کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2083445 1545336 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Use of a continuous twin screw granulation and drying system during formulation development and process optimization
ترجمه فارسی عنوان
استفاده از سیستم گرانولاسیون دوقلو و سیستم خشک کردن در طول توسعه فرمولاسیون و بهینه سازی فرآیند
کلمات کلیدی
گرانولاتور دوقلو مداوم و خشک کردن، روند روند، تکرارپذیری، کیفیت قرص و قرص، توسعه فرمولاسیون، بهینه سازی فرآیند
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوتکنولوژی یا زیست‌فناوری
چکیده انگلیسی


• Deviating quality attributes were obtained during the first 30 min of the 1 h run.
• No deviating granule and tablet quality was observed during the shutdown phase.
• Processing of material in a single cell was repeatable.
• Materials processed in a single cell were predictive for full-scale manufacturing.
• Tablet quality from ConsiGma™-1 system was predictive for ConsiGma™-25 system.

Since small scale is key for successful introduction of continuous techniques in the pharmaceutical industry to allow its use during formulation development and process optimization, it is essential to determine whether the product quality is similar when small quantities of materials are processed compared to the continuous processing of larger quantities. Therefore, the aim of this study was to investigate whether material processed in a single cell of the six-segmented fluid bed dryer of the ConsiGma™-25 system (a continuous twin screw granulation and drying system introduced by GEA Pharma Systems, Collette™, Wommelgem, Belgium) is predictive of granule and tablet quality during full-scale manufacturing when all drying cells are filled. Furthermore, the performance of the ConsiGma™-1 system (a mobile laboratory unit) was evaluated and compared to the ConsiGma™-25 system.A premix of two active ingredients, powdered cellulose, maize starch, pregelatinized starch and sodium starch glycolate was granulated with distilled water. After drying and milling (1000 μm, 800 rpm), granules were blended with magnesium stearate and compressed using a Modul™ P tablet press (tablet weight: 430 mg, main compression force: 12 kN). Single cell experiments using the ConsiGma™-25 system and ConsiGma™-1 system were performed in triplicate. Additionally, a 1 h continuous run using the ConsiGma™-25 system was executed. Process outcomes (torque, barrel wall temperature, product temperature during drying) and granule (residual moisture content, particle size distribution, bulk and tapped density, hausner ratio, friability) as well as tablet (hardness, friability, disintegration time and dissolution) quality attributes were evaluated.By performing a 1 h continuous run, it was detected that a stabilization period was needed for torque and barrel wall temperature due to initial layering of the screws and the screw chamber walls with material. Consequently, slightly deviating granule and tablet quality attributes were obtained during the start-up phase of the 1 h run. For the single cell runs, granule and tablet properties were comparable with results obtained during the second part of the 1 h run (after start-up). Although deviating granule quality (particle size distribution and Hausner ratio) was observed due to the divergent design of the ConsiGma™-1 unit and the ConsiGma™-25 system (horizontal set-up) used in this study, tablet quality produced from granules processed with the ConsiGma™-1 system was predictive for tablet quality obtained during continuous production using the ConsiGma™-25 system.

Figure optionsDownload high-quality image (125 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Pharmaceutics and Biopharmaceutics - Volume 89, January 2015, Pages 239–247
نویسندگان
, , , , , , , , ,