PREPARATION OF MICROCAPSULES MASKING THE BITTER TASTE OF ENOXACIN BY USING ONE CONTINUOUS PROCESS TECHNIQUE OF AGGLOMERATION AND MICROENCAPSULATION

被引:23
作者
UEDA, M
NAKAMURA, Y
MAKITA, H
KAWASHIMA, Y
机构
[1] Pharmaceutical Research Laboratories, Dainippon Pharmaceutical Co. Ltd, Osaka, 553, 1-5-51, Ebie Fukushima-ku
[2] Department of Pharmaceutical Engineering, Gifu Pharmaceutical University, Gifu, 502, 5-6-1, Mitahora-higashi
关键词
D O I
10.3109/02652049309015323
中图分类号
O69 [应用化学];
学科分类号
081704 [应用化学];
摘要
In order to mask the bitter taste of drugs, a novel microencapsulation process combined with the wet spherical agglomeration (WSA) technique was developed by using a modified phase separation method. The spherical agglomerates of enoxacin (ENX) with various additives including disintegrants were successfully produced in the system of acetone-n-hexane-ammonia water or acetone-n-hexane-distilled water by the WSA, using flocculation phenomena of particles in liquid. Resultant agglomerates could be microencapsulated continuously with Eudragit RS utilizing the phase separation method in the same system as agglomeration under stirring. 'Explosible' microcapsules which were free from the bitter taste could be produced in formulating finer particle size of ENX and 50 per cent of Primojel in core agglomerates, using distilled water as a bridging liquid, and treating with 20 per cent polymer coating level. These microcapsules were bioequivalent to the commercial ENX 1 00 mg tablets in beagle dogs. One continuous process technique of agglomeration and microencapsulation was useful for the design of ENX powders which masked the bitter taste and controlled the drug release rate.
引用
收藏
页码:461 / 473
页数:13
相关论文
共 7 条
[1]
Fukumori Y., Fukuda T., Hanyu Y., Takeuchi Y., Osako Y., Coating for pharmaceutical powders by fluidized bed process. I. Aqueous enteric coating with methacrylic acid-ethylacrylate copolymer and the dissolution behaviour of products, Chemical and Pharmaceutical Bulletin, 35, pp. 2947-2957, (1987)
[2]
Lehmann K., Dreher D., Coating of tablets and small particles with acrylic resins by fluid-bed technology, International Journal of Pharmaceutical Technology and Product Manufacture, 2, pp. 31-43, (1981)
[3]
Nakamura R., Yamaguchi T., Sekine Y., Hashimoto M., Determination of a new antibacterial agent (AT-2266) and its metabolites in plasma and urine by high-performance liquid chromatography, Journal of Chromatography, 278, pp. 321-328, (1983)
[4]
Samejima M., Hirata G., Koida Y., Rapid-release microcapsules containing ethylcellulose and carbonates, Jpn. Kokai Tokkyo Koho, (1982)
[5]
Ueda M., Nakamura Y., Makita H., Kawashima Y., One continuous process of agglomeration and microencapsulation for enoxacin. Preparation methods and mechanism of microencapsulation, Journal of Microencapsulation, 10, 1, pp. 25-34, (1993)
[6]
Ueda M., Nakamura Y., Makita H., Kawashima Y., Preparation and characteristics of microcapsules containing enoxacin by one continuous process of agglomeration and microencapsulation, Journal of Microencapsulation, 10, 2, pp. 171-180, (1993)
[7]
Yamamura T., Mori M., Tan T., Izutsu Y., Nakamura Y., Makita H., Imasato Y., Studies of nondisintegrating and matrix-types of fine granules, Journal of the Society of Powder Technology, Japan, 28, pp. 4-10, (1991)