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采用喷雾干燥技术开发地高辛干糖浆新型剂型。

Development of digoxin dry elixir as a novel dosage form using a spray-drying technique.

作者信息

Kim C K, Yoon Y S

机构信息

College of Pharmacy, Seoul National University, Shimlim-Dong, Kwanak-Gu, Korea.

出版信息

J Microencapsul. 1995 Sep-Oct;12(5):547-56. doi: 10.3109/02652049509006785.

Abstract

A rapidly absorbed new novel oral dosage form for digoxin termed 'digoxin dry elixir' was developed by the spray-drying technique. Digoxin, dextrin and sodium lauryl sulphate were dissolved in a ethanol-water mixture (20:25 w/w) and therefore spray-dried to form the digoxin dry elixir. According to scanning electron micrographs, digoxin dry elixir is spherical in shape with a smooth surface. The geometric mean diameter of dry elixir determined by laser particle size analysis was about 13 microns. The appearance and flow properties were almost unchanged and about 10% of ethanol contents in the dry elixir decreased during 180 days in a sealed bottle at room temperature. Comparative studies on the in vitro dissolution and in vivo absorption of digoxin in the form of digoxin dry elixir, digoxin elixir and digoxin powder were carried out. Digoxin in the dry elixirs was completely dissolved within 2 min. On the other hand, only about 87% of digoxin powder dissolved in 60 min. The initial dissolution rates of digoxin in the dry elixirs markedly increased in distilled water at 37 degrees C, which were over 100 fold higher than that of digoxin powder alone. The maximal plasma concentration of digoxin (Cmax) and area under the digoxin concentration-time curve from zero to 6 h (AUC0-6h) after the oral administration of digoxin dry elixir were almost 3.8 and 5.5 fold increased compared to digoxin powder alone. No significant difference of AUC0-6 h between dry elixir and elixir was observed, but the Cmax of digoxin in the form of dry elixir was significantly reduced compared to the digoxin elixir (0.57 versus 0.83). Digoxin dry elixir might be a useful solid dosage form to improve the dissolution rate and bioavailability of poorly water-soluble digoxin compared to digoxin powder alone. It also indicates that dry elixir might reduce the side effects in oral digitalis glycoside therapy compared to the digoxin elixir due to the reduction of Cmax.

摘要

一种名为“地高辛干糖浆”的新型口服地高辛剂型通过喷雾干燥技术得以开发,其吸收迅速。将地高辛、糊精和十二烷基硫酸钠溶解于乙醇 - 水混合物(20:25 w/w)中,随后进行喷雾干燥以形成地高辛干糖浆。根据扫描电子显微镜照片,地高辛干糖浆呈球形,表面光滑。通过激光粒度分析测定,干糖浆的几何平均直径约为13微米。其外观和流动性质几乎未变,在室温下密封瓶中放置180天期间,干糖浆中乙醇含量下降约10%。开展了关于地高辛干糖浆、地高辛糖浆和地高辛粉末形式的地高辛体外溶出度和体内吸收的对比研究。干糖浆中的地高辛在2分钟内完全溶解。另一方面,地高辛粉末在60分钟内仅约87%溶解。地高辛在干糖浆中的初始溶出速率在37℃蒸馏水中显著增加,比单独的地高辛粉末高出100多倍。口服地高辛干糖浆后,地高辛的最大血浆浓度(Cmax)以及地高辛浓度 - 时间曲线从零至6小时的面积(AUC0 - 6h)与单独的地高辛粉末相比,几乎分别增加了3.8倍和5.5倍。未观察到干糖浆和糖浆之间AUC0 - 6 h有显著差异,但干糖浆形式的地高辛Cmax与地高辛糖浆相比显著降低(0.57对0.83)。与单独的地高辛粉末相比,地高辛干糖浆可能是一种有用的固体剂型,可提高难溶性地高辛的溶出速率和生物利用度。这也表明,由于Cmax降低,与地高辛糖浆相比,干糖浆可能会减少口服洋地黄苷治疗中的副作用。

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