Thakore Samarth D, Reddy Katangur Vishruth, Dantuluri Ajay K, Patel Deepika, Kumawat Akshant, Sihorkar Vaibhav, Ghoroi Chinmay, Bansal Arvind K
Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Sector 67, S.A.S. Nagar, Mohali, Punjab, 160062, India.
Ashland (India) Pvt. Ltd., MN Park Synergy Square 3, Building No.2700, II Floor, Lalgadi Malakpet Village, Turkapally, Shamirpet, Hyderabad, Telangana, 500078, India.
Pharm Res. 2022 Dec;39(12):3241-3257. doi: 10.1007/s11095-022-03369-w. Epub 2022 Aug 25.
Pharmaceutical tablet manufacturing has seen a paradigm shift toward continuous manufacturing and twin-screw granulation-based technologies have catalyzed this shift. Twin-screw granulator can simultaneously perform unit operations like mixing, granulation, and drying of the granules. The present study investigates the impact of polymer concentration and processing parameters of twin-screw melt granulation, on flow properties and compaction characteristics of a model drug having high dose and poor tabletability. Acetaminophen (AAP) and polyvinylpyrrolidone vinyl acetate (PVPVA) were used as a model drug (90-95% w/w) and polymeric binder (5-10%w/w), respectively, for the current study. Feed rate (650-1150 g/h), extruder screw speed (150-300 rpm), and temperature (60-150°C) were used as processing variables. Results showed the reduction in particle size of drug in the extrudates (D of 15-25 μm from ~80 μm), irrespective of processing condition, while flow properties were a function of polymer concentration. Overall, good flowability of the products and their tablets with optimum tensile strength can be obtained through using high polymer concentration (i.e., 10% w/w), lower feed rate (650 g/h), lower extruder screw speed (150 rpm), and higher processing temperatures (up to 120°C). The findings from the current study can be useful for continuous manufacturing of tablets of high dose drugs with minimal excipient loading in the final dosage form.
药物片剂制造已朝着连续制造发生了范式转变,而基于双螺杆制粒的技术推动了这一转变。双螺杆制粒机可同时进行诸如混合、制粒以及颗粒干燥等单元操作。本研究考察了双螺杆熔融制粒的聚合物浓度和加工参数对一种高剂量且可压性差的模型药物的流动性和压片特性的影响。在本研究中,分别使用对乙酰氨基酚(AAP)和聚维酮醋酸乙烯酯(PVPVA)作为模型药物(90 - 95% w/w)和聚合物粘合剂(5 - 10% w/w)。进料速率(约650 - 1150 g/h)、挤出机螺杆转速(150 - 300 rpm)和温度(60 - 150°C)用作加工变量。结果表明,无论加工条件如何,挤出物中药物的粒径均减小(从约80μm减小至15 - 25μm),而流动性是聚合物浓度的函数。总体而言,通过使用高聚合物浓度(即10% w/w)、较低的进料速率(约650 g/h)、较低的挤出机螺杆转速(150 rpm)和较高的加工温度(高达120°C),可获得具有最佳拉伸强度的产品及其片剂的良好流动性。本研究的结果可用于最终剂型中辅料用量最少的高剂量药物片剂的连续制造。