Laboratory of Adaptive and Regenerative Biology, Brigham & Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Institute of Functional and Clinical Anatomy, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
J Biomed Mater Res B Appl Biomater. 2019 Apr;107(3):799-806. doi: 10.1002/jbm.b.34175. Epub 2018 Sep 25.
Pulmonary "air leaks," typically the result of pleural injury caused by lung surgery or chest trauma, result in the accumulation of air in the pleural space (pneumothorax). Air leaks are a major source of morbidity and prolonged hospitalization after pulmonary surgery. Previous work has demonstrated structural heteropolysaccharide (pectin) binding to the mouse pleural glycocalyx. The similar lectin-binding characteristics and ultrastructural features of the human and mouse pleural glycocalyx suggested the potential application of these polymers in humans. To investigate the utility of pectin-based polymers, we developed a simulacrum using freshly obtained human pleura. Pressure-decay leak testing was performed with an inflation maneuver that involved a 3 s ramp to a 3 s plateau pressure; the inflation was completely abrogated after needle perforation of the pleura. Using nonbiologic materials, pressure-decay leak testing demonstrated an exponential decay with a plateau phase in materials with a Young's modulus less than 5. In human pleural testing, the simulacrum was used to test the sealant function of four mixtures of pectin-based polymers. A 50% high-methoxyl pectin and 50% carboxymethylcellulose mixture demonstrated no sealant failures at transpleural pressures of 60 cmH O. In contrast, pectin mixtures containing 50% low-methoxyl pectin, 50% amidated low-methoxyl pectins, or 100% carboxymethylcellulose demonstrated frequent sealant failures at transpleural pressures of 40-50 cmH O (p < 0.001). Inhibition of sealant adhesion with enzyme treatment, dessication and 4°C cooling suggested an adhesion mechanism dependent upon polysaccharide interpenetration. We conclude that pectin-based heteropolysaccharides are a promising air-tight sealant of human pleural injuries. © 2018 Wiley Periodicals, Inc. J. Biomed. Mater. Res. Part B, 2018. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B: 799-806, 2019.
肺“气漏”通常是肺部手术或胸部外伤引起的胸膜损伤的结果,导致胸腔内积聚空气(气胸)。气漏是肺部手术后发病率和住院时间延长的主要原因。先前的工作已经证明了结构杂多糖(果胶)与小鼠胸膜糖萼结合。人和小鼠胸膜糖萼的类似凝集素结合特征和超微结构特征表明,这些聚合物在人类中具有潜在的应用。为了研究果胶基聚合物的应用,我们使用新鲜获得的人胸膜开发了一种模拟物。通过充气操作进行压力衰减漏检测试,充气操作涉及 3 秒斜坡到 3 秒平台压力;在胸膜穿孔后,充气完全被阻断。使用非生物材料,压力衰减漏检测试表明,在杨氏模量小于 5 的材料中,压力衰减漏检测试呈指数衰减,具有平台阶段。在人胸膜测试中,模拟物用于测试四种果胶基聚合物混合物的密封剂功能。50%高甲氧基果胶和 50%羧甲基纤维素混合物在跨胸膜压力为 60cmH O 时没有密封剂失效。相比之下,含有 50%低甲氧基果胶、50%酰胺化低甲氧基果胶或 100%羧甲基纤维素的果胶混合物在跨胸膜压力为 40-50cmH O 时经常发生密封剂失效(p<0.001)。酶处理、干燥和 4°C 冷却抑制密封剂粘附表明,粘附机制依赖于多糖互穿。我们得出结论,果胶基杂多糖是一种有前途的人胸膜损伤气密密封剂。