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载唑来膦酸的聚乳酸/聚己内酯/羟基磷灰石支架可加速大鼠桡骨缺损的再生,并提高其结构性能和功能能力。

Zoledronate loaded polylactic acid/polycaprolactone/hydroxyapatite scaffold accelerates regeneration and led to enhance structural performance and functional ability of the radial bone defect in rat.

作者信息

Oryan A, Hassanajili S, Sahvieh S

机构信息

Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Department of Chemical Engineering, School of Chemical and Petroleum Engineering, Shiraz University, Shiraz, Iran.

出版信息

Iran J Vet Res. 2023;24(2):122-125. doi: 10.22099/IJVR.2023.43807.6421.

Abstract

UNLABELLED

Abstract.

BACKGROUND

One of the most common concerns in the regeneration of massive bone defects necessitating surgery and bone grafts is the application of tissue engineering using drug delivery. Zoledronate is a well-known effective drug for the healing bone fractures in osteoporotic patients.

AIMS

An attempt was made to design a more efficient bone scaffold with polycaprolactone, polylactic acid, and hydroxyapatite.

METHODS

The scaffold was fabricated by freeze-drying and indirect 3D printing approaches. X-ray diffraction, Fourier transform infrared spectroscopy, rheometry, scanning electron microscopy, and neutral red tests were performed to characterize the scaffold. qRT-PCR was also done to define the osteoinductivity and angiogenic induction capacity of this scaffold. Forty rats were selected and randomly divided into four groups: the control group, which received no treatment, the autograft group, scaffold group, and Zol-loaded scaffold group (n=10 in each group). The injured area was studied by radiology, biomechanical analysis, histopathology, histomorphometry, immunohistochemistry, and CT scan analyses.

RESULTS

The qRT-PCR results demonstrated significantly higher expression levels of , , and markers in the scaffold group when compared to the control group (P<0.05). Histopathologically, the newly formed bone tissue was significantly detected in the Zol-loaded scaffold and autograft groups in comparison with the non-treated group (P<0.001). The immunohistochemistry (OC marker), biomechanical, and histomorphometric results indicated a significant improvement in the regeneration of the injured area in the groups treated with autologous bone and Zol-loaded scaffold compared to the non-treated group (P<0.05). The Zol-loaded scaffold accelerated bone regeneration, and led to enhanced structural performance and functional ability of the injured radial bone in rats.

摘要

未标注

摘要。

背景

在需要手术和骨移植的大块骨缺损再生中,最常见的问题之一是利用药物递送的组织工程应用。唑来膦酸盐是治疗骨质疏松症患者骨折的一种知名有效药物。

目的

尝试用聚己内酯、聚乳酸和羟基磷灰石设计一种更高效的骨支架。

方法

通过冷冻干燥和间接3D打印方法制备支架。进行X射线衍射、傅里叶变换红外光谱、流变学、扫描电子显微镜和中性红试验以表征支架。还进行了qRT-PCR以确定该支架的骨诱导性和血管生成诱导能力。选择40只大鼠并随机分为四组:对照组,不接受任何治疗;自体移植组、支架组和载唑来膦酸盐支架组(每组n = 10)。通过放射学、生物力学分析、组织病理学、组织形态计量学、免疫组织化学和CT扫描分析研究损伤区域。

结果

与对照组相比,qRT-PCR结果显示支架组中 、 和 标志物的表达水平显著更高(P < 0.05)。组织病理学上,与未治疗组相比,在载唑来膦酸盐支架组和自体移植组中明显检测到新形成的骨组织(P < 0.001)。免疫组织化学(OC标志物)、生物力学和组织形态计量学结果表明,与未治疗组相比,自体骨和载唑来膦酸盐支架治疗组损伤区域的再生有显著改善(P < 0.05)。载唑来膦酸盐支架加速了骨再生,并提高了大鼠损伤桡骨的结构性能和功能能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c681/10542868/c1b1d27c7619/ijvr-24-122-g001.jpg

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