氯胺酮
PLGA公司
乙二醇
化学
药理学
体内
纳米颗粒
止痛药
剂型
药物输送
材料科学
纳米技术
麻醉
医学
色谱法
有机化学
生物技术
生物
作者
Felicity Y. Han,Yun Liu,Vinod Kumar,Weizhi Xu,Guangze Yang,Chun‐Xia Zhao,Trent M. Woodruff,Andrew K. Whittaker,Maree T. Smith
标识
DOI:10.1016/j.ijpharm.2020.119291
摘要
Ketamine in sub-anaesthetic doses is an analgesic adjuvant with a morphine-sparing effect. Co-administration of a strong opioid with an analgesic adjuvant such as ketamine is a potential treatment option, especially for patients with cancer-related pain. A limitation of ketamine is its short in vivo elimination half-life. Hence, our aim was to develop biocompatible and biodegradable ketamine-loaded poly(ethylene glycol) (PEG)-block-poly(lactic-co-glycolic acid) (PLGA) nanoparticles for sustained release. Ketamine-encapsulated single polymer PEG-PLGA nanoparticles and double polymer PEG-PLGA/shellac (SH) nanoparticles with a high drug loading of 41.8% (drug weight/the total weight of drug-loaded nanoparticles) were prepared using a new sequential nanoprecipitation method. These drug-loaded nanoparticles exhibited a sustained-release profile for up to 21 days in vitro and for more than 5 days after intravenous injection in mice. Our study demonstrates that high drug loading and a sustained release profile can be achieved with ketamine-loaded PEG-PLGA nanoparticles prepared using this new nanoprecipitation method.
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