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基于酶联免疫吸附测定法检测含蛋白质样品中的庆大霉素和万古霉素。

ELISA-based detection of gentamicin and vancomycin in protein-containing samples.

作者信息

Odekerken Jim C E, Logister Dorien M W, Assabre Loubna, Arts Jacobus J C, Walenkamp Geert H I M, Welting Tim J M

机构信息

Laboratory for Experimental Orthopaedics, Department of Orthopaedic Surgery, Research School CAPHRI, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ Maastricht, The Netherlands.

出版信息

Springerplus. 2015 Oct 15;4:614. doi: 10.1186/s40064-015-1411-y. eCollection 2015.

Abstract

BACKGROUND

Orthopaedic implant infections are treated by surgical debridement, systematic antibiotic treatment or local antibiotic treatment with antibiotic-loaded beads. Currently antibiotic concentrations in wound exudate, serum, urine or tissue samples are determined with HPLC or fluorescent spectrometric assays. Both methods are heavily influenced due to proteins in the samples.

QUESTIONS/PURPOSES: Is ELISA capable to detect gentamicin and vancomycin in protein-containing samples like serum and wound exudate.

METHODS

Two specific competitive ELISA-assays were set-up to detect either gentamicin or vancomycin in protein-rich samples. An antibiotic-BSA hapten was generated as a coatable antigen and commercially available antibodies were applied for downstream immunodetection.

RESULTS

The developed ELISAs perform at a detection range of 2-500 ng/ml gentamycin and 20-5000 ng/ml vancomycin. Both ELISAs were capable of detecting these antibiotics in human serum and wound exudate without being compromised by the presence of proteins. We did not detect cross-reactivity for gentamicin in the vancomycin ELISA or vice versa.

CONCLUSIONS

The antibiotic ELISAs detect gentamicin and vancomycin at low concentrations in protein-rich samples and they can be used as a high throughput and cost-effective alternative for chromatographic or fluorescent methods.

CLINICAL RELEVANCE

These ELISAs can be used to detect very low gentamicin or vancomycin concentrations in clinical samples or assess novel orthopaedic antibiotic release systems in in vitro and in vivo studies.

摘要

背景

骨科植入物感染通过手术清创、全身抗生素治疗或使用载抗生素珠进行局部抗生素治疗。目前,伤口渗出液、血清、尿液或组织样本中的抗生素浓度通过高效液相色谱法(HPLC)或荧光光谱法测定。由于样本中的蛋白质,这两种方法都受到很大影响。

问题/目的:酶联免疫吸附测定(ELISA)能否检测血清和伤口渗出液等含蛋白质样本中的庆大霉素和万古霉素。

方法

建立了两种特异性竞争ELISA检测方法,以检测富含蛋白质样本中的庆大霉素或万古霉素。制备了一种抗生素-牛血清白蛋白(BSA)半抗原作为可包被抗原,并使用市售抗体进行下游免疫检测。

结果

所开发的ELISA在庆大霉素检测范围为2 - 500 ng/ml、万古霉素检测范围为20 - 5000 ng/ml时表现良好。两种ELISA都能够在人血清和伤口渗出液中检测到这些抗生素,且不受蛋白质存在的影响。我们在万古霉素ELISA中未检测到庆大霉素的交叉反应,反之亦然。

结论

抗生素ELISA能够在富含蛋白质的样本中检测低浓度的庆大霉素和万古霉素,它们可作为色谱法或荧光法的高通量且经济高效的替代方法。

临床意义

这些ELISA可用于检测临床样本中极低浓度的庆大霉素或万古霉素,或在体外和体内研究中评估新型骨科抗生素释放系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d719/4628023/423b8881a036/40064_2015_1411_Fig1_HTML.jpg

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