Nirajan Adhikari , Evgeniia Vorozhbit , Petr Kazarin , Gayathri Shivkumar , Darryl Drake , Jie Wang , Mrinal Shah , Sherwin Shang , Alina A. Alexeenko
{"title":"生物原料药冷冻和解冻的冷冻浓缩模型和实验测量。","authors":"Nirajan Adhikari , Evgeniia Vorozhbit , Petr Kazarin , Gayathri Shivkumar , Darryl Drake , Jie Wang , Mrinal Shah , Sherwin Shang , Alina A. Alexeenko","doi":"10.1016/j.ejpb.2025.114812","DOIUrl":null,"url":null,"abstract":"<div><div>The freezing and thawing process is a key determinant of the cryoconcentration distribution in pharmaceutical and biological bulk drug substances (BDS), which has a direct and inevitable impact on protein stability. Due to the critical influence of cryoconcentration — either stabilizing or destabilizing the protein depending on its distribution — understanding the specific mechanisms and changes occurring during freezing and thawing is essential for ensuring the stability of the BDS and, by extension, the drug product (DP). This work presents computational modeling of protein cryoconcentration induced by freezing and thawing in a two-liter plastic container. The study utilized fixed-grid modeling with a species segregation model to investigate freezing and thawing dynamics that lead to a shift in protein concentration distribution inside the container, simulating typical processing for pharmaceutical bulk drug substance. The model incorporates a partition coefficient to represent protein distribution between the BDS solution phase and the frozen ice phase. The solute (such as protein) partitioning during ice formation and gravity settlement of protein-rich liquid from the ice–liquid interface towards the bottom of a container creates cryoconcentration during freezing in an ultra-low temperature freezer. Simulations of previously frozen solution subjected to water-bath thawing at <span><math><mrow><mo>+</mo><mn>23</mn><mspace></mspace><mo>°</mo><mi>C</mi></mrow></math></span> showed a further increase of protein concentration at the bottom of the container due to the inability of the free convective currents set up during the thawing process to overcome the density based segregation. The modeling results were consistent with experimental measurements of freezing and thawing of Human serum albumin solution at 60 mg/mL in 2 L bottles, showing promise for the utilization of computational techniques to design process and equipment that reduces protein cryoconcentration and segregation gradients during freeze–thaw operation improving pharmaceutical manufacturing and product quality.</div></div>","PeriodicalId":12024,"journal":{"name":"European Journal of Pharmaceutics and Biopharmaceutics","volume":"215 ","pages":"Article 114812"},"PeriodicalIF":4.3000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cryoconcentration modeling and experimental measurements for freezing and thawing of a biologic bulk drug substance\",\"authors\":\"Nirajan Adhikari , Evgeniia Vorozhbit , Petr Kazarin , Gayathri Shivkumar , Darryl Drake , Jie Wang , Mrinal Shah , Sherwin Shang , Alina A. Alexeenko\",\"doi\":\"10.1016/j.ejpb.2025.114812\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The freezing and thawing process is a key determinant of the cryoconcentration distribution in pharmaceutical and biological bulk drug substances (BDS), which has a direct and inevitable impact on protein stability. Due to the critical influence of cryoconcentration — either stabilizing or destabilizing the protein depending on its distribution — understanding the specific mechanisms and changes occurring during freezing and thawing is essential for ensuring the stability of the BDS and, by extension, the drug product (DP). This work presents computational modeling of protein cryoconcentration induced by freezing and thawing in a two-liter plastic container. The study utilized fixed-grid modeling with a species segregation model to investigate freezing and thawing dynamics that lead to a shift in protein concentration distribution inside the container, simulating typical processing for pharmaceutical bulk drug substance. The model incorporates a partition coefficient to represent protein distribution between the BDS solution phase and the frozen ice phase. The solute (such as protein) partitioning during ice formation and gravity settlement of protein-rich liquid from the ice–liquid interface towards the bottom of a container creates cryoconcentration during freezing in an ultra-low temperature freezer. Simulations of previously frozen solution subjected to water-bath thawing at <span><math><mrow><mo>+</mo><mn>23</mn><mspace></mspace><mo>°</mo><mi>C</mi></mrow></math></span> showed a further increase of protein concentration at the bottom of the container due to the inability of the free convective currents set up during the thawing process to overcome the density based segregation. The modeling results were consistent with experimental measurements of freezing and thawing of Human serum albumin solution at 60 mg/mL in 2 L bottles, showing promise for the utilization of computational techniques to design process and equipment that reduces protein cryoconcentration and segregation gradients during freeze–thaw operation improving pharmaceutical manufacturing and product quality.</div></div>\",\"PeriodicalId\":12024,\"journal\":{\"name\":\"European Journal of Pharmaceutics and Biopharmaceutics\",\"volume\":\"215 \",\"pages\":\"Article 114812\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Pharmaceutics and Biopharmaceutics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0939641125001894\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmaceutics and Biopharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0939641125001894","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Cryoconcentration modeling and experimental measurements for freezing and thawing of a biologic bulk drug substance
The freezing and thawing process is a key determinant of the cryoconcentration distribution in pharmaceutical and biological bulk drug substances (BDS), which has a direct and inevitable impact on protein stability. Due to the critical influence of cryoconcentration — either stabilizing or destabilizing the protein depending on its distribution — understanding the specific mechanisms and changes occurring during freezing and thawing is essential for ensuring the stability of the BDS and, by extension, the drug product (DP). This work presents computational modeling of protein cryoconcentration induced by freezing and thawing in a two-liter plastic container. The study utilized fixed-grid modeling with a species segregation model to investigate freezing and thawing dynamics that lead to a shift in protein concentration distribution inside the container, simulating typical processing for pharmaceutical bulk drug substance. The model incorporates a partition coefficient to represent protein distribution between the BDS solution phase and the frozen ice phase. The solute (such as protein) partitioning during ice formation and gravity settlement of protein-rich liquid from the ice–liquid interface towards the bottom of a container creates cryoconcentration during freezing in an ultra-low temperature freezer. Simulations of previously frozen solution subjected to water-bath thawing at showed a further increase of protein concentration at the bottom of the container due to the inability of the free convective currents set up during the thawing process to overcome the density based segregation. The modeling results were consistent with experimental measurements of freezing and thawing of Human serum albumin solution at 60 mg/mL in 2 L bottles, showing promise for the utilization of computational techniques to design process and equipment that reduces protein cryoconcentration and segregation gradients during freeze–thaw operation improving pharmaceutical manufacturing and product quality.
期刊介绍:
The European Journal of Pharmaceutics and Biopharmaceutics provides a medium for the publication of novel, innovative and hypothesis-driven research from the areas of Pharmaceutics and Biopharmaceutics.
Topics covered include for example:
Design and development of drug delivery systems for pharmaceuticals and biopharmaceuticals (small molecules, proteins, nucleic acids)
Aspects of manufacturing process design
Biomedical aspects of drug product design
Strategies and formulations for controlled drug transport across biological barriers
Physicochemical aspects of drug product development
Novel excipients for drug product design
Drug delivery and controlled release systems for systemic and local applications
Nanomaterials for therapeutic and diagnostic purposes
Advanced therapy medicinal products
Medical devices supporting a distinct pharmacological effect.