Pharmacologie cellulaire et moléculaire, Louvain Drug Research Institute, Université catholique de Louvain, Brussels, Belgium.
Department of Clinical Pharmacology, Medical University of Vienna, ViennaAustria.
J Antimicrob Chemother. 2022 Sep 30;77(10):2742-2753. doi: 10.1093/jac/dkac286.
Temocillin plasma protein binding (PPB) in healthy individuals is reported to be ∼85% but had not been studied in patients.
To obtain normative data on temocillin PPB in patients in relation to infection and impact of co-medications widely used in ICU.
Plasma was obtained from healthy individuals (Group #1), non-ICU patients with UTI (Group #2), ICU patients with suspected/confirmed ventriculitis (Group #3) or with sepsis/septic shock (Group #4). Total and unbound temocillin concentrations were measured in spiked samples from temocillin-naive donors (in vitro) or in plasma from temocillin-treated subjects (in vivo). The impact of diluting plasma, using pharmaceutical albumin, or adding drugs potentially competing for PPB was tested in spiked samples. Data were analysed using a modified Hill-Langmuir equation taking ligand depletion into account.
Temocillin PPB was saturable in all groups, both in vitro and in vivo. Maximal binding capacity (Bmax) was 1.2-2-fold lower in patients. At 20 and 200 mg/L (total concentrations), the unbound fraction reached 12%-29%, 23%-42% and 32%-52% in Groups #2, #3, #4. The unbound fraction was inversely correlated with albumin and C-reactive protein concentrations. Binding to albumin was 2-3-fold lower than in plasma and non-saturable. Drugs with high PPB but active at lower molar concentrations than temocillin caused minimal displacement, while fluconazole (low PPB but similar plasma concentrations to temocillin) increased up to 2-fold its unbound fraction.
Temocillin PPB is saturable, 2-4-fold lowered in infected patients in relation to disease severity (ICU admission, hypoalbuminaemia, inflammation) and only partially reproducible with albumin. Competition with other drugs must be considered for therapeutic concentrations to be meaningful.
据报道,健康个体中单剂西司他丁的血浆蛋白结合率(PPB)约为 85%,但尚未在患者中进行研究。
获得与感染相关的患者中单剂西司他丁 PPB 的规范数据,并研究在 ICU 中广泛使用的合并用药对其的影响。
从健康个体(第 1 组)、非 ICU 尿路感染患者(第 2 组)、疑似/确诊脑室炎的 ICU 患者(第 3 组)或脓毒症/感染性休克的 ICU 患者(第 4 组)中采集血浆。在未使用单剂西司他丁的供体的添加样本(体外)或接受单剂西司他丁治疗的受试者的血浆(体内)中测量总浓度和游离单剂西司他丁浓度。在添加样本中测试了稀释血浆、使用药物白蛋白或添加可能竞争 PPB 的药物的影响。使用考虑配体消耗的改良 Hill-Langmuir 方程分析数据。
在所有组中,无论是在体外还是体内,单剂西司他丁的 PPB 均为饱和型。在患者中,最大结合能力(Bmax)降低了 1.2-2 倍。在 20 和 200mg/L(总浓度)时,游离分数分别达到第 2、3、4 组的 12%-29%、23%-42%和 32%-52%。游离分数与白蛋白和 C 反应蛋白浓度呈负相关。与血浆相比,与白蛋白的结合降低了 2-3 倍且非饱和型。与单剂西司他丁相比,具有高 PPB 但在较低摩尔浓度下具有活性的药物仅引起轻微的置换,而氟康唑(PPB 低但与单剂西司他丁的血浆浓度相似)可将其游离分数增加 2 倍。
单剂西司他丁的 PPB 为饱和型,与疾病严重程度(入住 ICU、低白蛋白血症、炎症)相关时,降低 2-4 倍,且仅部分可通过白蛋白重现。对于治疗浓度,必须考虑与其他药物的竞争。