Stearyl polyoxyethylene-grafted heparin nanogel for oral delivery of Cisplatin: enhanced drug loading capacity and anticancer efficacy

IF 2.8 4区 工程技术 Q2 POLYMER SCIENCE
Huong Nguyen Thi, Thanh Vu Minh, Dung Vu Van, Huyen La Thi, Hong Phong Le Thi, Van Toan Nguyen, Le Hang Dang, Ngoc Quyen Tran, Phuong Le Thi
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引用次数: 0

Abstract

In this work, novel nanoparticles based on stearyl polyoxyethylene ether (Brij S100) and heparin for oral delivery of cisplatin were developed. The Brij S100 was covalently grafted with heparin (Hep) via the help of cystamine as a linker molecule and the successful conjugation of Hep and Brij S100 was proved by FT-IR and 1H-NMR spectroscopy techniques. The Hep-Brij S100 copolymer was self-assembled to form the micelle structure at the minimum concentration (CMC value) of 392 ± 23 µg/ml. Cisplatin (Cis) was loaded into the Hep-Brij S100 nanogels with high drug loading content (4.88%) and efficiency (93.60%). The results of DLS and SEM revealed the nanoscale of particles (170.5 nm) with homogeneity of dispersed colloidal nanoparticles. The in vitro release of Cis from Hep-Brij S100 nanogel followed the Fickian diffusion. Furthermore, the pH-responsive release profile of Cis showed that Hep-Brij S100 nanoformulation was suitable for oral administration, without inducing any cytotoxic effect on normal cells, even at the high concentration (100 mg/ml). Importantly, the Hep-Brij S100/Cis nanomedicine exerted better cytotoxicity (IC50 = 3.26 ± 0.19 µg/mL) than that of the free Cis (52.81 ± 6.26 µg/mL) on MCF7-breast cancer cells. These results strongly indicated that Hep-Brij S100 nanogels possess great potential for the oral delivery of chemotherapies.

Graphical abstract

用于顺铂口服给药的硬脂酰聚氧乙烯移植肝素纳米凝胶:增强载药能力和抗癌效果
在这项工作中,基于硬脂酰聚氧乙烯醚(Brij S100)和肝素的新型纳米颗粒被开发用于口服顺铂。通过半胱胺作为连接分子,将Brij S100与肝素(Hep)共价接枝,并通过FT-IR和1H-NMR技术证明了Hep与Brij S100的成功偶联。Hep-Brij S100共聚物在最小浓度(CMC值)为392±23µg/ml时自组装形成胶束结构。顺铂(Cis)被装入Hep-Brij S100纳米凝胶中,载药量高(4.88%),效率高(93.60%)。DLS和SEM的结果表明,纳米级颗粒(170.5 nm)具有均匀的分散胶体纳米颗粒。Hep-Brij S100纳米凝胶中Cis的体外释放遵循菲氏扩散。此外,Cis的ph响应释放谱表明,Hep-Brij S100纳米制剂适合口服给药,即使在高浓度(100 mg/ml)下也不会对正常细胞产生任何细胞毒性作用。重要的是,Hep-Brij S100/Cis纳米药物对mcf7乳腺癌细胞的细胞毒性(IC50 = 3.26±0.19µg/mL)优于游离Cis(52.81±6.26µg/mL)。这些结果强烈表明Hep-Brij S100纳米凝胶在口服给药方面具有巨大的潜力。图形抽象
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来源期刊
Macromolecular Research
Macromolecular Research 工程技术-高分子科学
CiteScore
4.70
自引率
8.30%
发文量
100
审稿时长
1.3 months
期刊介绍: Original research on all aspects of polymer science, engineering and technology, including nanotechnology Presents original research articles on all aspects of polymer science, engineering and technology Coverage extends to such topics as nanotechnology, biotechnology and information technology The English-language journal of the Polymer Society of Korea Macromolecular Research is a scientific journal published monthly by the Polymer Society of Korea. Macromolecular Research publishes original researches on all aspects of polymer science, engineering, and technology as well as new emerging technologies using polymeric materials including nanotechnology, biotechnology, and information technology in forms of Articles, Communications, Notes, Reviews, and Feature articles.
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