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评估符合英国国民保健制度黄色封面文件要求的弹性输注装置中替莫西林的稳定性,用于门诊肠外抗菌治疗。

Evaluation of the stability of temocillin in elastomeric infusion devices used for outpatient parenteral antimicrobial therapy in accordance with the requirements of the UK NHS Yellow Cover Document.

机构信息

University of Queensland Centre for Clinical Research, Faculty of Medicine,the University of Queensland, Herston, Queensland, Australia

University of Queensland Centre for Clinical Research, Faculty of Medicine,the University of Queensland, Herston, Queensland, Australia.

出版信息

Eur J Hosp Pharm. 2023 Mar;30(e1):e76-e81. doi: 10.1136/ejhpharm-2022-003286. Epub 2022 May 24.

Abstract

OBJECTIVE

To evaluate the stability of temocillin solution in two elastomeric infusion devices - Easypump II LT 270-27- S and Dosi-Fusor L25915-250D1 for OPAT administration during 14 days of 5°C±3°C fridge storage followed by 24 hour exposure at an in-use temperature of 32°C, when reconstituted with 0.3% citrate buffer at pH7.

METHODS

Stability testing was conducted in accordance with standard protocols in the UK National Health Service Yellow Cover Document (YCD). A stability indicating assay method was applied using a high-performance liquid chromatography (HPLC) system with a photodiode array detector. Low (500 mg/240 mL), intermediate (4000 mg/240 mL) and high (6000 mg/240 mL) temocillin concentrations were tested in triplicate devices with duplicate samples taken at 11 time points during fridge storage and subsequent in-use temperature exposure.

RESULT

The percentage of temocillin remaining after 14 days of fridge storage was greater than 97% in both devices and at all concentrations tested. During subsequent in-use temperature exposure, a 95% stability limit was achieved for 12 hours except for the high concentration (25 mg/mL) in the Dosi-Fusor device. It met this criterion for only 10 hours - the percent of temocillin remaining at 12 hours was 94.5%. However, for all devices and the doses tested, the degradation of temocillin was <9% at the end of 24 hours in-use temperature exposure.

CONCLUSION

Temocillin reconstituted with 0.3% citrate buffer at pH7 in elastomeric infusion devices can be stored in a fridge (2°C-8°C) for 14 days meeting the YCD acceptance criteria. Considering <5% degradation, the current data supports twice daily dosing of temocillin within the OPAT setting. In jurisdictions where a <10% degradation limit is acceptable, once daily dosing with 24-hour continuous infusion may be considered. Temocillin is a useful alternative to other broad-spectrum anti-Gram-negative agents currently utilised in the OPAT setting and supports the wider antimicrobial stewardship agenda.

摘要

目的

评估替莫西林溶液在两种弹性输注装置——Easypump II LT 270-27-S 和 Dosi-Fusor L25915-250D1 中的稳定性,这两种装置用于 5°C±3°C 冰箱储存 14 天后,再在使用温度 32°C 下暴露 24 小时,在与 0.3%柠檬酸缓冲液(pH7)复溶后用于 OPAT 治疗。

方法

稳定性测试按照英国国家卫生服务部黄色封面文件(YCD)中的标准方案进行。使用高效液相色谱(HPLC)系统和光电二极管阵列检测器进行稳定性指示检测方法。在三个设备中重复测试低(500mg/240mL)、中(4000mg/240mL)和高(6000mg/240mL)浓度的替莫西林,在冰箱储存和随后的使用温度暴露期间,在 11 个时间点采集重复样本。

结果

在两种设备和所有测试浓度下,冰箱储存 14 天后,替莫西林的剩余百分比均大于 97%。在随后的使用温度暴露期间,除了 Dosi-Fusor 设备中的高浓度(25mg/mL)外,12 小时时达到 95%的稳定性限度。该设备仅满足 10 小时的标准,12 小时时替莫西林的剩余百分比为 94.5%。然而,对于所有设备和测试剂量,在 24 小时使用温度暴露结束时,替莫西林的降解率<9%。

结论

用 pH7 的 0.3%柠檬酸缓冲液复溶的替莫西林可在冰箱(2°C-8°C)中储存 14 天,符合 YCD 接受标准。考虑到<5%的降解,目前的数据支持在 OPAT 环境中每日两次给予替莫西林。在可接受<10%降解限度的司法管辖区,可考虑每日一次、24 小时持续输注。替莫西林是目前在 OPAT 环境中使用的其他广谱抗革兰氏阴性药物的有效替代品,支持更广泛的抗菌药物管理议程。

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