纳米材料的表面改性及其在生物技术中的应用

Hélio Ribeiro
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引用次数: 1

摘要

近几十年来,各科学技术领域对纳米材料的研究进行了广泛的探索。一些作者认为,碳纳米管的发现(Iijima[1])和石墨烯的发现(Geim和Novoselov[2])刺激了纳米技术的研究。与此同时,探针显微镜、扫描显微镜和透射显微镜的进步也有助于发现新的纳米结构,以及对其他尚未很好阐明的纳米结构的理解。人们期望碳纳米管、石墨烯、氢氮化硼、bnnt和金属纳米颗粒等纳米结构具有优异的物理化学性能和生物相容性。一方面,这些材料在纳米技术、生物工程和生物医学等领域具有巨大的应用潜力[4,5],如肿瘤标志物[6]、药物递送[7]、生物包装[8]、生物传感[9-11]、疫苗佐剂[5-12,13]等。然而,这些纳米颗粒在相关介质中的相容性和分散性是其潜在应用的基础。宿主生物系统与纳米颗粒之间的纳米工程界面涉及几个需要克服的挑战。例如,纳米颗粒的堆积或团聚过程不允许它们将预期的特性转移到系统中,导致分散介质不均匀,生物相容性最低。这些不希望的过程可以通过物理或化学方法修饰其表面,如共价或非共价功能化来克服。因此,我们的选择将取决于所研究的纳米粒子和生物系统。共价功能化取决于纳米颗粒与所选择的官能团之间的键合,根据选择性[3]。基于这种方法,不同的有机或无机官能团或纳米颗粒可以被锚定。例如,它可以被引入氧化碳纳米管或氧化石墨烯(GO)表面、烷氧基(-OR)、氨基(-NH2)、胺(-NHR)、烷基(-R)等官能团[14,15]、杂原子掺杂、金属纳米颗粒、生物分子和生物聚合物等表面。这些修饰过程显著改变了它们与介质的相互作用,使它们在水、共聚物或有机溶剂中具有大范围的溶解度。另一方面,纳米颗粒的非共价功能化过程强烈依赖于它们通过分子间力与宿主系统的物理相互作用,如范德华力、亲水性、疏水性、氢键和π-π相互作用等。利用分子(缀合物、表面活性剂等)的物理相互作用,它们以其受控的物理化学和生物特性均匀地分散在不同的介质中。
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Surface Modification and Application of Nanomaterials in Biotechnology
Many studies about nanomaterials have been widely explored in recent decades in different scientific and technological areas. Several authors consider that the discovery of CNTs by Iijima [1] and graphene by Geim and Novoselov [2], stimulated the studies in nanotechnology. Concomitantly, the advances in probe, scanning, and transmission microscopies, it has also contributed to the discovery of new nanostructures and the understanding of others that were not yet well elucidated. It was expected exceptional physico-chemical properties and biocompatibility of nanostructures such as CNTs, graphene, h-BN, BNNTs and metallic nanoparticles, among others [3]. On the one hand, these materials have an enormous potential range of applications in nanotechnology, bioengineering and biomedicine [4,5], such as tumor markers[6], drugs delivers [7], bio-packaging [8], biosensing [9-11], adjuvant in vaccines [5-12,13], among others. However, the compatibility and dispersion of these nanoparticles in the medium of interest are fundamental to their potential applications [3]. The nanoengineering interfaces between host biological system and nanoparticles involves several challenges that need to be overcome. For instance, there-stacking or agglomeration processes of nanoparticles do not allow them to transfer their expected properties to the system, resulting in an inhomogeneous dispersion medium with minimum of biocompatibility. These undesirable processes can be overcome by physical or chemical modification methodologies of their surfaces, such as covalent or non-covalent functionalization. Thus, our choices will depend on the nanoparticles and the biological system in study. The covalent functionalization depends on bonding between the nanoparticles and the functional groups that were chosen, according to the selectivity [3]. Based on this approach, different organic or inorganic functional groups or nanoparticles can be anchored. For instance, it can be introduced on surfaces of oxidized CNTs or graphene oxide (GO), functional groups such as alkoxy (-OR), amino (-NH2), amine (-NHR), alkyl (-R) [14,15], heteroatom doping, metallic nanoparticles, biomolecules and biopolymers, among others. These modifications process alter significantly their interactions with the medium leading them to a large range of solubility in water, co-polymers or organic solvents [3]. On the other hand, non-covalent functionalization processes of nanoparticles are strongly dependent of their physical interaction with host system through intermolecular forces, such as van der Waals, hydrophilic, hydrophobic, hydrogen bonding and π-π interactions, among others [16]. Taking advantages of these physical interactions of molecules (conjugated, surfactants etc), they form homogenously dispersion into different medium with their controlled physicochemical and biological properties [17].
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