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   <subfield code="a">Comparison of lung accumulation of cationic liposomes in normal rats and LPS-treated rats</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Susanne Herber-Jonat, Rashmi Mittal, Stefan Gsinn, Hermann Bohnenkamp, Eric Guenzi, Andreas Schulze]</subfield>
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   <subfield code="a">Objective: Cationic liposomes have been shown to target angiogenic endothelial cells in lungs and joints with evidence of chronic inflammation. We sought to determine whether cationic liposomes accumulate in acutely inflamed lung tissue. Subjects, treatment and methods: Acute lung injury was induced by intratracheal instillation of lipopolysaccharide (LPS) in Sprague Dawley rats. The controls received saline. Following instillation, the rats were ventilated for 5h. Four hours after LPS-instillation each rat received rhodamine-labeled, cationic liposomes intravenously. The liposomes were allowed to circulate for 1h. Thereafter, a bronchoalveolar lavage (BAL) was done and the lungs were perfused with saline and formalin. Accumulation of liposomes was assessed by quantitative confocal microscopy and determination of rhodamine-content in lung tissue. Results: LPS induced a significant increase in BAL white blood cell count (3,444±1,420 vs. 1,314±906*103/μl) and cytokines (IL-1β: 145.57 vs. 51.94pg/ml; TNF-α: 3,467.5 vs. 42.1pg/ml) as compared to controls. Cationic liposomes exhibited an accumulation up to twofold in the inflamed lung tissue as compared to healthy lungs (fluorescent pixels 2.93 vs. 1.90(%)). Conclusions: Our findings indicate that cationic liposomes accumulate in the acutely inflamed lung tissue. This uptake raises the possibility of using cationic liposomes to direct diagnostic/therapeutic agents selectively to the sites of acute inflammation in the lung.</subfield>
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   <subfield code="a">Springer Basel AG, 2010</subfield>
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   <subfield code="a">Drug delivery systems</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Drug targeting</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Liposomes</subfield>
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   <subfield code="a">Acute lung injury</subfield>
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   <subfield code="a">Endothelial cells</subfield>
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   <subfield code="a">ARDS : Acute respiratory distress syndrome</subfield>
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   <subfield code="a">BAL : Bronchoalveolar lavage</subfield>
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   <subfield code="a">LPS : Lipopolysaccharide from E. coli</subfield>
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   <subfield code="a">Herber-Jonat</subfield>
   <subfield code="D">Susanne</subfield>
   <subfield code="u">Division of Neonatology, University Children's Hospital, Perinatal Center, Ludwig-Maximilian-University Munich, Grosshadern, Marchioninistr.15, 81377, Munich, Germany</subfield>
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   <subfield code="a">Mittal</subfield>
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   <subfield code="a">Gsinn</subfield>
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   <subfield code="u">Division of Neonatology, University Children's Hospital, Perinatal Center, Ludwig-Maximilian-University Munich, Grosshadern, Marchioninistr.15, 81377, Munich, Germany</subfield>
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   <subfield code="u">Division of Research, MediGene AG, Martinsried, Germany</subfield>
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   <subfield code="t">Inflammation Research</subfield>
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