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迷你压片转移和放大的挑战:以氯沙坦钾为例的案例研究。

Challenges in the transfer and scale-up of mini-tableting: Case study with losartan potassium.

机构信息

Institute of Pharmaceutics and Biopharmaceutics, Heinrich Heine University, Universitätsstr. 1, 40225 Düsseldorf, Germany.

Institute of Pharmaceutics and Biopharmaceutics, Heinrich Heine University, Universitätsstr. 1, 40225 Düsseldorf, Germany.

出版信息

Eur J Pharm Biopharm. 2023 Nov;192:161-173. doi: 10.1016/j.ejpb.2023.10.001. Epub 2023 Oct 9.

Abstract

Mini-tablets (MTs) with losartan potassium were developed to treat the rare disease Epidermolysis Bullosa. The focus was placed on transfer and scale-up of a direct compressible formulation from the compaction simulator STYL'One Evo (CS) to the rotary tablet press Korsch XM 12 (RP). Transfer of tabletability and compactibility profiles from CS to RP did not show good agreement, e.g. at a tableting pressure of 125 MPa mean tensile strengths (TS) of 4 MPa on CS and 1-1.5 MPa on RP were reached. These results highlight the impact of the feed frame on final product qualities depending on process and material factors. In the scale-up studies the critical quality attributes (CQAs) mass variation, content uniformity, TS and disintegration time were investigated. After an appropriate run-up time, most CQAs reached a plateau, after reaching a balance between influx, efflux and distribution of lubricant in the feed frame. TS values of 1-2 MPa, disintegration times of max. 50 s, mass variation of 0.9-2.2 % (CV) and acceptance values below 15.0 were reached depending on chosen process parameters.

摘要

开发了载有氯沙坦钾的迷你片剂(MT)以治疗罕见疾病——大疱性表皮松解症。重点是将一种直接可压缩的配方从 compaction simulator STYL'One Evo(CS)转移并放大到旋转压片机 Korsch XM 12(RP)。从 CS 到 RP 的片剂可压性和可压缩性曲线的转移没有很好地一致,例如在 125 MPa 的压片压力下,CS 的平均拉伸强度(TS)为 4 MPa,而 RP 为 1-1.5 MPa。这些结果强调了进料器对最终产品质量的影响,具体取决于工艺和材料因素。在放大研究中,考察了关键质量属性(CQAs)的质量变化、含量均匀性、TS 和崩解时间。经过适当的运行时间后,大多数 CQAs 达到了一个平台,这是在进料器中润滑剂的流入、流出和分布之间达到平衡之后实现的。根据所选的工艺参数,达到了 1-2 MPa 的 TS 值、最大 50 s 的崩解时间、0.9-2.2%(CV)的质量变化和低于 15.0 的接受值。

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