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Formulation of a modified-release pregabalin tablet using hot-melt coating with glyceryl behenate.
Jeong, Kyu Ho; Woo, Hye Seung; Kim, Chae Jin; Lee, Kyung Hwa; Jeon, Jun Young; Lee, Sang Young; Kang, Jae-Hoon; Lee, Sangkil; Choi, Young Wook.
Afiliación
  • Jeong KH; Drug Delivery Research Laboratory, College of Pharmacy, Chung-Ang University, Dongjak-gu, Seoul 156-756, Republic of Korea.
  • Woo HS; Drug Delivery Research Laboratory, College of Pharmacy, Chung-Ang University, Dongjak-gu, Seoul 156-756, Republic of Korea.
  • Kim CJ; Drug Delivery Research Laboratory, College of Pharmacy, Chung-Ang University, Dongjak-gu, Seoul 156-756, Republic of Korea.
  • Lee KH; Drug Delivery Research Laboratory, College of Pharmacy, Chung-Ang University, Dongjak-gu, Seoul 156-756, Republic of Korea.
  • Jeon JY; Research Laboratories, ILDONG Pharmaceutical Co., Ltd., Hwaseong-si, Gyeonggi-do 445-170, Republic of Korea.
  • Lee SY; Research Laboratories, ILDONG Pharmaceutical Co., Ltd., Hwaseong-si, Gyeonggi-do 445-170, Republic of Korea.
  • Kang JH; Research Laboratories, ILDONG Pharmaceutical Co., Ltd., Hwaseong-si, Gyeonggi-do 445-170, Republic of Korea.
  • Lee S; College of Pharmacy, Keimyung University, Daegu 704-701, Republic of Korea.
  • Choi YW; Drug Delivery Research Laboratory, College of Pharmacy, Chung-Ang University, Dongjak-gu, Seoul 156-756, Republic of Korea. Electronic address: ywchoi@cau.ac.kr.
Int J Pharm ; 495(1): 1-8, 2015 Nov 10.
Article en En | MEDLINE | ID: mdl-26315121
ABSTRACT
A modified-release (MR) tablet of the anti-anxiety drug pregabalin (PRE) was prepared by hot-melt coating PRE with glyceryl behenate (GB) as a release retardant and compressing to form a matrix with microcrystalline cellulose (MCC) as a hydrophilic diluent. GB-coated PRE had a size in the range of 177-290 µm with good to acceptable flowability. Tablet hardness decreased slightly as GB content increased. PRE release from the tablet matrices was successfully modified by altering the ratio of MCC and GB, and it was found that dissolution- or diffusion-controlled release depended on the amount of GB used. Drug release was pH-independent. An accelerated stability test on the most promising MR tablet at 40°C and 75% relative humidity for 6 months showed no significant changes in PRE content, and the occurrence of total impurities--including PRE-lactam--was within acceptable limits. After oral administration of the selected MR tablet or a commercial IR capsule (Lyrica) to healthy human volunteers, pharmacokinetic parameters including Tmax, Cmax, AUC0-24, and T1/2 were compared. The confidence interval of AUC0-24 was within the adequate range, but that of Cmax was inadequate. This study demonstrated the potential use of GB for PRE-containing MR formulations.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Preparaciones de Acción Retardada / Ácidos Grasos / Liberación de Fármacos / Pregabalina Tipo de estudio: Clinical_trials Límite: Adult / Humans / Male Idioma: En Revista: Int J Pharm Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Preparaciones de Acción Retardada / Ácidos Grasos / Liberación de Fármacos / Pregabalina Tipo de estudio: Clinical_trials Límite: Adult / Humans / Male Idioma: En Revista: Int J Pharm Año: 2015 Tipo del documento: Article