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将分析程序整合到集中抗胚细胞化合物制备单位的常规操作中以实现残余复合药物的增值。

Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded Drugs.

作者信息

Aquino Rita Patrizia, Falcone Giovanni, Russo Paola, Dal Piaz Fabrizio, Auriemma Giulia, de Francesco Ferdinando Maria, Cascone Stefania, Nava Eduardo, Del Gaudio Pasquale

机构信息

Department of Pharmacy, University of Salerno, 84084 Fisciano, Italy.

Department of Medicine, Surgery and Dentistry, University of Salerno, 84084 Fisciano, Italy.

出版信息

Pharmaceutics. 2025 Jan 14;17(1):101. doi: 10.3390/pharmaceutics17010101.

Abstract

BACKGROUND/OBJECTIVES: Although extemporaneous formulations of anticancer drug products for personalized therapy are produced according to Good Hospital Pharmacy Manufacturing Practice, the lack of knowledge about drug stability under clinical conditions limits the second-time use of these highly costly medications in clinical practice. Therefore, the residual compounded drugs are considered waste and a cost item that negatively affects the healthcare system. In the context of the ever-increasing interest of the health system in applying practices in line with personalized medicine and spending review policies, this research aimed to demonstrate the feasibility of incorporating analytical techniques into daily routine practice. Specifically, the present research focused on fast stability analysis of Active Pharmaceutical Ingredients (APIs) in antiblastic residual compounded drugs with the purpose of demonstrating their potentialities as a resource for possible second-time use.

METHODS

Two different subsets of drug products were analyzed, i.e., medicines containing small molecules and medicines containing monoclonal antibodies. In relation to their different physicochemical properties, two analytical approaches were optimized and involved in the stability investigation: HPLC-DAD for small molecules and a combined approach of LC-MS/MS with size exclusion chromatography for monoclonal antibodies analysis.

RESULTS

Results underlined that the stability data, as available in the summary of product characteristics related to each medicine, do not completely describe the physicochemical shelf-life of anticancer compounded drugs.

CONCLUSIONS

In fact, for all tested products, our results suggested a longer shelf-life in comparison to the datasheet, giving hospital pharmacists the possibility to extend the clinical use of compounded drugs, improving the cost-benefit of anticancer personalized therapy.

摘要

背景/目的:尽管用于个性化治疗的抗癌药品临时制剂是按照良好医院药房生产规范生产的,但缺乏临床条件下药物稳定性的相关知识限制了这些高成本药物在临床实践中的二次使用。因此,剩余的配制药物被视为废物以及对医疗系统产生负面影响的成本项目。在卫生系统对符合个性化医疗和费用审查政策的实践应用兴趣日益增加的背景下,本研究旨在证明将分析技术纳入日常常规实践的可行性。具体而言,本研究聚焦于抗瘤残留配制药物中活性药物成分(API)的快速稳定性分析,目的是证明其作为可能二次使用资源的潜力。

方法

分析了两个不同的药品子集,即含有小分子的药物和含有单克隆抗体的药物。针对其不同的物理化学性质,优化了两种分析方法并将其用于稳定性研究:用于小分子的高效液相色谱-二极管阵列检测法(HPLC-DAD)以及用于单克隆抗体分析的液相色谱-串联质谱联用(LC-MS/MS)与尺寸排阻色谱相结合的方法。

结果

结果强调,与每种药物相关的产品特性摘要中提供的稳定性数据并未完全描述抗癌配制药物的物理化学保质期。

结论

事实上,对于所有测试产品,我们的结果表明其保质期比数据表中的更长,这使医院药剂师有可能延长配制药物的临床使用时间,提高抗癌个性化治疗的成本效益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a58/11769000/3711e218a707/pharmaceutics-17-00101-g001.jpg

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