首页> 外文期刊>International Journal of Pharmaceutics >Preparation and characterization of 4-dedimethylamino sancycline (CMT-3) loaded nanostructured lipid carrier (CMT-3/NLC) formulations
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Preparation and characterization of 4-dedimethylamino sancycline (CMT-3) loaded nanostructured lipid carrier (CMT-3/NLC) formulations

机译:负载4-去二甲氨基三环素(CMT-3)的纳米结构脂质载体(CMT-3 / NLC)制剂的制备和表征

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Chemically modified tetracyclines (CMTs) have been reported to strongly inhibit proliferation and metastasis of various cancers, but their efficacy is restricted by poor water solubility. In the present study, a hydrophilic 4-dedimethylamino sancycline (CMT-3) loaded nanostructured lipid carrier (CMT-3/NLC) was produced by high pressure homogenization (HPH). The physical properties of CMT-3/NLC formulations were characterized by dynamic light scattering (DLS), high efficiency liquid chromatography (HPLC), atomic force microscopy (AFM), scanning electron microscopy (SEM), small-angle neutron scattering (SANS), small-angle X-ray scattering (SAXS) and wide-angle X-ray powder diffraction (XRD). The lipid and surfactant ingredients, as well as drug/lipid concentrations (m/m) were optimized to produce stable and sustained NLC formulations. In vitro cytotoxicity of CMT-3/NLC against HeLa cells was evaluated by MTT assay. The diameter of CMT-3/NLC was found to increase from 153.1 ± 3.0 nm to a maximum of 168.5 ± 2.0 nm after 30 days of storage, while the entrapment efficiency remained constant at >90%. CMT-3/NLC demonstrated a burst-sustained release profile in release media with different pH, a property attributed to the 3-dimensional structure of CMT-3/NLC. Cell uptake and localization studies indicated that NLC reached the cytoplasm and could thereby facilitate CMT-3 entry into HeLa cells.
机译:据报道,化学修饰的四环素(CMT)可以强烈抑制各种癌症的增殖和转移,但是它们的功效因水溶性差而受到限制。在本研究中,通过高压均质化(HPH)制备了亲水的4-脱二甲基氨基三环素(CMT-3)负载的纳米结构脂质载体(CMT-3 / NLC)。通过动态光散射(DLS),高效液相色谱(HPLC),原子力显微镜(AFM),扫描电子显微镜(SEM),小角中子散射(SANS)对CMT-3 / NLC制剂的物理性质进行了表征,小角度X射线散射(SAXS)和广角X射线粉末衍射(XRD)。对脂质和表面活性剂成分以及药物/脂质浓度(m / m)进行了优化,以生产稳定且持续的NLC制剂。通过MTT分析评估了CMT-3 / NLC对HeLa细胞的体外细胞毒性。储存30天后,发现CMT-3 / NLC的直径从153.1±3.0 nm增加到最大168.5±2.0 nm,而包封效率保持恒定在> 90%。 CMT-3 / NLC在具有不同pH值的释放介质中表现出爆发持续释放特性,这归因于CMT-3 / NLC的3维结构。细胞摄取和定位研究表明NLC到达了细胞质,从而可以促进CMT-3进入HeLa细胞。

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