Chitosan Nanophormulations | Purpose | Findings | Refs. |
---|---|---|---|
Oral drugs semi-synthetic biopolymer chitosan complexes | Drug delivery developing | ↑Solubility, ↑formation and ↑stability of SSBC | [79] |
Rasagiline encapsulated chitosan-coated PLGA nanoparticles | Evaluation of encapsulation efficiency | ↑Bioavailability in the brain | [80] |
Chitosan, hydroxypropylmethylcellulose, pluronic F127, polyaniline, BCNU-Nano-co-Plex | Nose to brain drug delivery system developing | ↑ Release of bioactive agent | [81] |
Mnps coated with non-cross-linked chitosan | In vitro/Evaluating of rat aortic endothelial cells (ecs) viability In vivo/ evaluating issue distribution | no effect on cell viability ↑biocompatibility of MNPs | [82] |
Chitosan nanospheres with methotrexate | In vitro/ evaluating of nanoparticles containing methotrexate | Sustained release, ↑ Passive targeted delivery system for MTX, ↓ Side effects of the drug | [83] |
Chitosan/gelatin nanocarriers | In vitro evaluation /for calcium hydroxide delivery | ↑ Release of calcium ions | [84] |
Chitosan grafted halloysite nanotubes | In vitro/ evaluation of anticancer effect of curcumin on hepg2, mcf-7, sv-huc-1, ej, caski, hela cells | ↑ Anticancer effect ↑ Apoptosis | [85] |
Curcumin-loaded O-CMCS/n-zno nanocomposite | In vitro efficacy/ evaluation of delivery of curcumin on MA104 cells | ↑ Curcumin release | [87] |
Chitosan nanoparticles Chitosan beads | Betamethasone and teracycline encapsulation efficiency | Drug released from chitosan nanoparticles is lower than that released from chitosan beads | [88] |
Encapsulating chitosan (CS) nanoparticles (nps) | Chemotherapeutics targeted delivery | ↑ Tissue targeting ↑ Controlled drug release | [89] |
Pyrazolopyrimidine, pyrazolopyridine thioglycosides encapsulated by chitosan nanoparticles | In vitro efficacy/huh-7, mcf-7 cells | ↑ Anti-cancerous activity | [90] |
Raloxifene-encapsulated hyaluronic acid-decorated chitosan | In vitro efficacy/ lung a549 cancer cell line | ↑Cytotoxicity ↑ entrapment efficiency | [91] |
Self-aggregates from deoxycholic acid-modified chitosan | Delivery vehicle of genes | ↑Anti-cancer effect | [92] |
Cytarabine-loaded chitosan nanoparticles | Drug delivery system | ↑Anti-cancer effect | [93] |
10-hydroxycamptothecine nanoneedles Methotrexate-chitosan conjugate | Dual-drug delivery system | ↑Anti-cancer effect | [94] |
Fe3O4/carboxymethyl-chitosan nanoparticles | Model anti-tumour drug | ↑Cellular uptake ↓rapa drug damage | [95] |
Encapsulated Fe3O4-blf | In vivo /mice | Complete regression of the tumour | [96] |
Doxorubicin-loaded zein nanoparticles | In vitro/ cancer cells | ↑anti-cancer effect | [97] |
DTX-HGC nanoparticles | In vitro /A549 lung cancer cells | Antitumor efficacy | [98] |
Tamoxifen nanoformulations | In vitro efficacy/ rat intestinal tissue | ↑Drug permeated | [99] |
Letrozole with chitosan nanoparticles | Pharmaceutical carrier | ↑Anticancer efficacy | [100] |
Ciprofloxacin hydrochloride-loaded nanoparticles | Drug carrier | ↑Ciprofloxacin release | [101] |
5-fluorouracil CS-SPION | Drug carrier | ↑Drug loading efficiency | [106] |
Chitosan nanospheres with 5-FU | In vitro/ HT29 and PC-3 cells | ↓Tumour cell proliferation ↓HT29, PC-3 adhesion | [107] |
Chitosan-coated curcumin nanocrystals | In vitro and in vivo/murine model of lps induced endotoxemia | ↑Nrf2, ↑GST, ↑SOD, ↑NF-kB | [109] |
Simvastatin loaded nanoparticle | In vivo/mice | ↓Lipid profile | [125] |