Investigation of silicon oxide nanoparticle-enhanced self-healing hydrogel for cartilage repair and regeneration in rabbit earlobe models.

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Seyedeh-Sara Hashemi, Reza Alizadeh, Alireza Rafati, Aliakbar Mohammadi, Mojtaba Mortazavi, Mohammad Hashem Hashempur
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引用次数: 0

Abstract

This study developed an alginate, gelatine and chondroitin sulphate hydrogel incorporating silicon oxide nanoparticles to assess hydrogel morphology, cell proliferation and viability. The effectiveness of these hydrogels for cartilage repair was evaluated in vivo using male albino rabbits, divided into three groups: a control group without hydrogels, an observer group with hydrogels lacking nanoparticles and a treatment group with nanoparticle-enhanced hydrogels for post-injury repair. At 15, 30 and 60 days post-surgery, the rabbits were humanely euthanized and excised tissue samples were fixed in 10% formalin for histopathological analysis, then processed and embedded in paraffin for microscopic evaluation. Statistical analysis was performed using SPSS software with ANOVA and Tukey's post hoc test. Results indicated that the hydrogels supported cell viability and encouraged differentiation into chondrocyte-like phenotypes. Scanning electron microscopy confirmed the hydrogels' porosity and showed significant differences in cell survival rates compared to the control group, underscoring the potential of hydrogels in cartilage tissue engineering and regenerative repair strategies.

纳米氧化硅增强自愈水凝胶用于兔耳垂软骨修复和再生的研究。
本研究开发了一种海藻酸盐、明胶和硫酸软骨素水凝胶,其中含有氧化硅纳米颗粒,以评估水凝胶的形态、细胞增殖和活力。用雄性白化兔在体内评估这些水凝胶对软骨修复的有效性,将其分为三组:没有水凝胶的对照组,缺乏纳米颗粒的水凝胶观察组,以及纳米颗粒增强水凝胶用于损伤后修复的治疗组。术后15、30、60天对家兔进行人道安乐死,切除组织标本用10%福尔马林固定进行组织病理学分析,处理后包埋石蜡显微镜观察。统计学分析采用SPSS软件,采用方差分析和Tukey事后检验。结果表明,水凝胶支持细胞活力,促进细胞分化为软骨细胞样表型。扫描电镜(SEM)证实了水凝胶的多孔性,并显示与对照组相比,水凝胶的细胞存活率有显著差异,强调了水凝胶在软骨组织工程和再生修复策略中的潜力。
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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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