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Effect of polymorphism on in vitro-in vivo properties of carbamazepine conventional tablets

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Al-Azhar University – Gaza
Elqidra R.; Ünlü N.; Çapan Y.; Sahin G.; Dalkara T.; Hincal A.A.
Elqidra, R. (36643847900); Ünlü, N. (7003608097); Çapan, Y. (6603768177); Sahin, G. (58460193100); Dalkara, T. (7005158087); Hincal, A.A. (7006150494)
36643847900; 7003608097; 6603768177; 58460193100; 7005158087; 7006150494
2004
Journal of Drug Delivery Science and Technology
Effect of polymorphism on in vitro-in vivo properties of carbamazepine conventional tablets
14
2
147
153
Editions de Sante
Al-Azhar University, Faculty of Pharmacy, Gaza 07-823180, Gaza, PO Box 1277, Palestine; Hacettepe University, Faculty of Pharmacy, Dept. of Pharmaceutical Technology, 06100 Ankara, Turkey; Hacettepe University, Faculty of Medicine, Department of Neurology, 06100 Ankara, Turkey
Elqidra R., Al-Azhar University, Faculty of Pharmacy, Gaza 07-823180, Gaza, PO Box 1277, Palestine; Ünlü N., Hacettepe University, Faculty of Pharmacy, Dept. of Pharmaceutical Technology, 06100 Ankara, Turkey; Çapan Y., Hacettepe University, Faculty of Pharmacy, Dept. of Pharmaceutical Technology, 06100 Ankara, Turkey; Sahin G., Hacettepe University, Faculty of Medicine, Department of Neurology, 06100 Ankara, Turkey; Dalkara T., Hacettepe University, Faculty of Medicine, Department of Neurology, 06100 Ankara, Turkey; Hincal A.A., Hacettepe University, Faculty of Pharmacy, Dept. of Pharmaceutical Technology, 06100 Ankara, Turkey
N. Ünlü; Hacettepe University, Faculty of Pharmacy, Dept. of Pharmaceutical Technology, 06100 Ankara, Turkey; email: nursen@tr.net
14
10.1016/s1773-2247(04)50027-8
Bioavailability; Carbamazepine; In vitro dissolution; Polymorphism
acetonitrile; carbamazepine; water; area under the curve; article; blood sampling; clinical trial; concentration (parameters); controlled clinical trial; controlled study; crossover procedure; crystallization; differential scanning calorimetry; dose response; dose time effect relation; drug bioavailability; drug blood level; drug effect; drug formulation; genetic polymorphism; high performance liquid chromatography; human; human experiment; in vitro study; in vivo study; infrared spectroscopy; normal human; open study; powder; randomized controlled trial; statistical significance; tablet formulation; tablet property