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具有共价键合网络的壳聚糖/乙二醇二缩水甘油醚/阿莫西林水凝胶的超声触发阿莫西林释放

Ultrasound-Triggered Amoxicillin Release from Chitosan/Ethylene Glycol Diglycidyl Ether/Amoxicillin Hydrogels Having a Covalently Bonded Network.

作者信息

Tran Vo Tu Minh, Potiyaraj Pranut, Del Val Patricia, Kobayashi Takaomi

机构信息

Department of Energy and Environmental Science, Nagaoka University of Technology, 1603-1 Kamitomioka, Nagaoka, Niigata 940-2188, Japan.

Department of Materials Science, Chulalongkorn University, Faculty of Science, Pathum Wan, Bangkok 10330, Thailand.

出版信息

ACS Omega. 2023 Dec 19;9(1):585-597. doi: 10.1021/acsomega.3c06213. eCollection 2024 Jan 9.

Abstract

An antibiotic release system triggered by ultrasound (US) was investigated using chitosan (CS)/ethylene glycol diglycidyl ether (EGDE) hydrogel carriers with amoxicillin (Amox) drug. Different CS concentrations of 1.5, 2, 2.5, and 3 wt % were gelled with EGDE and Amox was entrapped in the hydrogel carrier; the accelerated release was observed as triggered by 43 kHz US exposure at different US output powers ranging from 0 to 35 W. Among these CS hydrogel systems, the degree of accelerated Amox release depended on the CS concentration for the hydrogelation and the matrix with 2 wt % CS exhibited efficient Amox release at 35 W US power with around 19 μg/mL. The drug released with time was fitted with Higuchi and Korsmeyer-Peppas models, and the enhancement was caused by US aiding drug diffusion within the hydrogel matrix by a non-Fickian diffusion mechanism. The US effect on the viscoelasticity of the hydrogel matrix indicated that the matrix became somewhat softened by the US exposure to the dense hydrogels for 2.5 and 3% CS/EGDE, while the degree of softening was slightly marked in the CS/EGDE hydrogels prepared with 1.5 and 2% CS concentration. Such US softening also aided drug diffusion within the hydrogel matrix, suggesting an enhanced Amox release.

摘要

利用壳聚糖(CS)/乙二醇二缩水甘油醚(EGDE)水凝胶载体与阿莫西林(Amox)药物,研究了一种由超声波(US)触发的抗生素释放系统。将1.5、2、2.5和3 wt%的不同CS浓度与EGDE进行凝胶化,并将Amox包封在水凝胶载体中;在0至35 W的不同超声输出功率下,通过43 kHz超声照射触发加速释放。在这些CS水凝胶系统中,Amox加速释放的程度取决于用于凝胶化的CS浓度,含2 wt% CS的基质在35 W超声功率下表现出高效的Amox释放,释放量约为19 μg/mL。随时间释放的药物符合Higuchi和Korsmeyer-Peppas模型,增强作用是由超声通过非菲克扩散机制辅助药物在水凝胶基质中扩散引起的。超声对水凝胶基质粘弹性的影响表明,对于2.5%和3% CS/EGDE的致密水凝胶,超声照射后基质会有所软化,而在CS浓度为1.5%和2%制备的CS/EGDE水凝胶中,软化程度稍明显。这种超声软化也有助于药物在水凝胶基质中扩散,表明Amox释放增强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b04/10785092/7c4ac8c89750/ao3c06213_0010.jpg

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