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基于拉曼光谱的聚乙二醇化还原氧化石墨烯的器官分布和清除检测及其生物学效应。

Raman spectroscopy for the detection of organ distribution and clearance of PEGylated reduced graphene oxide and biological consequences.

机构信息

Biomedical Technology Wing, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Poojapura, Trivandrum 695 012, Kerala, India.

Biomedical Technology Wing, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Poojapura, Trivandrum 695 012, Kerala, India.

出版信息

Biomaterials. 2017 Jul;131:121-130. doi: 10.1016/j.biomaterials.2017.03.043. Epub 2017 Mar 28.

Abstract

Graphene, a 2D carbon material has found vast application in biomedical field because of its exciting physico-chemical properties. The large planar sheet like structure helps graphene to act as an effective carrier of drug or biomolecules in enormous amount. However, limited data available on the biocompatibility of graphene upon interaction with the biological system prompts us to evaluate their toxicity in animal model. In this study organ distribution, clearance and toxicity of PEGylated reduced nanographene (PrGO) on Swiss Albino mice was investigated after intraperitoneal and intravenous administration. Biodistribution and blood clearance was monitored using confocal Raman mapping and indicated that PrGO was distributed on major organs such as brain, liver, kidney, spleen and bone marrow. Presence of PrGO in brain tissue suggests that it has the potential to cross blood brain barrier. Small amount of injected PrGO was found to excrete via urine. Repeated administration of PrGO induced acute liver injury, congestion in kidney and increased splenocytes proliferation in days following exposure. Hence the result of the study recommended that PrGO should undergo intensive safety assessment before clinical application or validated to be safe for medical use.

摘要

石墨烯是一种 2D 碳材料,由于其令人兴奋的物理化学特性,在生物医学领域得到了广泛的应用。其较大的平面片状结构有助于石墨烯作为大量药物或生物分子的有效载体。然而,由于与生物系统相互作用时石墨烯的生物相容性数据有限,促使我们在动物模型中评估其毒性。在这项研究中,研究了经 PEG 化还原纳米石墨烯(PrGO)经腹腔和静脉给药后在瑞士白化病小鼠中的器官分布、清除和毒性。使用共聚焦拉曼映射监测生物分布和血液清除,并表明 PrGO 分布在大脑、肝脏、肾脏、脾脏和骨髓等主要器官中。PrGO 存在于脑组织中表明它有可能穿过血脑屏障。通过尿液发现少量注射的 PrGO 被排出体外。重复给予 PrGO 可诱导急性肝损伤、肾脏充血和暴露后几天内脾细胞增殖增加。因此,研究结果建议在临床应用前或验证其对医疗用途安全之前,应对 PrGO 进行严格的安全性评估。

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