{"title":"透射低频拉曼光谱法定量模塑片中药物含量","authors":"Motoki Inoue, Tatsuya Akiyama, Toshiro Fukami","doi":"10.1039/d5an00079c","DOIUrl":null,"url":null,"abstract":"Orally disintegrating tablets (ODTs) are useful for elderly and pediatric patients suffering from difficulty in swallowing conventional tablets. Among various ODT preparing processes, wet tableting involves a process of the low-pressure compression of wet granules followed by drying, which is promising for the industrial production of medicines. Currently, the quality of wet molded tablets is analyzed via conventional high-performance liquid chromatography–based content uniformity tests. However, owing to the low compression pressure required the wet tableting process, integrating spectroscopic probes with the tableting process can be a potential technique for real-time quality assurance. This study explores the use of transmission low-frequency Raman spectroscopy as a nondestructive and efficient approach for quantifying active pharmaceutical ingredients (APIs) in molded tablets. Acetaminophen and D-mannitol were used as the model API and excipient, respectively. Tablets were prepared by compressing under 150 and 300 N followed by analysis using the partial least square regression method. The distinct spectral features of acetaminophen and D-mannitol enabled accurate quantification with good linear correlations (R2 = 0.98) and low root mean square prediction errors (1.59 for 150 N; 1.22 for 300 N). The method was effective under compressed forces, highlighting it as a real-time, nondestructive tool for quality control in pharmaceutical manufacturing. This approach aligns with continuous manufacturing and quality by design.","PeriodicalId":63,"journal":{"name":"Analyst","volume":"11 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quantification of drug contents in molded tablet using transmission low-frequency Raman spectroscopy\",\"authors\":\"Motoki Inoue, Tatsuya Akiyama, Toshiro Fukami\",\"doi\":\"10.1039/d5an00079c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Orally disintegrating tablets (ODTs) are useful for elderly and pediatric patients suffering from difficulty in swallowing conventional tablets. Among various ODT preparing processes, wet tableting involves a process of the low-pressure compression of wet granules followed by drying, which is promising for the industrial production of medicines. Currently, the quality of wet molded tablets is analyzed via conventional high-performance liquid chromatography–based content uniformity tests. However, owing to the low compression pressure required the wet tableting process, integrating spectroscopic probes with the tableting process can be a potential technique for real-time quality assurance. This study explores the use of transmission low-frequency Raman spectroscopy as a nondestructive and efficient approach for quantifying active pharmaceutical ingredients (APIs) in molded tablets. Acetaminophen and D-mannitol were used as the model API and excipient, respectively. Tablets were prepared by compressing under 150 and 300 N followed by analysis using the partial least square regression method. The distinct spectral features of acetaminophen and D-mannitol enabled accurate quantification with good linear correlations (R2 = 0.98) and low root mean square prediction errors (1.59 for 150 N; 1.22 for 300 N). The method was effective under compressed forces, highlighting it as a real-time, nondestructive tool for quality control in pharmaceutical manufacturing. This approach aligns with continuous manufacturing and quality by design.\",\"PeriodicalId\":63,\"journal\":{\"name\":\"Analyst\",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-05-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analyst\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5an00079c\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analyst","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5an00079c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Quantification of drug contents in molded tablet using transmission low-frequency Raman spectroscopy
Orally disintegrating tablets (ODTs) are useful for elderly and pediatric patients suffering from difficulty in swallowing conventional tablets. Among various ODT preparing processes, wet tableting involves a process of the low-pressure compression of wet granules followed by drying, which is promising for the industrial production of medicines. Currently, the quality of wet molded tablets is analyzed via conventional high-performance liquid chromatography–based content uniformity tests. However, owing to the low compression pressure required the wet tableting process, integrating spectroscopic probes with the tableting process can be a potential technique for real-time quality assurance. This study explores the use of transmission low-frequency Raman spectroscopy as a nondestructive and efficient approach for quantifying active pharmaceutical ingredients (APIs) in molded tablets. Acetaminophen and D-mannitol were used as the model API and excipient, respectively. Tablets were prepared by compressing under 150 and 300 N followed by analysis using the partial least square regression method. The distinct spectral features of acetaminophen and D-mannitol enabled accurate quantification with good linear correlations (R2 = 0.98) and low root mean square prediction errors (1.59 for 150 N; 1.22 for 300 N). The method was effective under compressed forces, highlighting it as a real-time, nondestructive tool for quality control in pharmaceutical manufacturing. This approach aligns with continuous manufacturing and quality by design.