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pAn efficient and long-acting local anesthetic: ropivacaine-loaded lipid-polymer hybrid nanoparticles for the control of pain/p

机译:>一种高效和长效的局部麻醉:加载Ropivaine加载的脂质 - 聚合物杂交纳米粒子,用于控制疼痛

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Purpose: Local anesthetics are used clinically for the control of pain following operation (including gastrointestinal surgery) or for the management of other acute and chronic pain. This study aimed to develop a kind of lipid-polymer hybrid nanoparticles (LPNs), which were constructed using poly(ethylene glycol)-distearoylphosphatidylethanolamine (PEG-DSPE) as the hydrophilic lipid shell and poly-ε-caprolactone (PCL) as the hydrophobic polymeric core. Methods: Ropivacaine (RPV) was entrapped in the LPNs (RPV-LPNs) and the physicochemical and biochemical properties such as size, zeta potential, drug release, and cytotoxicity were studied. The long-lasting effects and safety aspects of the LPNs were evaluated in vitro and in vivo. Results: The particle size and zeta potential of RPV-LPNs were 112.3±2.6 nm and -33.2±3.2 mV, with an entrapment efficiency (EE) of 90.2%±3.7%. Ex vivo permeation efficiency of LPNs was better than the drug solution. The RPV-LPNs exhibited a long-lasting in vivo anesthesia effect in both rats and mice. Conclusion: Considering the low cytotoxicity, the LPNs prepared here could be used as an efficient local anesthetic for the control of pain.
机译:目的:局部麻醉剂在临床上使用术后疼痛(包括胃肠外科)或用于管理其他急性和慢性疼痛。本研究旨在开发一种脂质 - 聚合物杂交纳米颗粒(LPN),其使用聚(乙二醇)-distearoylphosphatidyl乙醇胺(PEG-DSPE)作为亲水性脂壳和聚-ε-己内酯(PCL)作为疏水性构建聚合物核心。方法:研究罗哌卡因(RPV)捕获LPNS(RPV-LPN),研究了诸如尺寸,Zeta潜力,药物释放和细胞毒性的物理化学和生化特性。在体外和体内评估LPN的持久效果和安全方面。结果:RPV-LPN的粒度和Zeta电位为112.3±2.6nm和-33.2±3.2mV,夹带效率(EE)为90.2%±3.7%。 LPN的离体渗透效率优于药物溶液。 RPV-LPN在大鼠和小鼠中表现出持久的体内麻醉作用。结论:考虑到低细胞毒性,这里制备的LPN可用作控制疼痛的有效局部麻醉剂。

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