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载有维格列汀的三角型 DNA 纳米球,表面包覆有聚甲基丙烯酸乙酯,用于 2 型糖尿病的口服传递和更好的血糖控制。

Vildagliptin loaded triangular DNA nanospheres coated with eudragit for oral delivery and better glycemic control in type 2 diabetes mellitus.

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan; School of Chemistry and Chemical Engineering, Nanjing University, PR China.

Department of Pharmaceutical Chemistry, University College of Pharmacy, University of the Punjab, Lahore Pakistan.

出版信息

Biomed Pharmacother. 2018 Jan;97:1250-1258. doi: 10.1016/j.biopha.2017.11.059. Epub 2017 Nov 14.

Abstract

Diabetes mellitus type 2 is a multidimensional disease associated with poor glycemic control through compromised sensitivity of pancreatic islet α and β cells against glucose and dwindled secretion of insulin which is linked with the quantity of incretin hormones that are abridged by dipeptidyl peptidase-4 (DPP-4) in diseased condition. Vildagliptin (VG) inhibits DPP-4 therefore regulates the incretins that conversely maintains glycemic control. The safe reach and absorption of VG from intestine was dubious. Therefore we used Electrostatic Attraction Method to develop drug loaded DNA nanotechnology triangles coated by Eudragit (Eud) to make stable nanospheres of Vildagliptin (VG). We further analyzed the formulated nanospheres by AFM, XRD, DSC, SEM, TGA, ATR-FTIR and native PAGE. Additionally the efficacy of formulated nanospheres for drug release and glycemic control was assessed in Db/Db mouse. Our results showed that formulated nanospheres are smooth, spherical, stable and uniform in size ranging from 500 to 2000 nm with drug entrapment efficiency up to 95 ± 2% and extended drug release up to 15 ± 2 h. FTIR and DSC results confirmed the absence of VG-DNA-Eud interaction and XRD studies revealed a change in the crystalline status of the VG in nanospheres. Ex-vivo studies indicate that Eud-DNA-VG nanospheres effectively bypasses the acidic pH of the stomach and enhances glycemic control in Db/Db mouse without any risk of pancreatitis or pancreatic cancer. To the best of our knowledge, this is the first study conclusively reporting that VG loaded DNA Nano-architects coated with Eudragit are stable, safe and may improve therapeutic outcomes after oral delivery.

摘要

2 型糖尿病是一种多维疾病,与胰腺胰岛 α 和 β 细胞对葡萄糖的敏感性降低以及胰岛素分泌减少有关,而胰岛素分泌减少与在疾病状态下被二肽基肽酶-4(DPP-4)缩短的肠降血糖素激素的量有关。维格列汀(VG)抑制 DPP-4,因此调节肠降血糖素,从而反过来维持血糖控制。VG 从肠道的安全摄取和吸收是值得怀疑的。因此,我们使用静电吸引法开发载药 DNA 纳米技术三角形,并用 Eudragit(Eud)涂覆,制成维格列汀(VG)的稳定纳米球。我们进一步通过 AFM、XRD、DSC、SEM、TGA、ATR-FTIR 和天然 PAGE 对所制备的纳米球进行分析。此外,还在 Db/Db 小鼠中评估了所制备的纳米球用于药物释放和血糖控制的效果。我们的结果表明,所制备的纳米球光滑、球形、稳定且大小均匀,粒径范围为 500 至 2000nm,药物包封效率高达 95±2%,药物释放时间延长至 15±2h。FTIR 和 DSC 结果证实了 VG-DNA-Eud 相互作用的不存在,XRD 研究表明 VG 在纳米球中的晶体状态发生了变化。离体研究表明,Eud-DNA-VG 纳米球可有效绕过胃的酸性 pH 值,并在 Db/Db 小鼠中增强血糖控制,而不会增加胰腺炎或胰腺癌的风险。据我们所知,这是第一项明确报告 VG 负载的 DNA 纳米结构,用 Eudragit 涂层,稳定、安全,并可能改善口服给药后的治疗效果。

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