CARBON NANOCOMPOSITES IN MEDICINE: GRAPHENE AND POLYGRAPHENE AS POSSIBLE DRUG DELIVERY VEHICLE FOR INTESTINAL ONCOLOGY

A. Botin, D. Mashal, T. Popova, M.G.H. Rizk, A. Cordova
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Abstract

The paper considers one of the most important directions in modern pharmacology - targeted delivery of medicines, namely the directed transport of medicinal substance to given area of body, which is realized with help of carriers, which, as a rule, have sizes of tens or hundreds of nanometers, different nature and chemical structure. The delivery of antitumor drugs using nanoparticles is being discussed. Immobilization of drugs on nanocarriers makes it possible to increase their bioavailability. Various graphene derivatives - graphene oxide (GO) and reduced graphene oxide (RGO) - are being tested as carriers for drug delivery. There are several approaches for targeted drug delivery in oncology. The first, simple one is the attachment of both low– and high-molecular preparation to the surface of the carrier directly. The drug doxorubicin is firmly bound to surface of graphene oxide and is released only in acidic environment of tumor. The second, more complex method is to attach to surface of carrier not only active substance, but also guiding molecules - ligands. Sometimes ligand itself can be a drug at the same time. Polygraphene (PG) is an original modified analogue of thermally split graphite, obtained in the form of new form of expanded graphite, after repeated chemical modification and thermal activation, it is reduced to the characteristics of a layered material with stacks of carbon monolayers of smaller multiplicity (from 5 to 50), up to single sheets of graphene. The results of tests of PG as an effective basis for the immobilization of enzymes are presented, in particular, on the example of antitumor enzyme L-lysine-α-oxidase. These data indicate prospects of possible biomedical use of PG in oncology, namely, in treatment of intestinal cancer. Modified forms of graphene and polygraphene should be considered as new carrier of drugs.
碳纳米复合材料在医学中的应用:石墨烯和聚石墨烯可作为肠道肿瘤学的给药载体
本文探讨了现代药理学最重要的方向之一--靶向给药,即在载体的帮助下将药物定向输送到身体的特定部位,载体通常只有几十或几百纳米大小,具有不同的性质和化学结构。目前正在讨论使用纳米颗粒输送抗肿瘤药物的问题。将药物固定在纳米载体上可以提高药物的生物利用度。各种石墨烯衍生物--氧化石墨烯(GO)和还原氧化石墨烯(RGO)--正作为载体进行给药测试。在肿瘤学中,有几种靶向给药的方法。第一种简单的方法是将低分子和高分子制剂直接附着在载体表面。药物多柔比星被牢固地结合在氧化石墨烯表面,只有在肿瘤的酸性环境中才会释放出来。第二种更复杂的方法是在载体表面不仅附着活性物质,还附着引导分子--配体。有时,配体本身也可以同时是一种药物。聚石墨烯(PG)是热裂解石墨的一种原始改性类似物,以新形式的膨胀石墨获得,经过反复的化学改性和热活化,它被还原成具有较小倍数(从 5 到 50)的碳单层堆叠到单层石墨烯的分层材料的特征。本文以抗肿瘤酶 L-赖氨酸-α-氧化酶为例,介绍了将 PG 作为固定酶的有效基础的测试结果。这些数据预示着石墨烯在肿瘤学(即肠癌治疗)中的生物医学应用前景。石墨烯和聚石墨烯的改性形式应被视为新的药物载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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