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

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 co...

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Main Authors: Rita Patrizia Aquino, Giovanni Falcone, Paola Russo, Fabrizio Dal Piaz, Giulia Auriemma, Ferdinando Maria de Francesco, Stefania Cascone, Eduardo Nava, Pasquale Del Gaudio
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Pharmaceutics
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Online Access:https://www.mdpi.com/1999-4923/17/1/101
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author Rita Patrizia Aquino
Giovanni Falcone
Paola Russo
Fabrizio Dal Piaz
Giulia Auriemma
Ferdinando Maria de Francesco
Stefania Cascone
Eduardo Nava
Pasquale Del Gaudio
author_facet Rita Patrizia Aquino
Giovanni Falcone
Paola Russo
Fabrizio Dal Piaz
Giulia Auriemma
Ferdinando Maria de Francesco
Stefania Cascone
Eduardo Nava
Pasquale Del Gaudio
author_sort Rita Patrizia Aquino
collection DOAJ
description 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.
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spelling doaj-art-9afccd507a3a4ab8bf087b80756d9aba2025-01-24T13:45:57ZengMDPI AGPharmaceutics1999-49232025-01-0117110110.3390/pharmaceutics17010101Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded DrugsRita Patrizia Aquino0Giovanni Falcone1Paola Russo2Fabrizio Dal Piaz3Giulia Auriemma4Ferdinando Maria de Francesco5Stefania Cascone6Eduardo Nava7Pasquale Del Gaudio8Department of Pharmacy, University of Salerno, 84084 Fisciano, ItalyDepartment of Pharmacy, University of Salerno, 84084 Fisciano, ItalyDepartment of Pharmacy, University of Salerno, 84084 Fisciano, ItalyDepartment of Medicine, Surgery and Dentistry, University of Salerno, 84084 Fisciano, ItalyDepartment of Pharmacy, University of Salerno, 84084 Fisciano, ItalyPharmaceutical Department, Local Health Authority Naples 3 South, 80059 Torre Del Greco, ItalyPharmaceutical Department, Local Health Authority Naples 3 South, 80059 Torre Del Greco, ItalyPharmaceutical Department, Local Health Authority Naples 3 South, 80059 Torre Del Greco, ItalyDepartment of Pharmacy, University of Salerno, 84084 Fisciano, ItalyBackground/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.https://www.mdpi.com/1999-4923/17/1/101personalized medicineanticancer medicineshospital compounded drugsphysicochemical stability investigation
spellingShingle Rita Patrizia Aquino
Giovanni Falcone
Paola Russo
Fabrizio Dal Piaz
Giulia Auriemma
Ferdinando Maria de Francesco
Stefania Cascone
Eduardo Nava
Pasquale Del Gaudio
Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded Drugs
Pharmaceutics
personalized medicine
anticancer medicines
hospital compounded drugs
physicochemical stability investigation
title Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded Drugs
title_full Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded Drugs
title_fullStr Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded Drugs
title_full_unstemmed Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded Drugs
title_short Integrating Analytical Procedures in Routine Practices of Centralized Antiblastic Compounding Units for Valorization of Residual Compounded Drugs
title_sort integrating analytical procedures in routine practices of centralized antiblastic compounding units for valorization of residual compounded drugs
topic personalized medicine
anticancer medicines
hospital compounded drugs
physicochemical stability investigation
url https://www.mdpi.com/1999-4923/17/1/101
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