Optimized furosemide taste masked orally disintegrating tablets

被引:24
作者
Ibrahim, Mohamed Abbas [1 ,2 ]
Abou El Ela, Amal El Sayeh F. [1 ,3 ]
机构
[1] King Saud Univ, Dept Pharmaceut, Coll Pharm, Riyadh, Saudi Arabia
[2] Al Azhar Univ, Dept Pharmaceut & Ind Pharm, Coll Pharm, Assiut, Egypt
[3] Assiut Univ, Dept Pharmaceut, Coll Pharm, Assiut 71526, Egypt
关键词
Furosemide; Orally disintegrating tablets (ODTs); Eudragit E100; Optimization; Taste masking; Superdisinitgrant; CYCLODEXTRIN INCLUSION COMPLEX; SOLID DISPERSION; BIOAVAILABILITY; FORMULATION; MASKING; DRUGS;
D O I
10.1016/j.jsps.2017.04.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Optimized orally disintegrating tablets (ODTs) containing furosemide (FUR) were prepared by direct compression method. Two factors, three levels (3(2)) full factorial design was used to optimize the effect of taste masking agent (Eudragit E100; X1) and superdisintegarant; croscarmellose sodium (CCS; X2) on tablet properties. A composite was prepared by mixing ethanolic solution of FUR and Eudragit E100 with mannitol prior to mixing with other tablet ingredients. The prepared ODTs were characterized for their FUR content, hardness, friability and wetting time. The optimized ODT formulation (F1) was evaluated in term of palatability parameters and the in vivo disintegration. The manufactured ODTs were complying with the pharmacopeia guidelines regarding hardness, friability, weight variation and content. Eudragit E100 had a very slightly enhancing effect on tablets disintegration. However, the effects of both Eudragit E100 (X1) and CCS (X2) on ODTs disintegration time (Y1) were insignificant (p > 0.05). Moreover, X1 exhibited antagonistic effect on the dissolution after 5 and 30 min (D5 and D30, respectively), but only its effect on D30 is significant (p = 0.0004). Furthermore, the optimized ODTs formula showed good to acceptable taste in term of palatability, and in vivo disintegration time of this formula was about 10 s. (C) 2017 The Authors. Production and hosting by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:1055 / 1062
页数:8
相关论文
共 32 条
  • [1] Comparative effects of different cellulosic-based directly compressed orodispersable tablets on oral bioavailability of famotidine
    Abdelbary, A.
    Elshafeey, A. H.
    Zidan, G.
    [J]. CARBOHYDRATE POLYMERS, 2009, 77 (04) : 799 - 806
  • [2] [Anonymous], 2008, Guidance for Industry: E15 Definitions for Genomics biomarkers, pharmacogenomics, pharmacogenetics, genomic data and sample coding categories, P1
  • [3] Bandari S., 2008, Asian J Pharm, P1, DOI 10.22377/ajp.v2i1.159
  • [4] Chandrasekhar P., 2013, INT J PHARMACEUT, V3, P79
  • [5] Preparation and characterization of novel fast disintegrating capsules (Fastcaps) for administration in the oral cavity
    Ciper, M
    Bodmeier, R
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 303 (1-2) : 62 - 71
  • [6] Formulation of cyclodextrin inclusion complex-based orally disintegrating tablet of eslicarbazepine acetate for improved oral bioavailability
    Desai, Samixa
    Poddar, Aditi
    Sawant, Krutika
    [J]. MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2016, 58 : 826 - 834
  • [7] Disintegrating efficiency of croscarmellose sodium in a direct compression formulation
    Ferrero, C
    Munoz, N
    Velasco, MV
    MunozRuiz, A
    JimenezCastellanos, R
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 147 (01) : 11 - 21
  • [8] Physical properties of solid dispersion of a nonsteroidal anti-inflammatory drug (M-5011) with Eudragit E
    Horisawa, E
    Danjo, K
    Haruna, M
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (12) : 1271 - 1278
  • [9] Application of water-insoluble polymers to orally disintegrating tablets treated by high-pressure carbon dioxide gas
    Ito, Yoshitaka
    Maeda, Atsushi
    Kondo, Hiromu
    Iwao, Yasunori
    Noguchi, Shuji
    Itai, Shigeru
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2016, 511 (01) : 10 - 22
  • [10] Jagdale SC., 2010, J CHEM PHARM RES, V2, P65