2020
DOI: 10.1016/j.ijbiomac.2020.03.065
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Chitosan, N,N,N-trimethyl chitosan (TMC) and 2-hydroxypropyltrimethyl ammonium chloride chitosan (HTCC): The potential immune adjuvants and nano carriers

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Cited by 68 publications
(34 citation statements)
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“…The replacement of the primary amino group from C2 of chitosan with a quaternary amino group leads to the development of electrostatic bonds between the formed derivative and the sialic acid in the mucosa, improving the mucoadhesion, but also the immunostimulatory effect [ 34 ].…”
Section: Properties Of Chitosan and Its Derivativesmentioning
confidence: 99%
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“…The replacement of the primary amino group from C2 of chitosan with a quaternary amino group leads to the development of electrostatic bonds between the formed derivative and the sialic acid in the mucosa, improving the mucoadhesion, but also the immunostimulatory effect [ 34 ].…”
Section: Properties Of Chitosan and Its Derivativesmentioning
confidence: 99%
“…In the case of vaccines, a vehicle is needed to deliver the antigen and, preferably, to have a nonspecific immunostimulatory effect, which improves the efficiency of immunization [ 34 ]. To increase the immune response of vaccines, adjuvants are introduced into their component, increasing the potency and efficiency of immunization.…”
Section: Chitosan In the Development Of Intranasal Vaccinesmentioning
confidence: 99%
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“…This polymer was found to be suitable for preparing nanosystems such as polymeric NPs. In particular, Jin et al [27], prepared HACC-based NPs by ionotropic crosslinking with carboxymethyl chitosan (CMC) as a carrier of Newcastle disease virus (NDV) [69]. HACC has shown good antimicrobial and antifungal activity in itself, coupled with NDV activity.…”
Section: Quaternary Ammonium Chitosan Derivatives: Principal Charactementioning
confidence: 99%
“…In addition, chitosan can be easily functionalized to obtain the desired targeted delivery of therapeutic agents. Chemical modification of chitosan results in the formation of several derivatives [14] with improved solubility in several biological media (e.g., intestinal media-n-trimethyl chitosan chloride [15]) or enhanced mucoadhesiveness (thiolated chitosan [16]). The primary amine (-NH 2 ) groups of chitosan provide a reaction site for chemical modification, which can enhance the stability and drug encapsulation efficiency and thus open ways to various utilizations in pharmaceutical and medical fields [17].…”
Section: Introductionmentioning
confidence: 99%