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玉米醇溶蛋白和羟丙基甲基纤维素琥珀酸醋酸酯微纤维与苯甲酸甲硝唑和/或含甲硝唑的纤维素纳米原纤维结合用于潜在的牙周治疗。

Zein and hydroxypropyl methylcellulose acetate succinate microfibers combined with metronidazole benzoate and/or metronidazole-incorporated cellulose nanofibrils for potential periodontal treatment.

作者信息

Ferreira João O, Zambuzi Giovana C, Camargos Camilla H M, Carvalho Ana C W, Ferreira Maíra P, Rezende Camila A, de Freitas Osvaldo, Francisco Kelly R

机构信息

Science and Technology Center for Sustainability, Federal University of São Carlos, Rod. SP-264, km 110, Sorocaba 18052-780, SP, Brazil.

Department of Physical Chemistry, Institute of Chemistry, University of Campinas, 13083-970 Campinas, SP, Brazil; School of Fine Arts, Federal University of Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.

出版信息

Int J Biol Macromol. 2024 Mar;261(Pt 1):129701. doi: 10.1016/j.ijbiomac.2024.129701. Epub 2024 Jan 25.

Abstract

The development of flexible and porous materials to control antibacterial delivery is a pivotal endeavor in medical science. In this study, we aimed to produce long and defect-free fibers made of zein and hydroxypropyl methylcellulose acetate succinate (HPMCAS) to be used as a platform for the release of metronidazole (MDZ) and metronidazole benzoate (BMDZ) to be potentially used in periodontal treatment. Microfibers prepared via electrospinning under a 2:3 (w/w) zein to HPMCAS ratio, containing 0.5 % (w/w) poly(ethylene oxide) (PEO) and 1 % (w/w) cellulose nanofibril (CNF) were loaded with 40 % (w/w) MDZ, 40 % (w/w) BMDZ, or a combination of 20 % (w/w) of each drug. The addition of CNF improved the electrospinning process, resulting in long fibers with reduced MDZ and BMDZ surface crystallization. MDZ- and BMDZ-incorporated fibers were semicrystalline and displayed commendable compatibility among drugs, nanocellulose and polymeric chains. Release tests showed that zein/HPMCAS/PEO fibers without CNF and with 20 % (w/w) MDZ/ 20 % (w/w) BMDZ released the drug at a slower and more sustained rate compared to other samples over extended periods (up to 5 days), which is a favorable aspect concerning periodontitis treatment.

摘要

开发用于控制抗菌药物递送的柔性多孔材料是医学领域的一项关键工作。在本研究中,我们旨在制备由玉米醇溶蛋白和羟丙基甲基纤维素琥珀酸酯(HPMCAS)制成的长且无缺陷的纤维,用作甲硝唑(MDZ)和甲硝唑苯甲酸酯(BMDZ)释放的平台,潜在用于牙周治疗。通过静电纺丝制备的微纤维,其玉米醇溶蛋白与HPMCAS的比例为2:3(w/w),含有0.5%(w/w)的聚环氧乙烷(PEO)和1%(w/w)的纤维素纳米纤维(CNF),负载了40%(w/w)的MDZ、40%(w/w)的BMDZ或每种药物20%(w/w)的组合。CNF的添加改善了静电纺丝过程,得到了MDZ和BMDZ表面结晶减少的长纤维。负载MDZ和BMDZ的纤维是半结晶的,在药物、纳米纤维素和聚合物链之间表现出良好的相容性。释放测试表明,不含CNF且含有20%(w/w)MDZ/20%(w/w)BMDZ的玉米醇溶蛋白/HPMCAS/PEO纤维在较长时间(长达5天)内比其他样品以更缓慢和更持续的速率释放药物,这对于牙周炎治疗来说是一个有利的方面。

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