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载有庆大霉素的热固性水凝胶和可塑形复合支架:配方研究与生物学评估

Gentamicin-Loaded Thermosetting Hydrogel and Moldable Composite Scaffold: Formulation Study and Biologic Evaluation.

作者信息

Dorati Rossella, De Trizio Antonella, Genta Ida, Merelli Alessia, Modena Tiziana, Conti Bice

机构信息

Department of Drug Sciences, Pharmaceutical Chemistry Section, University of Pavia, Pavia, Italy; Department of Drug Sciences, Pharmacology Section, University of Pavia, Pavia, Italy.

Department of Drug Sciences, Pharmaceutical Chemistry Section, University of Pavia, Pavia, Italy.

出版信息

J Pharm Sci. 2017 Jun;106(6):1596-1607. doi: 10.1016/j.xphs.2017.02.031. Epub 2017 Mar 7.

Abstract

The aim was to design biodegradable drug delivery systems for gentamicin local delivery, meanwhile acting as scaffold for bone regeneration. Gentamicin-loaded thermosetting composite hydrogels were prepared combining chitosan with bovine bone substitutes (Orthoss® granules), beta-glycerophosphate as cross-linker, and lyophilized to obtain moldable composite scaffolds (moldable composite scaffold loaded with gentamicin [mCSG]). Diverse techniques for gentamicin loading into mCS were investigated by drug incorporation during hydrogel preparation or drug absorption on preformed mCS. Rheologic hydrogel characterization was performed. mCSGs were characterized for porosity, stability (water retention, water uptake), gentamicin release, cell seeding and proliferation, and antimicrobial effect on Escherichia coli ATCC 10356. Results show suitable gentamicin loadings were 4 mg in 1 mL thermosetting composite hydrogel starting solution, irreversible hydrogel thermosetting behavior, and cosolute effect of gentamicin on sol-gel transition. Positive results in terms of porosity (80%-86%), scaffold water uptake, and retention capability were obtained. Antibiotic in vitro release was completed in 4 h. Good cell seeding results were observed for mCSG1-5; mCSG3 and mCSG5 resulted the best as cell proliferation results. mCSG exerted bactericidal effect for 24 h, with superimposition of chitosan bacteriostatic effect in the first 4 h. The results lead to consider the drug delivery for reducing infection risk during bone open surgeries.

摘要

目的是设计用于庆大霉素局部递送的可生物降解药物递送系统,同时作为骨再生的支架。将壳聚糖与牛骨替代物(Orthoss®颗粒)、β-甘油磷酸作为交联剂相结合,制备负载庆大霉素的热固性复合水凝胶,并冻干以获得可成型的复合支架(负载庆大霉素的可成型复合支架 [mCSG])。通过在水凝胶制备过程中药物掺入或在预制的mCS上药物吸收,研究了将庆大霉素负载到mCS中的多种技术。进行了水凝胶流变学表征。对mCSG的孔隙率、稳定性(保水性、吸水性)、庆大霉素释放、细胞接种和增殖以及对大肠杆菌ATCC 10356的抗菌作用进行了表征。结果表明,在1 mL热固性复合水凝胶起始溶液中合适的庆大霉素负载量为^mg,水凝胶具有不可逆的热固性行为,以及庆大霉素对溶胶-凝胶转变的共溶质效应。在孔隙率(80%-86%)、支架吸水性和保留能力方面取得了积极结果。抗生素在体外4小时内释放完毕。观察到mCSG1-5的细胞接种效果良好;mCSG3和mCSG5在细胞增殖结果方面表现最佳。mCSG发挥杀菌作用24小时,在前4小时叠加了壳聚糖的抑菌作用。这些结果促使人们考虑在骨开放性手术期间进行药物递送以降低感染风险。

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