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Aerosol delivery of dry powder synthetic lung surfactant to surfactant-deficient rabbits and preterm lambs on non-invasive respiratory support

机译:将干粉合成肺表面活性剂气雾剂输送至缺乏表面活性剂的兔子和无创呼吸支持下的早产羔羊

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摘要

>Background: The development of synthetic lung surfactant for preterm infants has focused on peptide analogues of native surfactant proteins B and C (SP-B and SP-C). Non-invasive respiratory support with nasal continuous positive airway pressure (nCPAP) may benefit from synthetic surfactant for aerosol delivery. >Methods: A total of three dry powder (DP) surfactants, consisting of phospholipids and the SP-B analogue Super Mini-B (SMB), and one negative control DP surfactant without SMB, were produced with the Acorda Therapeutics ARCUS® Pulmonary Dry Powder Technology. Structure of the DP surfactants was compared with FTIR spectroscopy, in vitro surface activity with captive bubble surfactometry, and in vivo activity in surfactant-deficient adult rabbits and preterm lambs. In the animal experiments, intratracheal (IT) aerosol delivery was compared with surfactant aerosolization during nCPAP support. Surfactant dosage was 100 mg/kg of lipids and aerosolization was performed using a low flow inhaler. >Results: FTIR spectra of the three DP surfactants each showed secondary structures compatible with peptide folding as an α-helix hairpin, similar to that previously noted for surface-active SMB in other lipids. The DP surfactants with SMB demonstrated in vitro surface activity <1 mN/m. Oxygenation and lung function increased quickly after IT aerosolization of DP surfactant in both surfactant-deficient rabbits and preterm lambs, similar to improvements seen with clinical surfactant. The response to nCPAP aerosol delivery of DP surfactant was about 50% of IT aerosol delivery, but could be boosted with a second dose in the preterm lambs. >Conclusions: Aerosol delivery of DP synthetic surfactant during non-invasive respiratory support with nCPAP significantly improved oxygenation and lung function in surfactant-deficient animals and this response could be enhanced by giving a second dose. Aerosol delivery of DP synthetic lung surfactant has potential for clinical applications.
机译:>背景:用于早产儿的合成肺表面活性剂的开发侧重于天然表面活性剂蛋白B和C(SP-B和SP-C)的肽类似物。鼻腔持续气道正压通气(nCPAP)的无创呼吸支持可受益于合成表面活性剂进行气雾剂输送。 >方法:用三氟甲磺酸生产了总共三种由磷脂和SP-B类似物Super Mini-B(SMB)组成的干粉(DP)表面活性剂和一种不含SMB的阴性对照DP表面活性剂。 Acorda TherapeuticsARCUS®肺干粉技术。 DP表面活性剂的结构与FTIR光谱,俘获气泡表面活性法的体外表面活性以及缺乏表面活性剂的成年兔和早产羔羊的体内活性进行了比较。在动物实验中,在nCPAP支持期间将气管内(IT)气雾剂与表面活性剂气雾剂进行了比较。表面活性剂的剂量为100 mg / kg脂质,并使用低流量吸入器进行雾化。 >结果:三种DP表面活性剂的FTIR光谱均显示与肽折叠相容的二级结构,可折叠为α-螺旋发夹,类似于先前在其他脂质中对表面活性SMB的记录。具有SMB的DP表面活性剂的体外表面活性<1 mN / m。 IT表面活性剂缺乏的兔子和早产羔羊的DP表面活性剂经IT雾化后,氧合和肺功能迅速提高,与临床表面活性剂的改善相似。 DP表面活性剂对nCPAP气雾剂输送的响应约为IT气雾剂输送的50%,但在早产羔羊中加第二剂可以增强这种反应。 >结论:在使用nCPAP的无创呼吸支持过程中,DP合成表面活性剂的气雾剂可显着改善表面活性剂缺乏动物的氧合作用和肺功能,可通过再给予第二剂来增强这种反应。 DP合成肺表面活性剂的气溶胶输送具有临床应用潜力。

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