Huskey Mariah, Lewis Paul, Brown Stacy D
East Tennessee State University, Johnson City, USA.
Johnson City Medical Center, TN, USA.
Hosp Pharm. 2021 Oct;56(5):507-512. doi: 10.1177/0018578720925389. Epub 2020 May 31.
Use of ampicillin in outpatient parenteral antimicrobial therapy (OPAT) has historically been complicated by frequent dosing and limited stability. The purpose of this study was to evaluate stability of ampicillin using high-pressure liquid chromatography (HPLC) in an OPAT dosing model using continuous infusion at room temperature over 24 hours immediately following preparation compared with batches stored under refrigeration for 24 hours, 72 hours, and 7 days.
An HPLC method was developed and validated as stability indicating using guidance in USP general Chapter <1225>. Four ampicillin batches were prepared for each experimental condition (immediate use and refrigerated storage for 24 hours, 72 hours, and 7 days). A pump was used to recirculate the solutions through medical-grade tubing for 24 hours. Triplicate 1-mL aliquots were removed from each batch at time 0, 4, 8, 12, and 24 hours and analyzed for ampicillin concentration.
Each batch was assayed for initial concentration (20.34-21.50 mg/mL), and percent recovery compared with that concentration thereafter. For the duration of infusion, the average recoveries were 96.4%, 95.8%, 94.6%, and 90.3% for immediate use, 24-hour storage, 72-hour storage, and 7-day storage, respectively. The recovery remained above 90% for all batches and time points, except for 7-day storage, which fell below 90% after 4 hours of circulation.
Ampicillin can be prepared and stored in a refrigerator for up to 72 hours prior to continuously infusing at room temperature over 24 hours with less than a 10% loss of potency over the dosing period. This model supports twice weekly OPAT delivery of ampicillin.
在门诊胃肠外抗菌治疗(OPAT)中,氨苄西林的使用在历史上一直因给药频繁和稳定性有限而变得复杂。本研究的目的是在OPAT给药模型中,使用高压液相色谱法(HPLC)评估氨苄西林的稳定性。该模型为室温下连续输注24小时,药物在制备后立即使用,并与冷藏保存24小时、72小时和7天的批次进行比较。
根据美国药典通则<1225>中的指导原则,开发并验证了一种HPLC方法作为稳定性指示方法。针对每种实验条件(立即使用以及冷藏保存24小时、72小时和7天)制备了四批氨苄西林。使用一台泵使溶液通过医用级管道循环达24小时。在0、4、8、12和24小时从每批中取出1 mL的三份等分试样,并分析氨苄西林浓度。
对每批药物测定初始浓度(20.34 - 21.50 mg/mL),并在此后比较与该浓度相比的回收率百分比。在输注期间,立即使用、保存24小时、保存72小时和保存7天的平均回收率分别为96.4%、95.8%、94.6%和90.3%。除了保存7天的批次在循环4小时后回收率降至90%以下外,所有批次和时间点的回收率均保持在90%以上。
氨苄西林可以在冰箱中制备并保存长达72小时,然后在室温下连续输注24小时,给药期间效力损失小于10%。该模型支持每周两次的OPAT氨苄西林给药。