LAPSE:2025.0556
Published Article

LAPSE:2025.0556
Active Pharmaceutical Ingredients from Unused Solid Drugs
June 27, 2025
Abstract
The increased use of pharmaceuticals globally over the past two decades has contributed to an increase in unused pharmaceuticals and a corresponding surge in pharmaceutical waste. Thus, there is an impetus for the development of processes for the recovery of the active pharmaceutical ingredients (APIs) from these unused drugs. This study introduces a decision framework for solvent selection to enable the recovery of APIs using a general separation train where cooling crystallization is the final step. The framework is designed to base solvent selection not just on the solubilities of the formulation contents but also considers the overall recovery that can be achieved in the process. In addition, the environmental sustainability of the framework is analyzed using the process mass intensity metric (PMI). The effectiveness of this framework is demonstrated by using paracetamol (PA) as a model API in a formulation consisting of five of the excipients commonly found in PA formulations. The results show that selecting a solvent based on the dissolution of pharmaceutical tablets may not be the best possible approach, whereas choosing a solvent that maximizes the theoretical recovery is preferred.
The increased use of pharmaceuticals globally over the past two decades has contributed to an increase in unused pharmaceuticals and a corresponding surge in pharmaceutical waste. Thus, there is an impetus for the development of processes for the recovery of the active pharmaceutical ingredients (APIs) from these unused drugs. This study introduces a decision framework for solvent selection to enable the recovery of APIs using a general separation train where cooling crystallization is the final step. The framework is designed to base solvent selection not just on the solubilities of the formulation contents but also considers the overall recovery that can be achieved in the process. In addition, the environmental sustainability of the framework is analyzed using the process mass intensity metric (PMI). The effectiveness of this framework is demonstrated by using paracetamol (PA) as a model API in a formulation consisting of five of the excipients commonly found in PA formulations. The results show that selecting a solvent based on the dissolution of pharmaceutical tablets may not be the best possible approach, whereas choosing a solvent that maximizes the theoretical recovery is preferred.
Record ID
Keywords
API recovery, Process Design, Renewable and Sustainable Energy, Solvent Selection
Subject
Suggested Citation
Korde S, Menon A, Reklaitis GV, Nagy ZK. Active Pharmaceutical Ingredients from Unused Solid Drugs. Systems and Control Transactions 4:2516-2521 (2025) https://doi.org/10.69997/sct.174860
Author Affiliations
Korde S: Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, USA
Menon A: Agricultural & Biological Engineering, Purdue University, West Lafayette, IN, USA
Reklaitis GV: Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, USA
Nagy ZK: Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, USA
Menon A: Agricultural & Biological Engineering, Purdue University, West Lafayette, IN, USA
Reklaitis GV: Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, USA
Nagy ZK: Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, USA
Journal Name
Systems and Control Transactions
Volume
4
First Page
2516
Last Page
2521
Year
2025
Publication Date
2025-07-01
Version Comments
Original Submission
Other Meta
PII: 2516-2521-1277-SCT-4-2025, Publication Type: Journal Article
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LAPSE:2025.0556
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https://doi.org/10.69997/sct.174860
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[v1] (Original Submission)
Jun 27, 2025
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References Cited
- J. Natarajan, S. Altan, D. Raghavarao, Expiration Dating of Pharmaceutical Compounds in Relation to Analytical Variation, Degradation Rate, and Matrix Designs. Drug Inf. J. 31 589-595 (1997) https://doi.org/10.1177/009286159703100226
- R. C. Lyon, Stability profiles of drug products extended beyond labeled expiration dates. J. Pharm. Sci. 95 (2006) https://doi.org/10.1002/jps.20636
- J. Kim, O. De Jesus. http://www.ncbi.nlm.nih.gov/books/NBK568677/
- D. E. Pratama, W.-C. Hsieh, A. Elmaamoun, H. L. Lee, T. Lee, Recovery of Active Pharmaceutical Ingredients from Unused Solid Dosage-Form Drugs. ACS Omega 5 29147-29157 (2020) https://doi.org/10.1021/acsomega.0c03878
- A. T. Karunanithi, L. E. K. Achenie, R. Gani, A computer-aided molecular design framework for crystallization solvent design. Chem. Eng. Sci. 61 1247-1260 (2006) https://doi.org/10.1016/j.ces.2005.08.031
- S. K. Branch, Guidelines from the International Conference on Harmonisation (ICH). J. Pharm. Biomed. Anal. 38 798-805 (2005) https://doi.org/10.1016/j.jpba.2005.02.037
- S. Niazi, Handbook of Pharmaceutical Manufacturing Formulations. Boca Raton: CRC Press, 2004 https://doi.org/10.1201/9780203489581

