A pharmaceutical study on different approaches for itopride hydrochloride sustainment: In-vitro and in-vivo evaluation

被引:0
|
作者
机构
[1] Yehia, Soad A.
[2] El Shafeey, Ahmed H.
[3] El Meshad, Aliaa
[4] Al-Bialey, Hamoud A.
来源
Yehia, S. A. | 1600年 / Journal of Chemical and Pharmaceutical Research, 3/668 Malviya Nagar, Jaipur, Rajasthan, India卷 / 04期
关键词
Drug products - Drug dosage - Controlled drug delivery - Biochemistry - Granulation - Targeted drug delivery - Blending - Cellulose - Plastic coatings;
D O I
暂无
中图分类号
学科分类号
摘要
Recent trends indicate that dosage form drug delivery systems are especially suitable for achieving sustained or delayed release oral formulations with low risk of dose dumping, flexibility of blending to attain different release patterns as well as reproducibility. One of the approaches toward this goal was to develop and formulate extended release matrix oral tablets of itopride hydrochloride (ITO) as a highly water soluble drug and to increase its gastric retention time. Matrix tablets of (ITO) were developed using different methods such as: (wetting granulation, direct compression, and coating compression), by using different types of polymers (hydroxypropyl methyl cellulose (HPMC) K15M, hydroxypropyl cellulose (HPC) low viscosity, Eudragit&reg RL100, and Carnauba wax). The prepared tablets were evaluated according to various physicochemical characteristics such as: weight and thickness variation, drug content, hardness, friability, and in vitro drug release. Tablet weight variation ranged from 395 ± 0.34 to 409 ± 1.78 mg, thickness ranged from 3.16 ± 1.37 to 3.74 mm, drug content ranged from 94.5 ± 1.01% to 106.2 ± 0.08%, friability ranged from 0.04 ± 0.69 to 0.84 ± 0.45, and hardness ranged from 5.25 ± 0.25 to 8.80 ± 0.4 Kg/cm2. Results indicated that drug release depended upon method of preparation and polymer type. Furthermore, in vivo testing of the optimum sustained release tablet formulation (F23) using coating compression by HPMC as coat was performed in human subjects, and determined and compared to that of a commercial oral tablet (Ganaton&reg) as a reference formulation. The obtained the maximum plasma concentration (Cmax) and the area under the curve from zero to infinity (AUC (0-∞) values were higher following formulated tablet administration than after Ganaton&reg administration. The percentage relative bioavailability of ITO from the selected formula in human volunteers was found to be 243% compared to Ganaton&reg.
引用
收藏
相关论文
共 50 条
  • [41] In-vitro and in-vivo antibacterial activity evaluation of a polyurethane matrix
    Lee, SH
    Kim, SR
    Kim, JS
    Bae, HR
    Lee, CH
    Kim, DD
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (04) : 559 - 566
  • [42] IN-VITRO AND IN-VIVO EVALUATION OF PEPTIDE ISOSTERE THROMBIN INHIBITORS
    DEADMAN, J
    SCULLY, MF
    CHENG, I
    CLAESON, G
    PATEL, G
    ELGENDY, S
    KAKKAR, VV
    THROMBOSIS AND HAEMOSTASIS, 1993, 69 (06) : 669 - 669
  • [43] In-vivo evaluation of an in-vitro model for gingival abrasion.
    Kuytz, C
    Sener, B
    Imfeld, T
    JOURNAL OF DENTAL RESEARCH, 2001, 80 (04) : 1217 - 1217
  • [44] In-Vitro and In-vivo evaluation of controlled release erythromycin formulations
    Elkordy, A.
    Yusif, M.
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2007, 59 : A20 - A20
  • [45] In-vivo and in-vitro evaluation of therapeutic potential of β- Carotene in diabetes
    Vikram Nimbalkar
    Uttara Joshi
    Sachin Shinde
    Ganesh Pawar
    Journal of Diabetes & Metabolic Disorders, 2021, 20 : 1621 - 1630
  • [46] Optimization, in-vitro Release and in-vivo Evaluation of Gliquidone Nanoparticles
    Mohamed, Mohamed S.
    Abdelhafez, Wael A.
    Zayed, Gamal
    Samy, Ahmed M.
    AAPS PHARMSCITECH, 2019, 21 (02)
  • [47] IN-VITRO AND IN-VIVO EVALUATION OF COOLING EFFECT OF COLD CREAMS
    SCHNEIDE.MJ
    RITSCHEL, WA
    JOURNAL OF THE SOCIETY OF COSMETIC CHEMISTS, 1972, 23 (06): : 347 - &
  • [48] Optimization, in-vitro Release and in-vivo Evaluation of Gliquidone Nanoparticles
    Mohamed S. Mohamed
    Wael A. Abdelhafez
    Gamal Zayed
    Ahmed M. Samy
    AAPS PharmSciTech, 21
  • [49] IN-VITRO AND IN-VIVO EVALUATION OF A TEMPORARY BIODEGRADABLE WOUND DRESSING
    JURGENS, C
    BEUCHEL, M
    BISGWA, F
    DEKKER, A
    HAFEMANN, B
    KORTMANN, HR
    NIENDORF, A
    PARTECKE, BD
    PORTE, T
    SCHULTZ, JH
    UNFALLCHIRURG, 1995, 98 (04): : 241 - 247
  • [50] In-vitro and in-vivo evaluation of the antibacterial potential of Typha elephantina
    Ahmad, B.
    Yousafzai, A. M.
    Zeb, A.
    Khan, A. A.
    Attaullah, M.
    Ahmad, S.
    TROPICAL BIOMEDICINE, 2021, 38 (01) : 1 - 7