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Effect of formulation and process variables on lipid based sustained release tablets via continuous twin screw granulation: A comparative study

机译:连续双螺杆制粒对脂质基缓释片的制剂和工艺变量的影响:对比研究

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摘要

The current study’s aim is to prepare lipid based sustained release tablets via a twin-screw granulation technique and compare those dosage forms with conventional techniques, namely wet granulation and direct compression. The granules were successfully manufactured in a single-step, continuous twin-screw granulation process with a low proportion of binder (Klucel™ EF, HPC SSL) using Compritol® 888 ATO, Precirol® ATO 5 and Geleol™ as sustained release agents. The granules prepared showed good flow characteristics and compaction properties. DSC and XRD studies were conducted to characterize the granules prepared via a twin-screw granulation method and the results demonstrated the crystalline nature of lipids within the granules. FTIR data indicated that there were no interactions with the formulation components investigated. The formulations developed by all three methods were compressed into tablets with a mechanical strength of 14–16 KP. The tablets formulated were characterized for physicochemical properties, in vitro drug release studies, water uptake and erosion studies. These results showed that the drug was not completely released after 24h for tablets developed by the wet granulation process using all three lipids. The tablets prepared by the direct compression method demonstrated a burst release within 8 to 10h from Precirol ATO 5® and Geleol™ formulations compared to Compritol® 888 ATO. However, tablets prepared using twin-screw granulation exhibited sustained release of the drug over 24h and the water uptake and erosion results were in accordance with dissolution data. Stability data for 45 days at accelerated conditions (40 °C/75% RH) showed similar release profiles with f2 values above 50 for all of the twin screw granulation formulations, indicating the suitability of the process for formulating sustained release tablets. These findings of a single-step, continuous twin-screw granulation process are novel and demonstrate new opportunities for development of sustained release tablets.
机译:目前的研究目的是通过双螺杆造粒技术制备脂质基缓释片剂,并将这些剂型与常规技术(即湿法制粒和直接压片)进行比较。使用Compritol®888 ATO,Precirol®ATO 5和Geleol™作为缓释剂,以低比例的粘合剂(Klucel™EF,HPC SSL)通过一步,连续双螺杆制粒工艺成功制备了颗粒。制备的颗粒显示出良好的流动特性和压实性能。进行DSC和XRD研究以表征通过双螺杆造粒方法制备的颗粒,并且结果证明了颗粒内脂质的结晶性质。 FTIR数据表明与所研究的配方成分没有相互作用。通过这三种方法开发的制剂被压制成片剂,机械强度为14-16 KP。对所配制的片剂进行理化性质,体外药物释放研究,吸水率和侵蚀研究的特征。这些结果表明,对于使用这三种脂质的湿法制粒工艺开发的片剂,在24小时后药物并未完全释放。与888 ATO相比,通过直接压片法制备的片剂在8至10小时内即可从Precirol ATO5®和Geleol™制剂中爆发释放。然而,使用双螺杆制粒制备的片剂在24小时内显示出药物的持续释放,并且吸水率和侵蚀率结果与溶出度数据一致。在加速条件下(40°C / 75%RH)45天的稳定性数据显示,所有双螺杆造粒制剂的f2值均大于50,f2值相似,释放曲线相似,表明该制剂适合制备缓释片剂。单步连续双螺杆制粒过程的这些发现是新颖的,并证明了开发缓释片剂的新机会。

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