Research Article
BibTex RIS Cite

Formulation and evaluation of a bilayer tablet comprising of diclofenac potassium as orodispersible layer and diclofenac sodium as sustained release core

Year 2017, Volume: 21 Issue: 3, 707 - 716, 24.06.2017
https://doi.org/10.12991/marupj.323595

Abstract

Diclofenac a phenylacetic acid derivative has long been used
as an anti-inflammatory and analgesic drug to treat certain
conditions however its sustained release formulation with
immediate release loading dose is desirable. The rationale
of the current work was to develop and evaluate bilayer
tablets with diclofenac potassium as orodispersible layer and
diclofenac sodium as sustained release core. The diclofenac
sodium core was prepared by wet granulation method while the
orodispersible outer layer was prepared by direct compression
method using super disintegrant sodium starch glycolate. The
powder blends were then evaluated for both pre- compressional
and post compressional properties. The physical parameters
of both powders and tablets were in accordance with the
compendial standards. The orodispersible portion disintegrated
in less than 30sec releasing diclofenac potassium as the loading
dose while the core was able to sustain the release of diclofenac
sodium up to 10hrs in simulated intestinal fluid (pH 6.8). The
kinetic data revealed that the release pattern was best fitted into
Korsmeyer-Peppas model with non-fickian release. The outer
orodispersible layer of diclofenac potassium and sustained
release inner core of diclofenac sodium in a single tablet was
successfully formulated while sodium starch glycolate showed
to have good super disintegrant properties.

References

  • 1. Gwen M, Joseph RR. Sustained and Controlled-Release Drug Delivery Systems. In: Modern Pharmaceutics. Editors: Banker GS, Rhodes CT. Marcel Dekker Inc., New York. 1996, pp. 575- 587. 2. Nagaich U, Bharti C, Kumar Pal A, Neha Gulati N. diclofenac sodium loaded sustained release matrix tablet possessing natural and synthetic polymers: Formulation and in vitro characterization. Indian J Pharm Edu Res 2014; 48: 49-55. 3. Patel VF, Liu F, Brown MB. Advances in oral trans mucosal drug delivery. J Cont Drug Deliv 2011; 153: 106-16. 4. Bhushan SY, Sambhaji SP, Anant RP, Mahadik KR. New drug delivery system for elderly. Ind Drug 2003; 37: 312-8. 5. Behnke K, Sogaard J, Martin S, Bauml J, Ravindran AV, Agren H. Mirtazapine orally disintegrating tablet versus sertraline: A prospective onset of action study. J Clin Psychopharmacol 2003; 23: 358-64. 6. Zalte HD, Saudagar RB. Review on sustained release matrix tablet. Int J Pharm Bio Sci 2013; 3: 17-29. 7. Patil HG, Tiwari RV, Repka MA, Singh KK. Formulation and development of orodispersible sustained release tablet of domperidone. Drug Dev Ind Pharm 2016; 42: 906-15. 8. Gan TJ. Diclofenac: an update on its mechanism of action and safety profile. Curr Med Res Opin 2010; 26: 1715-31. 9. Billa N, Yuen KH, Khader MA, Omar A. Gamma-scintigraphic study of the gastrointestinal transit and in vivo dissolution of a controlled release diclofenac sodium formulation in xanthan gum matrices. Int J Pharm 2000; 201: 109-20. 10. Soppimath KS, Kulkarni AR, Aminabhavi TM. Encapsulation of antihypertensive drugs in cellulose-based matrix microspheres: Characterization and release kinetics of microspheres and tableted microspheres. J Microencapsul 2001; 18: 397–409. 11. Sung KC, Nixon PR, Skoug JW, Roburt JT, Gao P, Topp EM, Patel MV. Effects of formulation variables on drug and polymer release from HPMC based matrix tablets. Int J Pharm 1996; 142: 53-60. 12. Shoaib MH, Tazeen J, Merchant HA, Yousuf RI. Evaluation of drug release kinetics from ibuprofen matrix tablets using HPMC. Pak J Pharm Sci 2006; 19: 119-24. 13. Velasco M, Ford JL, Rowe P, Rajabi-Siahboomi AR. Influence of drug: Hydroxypropyl methylcellulose ratio, drug and polymer particle size and compression force on the release of diclofenac sodium from HPMC matrices. J Control Release 1999; 57: 75–85. 14. Stewart AG, Grant DJW, Newton JM. The release of a model low-dose drug (riboflavine) from hard gelatin capsule formulations. J Pharm Pharmacol 1979; 31: 1–6. 15. Khan KA, Rooke DJ. Effect of disintegrant type upon the relationship between compressional pressure and dissolution efficiency. J Pharm Pharmacol 1976; 28: 633-6 16. Cid E, Jaminet F. Influence of adjuvants on the dissolution rate and stability of acetylsalicylic acid in compressed tablets. J Pharm Belg 1971; 26: 38–48. 17. Addnan Abdullah MD, Bepary S, Shamsur Rouf AS. In vitro dissolution studies of different brands of sustained release diclofenac sodium matrix tablet available in Bangladesh. Pak J Pharm Sci 2008; 21: 70-8. 18. Chickpetty SM, Raga B, Nanjwade BK. Studies on development of novel combined time and pH dependent solventless compression coated delivery systems for colonic delivery of diclofenac sodium. Asian J Pharm Clin Res 2010; 32: 110-3. 19. Gohel MC, Parikh RK, Nagori SA, Jethwa BA. Fabrication and evaluation of bi-layer tablet containing conventional paracetamol and modified release diclofenac sodium. Indian J Pharm Sci 2010; 72: 191–6. 20. Mutalik S, Naha A, Usha AN, Ranjith AK, Musmade P, Manoj K, Anju P, Prasanna S. Preparation, in-vitro, preclinical and clinical evaluations of once daily sustained release tablets of aceclofenac. Arch Pharm Res 2007; 30: 222-34. 21. Xu GJ, Sunada H. Influence of formulation changes on drug release kinetics. Chem Pharm Bull 1995; 43: 438-87. 22. Singla AK, Medirata DK. Influence of sodium lauryl sulphate on indomethacin release pattern. Drug Dev Ind Pharm 1988; 14: 1883-8. 23. Higuchi T. Mechanism of rate of sustained action medication. J Pharm Sci 1963; 52: 1145-9. 24. Hixson AW, Crowell JH. Dependence of reaction velocity upon surface and agitation (I) theoretical consideration. Ind Eng Chem 1931; 23: 923-31. 25. Korsmeyer RW, von Meerwall E and Peppas NA. Solute and penetrant diffusion in swellable polymers. II. Verification of theoretical models. J Polym Sci Polym Phys Ed 1986; 24: 409- 34. 26. Murtaza G, Ahmad M, Shahnaz G. Microencapsulation of diclofenac sodium by nonsolvent addition technique. Trop J Pharm Res 2010; 9: 187-95. 27. The United States Pharmacopeia; The United States Pharmacopeial Convention: Twinbrook parkway, Rockville. 2009. 28. Kramar A, Turk S, Vrečer F. Statistical optimisation of diclofenac sustained release pellets coated with polymethacrylic films. Int J Pharm 2003; 256: 43–52.

Ağızda dağılan tabaka olarak diklofenak potasyum, geciktirilmiş salım çekirdeği olarak diklofenak sodyum içeren iki tabakalı tabletin formülasyonu ve değerlendirilmesi

Year 2017, Volume: 21 Issue: 3, 707 - 716, 24.06.2017
https://doi.org/10.12991/marupj.323595

Abstract

Diklofenak, bir fenilasetik asit türevi olup uzun yıllardan beri
antienfamatuvar ve analjezik bir ilaç olarak kullanılmaktadır
ancak bu etken maddeden hareketle hemen salım için yükleme
dozu içeren geciktirilmiş salım formülasyonunun hazırlanması
istenmektedir. Bu çalışmanın amacı, ağızda dağılan tabaka
olarak diklofenak potasyum, geciktirilmiş salım çekirdeği
olarak diklofenak sodyum içeren iki tabakalı tabletlerin
formülasyonu ve değerlendirilmesidir. Diklofenak sodyum
içeren çekirdek yaş granülasyon yöntemi ile hazırlanırken
ağızda dağılan dış tabaka direct basım yöntemiyle ve süper
dağıtıcı olarak sodyum nişasta glikolat varlığında hazırlandı.
Toz karışımı hem basım öncesi hem de basım sonrası özellikleri
açısından değerlendirildi. Toz karışımının ve tabletlerin fiziksel
özelliklerinin zorunlu standartlarla uyumlu olduğu görüldü.
Ağızda dağılan kısmın 30 saniyeden kısa bir sürede dağılarak
yükleme dozu olan diklofenak potasyumu saldığı, çekirdek
kısmının ise simule bağırsak sıvısında (pH 6.8), 10 saate kadar
diklofenak sodyum salınımı sağladığı tespit edildi. Kinetik ile
ilgili veriler incelendiğinde, tabletin non-fickian salım gösterdiği
ve Korsmeyer-Peppas modeline uygun olduğu tespit edildi. Tek
bir tablet içeriğinde, ağızda dağılan tabaka olarak diklofenak
potasyum, geciktirilmiş salım çekirdeği olarak diklofenak
sodyum içeren ve süper dağıtıcı olarak sodyum nişasta glikolat
içeren tabletlerin formülasyonu başarıyla yapıldı.

References

  • 1. Gwen M, Joseph RR. Sustained and Controlled-Release Drug Delivery Systems. In: Modern Pharmaceutics. Editors: Banker GS, Rhodes CT. Marcel Dekker Inc., New York. 1996, pp. 575- 587. 2. Nagaich U, Bharti C, Kumar Pal A, Neha Gulati N. diclofenac sodium loaded sustained release matrix tablet possessing natural and synthetic polymers: Formulation and in vitro characterization. Indian J Pharm Edu Res 2014; 48: 49-55. 3. Patel VF, Liu F, Brown MB. Advances in oral trans mucosal drug delivery. J Cont Drug Deliv 2011; 153: 106-16. 4. Bhushan SY, Sambhaji SP, Anant RP, Mahadik KR. New drug delivery system for elderly. Ind Drug 2003; 37: 312-8. 5. Behnke K, Sogaard J, Martin S, Bauml J, Ravindran AV, Agren H. Mirtazapine orally disintegrating tablet versus sertraline: A prospective onset of action study. J Clin Psychopharmacol 2003; 23: 358-64. 6. Zalte HD, Saudagar RB. Review on sustained release matrix tablet. Int J Pharm Bio Sci 2013; 3: 17-29. 7. Patil HG, Tiwari RV, Repka MA, Singh KK. Formulation and development of orodispersible sustained release tablet of domperidone. Drug Dev Ind Pharm 2016; 42: 906-15. 8. Gan TJ. Diclofenac: an update on its mechanism of action and safety profile. Curr Med Res Opin 2010; 26: 1715-31. 9. Billa N, Yuen KH, Khader MA, Omar A. Gamma-scintigraphic study of the gastrointestinal transit and in vivo dissolution of a controlled release diclofenac sodium formulation in xanthan gum matrices. Int J Pharm 2000; 201: 109-20. 10. Soppimath KS, Kulkarni AR, Aminabhavi TM. Encapsulation of antihypertensive drugs in cellulose-based matrix microspheres: Characterization and release kinetics of microspheres and tableted microspheres. J Microencapsul 2001; 18: 397–409. 11. Sung KC, Nixon PR, Skoug JW, Roburt JT, Gao P, Topp EM, Patel MV. Effects of formulation variables on drug and polymer release from HPMC based matrix tablets. Int J Pharm 1996; 142: 53-60. 12. Shoaib MH, Tazeen J, Merchant HA, Yousuf RI. Evaluation of drug release kinetics from ibuprofen matrix tablets using HPMC. Pak J Pharm Sci 2006; 19: 119-24. 13. Velasco M, Ford JL, Rowe P, Rajabi-Siahboomi AR. Influence of drug: Hydroxypropyl methylcellulose ratio, drug and polymer particle size and compression force on the release of diclofenac sodium from HPMC matrices. J Control Release 1999; 57: 75–85. 14. Stewart AG, Grant DJW, Newton JM. The release of a model low-dose drug (riboflavine) from hard gelatin capsule formulations. J Pharm Pharmacol 1979; 31: 1–6. 15. Khan KA, Rooke DJ. Effect of disintegrant type upon the relationship between compressional pressure and dissolution efficiency. J Pharm Pharmacol 1976; 28: 633-6 16. Cid E, Jaminet F. Influence of adjuvants on the dissolution rate and stability of acetylsalicylic acid in compressed tablets. J Pharm Belg 1971; 26: 38–48. 17. Addnan Abdullah MD, Bepary S, Shamsur Rouf AS. In vitro dissolution studies of different brands of sustained release diclofenac sodium matrix tablet available in Bangladesh. Pak J Pharm Sci 2008; 21: 70-8. 18. Chickpetty SM, Raga B, Nanjwade BK. Studies on development of novel combined time and pH dependent solventless compression coated delivery systems for colonic delivery of diclofenac sodium. Asian J Pharm Clin Res 2010; 32: 110-3. 19. Gohel MC, Parikh RK, Nagori SA, Jethwa BA. Fabrication and evaluation of bi-layer tablet containing conventional paracetamol and modified release diclofenac sodium. Indian J Pharm Sci 2010; 72: 191–6. 20. Mutalik S, Naha A, Usha AN, Ranjith AK, Musmade P, Manoj K, Anju P, Prasanna S. Preparation, in-vitro, preclinical and clinical evaluations of once daily sustained release tablets of aceclofenac. Arch Pharm Res 2007; 30: 222-34. 21. Xu GJ, Sunada H. Influence of formulation changes on drug release kinetics. Chem Pharm Bull 1995; 43: 438-87. 22. Singla AK, Medirata DK. Influence of sodium lauryl sulphate on indomethacin release pattern. Drug Dev Ind Pharm 1988; 14: 1883-8. 23. Higuchi T. Mechanism of rate of sustained action medication. J Pharm Sci 1963; 52: 1145-9. 24. Hixson AW, Crowell JH. Dependence of reaction velocity upon surface and agitation (I) theoretical consideration. Ind Eng Chem 1931; 23: 923-31. 25. Korsmeyer RW, von Meerwall E and Peppas NA. Solute and penetrant diffusion in swellable polymers. II. Verification of theoretical models. J Polym Sci Polym Phys Ed 1986; 24: 409- 34. 26. Murtaza G, Ahmad M, Shahnaz G. Microencapsulation of diclofenac sodium by nonsolvent addition technique. Trop J Pharm Res 2010; 9: 187-95. 27. The United States Pharmacopeia; The United States Pharmacopeial Convention: Twinbrook parkway, Rockville. 2009. 28. Kramar A, Turk S, Vrečer F. Statistical optimisation of diclofenac sustained release pellets coated with polymethacrylic films. Int J Pharm 2003; 256: 43–52.
There are 1 citations in total.

Details

Subjects Health Care Administration
Journal Section Articles
Authors

Jabbar Abbas This is me

Sajid Bashir This is me

Muhammad Samie This is me

Sadaf Laghari This is me

Nargis Aman This is me

Habib Ullah Jan This is me

İmran Nazir This is me

Publication Date June 24, 2017
Published in Issue Year 2017 Volume: 21 Issue: 3

Cite

APA Abbas, J., Bashir, S., Samie, M., Laghari, S., et al. (2017). Formulation and evaluation of a bilayer tablet comprising of diclofenac potassium as orodispersible layer and diclofenac sodium as sustained release core. Marmara Pharmaceutical Journal, 21(3), 707-716. https://doi.org/10.12991/marupj.323595
AMA Abbas J, Bashir S, Samie M, Laghari S, Aman N, Jan HU, Nazir İ. Formulation and evaluation of a bilayer tablet comprising of diclofenac potassium as orodispersible layer and diclofenac sodium as sustained release core. Marmara Pharm J. June 2017;21(3):707-716. doi:10.12991/marupj.323595
Chicago Abbas, Jabbar, Sajid Bashir, Muhammad Samie, Sadaf Laghari, Nargis Aman, Habib Ullah Jan, and İmran Nazir. “Formulation and Evaluation of a Bilayer Tablet Comprising of Diclofenac Potassium As Orodispersible Layer and Diclofenac Sodium As Sustained Release Core”. Marmara Pharmaceutical Journal 21, no. 3 (June 2017): 707-16. https://doi.org/10.12991/marupj.323595.
EndNote Abbas J, Bashir S, Samie M, Laghari S, Aman N, Jan HU, Nazir İ (June 1, 2017) Formulation and evaluation of a bilayer tablet comprising of diclofenac potassium as orodispersible layer and diclofenac sodium as sustained release core. Marmara Pharmaceutical Journal 21 3 707–716.
IEEE J. Abbas, “Formulation and evaluation of a bilayer tablet comprising of diclofenac potassium as orodispersible layer and diclofenac sodium as sustained release core”, Marmara Pharm J, vol. 21, no. 3, pp. 707–716, 2017, doi: 10.12991/marupj.323595.
ISNAD Abbas, Jabbar et al. “Formulation and Evaluation of a Bilayer Tablet Comprising of Diclofenac Potassium As Orodispersible Layer and Diclofenac Sodium As Sustained Release Core”. Marmara Pharmaceutical Journal 21/3 (June 2017), 707-716. https://doi.org/10.12991/marupj.323595.
JAMA Abbas J, Bashir S, Samie M, Laghari S, Aman N, Jan HU, Nazir İ. Formulation and evaluation of a bilayer tablet comprising of diclofenac potassium as orodispersible layer and diclofenac sodium as sustained release core. Marmara Pharm J. 2017;21:707–716.
MLA Abbas, Jabbar et al. “Formulation and Evaluation of a Bilayer Tablet Comprising of Diclofenac Potassium As Orodispersible Layer and Diclofenac Sodium As Sustained Release Core”. Marmara Pharmaceutical Journal, vol. 21, no. 3, 2017, pp. 707-16, doi:10.12991/marupj.323595.
Vancouver Abbas J, Bashir S, Samie M, Laghari S, Aman N, Jan HU, Nazir İ. Formulation and evaluation of a bilayer tablet comprising of diclofenac potassium as orodispersible layer and diclofenac sodium as sustained release core. Marmara Pharm J. 2017;21(3):707-16.