Zoltán Sávoly , Enikő Szilágyi , Dóra Kozák , Viktor Vásárhelyi , Hajnalka Szabados
{"title":"蛋白质样品中聚二烯基二甲基氯化铵测定方法的建立及其在单克隆抗体生产下游技术发展中的作用","authors":"Zoltán Sávoly , Enikő Szilágyi , Dóra Kozák , Viktor Vásárhelyi , Hajnalka Szabados","doi":"10.1016/j.jpba.2025.117113","DOIUrl":null,"url":null,"abstract":"<div><div>Poly(diallyldimethylammonium chloride) (pDADMAC) is a cationic polyelectrolyte bearing one positive charge per monomer unit. This structure enables its application as flocculating agent. It can be used in the downstream processing of biological drug production. Due to its potential toxicity, its concentration in the drug substance should be reduced to a sufficiently low level, which is realized by chromatographic steps of downstream processing. To prove proper clearance, appropriate analytical method should be developed, which should be able to measure low pDADMAC concentration in matrices with high protein content. It is a challenge due to the size and composition of pDADMAC. Its molar weight (∼300 kDa) is commensurable with that of mAbs (∼150 kDa) or rather their dimers. It hampers the applicability of size-exclusion chromatography. For reversed-phase HPLC the protein content of the samples should be removed, which is especially challenging due to electrostatic interaction between protein and the pDADMAC analyte. The development and qualification of an RP-HPLC method is presented in this study. The protein removal is realized by precipitation using ammonium sulfate, which is a quick and simple method. The method was found to be able to measure pDADMAC concentration accurately and precisely in samples with up to 85 g/L protein concentration.</div></div>","PeriodicalId":16685,"journal":{"name":"Journal of pharmaceutical and biomedical analysis","volume":"268 ","pages":"Article 117113"},"PeriodicalIF":3.1000,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Method development for poly(diallyldimethylammonium chloride) determination in proteinaceous samples and its role in downstream technology development of monoclonal antibody production\",\"authors\":\"Zoltán Sávoly , Enikő Szilágyi , Dóra Kozák , Viktor Vásárhelyi , Hajnalka Szabados\",\"doi\":\"10.1016/j.jpba.2025.117113\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Poly(diallyldimethylammonium chloride) (pDADMAC) is a cationic polyelectrolyte bearing one positive charge per monomer unit. This structure enables its application as flocculating agent. It can be used in the downstream processing of biological drug production. Due to its potential toxicity, its concentration in the drug substance should be reduced to a sufficiently low level, which is realized by chromatographic steps of downstream processing. To prove proper clearance, appropriate analytical method should be developed, which should be able to measure low pDADMAC concentration in matrices with high protein content. It is a challenge due to the size and composition of pDADMAC. Its molar weight (∼300 kDa) is commensurable with that of mAbs (∼150 kDa) or rather their dimers. It hampers the applicability of size-exclusion chromatography. For reversed-phase HPLC the protein content of the samples should be removed, which is especially challenging due to electrostatic interaction between protein and the pDADMAC analyte. The development and qualification of an RP-HPLC method is presented in this study. The protein removal is realized by precipitation using ammonium sulfate, which is a quick and simple method. The method was found to be able to measure pDADMAC concentration accurately and precisely in samples with up to 85 g/L protein concentration.</div></div>\",\"PeriodicalId\":16685,\"journal\":{\"name\":\"Journal of pharmaceutical and biomedical analysis\",\"volume\":\"268 \",\"pages\":\"Article 117113\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-08-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pharmaceutical and biomedical analysis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0731708525004546\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmaceutical and biomedical analysis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0731708525004546","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Method development for poly(diallyldimethylammonium chloride) determination in proteinaceous samples and its role in downstream technology development of monoclonal antibody production
Poly(diallyldimethylammonium chloride) (pDADMAC) is a cationic polyelectrolyte bearing one positive charge per monomer unit. This structure enables its application as flocculating agent. It can be used in the downstream processing of biological drug production. Due to its potential toxicity, its concentration in the drug substance should be reduced to a sufficiently low level, which is realized by chromatographic steps of downstream processing. To prove proper clearance, appropriate analytical method should be developed, which should be able to measure low pDADMAC concentration in matrices with high protein content. It is a challenge due to the size and composition of pDADMAC. Its molar weight (∼300 kDa) is commensurable with that of mAbs (∼150 kDa) or rather their dimers. It hampers the applicability of size-exclusion chromatography. For reversed-phase HPLC the protein content of the samples should be removed, which is especially challenging due to electrostatic interaction between protein and the pDADMAC analyte. The development and qualification of an RP-HPLC method is presented in this study. The protein removal is realized by precipitation using ammonium sulfate, which is a quick and simple method. The method was found to be able to measure pDADMAC concentration accurately and precisely in samples with up to 85 g/L protein concentration.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.