Coated hydralazine hydrochloride beads for sustained release after oral administration
被引:5
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作者:
Mughal, M. Akhlaq
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Univ Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
Univ Peshawar, Dept Pharm, Peshawar, PakistanUniv Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
Mughal, M. Akhlaq
[1
,2
]
Saripella, Kalyan K.
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Univ Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
Tech Operat, McNeil Consumer Healthcare, Ft Washington, PA 19034 USAUniv Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
Saripella, Kalyan K.
[1
,3
]
Kouba, Chahinaz
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Univ Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USAUniv Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
Kouba, Chahinaz
[1
]
Iqbal, Zafar
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机构:
Univ Peshawar, Dept Pharm, Peshawar, PakistanUniv Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
Iqbal, Zafar
[2
]
Neau, Steven H.
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Univ Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USAUniv Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
Neau, Steven H.
[1
]
机构:
[1] Univ Sci, Philadelphia Coll Pharm, Philadelphia, PA 19104 USA
[2] Univ Peshawar, Dept Pharm, Peshawar, Pakistan
[3] Tech Operat, McNeil Consumer Healthcare, Ft Washington, PA 19034 USA
Hydralazine hydrochloride is an antihypertensive used alone or in combination with isosorbide nitrate for the treatment of congestive heart failure. Since control of blood pressure should be continuous, sustained release delivery of this drug is considered therapeutically beneficial. Core beads for oral administration of this drug were prepared by extrusion-spheronization. Using experimental design to define the coat that was applied, the core beads were coated using a fluid bed coater to different coat thickness with combinations of two commercially available products dissolved in a hydroalcoholic solvent. The coat is a film with a combination of ethylcellulose and hydroxypropylcellulose that can provide desirable release profiles. Visually spherical and rugged bead products were obtained. Two products were identified that exhibited essentially a zero order release profile following a 2-h lag time with release of greater than 70% of the drug over the next 10 h in simulated intestinal fluid.
机构:
Department of Basic Science, Jilin Jianzhu University, 5088 Xincheng Street, ChangchunDepartment of Basic Science, Jilin Jianzhu University, 5088 Xincheng Street, Changchun
Li X.-D.
Zhai Q.-Z.
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机构:
Research Center for Nanotechnology, Changchun University of Science and Technology, 7186 Weixing Road, ChangchunDepartment of Basic Science, Jilin Jianzhu University, 5088 Xincheng Street, Changchun
机构:
Sookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
Sookmyung Womens Univ, Coll Pharm, Seoul 140742, South KoreaSookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
Kim, Hye Jin
Shin, Dae Hwan
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Sookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
Sookmyung Womens Univ, Coll Pharm, Seoul 140742, South KoreaSookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
Shin, Dae Hwan
Lim, Eun Ah
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机构:
Sookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
Sookmyung Womens Univ, Coll Pharm, Seoul 140742, South KoreaSookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
Lim, Eun Ah
Kim, Jin-Seok
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机构:
Sookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
Sookmyung Womens Univ, Coll Pharm, Seoul 140742, South KoreaSookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea