Department of Chemical Engineering, University of Chemistry and Technology, Technická 5, 166 28, Prague 6, Czech Republic.
Zentiva, k.s, U Kabelovny 130, 102 00, Prague 10, Czech Republic.
AAPS PharmSciTech. 2019 Jan 2;20(1):25. doi: 10.1208/s12249-018-1224-8.
The manufacture of personalised medicines where specific combinations of active pharmaceutical ingredients (APIs) and their dose within a tablet would be adjusted to the needs of individual patients, would require new manufacturing approaches compared to the established practice. In the case of low-dose formulations, the required precision of API content might not be achievable by traditional unit operations such as solid powder blending. The aim of the present work was to explore an alternative approach, based on the concept of pre-formulated placebo tablets containing mesoporous silica particles capable of absorbing APIs in the form of solutions, which can be precisely dosed at arbitrarily low quantities. The precision of the liquid dosing system has been validated; it was shown that the mechanical properties of the tablets were satisfactory even after multiple impregnation-drying cycles and that pharmacopoeia specifications on content uniformity could be met. Using model APIs, the spatial distribution of the API within the tablet after impregnation was investigated and shown to depend on the number and order of the impregnation-drying cycles. It was found that when an API was loaded to the tablet in a single step, a different dissolution profile was obtained compared to the same quantity dosed in multiple smaller steps. Overall, the approach of loading multiple API to a pre-formulated tablet at defined quantities using drop-on-demand liquid dosing was found to be feasible from the dose uniformity point of view. Further research should focus on potential API interactions and storage stability of tablets manufactured in this way.
个性化药物的制造,其中特定组合的活性药物成分 (APIs) 和片剂中的剂量将根据个体患者的需求进行调整,与既定的实践相比,需要新的制造方法。对于低剂量制剂,传统的单元操作(如固体粉末混合)可能无法实现 API 含量所需的精度。本工作的目的是探索一种替代方法,该方法基于含有介孔硅颗粒的预成型安慰剂片剂的概念,这些颗粒能够以溶液的形式吸收 API,可以精确地以任意低的量进行剂量。已经验证了液体计量系统的精度;结果表明,即使经过多次浸渍-干燥循环,片剂的机械性能也令人满意,并且可以满足药典关于含量均匀性的规定。使用模型 APIs ,研究了浸渍后 API 在片剂中的空间分布,结果表明其分布取决于浸渍-干燥循环的次数和顺序。结果发现,当 API 以单次加载到片剂中时,与以多个较小剂量给药相同数量的 API 相比,获得了不同的溶解曲线。总体而言,从剂量均匀性的角度来看,使用按需滴注的液体计量将多种 API 以定义的量加载到预成型片剂中的方法是可行的。进一步的研究应集中在以这种方式制造的片剂的潜在 API 相互作用和储存稳定性上。