Fiolet Anne-Sophie, Jandot Elise, Doucey Pauline, Crétet Coralie, Brunel Célia, Pivot Christine, Ghigo Jean-Marc, Beloin Christophe, Lebeaux David, Pirot Fabrice
Service Pharmaceutique, Plateforme FRIPHARM, Groupe Hospitalier Centre Edouard Herriot, Hospices Civils de Lyon, 5, Place d'Arsonval, F-69437 Lyon Cedex 03, France.
Unité de Génétique des Biofilms, Département de Microbiologie, Institut Pasteur, 28 rue du docteur Roux, F-75724 Paris Cedex 15, France.
J Pharm Anal. 2018 Dec;8(6):386-393. doi: 10.1016/j.jpha.2017.09.004. Epub 2017 Sep 25.
A lock solution composed of gentamicin sulfate (5 mg/mL) and ethylenediaminetetraacetic acid disodium salt (EDTA-Na, 30 mg/mL) could fully eradicate in vivo bacterial biofilms in totally implantable venous access ports (TIVAP). In this study, fabrication, conditioning and sterilization processes of antimicrobial lock solution (ALS) were detailed and completed by a stability study. Stability of ALS was conducted for 12 months in vial (25 °C ± 2 °C, 60% ± 5% relative humidity (RH), and at 40 °C ± 2 °C, RH 75% ± 5%) and for 24 h and 72 h in TIVAP (40 °C ± 2 °C, RH 75% ± 5%). A stability indicating HPLC assay with UV detection for simultaneous quantification of gentamicin sulfate and EDTA-Na was developed. ALS was assayed by ion-pairing high performance liquid chromatography (HPLC) needing gentamicin derivatization, EDTA-Na metallocomplexation of samples and gradient mobile phase. HPLC methods to separate four gentamicin components and EDTA-Na were validated. Efficiency of sterility procedure and conditioning of ALS was confirmed by bacterial endotoxins and sterility tests. Physicochemical stability of ALS was determined by visual inspection, osmolality, pH, and sub-visible particle counting. Results confirmed that the stability of ALS in vials was maintained for 12 months and 24 h and 72 h in TIVAP.
一种由硫酸庆大霉素(5毫克/毫升)和乙二胺四乙酸二钠盐(EDTA-Na,30毫克/毫升)组成的封管溶液能够完全根除全植入式静脉输液港(TIVAP)内的体内细菌生物膜。在本研究中,详细阐述了抗菌封管溶液(ALS)的制备、预处理和灭菌过程,并通过稳定性研究完成。ALS在小瓶中(25℃±2℃,相对湿度(RH)60%±5%)以及在40℃±2℃、RH 75%±5%条件下于TIVAP中分别进行了12个月、24小时和72小时的稳定性研究。开发了一种采用紫外检测的稳定性指示高效液相色谱(HPLC)法,用于同时定量硫酸庆大霉素和EDTA-Na。ALS通过离子对高效液相色谱法(HPLC)进行检测,该方法需要对庆大霉素进行衍生化、对样品进行EDTA-Na金属络合以及采用梯度流动相。验证了用于分离四种庆大霉素组分和EDTA-Na的HPLC方法。通过细菌内毒素和无菌试验确认了ALS无菌程序和预处理的有效性。通过目视检查、渗透压、pH值和亚可见颗粒计数来确定ALS的物理化学稳定性。结果证实,ALS在小瓶中的稳定性可维持12个月,在TIVAP中可维持24小时和72小时。