Resistance of different surfactant preparations to inactivation by meconium

被引:66
作者
Herting, E
Rauprich, P
Stichtenoth, G
Walter, G
Johansson, J
Robertson, B
机构
[1] Univ Gottingen, Dept Pediat, D-37075 Gottingen, Germany
[2] Karolinska Inst, Dept Woman & Child Hlth, Div Expt Perinatal Pathol, S-17176 Stockholm, Sweden
[3] Karolinska Inst, Dept Med Biochem & Biophys, S-17176 Stockholm, Sweden
关键词
D O I
10.1203/00006450-200107000-00010
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
A disease similar to acute respiratory distress syndrome may occur in neonates after aspiration of meconium. The aim of the study was to compare the inhibitory effects of human meconium on the following surfactant preparations suspended at a concentration of 2.5 mg/mL: Curosurf, Alveofact, Survanta, Exosurf, Pumactant, rabbit natural surfactant from bronchoalveolar lavage, and two synthetic surfactants based on recombinant surfactant protein-C (Venticute) or a leucine/lysine polypeptide. Minimum surface tension, determined with a pulsating bubble surfactometer, was increased >10 mN/m at meconium concentrations greater than or equal to0.04 mg/mL for Curosurf, Alveofact, or Survanta, greater than or equal to0.32 mg/mL for recombinant surfactant protein-C, greater than or equal to1.25 mg/mL for leucine/lysine polypeptide, and greater than or equal to 20 mg/mL for rabbit natural surfactant. The protein-free synthetic surfactants Exosurf and Pumactant did not reach minimum surface tension <10 mN/m even in the absence of meconium. We conclude that surfactant activity is inhibited by meconium in a dose-dependent manner. Recombinant surfactant protein-C and leucine/lysine polypeptide surfactant were more resistant to inhibition than the modified natural surfactants Curosurf, Alveofact, or Survanta but less resistant than natural lavage surfactant containing surfactant protein-A. We speculate that recombinant hydrophobic surfactant proteins or synthetic analogs of these proteins can be used for the design of new surfactant preparations that are relatively resistant to inactivation and therefore suitable for treatment of acute respiratory distress syndrome.
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页码:44 / 49
页数:6
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