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groups of the polysaccharide backbone allow chemical modification to develop nanoparticles with diverse structures. Some polysaccharides can be recognized by specific cell types so, these polysaccharides can be used to design targeted-drug delivery systems through receptor-mediated endocytosis [135]. Alginate, fucoidan, carrageenan, laminarin, and ulvan are natural polysaccharides mainly isolated from seaweed and these biopolymers can be used to obtain nanoparticles with the desired shape, size, and charge after modified via different techniques such as covalent cross-linking, ionic linking, self-assembly, and polyelectrolyte complexing. Fucoidan is a polysaccharide with anti-tumor activities and so, various fucoidan-based nanoparticles have been designed to encapsulate anticancer drugs [136–138]. Huang et al. designed pH-sensitive nanoparticles for oral drug delivery to protect drugs from deterioration. Also, the composite nanoparticles obtained by using positively charged chitosan and negatively charged fucoidan through the ionic-gelation method were used for the delivery of anti-cancer drug curcumin. The encapsulation efficiency of curcumin in chitosan-fucoidan nanoparticles was higher than 85% and the release of curcumin from the nanoparticles was found to be increased at pH 6.0 and 7.0 [139].

      Polysaccharide formulations can also be utilized in green pesticide technology by providing safer delivery of agrochemicals. Although agrochemicals enhance the crop yields, commonly used agrochemical formulations can contaminate the environment. The use of natural polysaccharides has been claimed to be used for the controlled-release of agrochemicals to reduce pollution and health hazards. Polysaccharides, in the structural forms such as micro- or nanoparticles, beads, or hydrogels, can reduce agrochemical leaching, volatilization, and degradation by providing slow release. For instance, while free chlorpyrifos is released in 1 day, 50% of the encapsulated insecticide chlorpyrifos is released in 5 days. Slow-release property of polysaccharide formulations can also enhance the water-holding capacity of the soil, besides polysaccharide-clay formulations can store ionic plant nutrients. In addition to protecting crops from pests and diseases, biopolysaccharide derived formulations can enhance infiltration rates, soil permeability and aeration, and microbial activity, and therefore enhance crop yield [140–142].

In the field of pharmaceuticals, nucleic acid delivery has gained increasing interest especially to be used for modulating cellular signals. For a safe and efficient intracellular delivery, nucleic acids have to be encapsulated in nanosized carriers. A novel process, termed caged nanoparticle encapsulation, has been developed for concentrated and unaggregated nucleic acid delivery by using hydrogels [143]. However, drug-loaded nanoparticles encounter numerous extracellular and intracellular barriers before arriving at the target site [144]. Many polysaccharides, like hyaluronic acid, alginate, and chitosan, are excellent bioadhesive materials. In addition, the presence of a dense layer of polysaccharides in a brush-like configuration on the nanocarrier surface can extend the circulation time of the carrier in the bloodstream before the clearance by mononuclear phagocyte system. Thus, the presence of polysaccharide in the nanostructure can also mitigate complement activation [144, 145]. Furthermore, in specific cell types, polysaccharides can be recognized by particular carbohydrate-binding cell-surface receptors, so polysaccharide moieties can provide targeted delivery for nucleic acids [146, 147]. For instance, dendritic-cell-associated C-type lectin-1 or dectin-1 receptor frequently expressed on antigen-presenting cells, thereby β-glucan containing nanoparticles can be used to treatment of inflammatory disorders which requires specific targeting to phagocytic cell types [144]. The other advantage of polysaccharides as carriers is they have various functional groups including hydroxyls, amines, carboxylic acids on the glycosidic units which can be easily modified. Thus, chemical modifications of polysaccharides have the potential to overcome specific obstacles of carrier systems such as insufficient nucleic acid binding, fast clearance by phagocytes and/or endosomal systems [144]. For example, although chitosan is an attractive polymer to use as a carrier for gene delivery, it is easily degraded by lysozymes or chitinases in the physiological environment thus, its transfection efficiency is very low. To overcome this limitation, derivatives of chitosan have been generated [143]. Galactosylated chitosan was shown to enhance the transfection efficiency of DNA and histidine-modified chitosan showed improved endosomal escape [148]. In another study, quaternized chitosan oligomers were reported as potential candidates for the delivery of DNA complexes because of their permanent positive charge [149]. Additionally, natural polysaccharides were also examined to investigate their RNA delivery potential. For instance, chitosan and hyaluronic acid, highly positively and negatively charged polysaccharides respectively, were studied as small interfering RNA (siRNA) carriers for gene silencing. Positively charged chitosan can stably interact with siRNA, therefore it can protect the nucleic acid from degradation but at the same time can also limit its release [150]. siRNA/chitosan complex was also shown to be prone to aggregation in the presence of serum proteins and also prone to be removed by the mononuclear phagocyte system [151, 152]. Lack of cell specificity, low stability at physiological pH, and weak buffering capacity are among the other limitations of chitosan-based delivery systems. However, anionic polysaccharides, like hyaluronic acid, usually require the presence of cationic components for more efficient interactions with siRNA. Besides, hyaluronic acid has the advantage that it can bind its specific receptors on certain cell types, therefore can provide targeted delivery. Accordingly, the development of carriers composed of both chitosan and hyaluronic acid can be advantageous for siRNA delivery whereby chitosan provides a strengthened siRNA binding while hyaluronic acid ensures high stability and targeting capacity [150].

      Improvements in drug delivery systems affect various fields of medicine. The design and development of innovative materials to be used in contact lenses is a rapidly evolving discipline. These materials are developing alongside the progress made in related biomaterials [153]. In ocular pharmacology, there is a growing interest for the development of innovative delivery systems for a convenient and sustained drug release, especially for chronic eye diseases that require the adoption of a strict insurmountable treatment strategy for a large part of the affected population, as in the case of glaucoma [154]. New and improved contact lens materials can be used for drug delivery to the eye for more effective treatments [155]. For example, Xin-Yuan and Tian-Wei described a chitosan/gelatin composite film that was prepared by the solvent evaporation method. They showed that the presence of gelatin enhanced water absorption and oxygen and solute permeability of chitosan composite film. With its transparency, flexibility, and biocompatibility, chitosan/gelatin film structure was suggested as potential contact lens material [156]. Furthermore, drug delivery to the eye is currently a hot topic [155, 157]. Therefore, the use of natural polysaccharide derived materials should also be considered in the form of contact lenses to treat ocular diseases.

As discussed here, natural polysaccharides are promising candidates for drug delivery, as well as nucleic acid delivery. The design and development of polysaccharide-based targeted nanoplatforms have been gaining a great deal of attention. Future works seem to be focused more on chemical modifications of polysaccharides for designing efficient nanocarriers to be used in clinical trials. Although studies with polysaccharide-based nanosystems show promising proof of concept results, the ultimate performance of these platforms must be established in clinical trials. Besides, bringing the advantages of different polysaccharides together to achieve more efficient and biocompatible hybrid carrier systems has to be considered for successful drug delivery applications.

       6.2.2.4 Therapeutics

      Several researches report that polysaccharides can be utilized for therapeutic purposes because of their several biological actions such as antioxidant, anticoagulant, antiviral, antidiabetic, antitumor, and immunostimulatory activities [100]. Medicinal polysaccharides also claimed as “biological response modifiers”, are that stimulate the immunological response to infection and disease [158].

      The primary effect of polysaccharides was identified as enhancing and/or activating immune response [103]. Lo et al. proposed that arabinose, mannose, xylose, and galactose are the main monosaccharide components contributing to macrophage stimulating activity while being the most common monosaccharide component, glucose showed no clear role in the immunoactivity of polysaccharides [100]. The immunomodulating activity of polysaccharides comprises the activation of macrophages, dendritic cells, tumor-infiltrating lymphocytes, natural killer cells, lymphocyte activated killer cells, and several cytokines such as interferons,

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