Substantiation of Production Technology of Tablets ‘AP-Helmin’

K. Semchenko, L. Vyshnevska, I. Gladukh
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Abstract

The aim. The purpose of this work is to substantiate the technology of “AP-helmin” tablets preparation and to establish the possible critical parameters of the production process.Materials and methods. Objects such as a mixture of pure substances albendazole and praziquantel in the ratio (1:4), tablet mass and tablet core samples were used in the research. The usual physicochemical and pharmacotechnological methods of the State Pharmacopoeia of Ukraine were used in the work, namely, the appearance, physical parameters, bulk density, compressibility, flowability, crushing force, determination of average mass, uniformity of mass, resistance to crushing and disintegration time were evaluated.Results. It was found that the mixture of active substances has poor flowability, indicating the need to enter the stage of wet granulation in the development of tablet technology with them.The wet granulation stage was carried out with the addition of such excipients as corn starch, microcrystalline cellulose 101 (MCC-101) and povidone (as a 10 % solution).Studies of the 4 samples of tablet mass allowed establishing the most rational composition for the formation of tablets-cores – sample number 4. The samples of composition No. 4 are white core tablets, homogeneous, without chips and cracks, and with respect to resistance to crushing and disintegration time meet the requirements of SPhU (96 N and 8 min 27 sec, respectively).The next stage of the study was the development of a common technology for the preparation of the tablets “AP-helmin”. In order to ensure proper consumer characteristics, the Opadry II ®YS-1-7027 White ("Colorcon") white coating was introduced.Conclusions. On the basis of the obtained results, a technological scheme of production was prepared taking into account the critical parameters and the forecasted control methods at different stages
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AP-Helmin片剂生产工艺的验证
的目标。本工作的目的是验证“AP-helmin”片剂的制备工艺,并确定可能的生产工艺关键参数。材料和方法。研究对象为阿苯达唑与吡喹酮按1:4比例混合的纯物质、片剂质量和片芯样品。采用乌克兰国家药典常用的物化药法,对其外观、物理参数、容重、可压缩性、流动性、破碎力、平均质量测定、质量均匀性、抗破碎性和崩解时间进行了评价。发现原料药混合后流动性较差,说明在片剂技术开发中需要进入湿造粒阶段。湿造粒阶段采用玉米淀粉、微晶纤维素101 (MCC-101)和聚维酮(10%溶液)等辅料进行。通过对4个片剂质量样品的研究,确定了片剂形成的最合理成分-岩心-样品号4。4号成分样品为白色芯片,均质,无碎裂,抗破碎性和崩解时间均满足SPhU要求(96 N, 8 min 27 sec)。研究的下一阶段是开发一种用于制备“AP-helmin”片剂的通用技术。为了确保适当的消费者特性,介绍了Opadry II®YS-1-7027白色(“Colorcon”)白色涂层。在此基础上,考虑关键参数和不同阶段的预测控制方法,制定了生产工艺方案
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