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• W4220682502 abstract "Abstract Background Owing to the limited amount of research, there are no nanoparticle-based anticancer agents that use hydrophilic drugs. Therefore, we developed irinotecan-loaded self-agglomerating hyaluronan nanoparticles (ISHNs). While irinotecan has high hydrophilicity, the resulting nanoparticle should possess high anticancer drug-loading capacity and allow selective targeting of the cluster of differentiation 44 (CD44) protein, which is overexpressed on the surface of tumor cells. Results The ISHNs were successfully made with hyaluronan (HA) as a targeting moiety, FeCl 3 as a binder, and D-glutamic acid (GA) as a stabilizer. The ISHNs self-agglomerated via chelating bonding and were lyophilized using a freeze dryer. The particle diameter and zeta potential of the ISHNs were 93.8 ± 4.48 nm and − 36.3 ± 0.28 mV, respectively; a relatively narrow size distribution was observed. The drug fixation yield and drug-loading concentration were 58.3% and 1.75 mg/mL, respectively. Affinity studies revealed a tenfold stronger targeting to H23 (CD44 + ) non-small-cell lung cancer (NSCLC) cells, than of A549 (CD44 − ) cells. Conclusion We developed irinotecan-loaded ISHNs, which comprised irinotecan hydrochloride as a water-soluble anticancer agent, HA as a targeting moiety, FeCl 3 as a binder for self-agglomeration, and GA as a stabilizer; HA is a binding material for CD44 in NSCLC cells. Owing to their ease of manufacture, excellent stability, non-cell toxicity and CD44-targeting ability, ISHNs are potential nanocarriers for passive and active tumor targeting." @default.
• W4220682502 created "2022-04-03" @default.
• W4220682502 creator A5034374409 @default.
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• W4220682502 date "2022-03-09" @default.
• W4220682502 modified "2023-09-26" @default.
• W4220682502 title "Hyaluronan self-agglomerating nanoparticles for non-small cell lung cancer targeting" @default.
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• W4220682502 doi "https://doi.org/10.1186/s12645-022-00115-0" @default.
• W4220682502 hasPublicationYear "2022" @default.
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