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本文引用的文献

1
Thirteen-week study of toxicity of fiber-like multi-walled carbon nanotubes with whole-body inhalation exposure in rats.大鼠全身吸入纤维状多壁碳纳米管毒性的 13 周研究。
Nanotoxicology. 2015 May;9(4):413-22. doi: 10.3109/17435390.2014.933903. Epub 2014 Jul 17.
2
Effect of force of microneedle insertion on the permeability of insulin in skin.微针插入力度对胰岛素经皮渗透性的影响。
J Diabetes Sci Technol. 2014 May;8(3):444-52. doi: 10.1177/1932296813519720. Epub 2014 Jan 21.
3
Cognitive deficits and decreased locomotor activity induced by single-walled carbon nanotubes and neuroprotective effects of ascorbic acid.单壁碳纳米管诱导的认知缺陷和运动活动减少以及抗坏血酸的神经保护作用。
Int J Nanomedicine. 2014 Feb 11;9:823-39. doi: 10.2147/IJN.S56339. eCollection 2014.
4
Microneedle assisted micro-particle delivery from gene guns: experiments using skin-mimicking agarose gel.微针辅助基因枪介导的微颗粒递药:应用于皮肤模拟琼脂糖凝胶的实验。
J Pharm Sci. 2014 Feb;103(2):613-27. doi: 10.1002/jps.23835. Epub 2014 Jan 7.
5
A concise review of carbon nanotube's toxicology.碳纳米管毒理学简要综述。
Nano Rev. 2013 Dec 3;4:21521. doi: 10.3402/nano.v4i0.21521.
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Potential of microneedle-assisted micro-particle delivery by gene guns: a review.基因枪介导的微针辅助微粒递送的潜力:综述
Drug Deliv. 2014 Dec;21(8):571-87. doi: 10.3109/10717544.2013.864345. Epub 2013 Dec 9.
7
Targeting colorectal cancer cells with single-walled carbon nanotubes conjugated to anticancer agent SN-38 and EGFR antibody.用与抗癌剂 SN-38 和 EGFR 抗体偶联的单壁碳纳米管靶向结直肠癌细胞。
Biomaterials. 2013 Nov;34(34):8756-65. doi: 10.1016/j.biomaterials.2013.07.067. Epub 2013 Aug 12.
8
Pulmonary toxicity of carbon nanotubes and asbestos - similarities and differences.碳纳米管和石棉的肺毒性——相似性和差异性。
Adv Drug Deliv Rev. 2013 Dec;65(15):2078-86. doi: 10.1016/j.addr.2013.07.014. Epub 2013 Jul 27.
9
Delivery of small interfering RNAs in human cervical cancer cells by polyethylenimine-functionalized carbon nanotubes.多聚乙烯亚胺功能化碳纳米管介导的小干扰 RNA 递送至人宫颈癌细胞。
Nanoscale Res Lett. 2013 Jun 6;8(1):267. doi: 10.1186/1556-276X-8-267.
10
Folate-conjugated PEG on single walled carbon nanotubes for targeting delivery of Doxorubicin to cancer cells.叶酸偶联的聚乙二醇修饰的单壁碳纳米管用于阿霉素靶向递送至癌细胞。
Macromol Biosci. 2013 Jun;13(6):735-44. doi: 10.1002/mabi.201200475. Epub 2013 Apr 24.

碳纳米管第二部分:药物和基因递送的卓越载体

Carbon nanotubes part II: a remarkable carrier for drug and gene delivery.

作者信息

Karimi Mahdi, Solati Navid, Ghasemi Amir, Estiar Mehrdad Asghari, Hashemkhani Mahshid, Kiani Parnian, Mohamed Elmira, Saeidi Ahad, Taheri Mahdiar, Avci Pinar, Aref Amir R, Amiri Mohammad, Baniasadi Fazel, Hamblin Michael R

机构信息

Iran University of Medical Sciences, School of Advanced Technologies in Medicine, Department of Nanotechnology , Tehran , Iran.

出版信息

Expert Opin Drug Deliv. 2015 Jul;12(7):1089-105. doi: 10.1517/17425247.2015.1004309. Epub 2015 Jan 22.

DOI:10.1517/17425247.2015.1004309
PMID:25613837
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4475451/
Abstract

INTRODUCTION

Carbon nanotubes (CNT) have recently been studied as novel and versatile drug and gene delivery vehicles. When CNT are suitably functionalized, they can interact with various cell types and are taken up by endocytosis.

AREAS COVERED

Anti-cancer drugs cisplatin and doxorubicin have been delivered by CNT, as well as methotrexate, taxol and gemcitabine. The delivery of the antifungal compound amphotericin B and the oral administration of erythropoietin have both been assisted using CNT. Frequently, targeting moieties such as folic acid, epidermal growth factor or various antibodies are attached to the CNT-drug nanovehicle. Different kinds of functionalization (e.g., polycations) have been used to allow CNT to act as gene delivery vectors. Plasmid DNA, small interfering RNA and micro-RNA have all been delivered by CNT vehicles. Significant concerns are raised about the nanotoxicology of the CNT and their potentially damaging effects on the environment.

EXPERT OPINION

CNT-mediated drug delivery has been studied for over a decade, and both in vitro and in vivo studies have been reported. The future success of CNTs as vectors in vivo and in clinical application will depend on achievement of efficacious therapy with minimal adverse effects and avoidance of possible toxic and environmentally damaging effects.

摘要

引言

碳纳米管(CNT)最近被作为新型多功能药物和基因递送载体进行研究。当碳纳米管经过适当功能化修饰后,它们能够与多种细胞类型相互作用并通过内吞作用被细胞摄取。

涵盖领域

抗癌药物顺铂和阿霉素已通过碳纳米管进行递送,还有甲氨蝶呤、紫杉醇和吉西他滨。抗真菌化合物两性霉素B的递送以及促红细胞生成素的口服给药都借助了碳纳米管。通常,靶向部分如叶酸、表皮生长因子或各种抗体被连接到碳纳米管 - 药物纳米载体上。已使用不同种类的功能化修饰(如聚阳离子)使碳纳米管充当基因递送载体。质粒DNA、小干扰RNA和微小RNA都已通过碳纳米管载体进行递送。人们对碳纳米管的纳米毒理学及其对环境的潜在破坏作用提出了重大担忧。

专家观点

碳纳米管介导的药物递送已研究了十多年,并且已有体外和体内研究报道。碳纳米管作为体内载体和临床应用未来的成功将取决于以最小的副作用实现有效治疗,并避免可能的毒性和环境破坏作用。