{"title":"Evaluation of Process Parameters for Continuous Manufacturing of Quetiapine Fumarate Immediate Release Tablets Using Twin Screw Wet Granulation.","authors":"Tejaswini Naguboyina, Preethi Lakkala, Siva Ram Munnangi, Sateesh Kumar Vemula, Michael Repka","doi":"10.1007/s11095-025-03859-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Granulation is one of the important unit operations in the manufacturing of solid dosage forms like tablets and capsules that regulate the quality of end products. It is a process of particle enlargement by agglomeration technique, which improves flow properties, compressibility, reduction of dust formation, drug content uniformity, dissolution rates, and overall product stability. Traditionally, it has been a batch process due to a better understanding of the process. However, there has been a shift towards continuous manufacturing using a Twin-screw granulator, which is more robust, scalable, and versatile for a wide range of applications.</p><p><strong>Methods: </strong>This work presents the innovative use of Twin screw wet granulation (TSWG) in the development of Quetiapine fumarate (QTF) immediate release tablets. Various process parameters (Screw configuration, liquid-to-solid (L/S) ratios), and binders (HPC and PVP) were evaluated to determine their effect on granule quality. Further, the obtained granules were tested for particle size distribution and flow properties.</p><p><strong>Results: </strong>A higher percentage of uniform-sized granules were yielded with three mixing zones even with a lower liquid addition compared to that of one mixing zone with a higher liquid addition. These granules were further tableted and tested for their hardness, friability, disintegration, and dissolution. The tablets disintegrated and released the drug (~ 95%) rapidly within 5 min in 0.1 N HCl due to QTF's high solubility and porosity of granules.</p><p><strong>Conclusions: </strong>Overall, the understanding of process parameters and their influence on granule and tablet characteristics would help establish a more robust and continuous manufacturing of dosage forms.</p>","PeriodicalId":20027,"journal":{"name":"Pharmaceutical Research","volume":"42 4","pages":"685-696"},"PeriodicalIF":3.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12055873/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11095-025-03859-7","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: Granulation is one of the important unit operations in the manufacturing of solid dosage forms like tablets and capsules that regulate the quality of end products. It is a process of particle enlargement by agglomeration technique, which improves flow properties, compressibility, reduction of dust formation, drug content uniformity, dissolution rates, and overall product stability. Traditionally, it has been a batch process due to a better understanding of the process. However, there has been a shift towards continuous manufacturing using a Twin-screw granulator, which is more robust, scalable, and versatile for a wide range of applications.
Methods: This work presents the innovative use of Twin screw wet granulation (TSWG) in the development of Quetiapine fumarate (QTF) immediate release tablets. Various process parameters (Screw configuration, liquid-to-solid (L/S) ratios), and binders (HPC and PVP) were evaluated to determine their effect on granule quality. Further, the obtained granules were tested for particle size distribution and flow properties.
Results: A higher percentage of uniform-sized granules were yielded with three mixing zones even with a lower liquid addition compared to that of one mixing zone with a higher liquid addition. These granules were further tableted and tested for their hardness, friability, disintegration, and dissolution. The tablets disintegrated and released the drug (~ 95%) rapidly within 5 min in 0.1 N HCl due to QTF's high solubility and porosity of granules.
Conclusions: Overall, the understanding of process parameters and their influence on granule and tablet characteristics would help establish a more robust and continuous manufacturing of dosage forms.
目的:造粒是制造固体剂型(如片剂和胶囊)的重要单元操作之一,可调节最终产品的质量。它是一个通过团聚技术将颗粒放大的过程,可以改善流动性能、可压缩性、减少粉尘形成、药物含量均匀性、溶解速度和整体产品稳定性。传统上,由于对过程有了更好的理解,它一直是批处理过程。然而,已经转向使用双螺杆造粒机进行连续制造,这对于广泛的应用来说更加强大,可扩展和通用。方法:采用双螺杆湿法造粒技术研制富马酸喹硫平(QTF)速释片。评估了各种工艺参数(螺杆配置、液固比(L/S))和粘合剂(HPC和PVP),以确定它们对颗粒质量的影响。进一步,对得到的颗粒进行了粒度分布和流动性能测试。结果:三个混合区即使在较低的液体添加量下,也比一个混合区在较高的液体添加量下产生的均匀颗粒的百分比更高。将这些颗粒进一步压片并测试其硬度、脆性、崩解性和溶出度。由于QTF颗粒的高溶解度和孔隙度,在0.1 N HCl中,片剂在5 min内迅速崩解并释放药物(~ 95%)。结论:总体而言,了解工艺参数及其对颗粒和片剂特性的影响将有助于建立更稳健和连续的剂型生产。
期刊介绍:
Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to:
-(pre)formulation engineering and processing-
computational biopharmaceutics-
drug delivery and targeting-
molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)-
pharmacokinetics, pharmacodynamics and pharmacogenetics.
Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.