Chen Pang, Mar Zin, Giannetti Anthony, Hughes Susan, Gilbert Justine, Zhao Fang
St. John Fisher College, Rochester, NY, USA.
University of Rochester Medical Center, Rochester, NY, USA.
Hosp Pharm. 2022 Feb;57(1):69-75. doi: 10.1177/0018578720973885. Epub 2020 Nov 25.
Compounded eye drop solutions of vancomycin hydrochloride have important clinical applications, such as postoperative antimicrobial prophylaxis and bacterial keratitis. There exists a plethora of data to support the use of various liquid vehicles to compound vancomycin hydrochloride eye drops. However, there are a number of limitations for implementation, especially the frequent shortage or discontinuation of the vehicle products. This study was designed to investigate the use of an OTC eye wash product as the evergreen vehicle and to evaluate the physical and chemical stability of the new formulation.
The Advance Eye Relief eye wash and vancomycin hydrochloride for injection vials were used to prepare 10 and 50 mg/mL vancomycin eye drop solutions. The solutions were packaged in Steri-Droppers bottles and stored in a freezer for 14 days followed by 28 days in refrigeration. The 14-day period of freezing was included to allow time for sterility testing. At pre-determined stability time points, samples were taken for visual inspection, pH and osmolality measurement, and analysis by a stability-indicating high performance liquid chromatography (HPLC) method.
Freshly prepared vancomycin eye drops were clear, colorless, and free of particulates. The pH readings were 7.03 and 6.28 for the 10 and 50 mg/mL solutions, respectively. The osmolality of both solutions were within the range of 300-330 mOsmol/kg and considered isotonic. Initial drug concentrations of all samples were confirmed by HPLC to be within 100%-103% of the label claims. Throughout the stability study period, there were no significant changes in the appearance, pH, or osmolality of any samples. The HPLC results also confirmed that the drug concentrations in all stability samples were within 98%-101% of the initial time zero values and no significant degradation product peaks were observed.
A new compounded vancomycin eye drop formulation was developed to mitigate vehicle sourcing issues. This eye drop formulation was easy to prepare, exhibited satisfactory properties for ophthalmic applications, and remained stable chemically and physically when stored for 14 days in freezer followed by 28 days in refrigerator.
盐酸万古霉素复方滴眼液制剂具有重要的临床应用,如术后抗菌预防和细菌性角膜炎。有大量数据支持使用各种液体载体来配制盐酸万古霉素滴眼液。然而,在实施过程中存在一些限制,特别是载体产品经常短缺或停产。本研究旨在探讨使用一种非处方洗眼产品作为长效载体,并评估新制剂的物理和化学稳定性。
使用Advance Eye Relief洗眼液和注射用盐酸万古霉素小瓶制备10和50mg/mL的万古霉素滴眼液溶液。将溶液包装在无菌滴管瓶中,先在冷冻室中储存14天,然后在冷藏室中储存28天。包含14天的冷冻期是为了留出时间进行无菌测试。在预先确定的稳定性时间点,取样进行外观检查、pH值和渗透压测量,并通过稳定性指示高效液相色谱(HPLC)法进行分析。
新制备的万古霉素滴眼液清澈、无色且无颗粒。10和50mg/mL溶液的pH值读数分别为7.03和6.28。两种溶液的渗透压均在300 - 330mOsmol/kg范围内,被认为是等渗的。所有样品的初始药物浓度经HPLC确认在标签标示值的100% - 103%范围内。在整个稳定性研究期间,任何样品的外观、pH值或渗透压均无显著变化。HPLC结果还证实,所有稳定性样品中的药物浓度在初始零时间值的98% - 101%范围内,未观察到显著的降解产物峰。
开发了一种新的复方万古霉素滴眼液制剂以缓解载体采购问题。这种滴眼液制剂易于制备,在眼科应用中表现出令人满意的性质,并且在冷冻室中储存14天,随后在冷藏室中储存28天时,在化学和物理性质上保持稳定。