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Design, in vitro release characterization and pharmacokinetics of novel controlled release pellets containing levodropropizine

机译:含左旋哌嗪嗪的新型控释微丸的设计,体外释放表征和药代动力学

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摘要

This study was performed to investigate the in vitro release characteristics of levodropropizine (LDP) from novel dual-coated sustained release (SR) pellets, and evaluate the pharmacokinetics of a novel controlled release (CR) preparation composed of the dual-coated SR pellets and immediate release (IR) LDP pellets. The dual-coated SR pellets composed of a drug-loaded nonpareil core, a sub-coating layer (HPMC 6cps) and an SR-coating layer (Aquacoat (R) ECD, Eudragit (R) RS 30D or Kollicoat (R) SR 30D) were prepared by a bottom-spray fluidized bed-coating method. The drug release from the dual-coated SR pellets coated with Aquacoat (R) ECD followed a zero-order profile in water, and the drug release was not affected by the coating level of the sub-coating layer and stable under the accelerated storage condition (40 degrees C, 75% RH) for 6 months. The CR preparation showed significantly decreased values of maximum drug concentration (C-max) and elimination rate (K) than the reference product (LEVOTUS (R) SYR) but the similar bioavailability (F = 95.43%). The novel CR preparation presents promising delivery of LDP with an immediate and sustained release manner, with similar clinical effect as the commercial IR product.
机译:进行这项研究的目的是从新型双重包衣缓释(SR)药丸中研究左旋洛哌嗪(LDP)的体外释放特性,并评估由双重包衣SR药丸和药物制成的新型控释(CR)制剂的药代动力学。立即释放(IR)LDP颗粒。双重涂层SR药丸由载药的无核芯,底涂层(HPMC 6cps)和SR涂层(Aquacoat(R)ECD,Eudragit(R)RS 30D或Kollicoat(R)SR 30D)组成通过底部喷雾流化床涂覆方法制备)。从涂有Aquacoat(R)ECD的双涂层SR药丸中释放的药物在水中呈零级分布,并且药物释放不受底涂层的包衣水平的影响,并且在加速储存条件下稳定(40摄氏度,相对湿度75%)放置6个月。 CR制剂显示最大药物浓度(C-max)和消除率(K)的值明显低于参考产品(LEVOTUS(R)SYR),但生物利用度相似(F = 95.43%)。新型CR制剂具有立即释放和持续释放方式的有希望的LDP递送效果,其临床效果与市售IR产品相似。

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