دورية أكاديمية

Amorphous Polymer–Phospholipid Solid Dispersions for the Co-Delivery of Curcumin and Piperine Prepared via Hot-Melt Extrusion

التفاصيل البيبلوغرافية
العنوان: Amorphous Polymer–Phospholipid Solid Dispersions for the Co-Delivery of Curcumin and Piperine Prepared via Hot-Melt Extrusion
المؤلفون: Kamil Wdowiak, Andrzej Miklaszewski, Judyta Cielecka-Piontek
المصدر: Pharmaceutics, Vol 16, Iss 8, p 999 (2024)
بيانات النشر: MDPI AG, 2024.
سنة النشر: 2024
المجموعة: LCC:Pharmacy and materia medica
مصطلحات موضوعية: curcumin, piperine, amorphous solid dispersion, phospholipids, hot-melt extrusion, supersaturation, Pharmacy and materia medica, RS1-441
الوصف: Curcumin and piperine are plant compounds known for their health-promoting properties, but their use in the prevention or treatment of various diseases is limited by their poor solubility. To overcome this drawback, the curcumin–piperine amorphous polymer–phospholipid dispersions were prepared by hot melt extrusion technology. X-ray powder diffraction indicated the formation of amorphous systems. Differential scanning calorimetry confirmed amorphization and provided information on the good miscibility of the active compound–polymer–phospholipid dispersions. Owing to Fourier-transform infrared spectroscopy, the intermolecular interactions in systems were investigated. In the biopharmaceutical properties assessment, the improvement in solubility as well as the maintenance of the supersaturation state were confirmed. Moreover, PAMPA models simulating the gastrointestinal tract and blood-brain barrier showed enhanced permeability of active compounds presented in dispersions compared to the crystalline form of individual compounds. The presented paper suggests that polymer–phospholipid dispersions advantageously impact the bioaccessibility of poorly soluble active compounds.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1999-4923
33936951
Relation: https://www.mdpi.com/1999-4923/16/8/999; https://doaj.org/toc/1999-4923
DOI: 10.3390/pharmaceutics16080999
URL الوصول: https://doaj.org/article/652fb6d4d95f4090b0a339369514635f
رقم الأكسشن: edsdoj.652fb6d4d95f4090b0a339369514635f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:19994923
33936951
DOI:10.3390/pharmaceutics16080999