong>of</strong> <strong>the</strong> retention curve with <strong>the</strong> ordinate, or is that <strong>the</strong> retention halftime? If <strong>the</strong>retention halftime is meant here that would be explainable since normally by instillation highdoses are delivered which result in overloaded areas with retarded clearance. Thus, it might bebetter to compare inhalation and instillation-associated retention kinetics by describing <strong>the</strong>respective retention halftimes.Line 18: The bulk <strong>of</strong> <strong>the</strong> instilled material certainly goes beyond <strong>the</strong> terminalbronchioles, o<strong>the</strong>rwise you would see all <strong>of</strong> it being cleared in a short time by <strong>the</strong> mucociliaryescalator. Of course, <strong>the</strong> very periphery <strong>of</strong> <strong>the</strong> lung is not well dosed, and as mentioned be<strong>for</strong>e,<strong>the</strong> coverage depends also on <strong>the</strong> instillation technique, i.e., synchronization with breathing ornot.Line 29: Disposition <strong>of</strong> particles is only one factor determining <strong>the</strong>ir biologicaleffects.Page 7-50, line 1-6: For a discussion <strong>of</strong> "human equivalent concentration (HEC)" EPA'sRfC document should also be quoted here. Fur<strong>the</strong>rmore, earlier in this section, emphasis was on<strong>the</strong> lung burden expressed as per unit lung surface area as being more appropriate, whereas here<strong>the</strong> amount per gram <strong>of</strong> lung is indicated. This might be confusing <strong>for</strong> <strong>the</strong> reader.Lines 13-19: The Asgharian 2000 reference is missing in <strong>the</strong> reference list, is thata publication describing <strong>the</strong> MPPDep model which should be mentioned here as well?As a general comment on this section, it should also be stated in a concludingsummarizing paragraph that all models are just that: models. They have inherent uncertainties,which can be large and differences between model results can probably most <strong>of</strong> <strong>the</strong> time beexplained by <strong>the</strong>se uncertainties.A - 67

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