Optimasi Polyvinilpyrolidone K-30 dan Sodium Starch Glycolate pada Tablet Likuisolid Simvastatin dengan Desain Faktorial

  • Agne Yuliana Nursatriya Fakultas Farmasi Universitas Jember
  • Lusia Oktora Ruma Kumala Sari Fakultas Farmasi Universitas Jember
  • Dwi Nurahmanto Fakultas Farmasi Universitas Jember

Abstract

The liquisolid technique is one way to increase the drug dissolution rate, which has low solubility in water and can improve drug flow properties. This research aims to determine the optimum composition of a combination of polymer PVP K-30 and SSG on a liquisolid simvastatin tablet with a factorial design. The factorial design method is used to determine the effect of the concentration of two factors, namely PVP K-30 and SSG, on the response of hardness, friability, disintegration time, and dissolution. PVP K-30 acts as a binder, and SSG works as a disintegration, determines the optimum formula using expert design software version 1. The result showed that all formulas meet the requirements of hardness values (4-8 kg), friability (<1%), disintegration time of no more than 15 minutes, and dissolution in 30 minutes. The use of PVP K-30 concentration of 6 mg and SSG 24 mg indicated the optimum formula with a desirability value of 0,806.

References

[1] Shah VP, Amidon GL. A theoretical basis for a biopharmaceutic drug classification : the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm res. 2014.12: 413 – 420.
[2] Sahu V, Ghuge N, Bakde BV. A New Thechnique For Enahancement Of Drug Dissolutionf Drug Dissolution. International Journal Of Pharmaceutical Sciences And Research, 2012. 4(974): 302–306.
[3] Vranikova B, Gajdziok J. Liquisolid systems and aspects influencing their research and development. Acta Pharm, 2013. 63:447–465.
[4] Javandest Y, Jafari-navimipour B, Nokhodchi A. Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug ( carbamazepine ). Iranian Journal Of Pharmaceutical Research. 2007.341: 26–34.
[5] Rowe RC, Sheskey D, Quin PJ. Handbook of pharmaceutical excipients. Pharmaceutical Press and American Pharmacist Association. 2009. 6 edition. USA.
[6] Fatmawati DA, Widjaja B, Setyawan D. Optimasi tablet levofloksasin yang mengandung bahan pengikat pvp k-30 dan disintegran vivasol. Jurnal Sains Farmasi Dan Klinik, 2017. 4: 9–15.
[7] Pahwa R, Gupta N. Super disintegrants In The Development Of Orally Disintegrating Tablets. International Journal Of Pharmaceutical Sciences And Research, 2011. 2(11): 2767–2780.
[8] Bala R, Khanna S, Pawar P. Polymers in Fast Disintegratig Tablets-A Review. Asian Journal of Pharmaceutical and Clinical Research 2012.
[9] Yadav V, Yadav A. Improvement of solubility and dissolution of indomethacin by liquisolid and compaction granulation technique. Journal Of Pharmaceutical Sciences And Research, 2009. 1(2):4 4–51.
Published
2024-08-08
How to Cite
NURSATRIYA, Agne Yuliana; SARI, Lusia Oktora Ruma Kumala; NURAHMANTO, Dwi. Optimasi Polyvinilpyrolidone K-30 dan Sodium Starch Glycolate pada Tablet Likuisolid Simvastatin dengan Desain Faktorial. Pustaka Kesehatan, [S.l.], v. 11, n. 3, p. 200-206, aug. 2024. ISSN 2721-3218. Available at: <https://jurnal.unej.ac.id/index.php/JPK/article/view/18320>. Date accessed: 22 nov. 2024. doi: https://doi.org/10.19184/pk.v11i3.18320.