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含盐酸米诺环素的抗菌胶原复合膜。

Antibacterial Collagen Composite Membranes Containing Minocycline.

机构信息

College of Dentistry, University of Tennessee Health Science Center, Memphis TN 38163 USA.

Harrison School of Pharmacy, Auburn University, Auburn, AL 36849 USA.

出版信息

J Pharm Sci. 2021 May;110(5):2177-2184. doi: 10.1016/j.xphs.2020.12.026. Epub 2020 Dec 26.

Abstract

Collagen membranes have been used as bioresorbable barrier membranes in guided tissue/bone regeneration. However, the collagen membranes currently used in clinics lack an active antibacterial function, although infection at surgical sites presents a realistic challenge for guided tissue/bone regeneration. In this study, we successfully prepared novel and advanced collagen composite membranes from collagen and complexes of heparin and chelates of minocycline and Ca ions. These membranes were characterized for chemical structures, morphology, elemental compositions and tensile strength. In vitro release studies were conducted to evaluate the release kinetics of minocycline from these membranes. Agar disk diffusion assays were used to assess their sustained antibacterial capability against model pathogenic bacteria Staphylococcus aureus. The chemical and physical characterization confirmed the successful synthesis of minocycline-loaded collagen composite membranes, namely NCCM-1 and NCCM-2. Both membranes had weaker tensile strength as compared with commercial collagen membranes. They achieved sustained release of minocycline for at least 4 weeks in simulated body fluid (pH 7.4) at 37°C. Moreover, both membranes demonstrated potent sustained antibacterial effects against Staphylococcus aureus. These results suggested that the advanced collagen composite membranes containing minocycline can be exploited as novel guided tissue regeneration membranes or wound dressing by providing additional antibacterial functions.

摘要

胶原蛋白膜已被用作引导组织/骨再生的生物可吸收屏障膜。然而,尽管手术部位的感染是引导组织/骨再生的一个现实挑战,但目前临床上使用的胶原蛋白膜缺乏主动的抗菌功能。在这项研究中,我们成功地从胶原蛋白和肝素复合物以及米诺环素和 Ca 离子的螯合物制备了新型先进的胶原蛋白复合膜。对这些膜的化学结构、形态、元素组成和拉伸强度进行了表征。进行了体外释放研究以评估米诺环素从这些膜中的释放动力学。琼脂圆盘扩散试验用于评估它们对金黄色葡萄球菌等模型病原菌的持续抗菌能力。化学和物理特性分析证实了载米诺环素的胶原蛋白复合膜(即 NCCM-1 和 NCCM-2)的成功合成。与商业胶原蛋白膜相比,这两种膜的拉伸强度都较弱。它们在 37°C 下的模拟体液(pH 7.4)中至少可实现 4 周的米诺环素持续释放。此外,这两种膜均对金黄色葡萄球菌表现出强大的持续抗菌作用。这些结果表明,载有米诺环素的先进胶原蛋白复合膜可通过提供额外的抗菌功能被开发为新型引导组织再生膜或伤口敷料。

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