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载有右美托咪定的纳米微球联合经皮穴位电刺激对老年髋部骨折患者术后认知功能的影响。

The Impact of Dexmedetomidine-loaded Nano-microsphere Combined with Percutaneous Acupoint Electrical Stimulation on the Postoperative Cognitive Function of Elderly Patients with Hip Fracture.

机构信息

Department of Anesthesiology, Jingmen Hospital of Traditional Chinese Medicine, Jingmen, 448000, China.

Department of Anesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.

出版信息

Cell Mol Biol (Noisy-le-grand). 2022 Mar 31;68(3):77-85. doi: 10.14715/cmb/2022.68.3.10.

Abstract

To explore the impact of nano-microsphere loaded with dexmedetomidine (DEX) combined with percutaneous acupoint electrical stimulation on the postoperative cognitive function of elderly patients with hip fracture. The free base was prepared by the alkali precipitation method in this research, and then the drug was loaded into PLGA microspheres to construct the drug sustained-release system. The PLAG microspheres loaded with DEX (MS/DEX) were prepared by the O/W emulsion volatilization method and then Gel-(DEX-MS/BUP) suspension was obtained. A scanning electron microscope (SEM) was used to analyze the characterization of the prepared drug-loaded nano-microsphere, rheological analysis was performed on the copolymer solution, and in vivo release and degradation, experiments were carried out. Wistar rats were randomly divided into four groups (n=ten). After the sciatic nerve block model was established, the block time was observed after the injection of each sustained-release agent. The results showed that the gel-forming temperature of Gel and Gel-(DEX-MS/BUP) were 27.3°C and 26.3°C, respectively. Both MS/BUP and Gel-(DEX-MS/BUP) drugs could completely enter the blocking state. There was no loss of motor function in the rats after GEL-DEX. The clinical trials showed that Gel-(DEX-MS/BUP) system had good in situ and sustained release effects, and the analgesic effect of local anesthesia was significantly improved.

摘要

探讨载盐酸右美托咪定(DEX)纳米微球联合经皮穴位电刺激对老年髋部骨折患者术后认知功能的影响。本研究采用碱沉淀法制备游离碱,然后将药物载入 PLGA 微球构建药物缓释系统。采用 O/W 乳液挥发法制备载 DEX 的 PLAG 微球(MS/DEX),然后得到 Gel-(DEX-MS/BUP)混悬液。采用扫描电子显微镜(SEM)分析所制备的载药纳米微球的特征,对共聚物溶液进行流变分析,并进行体内释放和降解实验。Wistar 大鼠随机分为四组(n=10)。建立坐骨神经阻滞模型后,观察注射每种缓释剂后的阻滞时间。结果表明,Gel 和 Gel-(DEX-MS/BUP)的胶凝温度分别为 27.3°C 和 26.3°C。MS/BUP 和 Gel-(DEX-MS/BUP)药物均可完全进入阻滞状态。GEL-DEX 后大鼠无运动功能丧失。临床试验表明,Gel-(DEX-MS/BUP)系统具有良好的原位和持续释放效果,局部麻醉的镇痛效果显著提高。

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