| Literature DB >> 24892632 |
Daquan Chen1, Shengnan Lian1, Jingfang Sun1, Zongliang Liu1, Feng Zhao1, Yongtao Jiang1,2, Mingming Gao3, Kaoxiang Sun1,2, Wanhui Liu1,2, Fenghua Fu1,2.
Abstract
In this study, to develop a multifunctional targeting nano-carrier drug delivery system for cancer therapy, the novel pH-sensitive ketal based oligosaccharides of hyaluronan (oHA) conjugates were synthesized by chemical conjugation of hydrophobic menthone 1,2-glycerol ketal (MGK) to the backbone of oHA with the histidine as the linker of proton sponge effect. The multifunctional oHA conjugates, oHA-histidine-MGK (oHM) carried the pH-sensitive MGK as hydrophobic moieties and oHA as the target of CD44 receptor. The oHM could self-assemble to nano-sized spherical shape with the average diameters of 128.6 nm at pH 7.4 PBS conditions. The oHM nanoparticles (oHMN) could release encapsulated curcumin (Cur) with 82.6% at pH 5.0 compared with 49.3% at pH 7.4. The results of cytotoxicity assay indicated that encapsulated Cur in oHMN (Cur-oHMN) were stable and have less toxicity compared to Cur suspension. The anti-tumor efficacy in vivo suggested that Cur-oHMN suppressed tumor growth most efficiently. These results present the promising potential of oHMN as a stable and effective nano-sized pH-sensitive drug delivery system for cancer treatment.Entities:
Keywords: 2-glycerol ketal (oHM); Drug delivery; nanoparticles; oHA-histidine– menthone 1; oligosaccharides of hyaluronan (oHA); pH-sensitive
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Year: 2014 PMID: 24892632 DOI: 10.3109/10717544.2014.917130
Source DB: PubMed Journal: Drug Deliv ISSN: 1071-7544 Impact factor: 6.419