“…Unfortunately, the poor solubility and the restricted drug-loading efficiency of native chitosan limit its applications in biomedical research. By modifying the structure of chitosan with hydrophilic groups, the solubility and the physicochemical properties of chitosan are greatly improved. − Nanoparticles prepared based on these chitosan derivatives further enhance the adsorption of antigen vaccines at the mucosal site and promote the uptake efficiency of vaccines by cells, broadening the usage of chitosan in the field of vaccine research. , Current studies mainly focus on the effective preparation of nano-carriers and the optimization of parametric properties, while the immunomodulatory function of nano-carriers themselves is still in the early research stage.…”
Nasal administration for vaccine delivery is a novel non-invasive vaccine administration approach that can induce local or systemic immune responses and overcome the disadvantages caused by traditional injectable administration. However, mucosal vaccine and adjuvant delivery systems with sustained-release ability and enhanced immune effects at mucosal sites have still been highly demanded. In this work, N-2-hydroxypropyl trimethyl ammonium chloride chitosan/N,O-carboxymethyl chitosan nanoparticles (N-2-HACC/CMCS NPs) with excellent mucosal absorption, high drug loading capacity, and enhanced immune responses were prepared by the ionic cross-linking method. To evaluate the potential capacity of the N-2-HACC/CMCS NPs as a vaccine adjuvant and the molecular mechanism for the induction of enhanced mucosal and systemic immune responses, bovine serum albumin (BSA) was employed as a general model antigen and loaded into the N-2-HACC/CMCS NPs to prepare a BSA-loaded N-2-HACC/CMCS adjuvant vaccine (N-2-HACC/CMCS/BSA NPs). It was well demonstrated that the N-2-HACC/CMCS/BSA NPs with great biostability and mucosal absorption could effectively promote the proliferation of lymphocytes and the secretion of related pro-inflammatory factors, resulting in the stimulation of specific mucosal and systemic immune responses. This study revealed that the chitosan-based nano-delivery system can act as the mucosal vaccine adjuvant and possesses great promise in viral infectious diseases and immunization therapy.
“…Unfortunately, the poor solubility and the restricted drug-loading efficiency of native chitosan limit its applications in biomedical research. By modifying the structure of chitosan with hydrophilic groups, the solubility and the physicochemical properties of chitosan are greatly improved. − Nanoparticles prepared based on these chitosan derivatives further enhance the adsorption of antigen vaccines at the mucosal site and promote the uptake efficiency of vaccines by cells, broadening the usage of chitosan in the field of vaccine research. , Current studies mainly focus on the effective preparation of nano-carriers and the optimization of parametric properties, while the immunomodulatory function of nano-carriers themselves is still in the early research stage.…”
Nasal administration for vaccine delivery is a novel non-invasive vaccine administration approach that can induce local or systemic immune responses and overcome the disadvantages caused by traditional injectable administration. However, mucosal vaccine and adjuvant delivery systems with sustained-release ability and enhanced immune effects at mucosal sites have still been highly demanded. In this work, N-2-hydroxypropyl trimethyl ammonium chloride chitosan/N,O-carboxymethyl chitosan nanoparticles (N-2-HACC/CMCS NPs) with excellent mucosal absorption, high drug loading capacity, and enhanced immune responses were prepared by the ionic cross-linking method. To evaluate the potential capacity of the N-2-HACC/CMCS NPs as a vaccine adjuvant and the molecular mechanism for the induction of enhanced mucosal and systemic immune responses, bovine serum albumin (BSA) was employed as a general model antigen and loaded into the N-2-HACC/CMCS NPs to prepare a BSA-loaded N-2-HACC/CMCS adjuvant vaccine (N-2-HACC/CMCS/BSA NPs). It was well demonstrated that the N-2-HACC/CMCS/BSA NPs with great biostability and mucosal absorption could effectively promote the proliferation of lymphocytes and the secretion of related pro-inflammatory factors, resulting in the stimulation of specific mucosal and systemic immune responses. This study revealed that the chitosan-based nano-delivery system can act as the mucosal vaccine adjuvant and possesses great promise in viral infectious diseases and immunization therapy.
“…This temperature-responsive and good biocompatibility characteristic have led to Pluronic F127’s wide range of applications in biology. − Our design strategies for preparing high-strength and printable hydrogel were that hydrogel could form hydrophobic/hydrophilic zones. So, we chose PEG as the hydrophilic constructional element rather than other biomaterials, such as polysaccharides, and proteins, owing to its good biocompatibility, water solubility, and pH insensitivity. − Otherwise, to increase the product’s durability, hydrogel should have characteristics like self-healing abilities. , Herein, the acylhydrazone bond was introduced into the hydrogel’s design, which was formed by the reaction of the acylhydrazine and benzaldehyde terminals. − …”
Constructing hydrogels, which exhibit ultrastretchable and energy dissipation ability, are suitable for engineering. However, the hydrogel exhibited both ultrastretchable and flowable properties, which were usually contradictory in hydrogel design. It remains a challenge to achieve a hydrogel with a highstrength property and a 3D printable capacity. Herein, hydrogel tPEG-az-F127 was prepared by condensation of acylhydrazineterminated three-armed PEG and benzaldehyde-terminated Pluronic F127, exhibiting high stretchability and 3D printable capability. These outstanding performances of hydrogel resulted from dynamic reversible covalent-bond of acylhydrazone bond and hydrophilicity−hydrophobicity transformation of Pluronic F127 moiety. Furthermore, the technical conditions for preparing the hydrogel, such as solid concentrations and gelation time, were optimized by the optical rheometer experiment. The principles of the switch-mode hydrogel, which can switch between highstretchability and printability, have been comprehensively studied with dynamic light scattering (DLS), swelling, tensile and rheological tests. Furthermore, as the temperature increases from 10 to 25 °C, the hydrogel tPEG-az-F127-20 exhibits a rapid storage modulus (G′) change from 1 and 40 kPa, which is attributed to the thermal-driven increasing hydrophobicity of Pluronic F127 moiety. According to the thermosensitive switch-mode hydrogel, a pneumatical-type 3D printing was conducted to fabricate constructs of good shape and stability within human body temperature, which will be a potential candidate for 3D printable ink in the fields of tissue engineering.
“…biocompatibility, biodegradability, non-toxicity and low immunogenicity, makes chitosan the second most abundant natural polymer in the world (Cao et al, 2018. Chitosan is a weak base, which is soluble in an aqueous acidic media and produces highly viscous solutions suitable for the preparation of free films and coatings (Rahmouni et al, 2018). Chitosan exhibits excellent mucoadhesive properties due to presence of reactive hydroxyl and amino groups providing excessive hydrogen bonding as well as a positive charge, resulting in a unique linear polycation with a high charge density (Agarwal et al, 2018).…”
Section: Discussionmentioning
confidence: 99%
“…Its unique properties such as biocompatibility, biodegradability, non-toxicity and low immunogenicity make chitosan the second most abundant natural polymer in the world [130,131], and due to its weak alkaline nature, chitosan is solubilized by aqueous acidic media and produces highly viscous solutions suitable for the preparation of free films and coatings [132].…”
Section: Methodsmentioning
confidence: 99%
“…From the pharmaceutical aspect, both polymeric micro-and nanoparticles are of emerging interest since they show better stability and therefore better preservation capacity against the degrading effect of the GI environment compared to the carriers of fatty origin, such as liposomes [132]. The effectiveness of protein drugs may be improved successfully with both micro-and nanoencapsulation [133] via protection from hydrolysis and proteolytic enzymes and the improvement of their absorption, in addition to their mucoadhesive properties and permeation enhancing characteristics [134].…”
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