Evidence map›Paper›PMID 40458932›Full record

ArticleAnalytical chemistry2025

Therapeutic Drug Monitoring of Amikacin and Colistin in Patients with Multidrug-Resistant Gram-Negative Infections Using a Portable Plasmonic Biosensor.

Alejandro Astúa, Maria Carmen Estevez, Sonia Luque, Santiago Grau, Luisa Sorlí, Milagro Montero, Juan P Horcajada, Laura M Lechuga

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Alejandro AstúaNanobiosensors and Bioanalytical Applications Group, Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC, CIBER-BBN, BIST, Bellaterra 08193, Spain.
Maria Carmen EstevezNanobiosensors and Bioanalytical Applications Group, Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC, CIBER-BBN, BIST, Bellaterra 08193, Spain.ORCID 0000-0003-3694-7186
Sonia LuquePharmacy Service, Hospital del Mar, Hospital del Mar Research Institute, Universitat Pompeu Fabra (UPF), Barcelona 08003, Spain.
Santiago GrauPharmacy Service, Hospital del Mar, Hospital del Mar Research Institute, Universitat Pompeu Fabra (UPF), Barcelona 08003, Spain.
Luisa SorlíInfectious Diseases Service, Hospital del Mar, Hospital del Mar Research Institute, Universitat Pompeu Fabra (UPF), Barcelona 08003, Spain.
Milagro MonteroInfectious Diseases Service, Hospital del Mar, Hospital del Mar Research Institute, Universitat Pompeu Fabra (UPF), Barcelona 08003, Spain.
Juan P HorcajadaInfectious Diseases Service, Hospital del Mar, Hospital del Mar Research Institute, Universitat Pompeu Fabra (UPF), Barcelona 08003, Spain.
Laura M LechugaNanobiosensors and Bioanalytical Applications Group, Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC, CIBER-BBN, BIST, Bellaterra 08193, Spain.ORCID 0000-0001-5187-5358

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innovative diagnostic tools that enhance antibiotic routine monitoring can improve the management of infections caused by antibiotic-resistant bacteria. Therapeutic drug monitoring (TDM) involves measuring drug levels in the patient bloodstream to ensure optimal efficacy and safety, particularly for drugs with a narrow therapeutic index (TI), assisting in dosage control and toxicity risk management. Amikacin (AK) and colistin (CS) are crucial antibiotics for treating multidrug-resistant (MDR) bacteria but they have side effects that require a precise TDM to try to minimize them. Current analytical techniques like immunoassays, high-performance liquid chromatography (HPLC), and liquid chromatography-mass spectrometry (LC-MS) are gold standards for the antibiotic analysis, but they may require transferring the human samples to centralized facilities, delaying crucial results and turnaround time. In contrast, plasmonic biosensors offer advantages for clinical diagnostics, enabling real-time drug detection with minimal sample volume and processing, being ideal for point-of-care applications. We have implemented plasmonic biosensors to quantify and rapidly monitor blood levels of amikacin and colistin. The biosensors provide high specificity and sensitivity, with limits of detection (LOD) of 0.92 ng/mL (1.57 nM) for amikacin and 9.11 pg/mL (7.88 pM) for colistin in blood serum. Statistics analyses demonstrated a strong correlation between the biosensor evaluation and the standard analytical methods (Spearman's correlation coefficient of 0.9171 (

Indexed as

AmikacinAnti-Bacterial AgentsBiosensing TechniquesColistinDrug MonitoringDrug Resistance, Multiple, BacterialGram-Negative Bacterial InfectionsHumansAmikacinAnti-Bacterial AgentsColistin

Identifiers

PMID40458932
PMCPMC12177867

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.