Yoo Okhee, Salman Sam, Hla Thel K, Osowicki Joshua, Page-Sharp Madhu, Marsh Julie A, Barr Renae, Azzopardi Kristy, Morici Michael, Batty Kevin T, Enkel Stephanie L, Kado Joseph, Hatchuel Lara, Fulurija Alma, McCarthy James S, Snelling Thomas, Steer Andrew C, Carapetis Jonathan, Manning Laurens
Wesfarmers Centre for Vaccines and Infectious Diseases, The Kids Research Institute, Nedlands, Western Australia, Australia.
Pharmacy, School of Allied Health, University of Western Australia, Perth, Western Australia, Australia.
Antimicrob Agents Chemother. 2025 Jul 2;69(7):e0026925. doi: 10.1128/aac.00269-25. Epub 2025 May 20.
Although benzylpenicillin (penicillin G) is listed by the World Health Organization as an Essential Medicine, dose optimization is a persistent challenge, especially for long-acting intramuscular formulations. Maintaining sustained antibiotic exposure at target concentrations is crucial for secondary chemoprophylaxis of rheumatic heart disease and treatment of syphilis. This study compared the pharmacokinetic profile of continuous low-dose benzylpenicillin infusions with a standard-dose bolus and evaluated which renal function marker (serum creatinine, cystatin C, or combined e-glomerular filtration rate [eGFR]) best predicted clearance. Healthy adult volunteers received a single 600 mg IV benzylpenicillin bolus followed by randomization to continuous infusions targeting steady-state concentrations of 3, 6, 9, 12, or 20 ng/mL. Plasma benzylpenicillin concentrations were measured by liquid chromatography-mass spectrometry. Population pharmacokinetic analysis was performed using NONMEM by incorporating both bolus and infusion data, and various GFR estimations were evaluated as covariates for clearance. Data from 72 participants were analyzed, including 504 bolus and 389 continuous infusion samples. A two-compartment model improved fit when the ratio of central volume of distribution between bolus and low-dose infusion was incorporated, and clearance differences at steady state plasma concentration of 3 ng/mL were accounted for. Of the GFR estimations, cystatin C-based eGFR significantly enhanced model fit compared with creatinine-based equations. Benzylpenicillin pharmacokinetics at very low concentrations demonstrated both a higher volume of distribution and increased clearance. Cystatin C-based eGFR may more accurately predict benzylpenicillin clearance, enabling precision dosing for long-acting preparations used for treatment of syphilis and prevention of rheumatic fever.
尽管苄星青霉素(青霉素G)被世界卫生组织列为基本药物,但剂量优化一直是个挑战,尤其是长效肌内注射制剂。在目标浓度下维持持续的抗生素暴露对于风湿性心脏病的二级化学预防和梅毒治疗至关重要。本研究比较了持续低剂量苄星青霉素输注与标准剂量推注的药代动力学特征,并评估了哪种肾功能标志物(血清肌酐、胱抑素C或合并的估算肾小球滤过率[eGFR])能最佳预测清除率。健康成年志愿者接受单次600mg静脉注射苄星青霉素推注,随后随机分为持续输注组,目标稳态浓度分别为3、6、9、12或20ng/mL。采用液相色谱 - 质谱法测定血浆苄星青霉素浓度。通过纳入推注和输注数据,使用NONMEM进行群体药代动力学分析,并评估各种肾小球滤过率估算值作为清除率的协变量。分析了72名参与者的数据,包括504次推注和389次持续输注样本。当纳入推注和低剂量输注之间中央分布容积的比例,并考虑稳态血浆浓度为3ng/mL时的清除率差异时,二室模型拟合效果更佳。在肾小球滤过率估算值中,基于胱抑素C的eGFR与基于肌酐的方程相比,显著提高了模型拟合度。极低浓度下苄星青霉素的药代动力学显示分布容积更大且清除率增加。基于胱抑素C的eGFR可能更准确地预测苄星青霉素清除率,从而为用于梅毒治疗和风湿热预防的长效制剂实现精准给药。