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Nanobiotechnology in Diagnosis, Drug Delivery and Treatment. Группа авторовЧитать онлайн книгу.

Nanobiotechnology in Diagnosis, Drug Delivery and Treatment - Группа авторов


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In addition, the large internal surface area and pore capacity of mesoporous materials allow a high loading of cargo molecules and also prevent them from escaping into water easily by dissolving in an aqueous environment (Jafari et al. 2019). These advantages enhance the effectiveness of the MSNP‐based delivery system and allow a specific amount of drugs to reach their therapeutic target (Li et al. 2012).

      1.2.1.3 Superparamagnetic Nanoparticles

      Among the inorganic nanoparticles, superparamagnetic nanoparticles (Figure 1.1c) are considered the most unique nanoparticles due to their strong magnetic properties. These nanoparticles were for the first time used in the late 1980s for biomedical applications (Stark et al. 1988). Usually, the core of these nanoparticles consists of metal molecules of nickel, cobalt, or iron oxide (Fe3O4 magnetite, which is the most commonly used metal). As mentioned above, superparamagnetic nanoparticles are considered most unique because the surface of these nanoparticles can be easily modified by coating the core with various organic polymers like dextran, starch, alginate, inorganic metals, oxides (silica, alumina), etc. (Núñez et al. 2018).

      Superparamagnetic nanoparticles can be promisingly used for the diagnosis of various diseases including cancer (tumors) by conjugating with various bioactive ligands (Anderson et al. 2019). To date, a number of approaches have been developed for the fabrication of superparamagnetic nanoparticles which have the potential ability to distinguish cancerous tissue from healthy tissue. In addition, these nanoparticles can be used for magnetic resonance imaging (MRI) of tumor tissue, cell labeling, and drug delivery in different diseases (Núñez et al. 2018; Anderson et al. 2019).

      1.2.1.4 Quantum Dots

      1.2.1.5 Graphene

      Graphene is an atom‐thick monolayer of carbon atoms arranged in a two‐dimensional honeycomb structure (Figure 1.1e) (Novoselov et al. 2004). Generally, graphene has been extensively used for a wide array of applications in many fields such as quantum physics, nanoelectronic devices, transparent conductors, energy research, catalysis, etc. (Wang et al. 2011; Huang et al. 2012). However, according to recent technological advancements graphene, graphene oxide, and reduced graphene oxide have shown promising applications in the biomedical field and hence have attracted significant interest worldwide (Gonzalez‐Rodriguez et al. 2019; Yang et al. 2019). Due to its excellent physicochemical and mechanical properties, single‐layered graphene has been widely utilized as a novel nanocarrier for drug and gene delivery in different diseases (Núñez et al. 2018).

      1.2.1.6 Carbon Nanotubes (CNTs)

      CNTs are cylindrical nanomaterials that consist of rolled‐up sheets of graphene (single‐layer carbon atoms). Depending on their structure CNTs can be divided into two types, namely single‐walled carbon nanotubes (SWCNTs) (Figure 1.1f), which usually have diameter of less than 1 nm, and multi‐walled carbon nanotubes (MWCNTs) (Figure 1.1g), which are composed of many concentrically interlinked nanotubes, usually having a diameter size of more than 100 nm (Hsu and Luo 2019). CNTs are considered as one of the stiffest and strongest fibers having novel exceptional characteristics and a unique physicochemical framework, which makes them suitable candidates for efficient delivery of different therapeutic drugs/molecules for various biomedical applications (Vengurlekar and Chaturvedi 2019). Figure 1.1 represents the schematic illustration of various inorganic nanomaterials.

      1.2.2 Organic Nanomaterials

      1.2.2.1 Polymeric Nanoparticles

Schematic illustrations of various organic nanomaterials. (a) Nanocapsule, (b) nanosphere, (c) polymeric micelle, (d) liposome, (e) solid-lipid nanoparticle, (f) dendrimer.

      1.2.2.2 Polymeric Micelles

      1.2.2.3 Liposomes


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