2021
DOI: 10.3390/ijms22179652
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Advances in Chitosan-Based Nanoparticles for Drug Delivery

Abstract: Nanoparticles (NPs) have an outstanding position in pharmaceutical, biological, and medical disciplines. Polymeric NPs based on chitosan (CS) can act as excellent drug carriers because of some intrinsic beneficial properties including biocompatibility, biodegradability, non-toxicity, bioactivity, easy preparation, and targeting specificity. Drug transport and release from CS-based particulate systems depend on the extent of cross-linking, morphology, size, and density of the particulate system, as well as phys… Show more

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Cited by 298 publications
(145 citation statements)
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References 233 publications
(418 reference statements)
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“…Moreover, CS can open the TJs between epithelial cells and inhibit the P-glycoprotein (P-gp) efflux transporter of epithelial cells, thus significantly facilitating the encapsulated molecules by the paracellular transport mechanism [69,70]. [71].…”
Section: Chitosan Nanoparticles For Oral Deliverymentioning
confidence: 99%
See 1 more Smart Citation
“…Moreover, CS can open the TJs between epithelial cells and inhibit the P-glycoprotein (P-gp) efflux transporter of epithelial cells, thus significantly facilitating the encapsulated molecules by the paracellular transport mechanism [69,70]. [71].…”
Section: Chitosan Nanoparticles For Oral Deliverymentioning
confidence: 99%
“…The PS of CS-NPs is directly dependent on the CS concentration in the formulation. Moreover, CS-NPs with high-molecular weight CS show a significantly higher PS compared to CS-NPs prepared with low-molecular weight CS [71]. The absorption of NPs by epithelial cells or M cells after oral administration greatly depends on the PS of NPs, which can affect the oral absorption efficiency as well as the speed of absorption.…”
Section: Phytochemical-loaded Cs-nps For Improved Oral Bioavailability and Bioactivitymentioning
confidence: 99%
“…The active functional groups from the structure of chitosan can undergo reactions such as hydroxylation, carboxylation, alkylation, acylation, and esterification that help introduce pendant groups, destroy the crystal structure, and consequently enhance the solubility of the resulted material. This possibility of facile modification expands the chitosan application range and dosage form [23,66,67].…”
Section: Natural Polymers 211 Chitosanmentioning
confidence: 99%
“…In the last decade, great efforts have been focused on increasing the bioavailability and solubility of poorly soluble drugs. Generally, the developed techniques tried to enhance the drug dissolution rate by introducing the drug into a solid dispersion [ 1 , 2 , 3 ].…”
Section: Introductionmentioning
confidence: 99%