Fabrication of 3D-printed scaffolds loaded with gallium acetylacetonate for potential application in osteoclastic bone resorption.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Evin Hessel, Pratyusha Ghanta, Timothy Winschel, Larissa Melnyk, Moses O Oyewumi
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引用次数: 0

Abstract

We recently reported the potential of a new gallium compound, gallium acetylacetonate (GaAcAc) in combating osteoclastic bone resorption through inhibition of osteoclast differentiation and function. Herein, we focused on 3D-printed polylactic acid scaffolds that were loaded with GaAcAc and investigated the impact of scaffold pretreatment with polydopamine (PDA) or sodium hydroxide (NaOH). We observed a remarkable increase in scaffold hydrophilicity with PDA or NaOH pretreatment while biocompatibility and in vitro degradation were not affected. NaOH-pretreated scaffolds showed the highest amount of GaAcAc loading when compared to other scaffolds (p < 0.05). NaOH-pretreated scaffolds with GaAcAc loading showed effective reduction of osteoclast counts and size. The trend was supported by suppression of key osteoclast differentiation markers such as NFAT2, c-Fos, TRAF6, & TRAP. All GaAcAc-loaded scaffolds, regardless of surface pretreatment, were effective in inhibiting osteoclast function as evidenced by reduction in the number of resorptive pits in bovine cortical bone slices (p < 0.01). The suppression of osteoclast function according to the type of scaffold followed the ranking: GaAcAc loading without surface pretreatment > GaAcAc loading with NaOH pretreatment > GaAcAc loading with PDA pretreatment. Additional studies will be needed to fully elucidate the impact of surface pretreatment on the efficacy and safety of GaAcAc-loaded 3D-printed scaffolds.

制作负载乙酰丙酮镓的三维打印支架,在破骨细胞骨吸收中的潜在应用
我们最近报道了一种新型镓化合物乙酰丙酮镓(GaAcAc)通过抑制破骨细胞的分化和功能来对抗破骨细胞骨吸收的潜力。在此,我们重点研究了负载乙酰丙酮镓的三维打印聚乳酸支架,并探讨了用多巴胺(PDA)或氢氧化钠(NaOH)预处理支架的影响。我们观察到,PDA 或 NaOH 预处理可显著增加支架的亲水性,而生物相容性和体外降解不受影响。与其他支架相比,NaOH预处理的支架显示出最高的GaAcAc负载量(NaOH预处理的GaAcAc负载量>PDA预处理的GaAcAc负载量)。要全面阐明表面预处理对负载GaAcAc的三维打印支架的有效性和安全性的影响,还需要进行更多的研究。
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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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