2014
DOI: 10.1016/b978-0-12-800148-6.00011-0
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Chitosan-Based Nanoparticles for Mucosal Delivery of RNAi Therapeutics

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Cited by 31 publications
(18 citation statements)
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“…33,34 Martirosyan et al utilized the mucoadhesive properties of chitosan for the delivery of siRNA across the mucosal surfaces following local administration. 35 Prego et al reported that chitosan NPs increased the intestinal absorption of salmon calcitonin, due to their mucoadhesive character and intimate interaction with the intestinal barrier. 36…”
Section: Mucosal Drug Deliverymentioning
confidence: 99%
“…33,34 Martirosyan et al utilized the mucoadhesive properties of chitosan for the delivery of siRNA across the mucosal surfaces following local administration. 35 Prego et al reported that chitosan NPs increased the intestinal absorption of salmon calcitonin, due to their mucoadhesive character and intimate interaction with the intestinal barrier. 36…”
Section: Mucosal Drug Deliverymentioning
confidence: 99%
“…The reported Mg-based micromotors rely on the combination of a CLR-loaded poly(lactic-co-glycolic acid) (PLGA) layer and a chitosan polymer layer covering on a propellant Mg core to offer high drug-loading capacity, along with biodegradability. The positively charged chitosan outer coating enables adhesion of the motor onto the stomach wall 35 , facilitating efficient localized autonomous release of CLR from the PLGA polymer coating. In contrast to acid suppression by PPIs, Mg-based micromotors can temporally and physically alter the local acidic environment by quickly depleting protons while propelling within the stomach 24 .…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, developing formulations that are suitable and can be applied to oral delivery of miRNAs is highly sought. Literature has identified that chitosan [80], mannose modified chitosan [81], bovine milk-derived exosomes [82], bovine lactoferrin [83], lipidic [84], and PLGA-based nanoformulations [85] are employed for effective oral delivery of miRNAs/therapeutics. Hence, developing oral nanoformulation(s) of miRNAs is achievable and is highly recommended for its successful implementation into the clinic.…”
Section: Expert Opinionmentioning
confidence: 99%