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首页> 外文期刊>Materials science & engineering >Ultrasonically assisted preparation of poly (acrylic acid)/calcium phosphate hybrid nanogels as pH-responsive drug carriers
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Ultrasonically assisted preparation of poly (acrylic acid)/calcium phosphate hybrid nanogels as pH-responsive drug carriers

机译:超声辅助制备聚丙烯酸酯/磷酸钙杂化纳米凝胶作为pH响应药物载体

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摘要

Biocompatible, biodegradable and stimuli-responsive nanomaterials can be used as drug carriers and to achieve controlled drug delivery, which is crucial for treating tumors and lowering drug side effects. Calcium phosphate (CaP) nanoparticles and poly(acrylic acid) (PAA) hydrogels can be used as biocompatible and pH-responsive drug carriers. In this study, based on the ultrasound effect, PAA/CaP hybrid nanogels (approximately 100 nm, PDI < 0.2) are obtained via the cross-linking of CaP nanoparticles and PAA molecules between the Ca~(2+) ions and -COOH groups. The PAA/CaP hybrid nanogels show good stability in biological media as well as no hemolysis and no cytotoxicity to L02 cells. Moreover, the PAA/CaP hybrid nanogels display an enhanced loading capacity (approximately 32%) for doxorubicin hydrochloride (DOX) compared to pure CaP nanoparticles (approximately 7.5%) and a pH-controlled drug release due to their dissolution in acidic environment. DOX can be delivered into cancer cells by the PAA/CaP hybrid nanogels, which show an inhibitory effect comparable to that of free DOX, although the inhibitory effect is delayed due to the slow release of DOX from the carriers. Jn vivo, the PAA/CaP hybrid nanogels cannot avoid the capture by the reticuloendothelial system; however, they show passive tumor targeting ability. In brief, the biocompatible, biodegradable and pH-responsive PAA/CaP hybrid nanogels have the potential to act as drug carriers for controlled drug release.
机译:具有生物相容性,可生物降解和刺激反应的纳米材料可以用作药物载体并实现受控的药物输送,这对于治疗肿瘤和降低药物副作用至关重要。磷酸钙(CaP)纳米颗粒和聚丙烯酸(PAA)水凝胶可用作生物相容性和pH响应药物载体。在这项研究中,基于超声效应,通过Ca〜(2+)离子与-COOH基团之间的CaP纳米颗粒和PAA分子的交联,获得了PAA / CaP杂化纳米凝胶(约100 nm,PDI <0.2)。 。 PAA / CaP杂化纳米凝胶在生物介质中显示出良好的稳定性,并且不溶血,对L02细胞无细胞毒性。此外,与纯CaP纳米颗粒(约7.5%)相比,PAA / CaP杂化纳米凝胶显示出对盐酸阿霉素(DOX)的增强的负载能力(约32%),并且由于它们在酸性环境中的溶解而可控制pH释放。 DOX可以通过PAA / CaP杂合纳米凝胶传递到癌细胞中,PAN / CaP杂合纳米凝胶显示出与游离DOX相当的抑制作用,尽管由于DOX从载体中缓慢释放而使抑制作用延迟。在体内,PAA / CaP杂化纳米凝胶无法避免被网状内皮系统捕获。但是,它们显示出被动的肿瘤靶向能力。简而言之,具有生物相容性,可生物降解且对pH敏感的PAA / CaP杂合纳米凝胶具有充当药物载体以控制药物释放的潜力。

著录项

  • 来源
    《Materials science & engineering》 |2017年第11期|688-697|共10页
  • 作者单位

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Biomedical Materials and Engineering Research Center of Hubei Province, Wuhan University of Technology, Wuhan 430070, PR China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Biomedical Materials and Engineering Research Center of Hubei Province, Wuhan University of Technology, Wuhan 430070, PR China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Biomedical Materials and Engineering Research Center of Hubei Province, Wuhan University of Technology, Wuhan 430070, PR China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Biomedical Materials and Engineering Research Center of Hubei Province, Wuhan University of Technology, Wuhan 430070, PR China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Biomedical Materials and Engineering Research Center of Hubei Province, Wuhan University of Technology, Wuhan 430070, PR China;

    Faculty of Applied Sciences, Sabaragamuwa University of Sri Lanka, 70140 Belihuloya, Sri Lanka;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Biomedical Materials and Engineering Research Center of Hubei Province, Wuhan University of Technology, Wuhan 430070, PR China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Ultrasonic synthesis; Poly(acrylic acid); Calcium phosphate; Hybrid nanogels; pH-sensitive drug carriers; Controlled delivery;

    机译:超声波合成;聚丙烯酸磷酸钙;杂化纳米凝胶;pH敏感药物载体;控制交货;

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