Design and Evaluation of Sustained Release Bilayer Tablets of Oxcarbazepine

被引:0
作者
Ameen, Muath Sheet Mohammed [1 ]
Ibrahim, Naz Jamal [2 ]
Omar, Thamer A. [3 ,4 ]
机构
[1] Knowledge Univ, Coll Pharm, Dept Pharm, Erbil, Iraq
[2] Hawler Med Univ, Coll Pharm, Dept Pharmaceut, Erbil, Iraq
[3] Univ Mosul, Coll Pharm, Mosul, Iraq
[4] Rutgers State Univ, Chem & Biochem Engn, 98 Brett Rd, Piscataway, NJ 08854 USA
关键词
Bilayer tablets; Oxcarbazepine; Formulation; Direct compaction; Sustained release; IN-VITRO EVALUATION; EUDRAGIT(R) RS-PO; MATRIX; MICROSPHERES; CARBAMAZEPINE; SOLUTE;
D O I
10.1007/s12247-022-09694-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective The aim of the present study is to modify the release profile of oxcarbazepine by formulating it as a bilayer tablet using direct compression method with dual compression. Methods In the bilayer system, the immediate release layer was formulated using four types of disintegrants, sodium starch glycolate (SSG), croscarmellose sodium (CCS), cross-linked polyvinylpyrrollidone (crospovidone), and starch. It was found that immediate release layer containing sodium starch glycolate gave faster disintegration time. Therefore, sodium starch glycolate was utilized in the preparation of bilayer tablets in this study. The sustained release layer was prepared utilizing three hydrophobic polymers, two of them are acrylics (Eudragit RS (R), Eudragit RL (R)) and the third one is ethyl cellulose. The prepared bilayer tablets were evaluated for hardness, friability, weight variation, content uniformity, and dissolution profile. Results The results showed that combination of Eudragit RL (R) with Eudragit RS (R) in ratio of 2:1 gave the best modified release profile. Also, using di calcium phosphate as a binder and microcrystalline cellulose (Avicel PH 101) as a diluent resulted in a slower release profile comparing with other formulas. Based on the integral 2 similarity factor value comparing with reference standard curve, F15, which contains Eudragit RL (R) and RS (R) in ratio of 2:1 with mannitol as a diluent and Avicel 102 as a binder, was selected as the best optimized formula. Drug release followed diffusion mechanism rather than erosion mechanism. Furthermore, FTIR spectra showed no possibility of chemical interaction between the drug and polymers, which were used in preparation of bilayer tablet. Stability studies of bilayer tablets under accelerated conditions indicated that the shelf life of the prepared tablets was 3 years and 5 months at 25 degrees C. However, stability of optimized formula in day light at room temperature revealed that the shelf life of oxcarbazepine is 1 year and 9 months. Conclusion The results of this study clearly demonstrate that oxcarbazepine can be successfully prepared as a bilayer modified release tablet.
引用
收藏
页码:1213 / 1228
页数:16
相关论文
共 50 条
  • [31] Evaluation of hydrophilic, hydrophobic and waxy matrix excipients for sustained release tablets of Venlafaxine hydrochloride
    Yadav, Kiran
    Yadav, Deepak
    Srivastava, Anand Kumar
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2013, 39 (08) : 1197 - 1206
  • [32] Design and Evaluation of Sustained Release of Ornidazole by Dental Inserts
    Harika, Sunchu
    Kumar, Y. Shravan
    Rao, Y. Madhusudhan
    Sriram, Pavani
    Shankar, Uma
    CURRENT DRUG METABOLISM, 2021, 22 (07) : 572 - 580
  • [33] Formulation Development and Evaluation of Carbamazepine Sustained Release Matrix Tablets Using Natural Gums
    Roohullah
    Iqbal, Zafar
    Baseer, Abdul
    Rasheed, Abdur
    Sadozai, Sajid Khan
    Khan, Saeed Ahmed
    Majeedullah
    Badshah, Munair
    Nasim, Muhammad Jawad
    LATIN AMERICAN JOURNAL OF PHARMACY, 2021, 40 (04): : 813 - 821
  • [34] Design and In-vitro Evaluation of Sustained Release Floating Tablets of Metformin HCl Based on Effervescence and Swelling
    Senjoti, Faria Gias
    Mahmood, Syed
    Jaffri, Juliana Md.
    Mandal, Uttam Kumar
    IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH, 2016, 15 (01): : 53 - 70
  • [35] Preparation and Optimization of Immediate Release/Sustained Release Bilayered Tablets of Loxoprofen Using Box-Behnken Design
    Tak, Jin Wook
    Gupta, Biki
    Thapa, Raj Kumar
    Woo, Kyu Bong
    Kim, Sung Yub
    Go, Toe Gyeong
    Choi, Yongjoo
    Choi, Ju Yeon
    Jeong, Jee-Heon
    Choi, Han-Gon
    Yong, Chul Soon
    Kim, Jong Oh
    AAPS PHARMSCITECH, 2017, 18 (04): : 1125 - 1134
  • [36] Evaluation of Release Patterns of Diclofenac Sodium Sustained Release Tablets Available In Pakistani Market
    Zafar, Farya
    Ali, Huma
    Shah, Shabana N.
    Bushra, Rabia
    Yasmin, Riffat
    Naqvi, Ghazala R.
    Shareef, Huma
    LATIN AMERICAN JOURNAL OF PHARMACY, 2014, 33 (05): : 759 - 765
  • [37] FORMULATION DEVELOPMENT AND EVALUATION OF SUSTAINED RELEASE MATRIX TABLETS OF VERAPAMIL HYDROCHLORIDE
    Reddy, Kondeti Ranjith
    Rathnam, Grace
    Kiran, I.
    Raju, Shalem
    Mulpuri, Kranti Sri
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2014, 5 (05): : 2066 - 2073
  • [38] Formulation and In Vitro Characterization of Sustained Release Tablets of Lornoxicam
    Noreen, Misbah
    Farooq, Muhammad A.
    Ghayas, Sana
    Bushra, Rabia
    Yaqoob, Naeem
    Abrar, Muhammad A.
    LATIN AMERICAN JOURNAL OF PHARMACY, 2019, 38 (04): : 701 - 711
  • [39] In Vitro Evaluation of Commercially Available Theophylline Sustained Release Tablets in Pakistan
    Ranjha, Nazar M.
    Mudassir, Jahanzeb
    Abbas, Tanveer
    Siam, Mohammad A. F.
    Hussain, Abid
    LATIN AMERICAN JOURNAL OF PHARMACY, 2010, 29 (06): : 869 - 875
  • [40] New Generation of Orally Disintegrating Tablets for Sustained Drug Release: A Propitious Outlook
    Elwerfalli, Arwa Matoug
    Ghanchi, Zabir
    Rashid, Fatema
    Alany, Raid G.
    ElShaer, Amr
    CURRENT DRUG DELIVERY, 2016, 12 (06) : 652 - 667