FORMULATION AND EVALUATION OF CARVEDILOL SUBLINGUAL TABLET

被引:0
|
作者
Siji, C. [1 ]
Augusthy, Ann Rose [2 ]
Vipin, K. V. [2 ]
机构
[1] Natl Coll Pharm, Manassery, Kerala, India
[2] Acad Pharmaceut Sci, Pariyaram, Kerala, India
来源
关键词
Carvedilol; Sublingual tablet; Super disintegrants; Bioavailability;
D O I
10.5281/zenodo.1185156
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Carvedilol is an oral antihypertensive agent. Due to its poor water solubility it posses problems of variable bioavailability and bioequivalence. In the present work an attempt was done to develop sublingual tablets of carvedilol using different superdisintegrants like crosscarmellose sodium, crosspovidone and sodium starch glycolate in different ratios. As carvedilol is a poor soluble drug the solubility was enhanced by solid dispersion method. Tablets were prepared by direct compression technique. Prepared tablets were evaluated for thickness, uniformity of weight, hardness, friability, wetting time, in-vitro disintegration time, drug content and in vitro drug release. All the formulations were evaluated for the characteristics of sublingual tablets mainly in terms of. disintegration time and dissolution studies. Out of the 7 formulation, formulation F7 shows the maximum drug release. The formulation F7 consist of super disintegrant crosscarmellose sodium 5% and drug polymer in the ratio 1:4.From the literature it was evident that drug release was increased with increase in concentration of the polymer. So the formulation F7 was optimized as the best formulation.
引用
收藏
页码:1043 / 1050
页数:8
相关论文
共 50 条
  • [31] Ternary complexation of carvedilol, β-cyclodextrin and citric acid for mouth-dissolving tablet formulation
    Pokharkar, Varsha
    Khanna, Abhishek
    Venkatpurwar, Vinod
    Dhar, Sheetal
    Mandpe, Leenata
    ACTA PHARMACEUTICA, 2009, 59 (02) : 121 - 132
  • [32] FORMULATION DEVELOPMENT AND IN VITRO CHARACTERIZATION OF CARVEDILOL SUSTAIN RELEASE TABLET BY USING LIQUISOLID TECHNIQUE
    Patel, Tushar N.
    Sheth, Zankhana P.
    Patel, Bhagirath K.
    Patel, Pritesh
    PHARMACOPHORE, 2014, 5 (04): : 451 - 466
  • [33] FORMULATION, EVALUATION AND OPTIMIZATION OF FLOATING MATRIX TABLETS OF CARVEDILOL
    Jamshiya, E.
    Anju, P.
    INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 5 (02): : 1146 - 1158
  • [34] Formulation and In vitro Evaluation of Carvedilol Transdermal Delivery System
    Aparna, Pisipati
    Divya, Lyadella
    Bhadrayya, Kalva
    Subrahmanyam, Chavali V. S.
    TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, 2013, 12 (04) : 461 - 467
  • [35] Formulation and Evaluation of Cyclodextrin Inclusion Complex Tablets of Carvedilol
    Raj, R. Arun
    Nair, Sruthy S.
    Harindran, Jyoti
    ASIAN JOURNAL OF PHARMACEUTICS, 2016, 10 (02) : 84 - 94
  • [36] Pharmaceutical and pharmacokinetic characterization of a novel sublingual buprenorphine/naloxone tablet formulation in healthy volunteers
    Fischer, Andreas
    Jonsson, Martin
    Hjelmstrom, Peter
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2015, 41 (01) : 79 - 84
  • [37] DEVELOPMENT AND IN VITRO EVALUATION OF MICRONIZED SUSTAINED RELEASE MATRIX TABLET OF CARVEDILOL
    Chatterjee, B.
    Pal, T. K.
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2010, 1 (10): : 96 - 102
  • [38] Formulation and Evaluation of Fexofenadine Mouth Dissolving Tablet
    Solanki, S. S.
    Garud, N.
    Garud, A.
    Kannojia, P.
    Tomar, V.
    Dahima, Rashmi
    INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 71 (02) : 178 - 178
  • [39] FORMULATION AND EVALUATION OF MOUTH DISSOLVING TABLET OF LOPERAMIDE
    Gautam, Surya Prakash
    Rai, Janki Prasad
    Billshaiya, Uma
    Jain, Nilesh
    Vikram, Pradeep
    Jain, Deepak Kumar
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2013, 4 (05): : 1782 - 1788
  • [40] Formulation and evaluation of floating matrix tablet of stavudine
    Prajapati, Pankaj H.
    Nakum, Vijay V.
    Patel, Chhagan N.
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL INVESTIGATION, 2012, 2 (02) : 83 - 89