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通过冷烧结制备的用于药物递送和骨组织工程应用的磷灰石/壳聚糖复合材料

Apatite/Chitosan Composites Formed by Cold Sintering for Drug Delivery and Bone Tissue Engineering Applications.

作者信息

Galotta Anna, Demir Öznur, Marsan Olivier, Sglavo Vincenzo M, Loca Dagnija, Combes Christèle, Locs Janis

机构信息

Department of Industrial Engineering, University of Trento, Via Sommarive 9, 38123 Trento, Italy.

Institute of Biomaterials and Bioengineering, Faculty of Natural Sciences and Technology, Riga Technical University, Pulka St. 3, LV-1007 Riga, Latvia.

出版信息

Nanomaterials (Basel). 2024 Feb 28;14(5):441. doi: 10.3390/nano14050441.

Abstract

In the biomedical field, nanocrystalline hydroxyapatite is still one of the most attractive candidates as a bone substitute material due to its analogies with native bone mineral features regarding chemical composition, bioactivity and osteoconductivity. Ion substitution and low crystallinity are also fundamental characteristics of bone apatite, making it metastable, bioresorbable and reactive. In the present work, biomimetic apatite and apatite/chitosan composites were produced by dissolution-precipitation synthesis, using mussel shells as a calcium biogenic source. With an eye on possible bone reconstruction and drug delivery applications, apatite/chitosan composites were loaded with strontium ranelate, an antiosteoporotic drug. Due to the metastability and temperature sensitivity of the produced composites, sintering could be carried out by conventional methods, and therefore, cold sintering was selected for the densification of the materials. The composites were consolidated up to ~90% relative density by applying a uniaxial pressure up to 1.5 GPa at room temperature for 10 min. Both the synthesised powders and cold-sintered samples were characterised from a physical and chemical point of view to demonstrate the effective production of biomimetic apatite/chitosan composites from mussel shells and exclude possible structural changes after sintering. Preliminary in vitro tests were also performed, which revealed a sustained release of strontium ranelate for about 19 days and no cytotoxicity towards human osteoblastic-like cells (MG63) exposed up to 72 h to the drug-containing composite extract.

摘要

在生物医学领域,纳米晶羟基磷灰石因其在化学成分、生物活性和骨传导性方面与天然骨矿物质特征相似,仍然是最具吸引力的骨替代材料候选者之一。离子取代和低结晶度也是骨磷灰石的基本特征,使其具有亚稳定性、生物可吸收性和反应活性。在本工作中,以贻贝壳作为钙生物源,通过溶解-沉淀合成法制备了仿生磷灰石和磷灰石/壳聚糖复合材料。着眼于可能的骨重建和药物递送应用,将抗骨质疏松药物雷奈酸锶负载到磷灰石/壳聚糖复合材料中。由于所制备复合材料的亚稳定性和温度敏感性,可以采用传统方法进行烧结,因此选择冷烧结来致密化材料。通过在室温下施加高达1.5 GPa的单轴压力10分钟,将复合材料致密化至相对密度约90%。从物理和化学角度对合成的粉末和冷烧结样品进行了表征,以证明从贻贝壳有效制备了仿生磷灰石/壳聚糖复合材料,并排除烧结后可能的结构变化。还进行了初步的体外试验,结果显示雷奈酸锶持续释放约19天,并且对暴露于含药复合材料提取物长达72小时的人成骨样细胞(MG63)没有细胞毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3e4/10934113/d188eb1cac99/nanomaterials-14-00441-g001.jpg

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