Scholarlink

<p>Diabetes-induced cognitive dysfunction remains an unaddressed medical concern across the globe with limited options left with conventional drug therapy. Piracetam, the first identified nootropic agent has been repurposed in the current study via solid-lipid nanoparticle against streptozotocin-induced cognitive dysfunction in rats. Experimental piracetam loaded solid-lipid nanoparticles (PSLNs) were developed by conventional nanoprecipitation method and characterized in terms of SEM, AFM, DLS, zeta potential, drug loading efficiency etc. <i>In vivo</i> efficacy of the selected PSLNs was analysed. Various biochemical parameters were analysed along with histopathology and brain pharmacokinetic studies. Experimental PSLNs were spherical, nanosized, homogenous (PDI: 0.21 ± 0.5) with −&#xa0;38.2 ± 0.3&#xa0;mV surface charge. Following administration, selected PSLNs brought significant improvement in behavioural and memory function as compared to plain piracetam and control rat groups. Modulation in key enzyme/ protein expression in terms of SOD, CAT, GSH was observed <i>in vivo</i> in PSLNs treated rats. Histopathology of brain tissue in AD rats indicated revival of normal tissue architecture in PSLNs treated group as compared to piracetam/control groups. Key brain pharmacokinetic parameters like AUC, AUMC, MRT etc. were substantially improved for PSLNs than plain piracetam, signifying higher accumulation and retention of the drug following nanoencapsulation. However, futuristic studies are necessary to establish PSLNs as a potent modality against diabetes-induced cognitive dysfunction in clinical settings.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Solid lipid nanoparticles enhance piracetam’s neuroprotective action in streptozotocin-induced cognitive dysfunction

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月29日

查看全文
  • Abhishek Mishra,
  • Bhabani Sankar Satapathy,
  • Pratap Kumar Sahu

摘要

Diabetes-induced cognitive dysfunction remains an unaddressed medical concern across the globe with limited options left with conventional drug therapy. Piracetam, the first identified nootropic agent has been repurposed in the current study via solid-lipid nanoparticle against streptozotocin-induced cognitive dysfunction in rats. Experimental piracetam loaded solid-lipid nanoparticles (PSLNs) were developed by conventional nanoprecipitation method and characterized in terms of SEM, AFM, DLS, zeta potential, drug loading efficiency etc. In vivo efficacy of the selected PSLNs was analysed. Various biochemical parameters were analysed along with histopathology and brain pharmacokinetic studies. Experimental PSLNs were spherical, nanosized, homogenous (PDI: 0.21 ± 0.5) with − 38.2 ± 0.3 mV surface charge. Following administration, selected PSLNs brought significant improvement in behavioural and memory function as compared to plain piracetam and control rat groups. Modulation in key enzyme/ protein expression in terms of SOD, CAT, GSH was observed in vivo in PSLNs treated rats. Histopathology of brain tissue in AD rats indicated revival of normal tissue architecture in PSLNs treated group as compared to piracetam/control groups. Key brain pharmacokinetic parameters like AUC, AUMC, MRT etc. were substantially improved for PSLNs than plain piracetam, signifying higher accumulation and retention of the drug following nanoencapsulation. However, futuristic studies are necessary to establish PSLNs as a potent modality against diabetes-induced cognitive dysfunction in clinical settings.