Your browser doesn't support javascript.
loading
Oral Delivery of Honokiol Microparticles for Nonrapid Eye Movement Sleep.
Yang, Yang; Wang, Tianxiao; Guan, Juan; Wang, Juan; Chen, Junyi; Liu, Xiaoqin; Qian, Jun; Xu, Xinhong; Qu, Weimin; Huang, Zhili; Zhan, Changyou.
Afiliación
  • Chen J; School of Pharmacy and Key Laboratory of Smart Drug Delivery, Ministry of Education , Fudan University , Shanghai 201203 , China.
  • Liu X; Department of Pharmaceutical Engineering , Chongqing Chemical Industry Vocational College , Chongqing 401220 , China.
  • Qian J; School of Pharmacy and Key Laboratory of Smart Drug Delivery, Ministry of Education , Fudan University , Shanghai 201203 , China.
  • Qu W; State Key Laboratory of Medical Neurobiology, and Institutes of Brain Science and Collaborative Innovation Center for Brain Science , Fudan University , Shanghai 200032 , China.
  • Huang Z; State Key Laboratory of Medical Neurobiology, and Institutes of Brain Science and Collaborative Innovation Center for Brain Science , Fudan University , Shanghai 200032 , China.
  • Zhan C; School of Pharmacy and Key Laboratory of Smart Drug Delivery, Ministry of Education , Fudan University , Shanghai 201203 , China.
Mol Pharm ; 16(2): 737-743, 2019 02 04.
Article en En | MEDLINE | ID: mdl-30652875
Honokiol (HNK) is a small-molecule lignin extracted from Magnolia Officinalis, demonstrating high potency in promoting nonrapid eye movement (NREM) sleep by modulating the benzodiazepine site of the GABAA receptor. However, the clinical use of HNK in the treatment of insomnia is restricted by its extremely low oral bioavailability. In the present work, enhanced oral bioavailability of HNK was achieved by loading it into poly lactide-glycolide acid microparticles (HNK-MP). After oral administration, HNK-MP demonstrated 15-fold increase of AUC0-12 h in comparison to free HNK. The maximum blood concentration ( Cmax) of HNK in HNK-MP-treated rats was 3.6 µg/mL at 2 h after oral administration, which was 6.5-fold of that in free HNK-treated rats. Oral administration of HNK-MP (20 mg/kg) efficiently increased NREM sleep by 60% by enhancing the transition from wakefulness to NREM sleep in rats. The biosafety of HNK-MP was assessed in vivo, and no damage occurred in the gastrointestinal tract. The present study provides a promising oral HNK formulation for the treatment of insomnia.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 15_ODS3_global_health_risks Problema de salud: 15_riscos_biologicos Asunto principal: Compuestos de Bifenilo / Lignanos / Movimientos Oculares Límite: Animals Idioma: En Revista: Mol Pharm Asunto de la revista: BIOLOGIA MOLECULAR / FARMACIA / FARMACOLOGIA Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 15_ODS3_global_health_risks Problema de salud: 15_riscos_biologicos Asunto principal: Compuestos de Bifenilo / Lignanos / Movimientos Oculares Límite: Animals Idioma: En Revista: Mol Pharm Asunto de la revista: BIOLOGIA MOLECULAR / FARMACIA / FARMACOLOGIA Año: 2019 Tipo del documento: Article
...