Abstract |
We determined whether microcrystalline cellulose (MCC), a component of pharmaceutical tablets, induces pulmonary changes. In vivo [resistive and viscoelastic pressures (DeltaP(1) and DeltaP(2)), static elastance (E(L))] and in vitro [tissue resistance (R), elastance (E), and hysteresivity (eta)] lung mechanics, histology, and bronchoalveolar lavage fluid (BALF) were analyzed 3h, 24h, and 3, 15 and 30 days after intratracheal instillation of saline (C) or MCC in BALB/c mice. DeltaP(1) increased at 3h, remaining higher than C until day 3, while E(L) and DeltaP(2) increased only at 24h. At 3 days all mechanical parameters returned to baseline. R and E increased only at 24h. MCC increased alveolar collapse and the number of neutrophils in BALF at 3h, until 3 and 15 days, respectively. At 3 days MCC migrate from the airways into the parenchyma, where they were observed until 30 days. In conclusion, microcrystalline cellulose yielded an acute and self-limited inflammation that impaired lung mechanics.
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Authors | L K S Nagato, M G F Lourenço, R A Cadete, J H P Leite-Júnior, V L G Koatz, P R M Rocco, D S Faffe, W A Zin |
Journal | Respiratory physiology & neurobiology
(Respir Physiol Neurobiol)
Vol. 164
Issue 3
Pg. 331-7
(Dec 31 2008)
ISSN: 1569-9048 [Print] Netherlands |
PMID | 18782634
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Excipients
- Cellulose
- microcrystalline cellulose
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Topics |
- Airway Resistance
(drug effects, physiology)
- Animals
- Bronchoalveolar Lavage Fluid
- Cellulose
(adverse effects)
- Excipients
(adverse effects)
- Inflammation
(chemically induced, physiopathology)
- Linear Models
- Lung
(pathology, physiopathology)
- Mice
- Mice, Inbred BALB C
- Pulmonary Alveoli
(pathology)
- Pulmonary Atelectasis
(chemically induced)
- Random Allocation
- Respiratory Mechanics
- Time Factors
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