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不同雾化器在腹腔内压力雾化化疗(PIPAC)临床应用中的性能。

Performance of different nebulizers in clinical use for Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC).

机构信息

Topas GmbH, Dresden, Germany.

Research Group Mechanical Process Engineering, Institute of Process Engineering and Environmental Technology, Technische Universität Dresden, Dresden, Germany.

出版信息

PLoS One. 2024 May 2;19(5):e0300241. doi: 10.1371/journal.pone.0300241. eCollection 2024.

Abstract

OBJECTIVE

Technical ex-vivo comparison of commercial nebulizer nozzles used for Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC).

METHODS

The performance of four different commercial nebulizer nozzles (Nebulizer; HurriChemTM; MCR-4 TOPOL®; QuattroJet) was analysed concerning: i) technical design and principle of operation, ii) operational pressure as function of the liquid flow rate, iii) droplet size distribution via laser diffraction spectrometry, iv) spray cone angle, spray cone form as well as horizontal drug deposition by image-metric analyses and v) chemical resistance via exposing to a cytostatic solution and chemical composition by means of spark optical emission spectral analysis.

RESULTS

The Nebulizer shows quasi an identical technical design and thus also a similar performance (e.g., mass median droplet size of 29 μm) as the original PIPAC nozzles (MIP/ CapnoPen). All other nozzles show more or less a performance deviation to the original PIPAC nozzles. The HurriChemTM has a similar design and principle of operation as the Nebulizer, but provides a finer aerosol (22 μm). The principle of operation of MCR-4 TOPOL® and QuattroJet differ significantly from that of the original PIPAC nozzle technology. The MCR-4 TOPOL® offers a hollow spray cone with significantly larger droplets (50 μm) than the original PIPAC nozzles. The QuattroJet generates an aerosol (22 μm) similar to that of the HurriChemTM but with improved spatial drug distribution.

CONCLUSION

The availability of new PIPAC nozzles is encouraging but can also have a negative impact if their performance and efficacy is unknown. It is recommended that PIPAC nozzles that deviate from the current standard should be subject to bioequivalence testing and implementation in accordance with the IDEAL-D framework prior to routine clinical use.

摘要

目的

对用于腹腔内加压雾化化疗(PIPAC)的商业雾化器喷嘴进行技术离体比较。

方法

分析了四种不同商业雾化器喷嘴(雾化器;HurriChemTM;MCR-4 TOPOL®;QuattroJet)的性能:i)技术设计和操作原理,ii)作为液体流量函数的操作压力,iii)通过激光衍射光谱法测量的液滴尺寸分布,iv)通过图像测量分析测量的喷雾锥角、喷雾锥形状以及水平药物沉积,v)通过暴露于细胞毒性溶液和火花发射光谱分析进行的化学抗性分析。

结果

雾化器的技术设计几乎相同,因此性能也相似(例如,质量中值液滴尺寸为 29μm),与原始 PIPAC 喷嘴(MIP/CapnoPen)相似。所有其他喷嘴或多或少地表现出与原始 PIPAC 喷嘴的性能偏差。HurriChemTM 的设计和操作原理与雾化器相似,但提供更精细的气溶胶(22μm)。MCR-4 TOPOL®和 QuattroJet 的操作原理与原始 PIPAC 喷嘴技术有很大不同。MCR-4 TOPOL®提供空心喷雾锥,液滴明显大于原始 PIPAC 喷嘴(50μm)。QuattroJet 产生的气溶胶(22μm)与 HurriChemTM 相似,但空间药物分布得到改善。

结论

新的 PIPAC 喷嘴的可用性令人鼓舞,但如果其性能和功效未知,也可能产生负面影响。建议与当前标准偏离的 PIPAC 喷嘴应进行生物等效性测试,并根据 IDEAL-D 框架在常规临床使用之前进行实施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43de/11065249/654c9371bd1e/pone.0300241.g001.jpg

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