Accelerate development of topical cream drug product using a common platform base formulation

关键质量属性 剂型 药物制剂 工艺工程 化学 色谱法 计算机科学 工程类 粒径 物理化学
作者
Dimple Modi,Himanshu Sharma,Graeme Campbell
出处
期刊:Pharmaceutical Development and Technology [Taylor & Francis]
卷期号:25 (6): 767-778 被引量:3
标识
DOI:10.1080/10837450.2020.1741617
摘要

The aim of this work was to identify stable topical platform cream formulations (placebo creams without active drug substance) using the quality attributes of cream consistency, droplet size distribution (<1 μm), and separation or instability index of <0.1 to accelerate the development of topical cream drug product. The formulations were developed with six emulsifier systems that were screened in three different solvent systems across a range of emulsifier ratios. Each formulation was characterized by microscopy, separation index, and consistency. The results showed that there are three emulsifier combination (PEG 40 stearate:GMS, S21:S2, and PEG 40 stearate:Span 60) that works well with the solvent systems. Platform cream formulations F4, F15, F33, F40, F52, F69, F77, F87, and F106 were found to meet the three criteria for a long-term stable platform cream formulation. Formulation development for topical administered drug product can be very time consuming, expensive, and resourceful in identifying a chemically and physically stable product. In early development, where it can take 1–2 years to develop a first time in human (FTIH) formulation for a new chemical entity. The use of the platform base cream formulations will expedite the early development timeline for new chemical entity by 3–6 months.

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