Department of Textile and Fibre Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, Delhi 110016, India.
Department of Biochemical Engineering and Biotechnology, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, Delhi 110016, India.
Int J Pharm. 2023 Feb 25;633:122611. doi: 10.1016/j.ijpharm.2023.122611. Epub 2023 Jan 13.
High internal phase emulsion (HIPE) templated poly (ɛ-caprolactone) (PCL) scaffolds have gained widespread attention for large-sized bone defects due to its tuneable 3D architecture and ease of fabricating crosslinked PCL (cPCL) scaffolds. However, extremely high stabilizer (surfactant or nanoparticle) concentration and negligence of microenvironment for regeneration sites like alveolar bones have restrained industrial acceptance of these scaffolds. Herein, we demonstrated the fabrication of nanocomposite cPCL scaffolds within Pickering HIPE templates stabilized using modified silica nanoparticles (mSiNP) concentrations as low as 0.1 to 1.0 wt%. Using an unconventional approach, the mSiNP Pickering stabilizer was added in dispersed phase, contradicting Bancroft's rule. The colloidal stability was attained due to faster drifting of mSiNP towards the interface when it was dispersed in silicone oil. Scaffolds with tuneable properties were fabricated by controlling the mSiNP concentration and ϕ. Further, cPCL scaffolds were functionalized using clove oil (CO) to improve their efficiency in eradicating S. aureus and E. coli by disrupting their cellular integrity. Additionally, formation of biofilm on the surface of the scaffolds was successfully inhibited by the incorporation of CO. CO-functionalized scaffolds demonstrated excellent cytocompatibility towards MG-63 cells allowing their successful adhesion and proliferation on the surface of the scaffolds.
高内相比乳液 (HIPE) 模板聚 (ε-己内酯) (PCL) 支架由于其可调节的 3D 结构和易于制造交联 PCL (cPCL) 支架,因此在大型骨缺损方面得到了广泛关注。然而,由于极高的稳定剂(表面活性剂或纳米粒子)浓度以及对肺泡骨等再生部位微环境的忽视,限制了这些支架在工业上的应用。在此,我们展示了使用改性二氧化硅纳米粒子 (mSiNP) 浓度低至 0.1 至 1.0 wt% 的 Pickering HIPE 模板内制备纳米复合 cPCL 支架。使用一种非传统的方法,将 mSiNP Pickering 稳定剂添加到分散相中,与 Bancroft 规则相矛盾。由于 mSiNP 在硅油中分散时更快地漂移到界面,因此实现了胶体稳定性。通过控制 mSiNP 浓度和 ϕ 可以制备具有可调性质的支架。此外,通过丁香油 (CO) 对 cPCL 支架进行功能化,以破坏其细胞完整性来提高其根除金黄色葡萄球菌和大肠杆菌的效率。此外,通过掺入 CO 成功抑制了支架表面生物膜的形成。CO 功能化支架对 MG-63 细胞表现出良好的细胞相容性,允许它们在支架表面成功粘附和增殖。