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新型载有丁丙诺啡的利福平/聚乙二醇/海藻酸钠纳米粒子的杂交体的制备方法。

New method of creating hybrid of buprenorphine loaded rifampin/polyethylene glycol/alginate nanoparticles.

机构信息

Department of Chemical Engineering, North Tehran Branch, Islamic Azad University, P.O. Box 1651153311, Tehran, Iran.

Department of Chemical Engineering, North Tehran Branch, Islamic Azad University, P.O. Box 1651153311, Tehran, Iran.

出版信息

Int J Biol Macromol. 2020 Sep 15;159:204-212. doi: 10.1016/j.ijbiomac.2020.05.065. Epub 2020 May 19.

Abstract

An indicator for cytochrome P450 enzymes which have the most fundamental role in methadone metabolism in the liver. In this study preparation in vitro, in vivo release and biological activities of FeO@ZnO/rifampin/polyethylene glycol/buprenorphine/alginate nanoparticles investigated. Rifampin is activator for the cytochrome P-3 enzymes which can detoxify residual drugs in the liver. This paper examines the changes pH, absorption rate, drug release, in vivo test (30 rats) in selected Wistar rats. All rats were either orally addicted to morphine after 21 days. After establishing dependence based on an observation of behavioral parameters the ability to quit the new drug was evaluated. In vitro and in vitro tests on antibacterial activity and multiple intestinal inflammation in addicts were conducted. Recent drug delivery systems that use polymers cause more sustainability of drug in the body and also prevent drug interactions. This research showed the success of decreasing consumption dose of the drug from 0.004 to 0.0005 mg, increasing lifetime from 24 to 32 h to 72-96 h, and decreasing the number of hepatic tissues that were damaged. The results of this investigation were confirmed by clinical tests and the dyeing process of mason tri‑chromium and hematoxylin and eosin.

摘要

一种细胞色素 P450 酶的指示剂,在肝脏中对美沙酮代谢起着最基本的作用。本研究采用体外制备、体内释放和生物活性方法,研究了 FeO@ZnO/利福平/聚乙二醇/丁丙诺啡/海藻酸钠纳米粒子。利福平是细胞色素 P-3 酶的激活剂,可解毒肝脏中的残留药物。本文研究了所选 Wistar 大鼠的 pH 值、吸收速率、药物释放、体内试验(30 只大鼠)的变化。所有大鼠在 21 天后均经口滥用吗啡。在基于行为参数观察建立依赖性后,评估了停止新药物的能力。对吸毒者进行了体外和体外抗菌活性和多发性肠炎症试验。最近使用聚合物的药物输送系统可使药物在体内更具可持续性,并防止药物相互作用。这项研究表明,成功地将药物的消耗剂量从 0.004 降低到 0.0005mg,将半衰期从 24 小时增加到 32 小时增加到 72-96 小时,并减少了受损的肝组织数量。这项研究的结果通过临床测试和三铬酸甲和苏木精伊红染色过程得到了证实。

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