美金刚和多奈哌齐负载3D支架的设计与表征。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Betül Topçu İnce, Samuel Guieu, Selin Seda Timur, Tuba Reçber, Emirhan Nemutlu, Maria Helena Vaz Fernandes, Hakan Eroğlu
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引用次数: 0

摘要

美金刚盐酸(Memantine HCl, MEM)和多奈哌齐盐酸(Donepezil HCl, DON)被广泛单独或联合用于治疗阿尔茨海默病,一些研究表明,这些药物还可能预防骨折和促进骨再生。为此,我们研制了基于纤维的3D支架,用于局部递送MEM/DON,以改善骨折的再生过程。首先采用静电纺丝法制备聚(ε-己内酯)(PCL)基MEM/ don负载纳米纤维膜,然后采用热诱导自团聚(TISA)方法将这些纳米纤维膜转化为三维支架。经过这两步后的包封率在20%左右。分析证实,3D支架具有类似于细胞外基质的形态,其亲水性、溶胀率、孔隙率和降解率足以用于骨组织再生。释放研究表明,支架提供药物的初始爆发性释放,随后持续释放21天。这些3D支架没有显示出对L-929细胞系的任何细胞毒性作用,并且随着时间的推移增加了细胞活力,表明它们可以用于组织工程应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design and characterization of memantine and donepezil loaded 3D scaffolds.

Memantine HCl (MEM) and Donepezil HCl (DON) are widely used separately and in combination to treat Alzheimer's disease, and some studies suggest that these drugs may also prevent bone fractures and promote bone regeneration. For this purpose, we formulated fiber-based 3D scaffolds for local delivery of MEM/DON to improve the regeneration process of bone fractures. First, Poly (ε-caprolactone) (PCL)-based MEM/DON-loaded nanofibrous membranes were produced by electrospinning, and then these nanofibrous membranes were transformed into 3D scaffolds using the thermally induced self-agglomeration (TISA) method. Encapsulation efficiency after these two steps was found to be around 20%. Analyses confirmed that the 3D scaffolds have a morphology similar to the extracellular matrix, and that their hydrophilicity, swelling ratio, porosity, and degradation rate were adequate for bone tissue regeneration. Release studies show that the scaffolds provide an initial burst release of the drugs, followed by a sustained release for 21 days. These 3D scaffolds did not show any cytotoxic effect on the L-929 cell line, and increased cell viability over time indicates that they can be used in tissue engineering applications.

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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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