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核心材料表面性质对热熔包衣多颗粒系统稳定性的影响

Impact of Surface Properties of Core Material on the Stability of Hot Melt-Coated Multiparticulate Systems.

作者信息

Schertel Sonja, Salar-Behzadi Sharareh, Zimmer Andreas

机构信息

Department of Pharmaceutical Technology and Biopharmacy, Institute of Pharmaceutical Science, University of Graz, 8010 Graz, Austria.

Hermes Arzneimittel GmbH, Division Hermes Pharma, 82049 Pullach, Germany.

出版信息

Pharmaceutics. 2021 Mar 10;13(3):366. doi: 10.3390/pharmaceutics13030366.

Abstract

Hot melt coating (HMC) of an active pharmaceutical ingredient (API) powder with lipid-based excipients is an innovative method for manufacturing patient-convenient dosage forms. However, drug release instability is still its main industrial challenge. The correlation between the unstable pharmaceutical product performance with the solid-state alteration of lipids is currently well-investigated. The remaining problem is the inconsistent release alteration of different APIs coated with the same lipid after storage, such as faster release in some cases and slower release in others. The interaction between API surface and lipid-based coating and its alteration during storage were investigated in this work. The surface properties of five different APIs and the coating composition of tripalmitin and polysorbate 65 were screened via Washburn and pendant drop methods, respectively. Metformin hydrochloride and hydrochlorothiazide particles were each coated with the coating composition. The water sorption alteration of coated particles and the crystal growth of tripalmitin in the coating after storage were measured via tensiometry and X-ray diffraction. The cleavage work necessary to overcome the adhesion of coating composition on the core surface was calculated for each API. The accelerated release of the polar core (metformin) after storage was correlated with a low cleavage work and a distinctive phase separation. In contrast, a decelerated release of the hydrophobic core (hydrochlorothiazide) was favored by the crystal growth of the lipid-based coating. The gained knowledge can be used to design the product stability during the formulation development.

摘要

用脂质类辅料对活性药物成分(API)粉末进行热熔包衣(HMC)是一种生产方便患者剂型的创新方法。然而,药物释放不稳定仍是其主要的工业挑战。目前已对不稳定药品性能与脂质固态变化之间的相关性进行了充分研究。剩下的问题是,相同脂质包衣的不同API在储存后释放变化不一致,例如在某些情况下释放较快,而在其他情况下释放较慢。本研究考察了API表面与脂质包衣之间的相互作用及其在储存过程中的变化。分别通过Washburn法和悬滴法筛选了五种不同API的表面性质以及三棕榈酸甘油酯和聚山梨醇酯65的包衣组成。将盐酸二甲双胍和氢氯噻嗪颗粒分别用该包衣组成进行包衣。通过张力测定法和X射线衍射法测定了包衣颗粒的吸水变化以及储存后包衣中三棕榈酸甘油酯的晶体生长情况。计算了每种API克服包衣组合物与核心表面粘附所需的裂解功。储存后极性核心(二甲双胍)的加速释放与低裂解功和明显的相分离有关。相反,基于脂质的包衣晶体生长有利于疏水性核心(氢氯噻嗪)的释放减缓。所获得的知识可用于在制剂开发过程中设计产品稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b98/8001618/b09b8dd6afff/pharmaceutics-13-00366-g001.jpg

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