Impact of surfactant raw material variability on extrudate clarity appearance (transparency) in HME continuous manufacturing.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Claudia A Lohmann, Esther Bochmann, Samuel O Kyeremateng
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引用次数: 0

Abstract

The appearance of an extrudate formulation was monitored during hot-melt extrusion (HME) continuous manufacturing over 3 days. The formulation matrix consisted of a polymeric component, copovidone, and a low molecular weight surfactant, polysorbate 80. Based on studies prior to the continuous manufacturing, the desired appearance of the target extrudate is translucent. Although process parameters such as feed rate and screw speed were fixed during the continuous manufacturing, the extrudate appearance changed over time from turbid to translucent. For root-cause investigation, the extrudates were analyzed offline by differential scanning calorimetry (DSC) and advanced polymer chromatography (APC). Although the polysorbate 80 content of both turbid and translucent extrudates was within target, the glass transition temperature of the turbid extrudate was 2 °C above expected value. The observed turbidity was traced to lot-to-lot variability of the polysorbate 80 used in the continuous manufacturing, where APC analysis revealed that the relative content of the low molecular weight component varied from 23% to 27% in correlation with the evolution from turbid to translucent extrudates. This work stresses the importance of taking feeding material variability into account during continuous manufacturing.

在高密度聚乙烯连续生产过程中,表面活性剂原料的变化对挤出物清澈外观(透明度)的影响。
在为期三天的热熔挤出(HME)连续生产过程中,对挤出配方的外观进行了监测。配方基质由聚合物成分聚维酮和低分子量表面活性剂聚山梨醇酯 80 组成。根据连续生产前的研究,目标挤出物的理想外观是半透明的。虽然在连续生产过程中喂料速率和螺杆速度等工艺参数是固定的,但挤出物的外观随着时间的推移从浑浊变为半透明。为了找出根本原因,我们采用差示扫描量热法(DSC)和高级聚合物色谱法(APC™)对挤出物进行了离线分析。虽然浑浊和半透明挤出物中的聚山梨醇酯 80 含量都在目标范围内,但浑浊挤出物的玻璃化转变温度比预期值高 2 °C。观察到的浑浊现象可追溯到连续生产过程中使用的聚山梨醇酯 80 的批次间差异,APC™ 分析显示,低分子量成分的相对含量从 23% 到 27% 不等,这与挤出物从浑浊到半透明的演变过程相关。这项工作强调了在连续生产过程中考虑喂料材料变化的重要性。
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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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