Optimation of Avicel PH 102 with Cab-O-Sil M-5P Ratio and Crospovidone Concentration on Liquisolid System Piroxicam Tablet

https://doi.org/10.22146/farmaseutik.v13i1.38466

T.N. Saifullah Sulaiman(1*), Rani Puspita(2), Mutmainah Mutmainah(3)

(1) Fakultas Farmasi, Universitas Gadjah Mada Yogyakarta
(2) Sekolah Tinggi Ilmu Farmasi “Yayasan Pharmasi” Semarang
(3) Sekolah Tinggi Ilmu Farmasi “Yayasan Pharmasi” Semarang
(*) Corresponding Author

Abstract


Piroxicam is slightly soluble, so it should be developed in a liquisolid system of tablet dosage form to increase its solubility in gastrointestinal tract. Factorial design was applied to optimize the formula of liquisolid system piroxicam tablet by using four formulas: run  I (18%A-2%B), run II (45%A-2%B), run III (18%A-5%B), and run IV (45%A-5%B). Component A is the ratio of Avicel PH 102 with Cab-O-Sil M-5P whether B is the concentration of crospovidone. Optimum formula was determined by superimposed contour plot from various parameters: hardness, friability, disintegrating time, and dissolution concentration (C45) using Design Expert software. Based on superimposed contour plot, optimum formula area was obtained in the range of 18-45 of Avicel PH 102 with Cab-O-Sil M-5P ratio and 2-5% of crospovidone concentration.


Keywords


Piroxicam, Avicel PH 102, Cab-O-Sil M-5P, crospovidone, liquisolid

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References

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DOI: https://doi.org/10.22146/farmaseutik.v13i1.38466

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