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Total flucloxacillin plasma concentrations poorly reflect unbound concentrations in hospitalized patients with
Paul Ken Leong Chin1,2, Philip George Drennan2, Sharon Jane Gardiner3
1Department of Medicine, University of Otago, Christchurch, New Zealand.
Aims:
Flucloxacillin dosing may be guided by measurement of its total plasma concentrations. Flucloxacillin is highly protein bound with fraction unbound in plasma (fu ) of around 0.04 in healthy individuals. The utility of measuring unbound flucloxacillin concentrations for patients outside the intensive care unit (ICU) is not established. We aimed to compare flucloxacillin fu in non-ICU hospitalised patients against healthy volunteers, and to examine the performance of a published model for predicting unbound concentrations, using total flucloxacillin and plasma albumin concentrations.
Methods:
Data from 12 healthy volunteers (248 samples) and 47 hospitalized patients (61 samples) were examined. Plasma flucloxacillin concentrations were measured using a validated liquid chromatography-tandem mass spectrometry method. Flucloxacillin fu for the two groups was compared using a generalized estimating equation model to account for clustered observations. The performance of the single protein binding site prediction model in hospitalized patients was compared with measured unbound concentrations using Bland-Altman plots.
Results:
The median (range) flucloxacillin fu for healthy (median albumin 45 g l-1 ) and hospitalized individuals (median albumin 30 g l-1 ) were 0.04 (0.02-0.07) and 0.10 (0.05-0.37), respectively (P < 0.0001). The prediction model underpredicted unbound flucloxacillin concentrations with a mean bias (95% limits of agreement) of -54% (-137%, +30%).
Conclusions:
The flucloxacillin fu values observed in our cohort of hospitalized patients had a wide range and were greater than those of healthy individuals. Unbound flucloxacillin plasma concentrations were predicted poorly by the model. Instead, unbound concentrations should be measured to guide dosing.
Insights
Hospitalized patients have higher unbound flucloxacillin levels than healthy individuals. Measuring unbound flucloxacillin concentrations is recommended for guiding patient dosing, as prediction models are inaccurate.
Area of Science:
- Pharmacokinetics and Pharmacodynamics
- Clinical Pharmacy
- Antibiotic Stewardship
Background:
- Flucloxacillin dosing is often guided by total plasma concentrations.
- Flucloxacillin is highly protein-bound, with a fraction unbound (fu) around 0.04 in healthy individuals.
- The utility of measuring unbound flucloxacillin concentrations in non-intensive care unit (ICU) hospitalized patients is not established.
Purpose of the Study:
- To compare flucloxacillin fu in non-ICU hospitalized patients versus healthy volunteers.
- To evaluate the performance of a published model for predicting unbound flucloxacillin concentrations in hospitalized patients.
Main Methods:
- Analyzed data from 12 healthy volunteers and 47 hospitalized patients.
- Measured plasma flucloxacillin concentrations using liquid chromatography-tandem mass spectrometry.
- Compared flucloxacillin fu between groups and assessed prediction model performance using Bland-Altman plots.
Main Results:
- Median flucloxacillin fu was significantly higher in hospitalized patients (0.10) compared to healthy individuals (0.04).
- Hospitalized patients exhibited a wider range of flucloxacillin fu (0.05-0.37) than healthy individuals (0.02-0.07).
- The prediction model underpredicted unbound flucloxacillin concentrations with a mean bias of -54%.
Conclusions:
- Flucloxacillin fu is higher and more variable in hospitalized patients than in healthy individuals.
- A published prediction model performed poorly in estimating unbound flucloxacillin concentrations.
- Direct measurement of unbound flucloxacillin concentrations is recommended for optimizing patient dosing.
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