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通过Seraph 100微结合亲和血液滤器清除抗感染药物。

elimination of anti-infective drugs by the Seraph 100 Microbind affinity blood filter.

作者信息

Schmidt Julius J, Eden Gabriele, Seffer Malin-Theres, Winkler Manuela, Kielstein Jan T

机构信息

Department of Nephrology and Hypertension, Hannover Medical School, Hannover, Germany.

Medical Clinic V, Nephrology | Rheumatology | Blood Purification, Academic Teaching Hospital Braunschweig, Braunschweig, Germany.

出版信息

Clin Kidney J. 2020 May 21;13(3):421-424. doi: 10.1093/ckj/sfaa063. eCollection 2020 Jun.

Abstract

BACKGROUND

In August 2019, the European Union licensed the first ever haemoperfusion device aimed to reduce pathogens in the blood. The core of the adsorber consists of ultra-high molecular weight polyethylene beads with endpoint-attached heparin. These beads utilize pathogen inherent adhesion mechanisms to reduce pathogen load. So far, it is unknown whether the device has an effect on anti-infective drug concentrations. The aim of this study was to investigate the adsorption of multiple anti-infective drugs from human plasma.

METHODS

In this study, 18 anti-infective drugs were administered to human donor plasma and pumped through the heparin-coated pathogen adsorber (Seraph 100 MicrobindAffinity Blood Filter; ExThera Medical Corp., Martinez, CA, USA) at a plasma flow rate of 250 mL/min for 60 min. Pre- and post-adsorber plasma samples were quantified after 5, 15, 30 and 60 min.

RESULTS

We found a reduction ratio (RR) in anti-infective plasma levels between -1% and 62%. This decrease occurred mainly in the first 5 min of the experiment (RR -4 to 62%). Mean plasma clearance rates ranged between -11.93 mL/min (fluconazole) and 4.86 mL/min (clindamycin). The highest RRs were measured for aminoglycosides (tobramycin 62% and gentamycin 59%).

CONCLUSIONS

The elimination of anti-infective drugs by the Seraph is neglectable in all but 2 of 18 of the investigated substances. Aminoglycosides may be adsorbed by the device during their first pass.

摘要

背景

2019年8月,欧盟批准了首个旨在减少血液中病原体的血液灌流装置。吸附器的核心由带有末端连接肝素的超高分子量聚乙烯珠组成。这些珠子利用病原体固有的粘附机制来降低病原体负荷。到目前为止,该装置是否会对抗感染药物浓度产生影响尚不清楚。本研究的目的是调查从人血浆中吸附多种抗感染药物的情况。

方法

在本研究中,将18种抗感染药物施用于人供体血浆,并以250 mL/min的血浆流速泵入肝素包被的病原体吸附器(Seraph 100 MicrobindAffinity血液过滤器;ExThera Medical Corp.,美国加利福尼亚州马丁内斯)60分钟。在5、15、30和60分钟后对吸附器前后的血浆样本进行定量。

结果

我们发现抗感染血浆水平的降低率(RR)在-1%至62%之间。这种降低主要发生在实验的前5分钟(RR -4%至62%)。平均血浆清除率在-11.93 mL/min(氟康唑)至4.86 mL/min(克林霉素)之间。氨基糖苷类药物的RR最高(妥布霉素为62%,庆大霉素为59%)。

结论

在18种被研究物质中,除2种外,Seraph对抗感染药物的清除作用可忽略不计。氨基糖苷类药物在首次通过时可能会被该装置吸附。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e2d/7367135/bb969dccd3cc/sfaa063f1.jpg

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