Formulation and in vitro evaluation of sustained release matrix tablets using cross-linked natural gum

被引:0
作者
Jamil, Qurrat Ul Ain [1 ,4 ]
Masood, Muhammad Irfan [1 ]
Jamil, Muhammad Nauman [2 ]
Masood, Imran [3 ]
Iqbal, Shahid Muhammad [4 ]
机构
[1] Univ Vet & Anim Sci, Inst Pharmaceut Sci, Lahore, Pakistan
[2] Univ Sargodha, Fac Pharm, Sargodha, Pakistan
[3] Islamia Univ Bahawalpur, Fac Pharm & Alternat Med, Bahawalpur, Pakistan
[4] Drugs Regulatory Author Pakistan, Islamabad, Pakistan
关键词
Sustained release tablet; isoniazid; dissolution release profile; release models; swelling index; OPTIMIZATION;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polysaccharide gums because of their biocompatibility, biodegiadability and non-immunogenic properties are considered as the best choice for preparing sustained release tablets as compared to their synthetic counterpart. The cross linking of natural gums in matrix tablets increase the sustained release property of matrix tablets. Isoniazid is a first line therapy of tuberculosis, belongs to BCS I with half-life of 3-4 hours. These characteristics make isoniazid a good candidate for sustained release dosage form. Karaya gum crossed linked with trisodium tri metaphosphate was used as release rate retardant for preparing isoniazid cross-linked matrix tablet. Total 8 sustained release formulations were prepared. Both granules and tablets were evaluated under in vitro condition against different parameters. Dissolution studies were performed with all eight formulations for 12 hours using USP apparatus I. Four formulations designated as F1, F2, F3, F4 have drug and karaya gum while other four formulations F5, F6, F7, F8 have drug and crossed linked polymer in ratios of 1:1, 1:2, 1:3 and 1:4 respectively. Dissolution data was analyzed by using different kinetic models. Best fit model for most efficient formulation was zero order while release mechanism was super case I. Formulation 8 showed sufficiently slow release kinetics and about 83% of drug was released in 10 hours, indicating that cross-linked karaya gum proved efficient in preparing sustained release tablets.
引用
收藏
页码:355 / 362
页数:8
相关论文
共 23 条
  • [1] Natural gums and modified natural gums as sustained-release carriers
    Bhardwaj, T
    Kanwar, M
    Lal, R
    Gupta, A
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (10) : 1025 - 1038
  • [2] Formulation development and optimization of sustained release matrix tablet of Itopride HCl by response surface methodology and its evaluation of release kinetics
    Bose, Anirbandeep
    Wong, Tin Wui
    Singh, Navjot
    [J]. SAUDI PHARMACEUTICAL JOURNAL, 2013, 21 (02) : 201 - 213
  • [3] Noncompliance with directly observed therapy for tuberculosis - Epidemiology and effect on the outcome of treatment
    Burman, WJ
    Cohn, DL
    Rietmeijer, CA
    Judson, FN
    Sbarbaro, JA
    Reves, RR
    [J]. CHEST, 1997, 111 (05) : 1168 - 1173
  • [4] The comparative pharmacokinetics of modified-release and immediate-release paracetamol in a simulated overdose model
    Chiew, Angela
    Day, Peter
    Salonikas, Chris
    Naidoo, Daya
    Graudins, Andis
    Thomas, Rebecca
    [J]. EMERGENCY MEDICINE AUSTRALASIA, 2010, 22 (06) : 548 - 555
  • [5] Modeling and comparison of dissolution profiles
    Costa, P
    Manuel, J
    Lobo, S
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (02) : 123 - 133
  • [6] Polysaccharide hydrogels for modified release formulations
    Coviello, Tommasina
    Matricardi, Pietro
    Marianecci, Carlotta
    Alhaique, Franco
    [J]. JOURNAL OF CONTROLLED RELEASE, 2007, 119 (01) : 5 - 24
  • [7] THE EFFECTS OF DIETARY GUM KARAYA (STERCULIA) IN MAN
    EASTWOOD, MA
    BRYDON, WG
    ANDERSON, DMW
    [J]. TOXICOLOGY LETTERS, 1983, 17 (1-2) : 159 - 166
  • [8] Formulation and optimization of orodispersible tablets of flutamide
    Elkhodairy, Kadria A.
    Hassan, Maha A.
    Afifi, Samar A.
    [J]. SAUDI PHARMACEUTICAL JOURNAL, 2014, 22 (01) : 53 - 61
  • [9] Emami J, 2008, IRAN J PHARM RES, V7, P247
  • [10] Gohel MC, 2007, AAPS PHARMSCITECH, V8