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基于速溶片的片剂配方与研发以及从实验室规模放大至生产规模

Formulation and development of tablets based on Ludipress and scale-up from laboratory to production scale.

作者信息

Heinz R, Wolf H, Schuchmann H, End L, Kolter K

机构信息

BASF Aktiengesellschaft, Ludwigshafen, Germany.

出版信息

Drug Dev Ind Pharm. 2000 May;26(5):513-21. doi: 10.1081/ddc-100101262.

Abstract

In spite of the wealth of experience available in the pharmaceutical industry, tablet formulations are still largely developed on an empirical basis, and the scale-up from laboratory to production is a time-consuming and costly process. Using Ludipress greatly simplifies formulation development and the manufacturing process because only the active ingredient Ludipress and a lubricant need to be mixed briefly before being compressed into tablets. The studies described here were designed to investigate the scale-up of Ludipress-based formulations from laboratory to production scale, and to predict changes in tablet properties due to changes in format, compaction pressure, and the use of different tablet presses. It was found that the tensile strength of tablets made of Ludipress increased linearly with compaction pressures up to 300 MPa. It was also independent of the geometry of the tablets (diameter, thickness, shape). It is therefore possible to give an equation with which the compaction pressure required to achieve a given hardness can be calculated for a given tablet form. The equation has to be modified slightly to convert from a single-punch press to a rotary tableting machine. Tablets produced in the rotary machine at the same pressure have a slightly higher tensile strength. The rate of increase in pressure, and therefore the throughput, has no effect on the tensile strength of Ludipress tablets. It is thought that a certain minimum dwell time is responsible for this difference. The production of tablets based on Ludipress can be scaled up from one rotary press to another without problem if the powder mixtures are prepared with the same mixing energy. The tensile strength curve determined for tablets made with Ludipress alone can also be applied to tablets with a small quantity (< 10%) of an active ingredient.

摘要

尽管制药行业已有丰富的经验,但片剂配方的开发在很大程度上仍基于经验,而且从实验室规模扩大到生产规模是一个耗时且成本高昂的过程。使用速溶片辅料(Ludipress)极大地简化了配方开发和制造过程,因为只需将活性成分速溶片辅料和一种润滑剂简单混合,然后压制成片即可。此处描述的研究旨在探讨基于速溶片辅料的配方从实验室规模扩大到生产规模的情况,并预测由于剂型、压制压力和使用不同压片机而导致的片剂性质变化。研究发现,由速溶片辅料制成的片剂的抗张强度在压制压力达到300兆帕之前随压制压力呈线性增加。它也与片剂的几何形状(直径、厚度、形状)无关。因此,可以给出一个方程,利用该方程可以为给定的片剂形式计算出达到给定硬度所需的压制压力。从单冲压片机转换为旋转压片机时,该方程必须稍作修改。在相同压力下,旋转压片机生产的片剂具有稍高的抗张强度。压力增加的速率以及由此产生的产量对速溶片辅料片剂的抗张强度没有影响。据认为这种差异是由一定的最短保压时间造成的。如果以相同的混合能量制备粉末混合物,基于速溶片辅料的片剂生产可以毫无问题地从一台旋转压片机扩大到另一台旋转压片机。仅由速溶片辅料制成片剂所确定的抗张强度曲线也可应用于含有少量(<10%)活性成分的片剂。

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