Table 1.
Examples of polysaccharides-based nanoparticles.
Materials | Composition of Nanoparticles | Significances | Ref. |
---|---|---|---|
Chitosan | Ascorbic acid, pentasodium tripolyphosphate | Antioxidative; reduced viability of cervical cancer cells; nontoxic to human normal cells | [40] |
EGFR binding peptide, PEG2000, Mad2 siRNA | Selective uptake by NSCLC cells; stronger tumor inhibition in a drug-resistant model | [41,42] | |
Folate, curcumin | Targeted folate receptors; enhanced toxicity to breast cancer cells; controlled release in acidic environments | [43] | |
Glycyrrhetinic acid, doxorubicin | Enhanced cellular uptake and cytotoxicity of doxorubicin | [45] | |
PNVCL, cell-penetrating peptide, doxorubicin | Controlled in acidic and hyperpyrexic conditions; selective cellular uptake; stronger tumor inhibition and lower systemic toxicity | [47] | |
Hyaluronic acid | Cisplatin, siRNA, near IR dye indocyanine green (ICG), various fatty amines or cationic polyamines | Targeted CD44 receptors; effective in combination treatments against resistant cancers | [48,49] |
L-lysine methyl ester, lipoic acid, doxorubicin | Controlled release of doxorubicin triggered by GSH; targeted CD44 receptors | [50] | |
PEGylated cationic quaternary amine, n-octyl acrylate segments, doxorubicin | Controlled release in acidic environments; antibacterial; overcame bacteria-induced tumor resistance | [51] | |
Glycyrrhetinic acid, L-histidine, doxorubicin | Controlled release in acidic environments; improved antitumor efficacy of doxorubicin | [52] | |
Polycaprolactone, 2-(Pyridyldithio)-ethylamine, doxorubicin | Improved performance of doxorubicin; targeted delivery; controlled release in acidic environments | [53] | |
Dodecylamide, docetaxel | Inhibited the growth of A549 cells; stable in human plasma | [54] | |
PLGA, PEI, docetaxel, α-naphthoflavone | Overcame the multidrug resistance; improved bioavailability of docetaxel | [55] | |
Alginate | Thiolated sodium alginate, fluorescein-labeled wheat germ agglutinin (fWGA), docetaxel | Selective uptake by cancer cells; stronger cytotoxicity toward HT-29 cells; degraded by GSH | [62] |
Disulfide crosslinked alginate, doxorubicin | Improved safety profile of doxorubicin; selective uptake by cancer cells; | [64] | |
Poly(allylamine hydrochloride), poly(4-styrenesulfonic acid-co-maleic acid) sodium salt, paclitaxel | Selective uptake by HT-29 cells; induced cell death to the cancer cells | [65] | |
pheophorbide A, doxorubicin | GSH dose-dependent release manner of payloads; accumulated in the tumor site; combination of chemotherapy and photodynamic therapy | [66] | |
Dextran | Carboxymethyl dextran, lithocholic acid, doxorubicin | Release triggered by GSH; improved therapeutic efficacy and biodistribution profile of doxorubicin | [68] |
Curcumin, methotrexate | Sustained release; synergistic effect in treating MCF-7 cells. | [72] | |
Chlorin e6, gold nanoparticles | Efficient cellular uptake; no leakage; accumulation of chlorin e6 at tumor site | [73] | |
Dextran acrylate, stearyl amine microRNAs | Stabilized and delivered microRNAs into the carcinoma cells; suppressed osteosarcoma cell proliferation | [74] | |
PEGylated dextran, siRNA | Changed biodistribution and cellular uptake without affecting cytotoxicity | [75] | |
Folic acid, doxorubicin | Enhanced tumor inhibition; targeting folate receptors | [76] |