Formulation of Ibuprofen Orally Disintegrating Tablets (ODT) Using a Combination of Cassava Starch (Manihot esculenta Crantz) and Mannitol as a Superdisintegrant

Authors

  • Adika Madani Institut Kesehatan Mitra Bunda Batam
  • Tommy Julianto Institut Kesehatan Mitra Bunda Batam
  • Sulastari Cahyani Institut Kesehatan Mitra Bunda Batam
  • Sri Budiasih Institut Kesehatan Mitra Bunda Batam

DOI:

https://doi.org/10.35451/jfm.v9i1.3998

Keywords:

Ibuprofen, Orally Disintegrating Tablet (ODT), Cassava Starch, Mannitol, Co-processing

Abstract

Background: Orally Disintegrating Tablets (ODT) are solid dosage forms designed to disintegrate rapidly in the oral cavity, making them highly beneficial for patients with swallowing difficulties. Aim: This study aimed to determine the formulation and evaluate the physical properties of Ibuprofen ODTs using a co-processed combination of cassava starch (Manihot esculenta Crantz) and mannitol as a superdisintegrant. Methods: The study was conducted experimentally using direct compression with varying ratios of cassava starch and mannitol in a co-milled physical mixture. Pre-compression evaluation included flow properties, angle of repose, compressibility index, and moisture content; tablet evaluation included weight and size uniformity, hardness, friability, disintegration time, stability, and dissolution. Results: F3 showed a disintegration time of 151.33 seconds (2.52 min) and the highest ibuprofen dissolution at 60 min (79.01%), compared with F1 (60.44%) and F2 (49.82%). Tablet hardness ranged from 3.33 to 3.70 kg, while friability was <1% for all formulations. Conclusion: The cassava starch–mannitol combination can be used in ibuprofen ODT formulations, although further optimization of mechanical strength and dissolution is required.

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References

[1] Qiu, Y., Chen, Y., Zhang, G. G., Liu, L., & Porter, W. R. (Eds.). (2017). Developing solid oral dosage forms: Pharmaceutical theory and practice (2nd ed.). San Diego: Academic Press.

[2] Katzung, B. G. (2018). Basic and Clinical Pharmacology (14th ed.). McGraw-Hill Education.

[3] Allen, L. V., & Ansel, H. C. (1989). Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems (10th ed.). Wolters Kluwer Health.

[4] Be Miller, J. N., & Whistler, R. L. (Eds.). (2009). Starch: Chemistry and Technology (3rd ed.). Academic Press.

[5] Ghourichay, M. P., Kiaie, S. H., Nokhodchi, A., & Javadzadeh, Y. (2021). Formulation and quality control of orally disintegrating tablets (ODTs): Recent advances and perspectives. BioMed Research International, 2021, 6618934. https://doi.org/10.1155/2021/6618934

[6] Adeoye, O., & Alebiowu, G. (2014). Evaluation of coprocessed disintegrants produced from tapioca starch and mannitol in orally disintegrating paracetamol tablet. Acta Poloniae Pharmaceutica – Drug Research, 71(5), 803–810.

[7] Grace, M. R. (2019). Cassava Processing. FAO Plant Production and Protection Series No. 3. Rome: Food and Agriculture Organization of the United Nations.

[8] Kementerian Kesehatan Republik Indonesia. (2020). Farmakope Indonesia Edisi VI. Jakarta: Kementerian Kesehatan Republik Indonesia.

[9] Lachman, L., Lieberman, H. A., & Kanig, J. L. (2008). The Theory and Practice of Industrial Pharmacy (3rd ed.). Lea & Febiger.

[10] Aulton, M. E., & Taylor, K. M. G. (2018). Aulton's pharmaceutics: The design and manufacture of medicines (5th ed.). Edinburgh: Elsevier.

[11] McSweeney, M., Fleming, A., & Binks, B. (2020). Pharmaceutical formulation design: Usable approaches. CRC Press.

[12] Augsburger, L. L., & Hoag, S. W. (Eds.). (2008). Pharmaceutical dosage forms: Tablets (3rd ed., Vol. 1). New York: Informa Healthcare.

[13] Pathak, T., Gehalot, N., Jain, V., & Mahajan, S. (2023). A review on orodispersible tablet. International Journal of Pharmaceutical Sciences and Medicine, 8(4), 41–51. https://doi.org/10.47760/IJPSM.2023.V08I04.004

[14] Rohmani, S., & Rosyanti, H. (2019). Perbedaan metode penambahan bahan penghancur secara intragranular-ekstragranular terhadap sifat fisik serta profil disolusi tablet ibuprofen. JPSCR: Journal of Pharmaceutical Science and Clinical Research, 4(2), 95–108. https://doi.org/10.20961/jpscr.v4i2.33622

[15] Husni, P., Fadhiilah, M. L., & Hasanah, U. (2020). Formulasi dan uji stabilitas fisik granul instan serbuk kering tangkai genjer (Limnocharis flava (L.) Buchenau.) sebagai suplemen penambah serat. Jurnal Ilmiah Farmasi Farmasyifa, 3(1), 1–8. https://doi.org/10.29313/JIFF.V3I1.5163

[16] Swain, R. P., Satish, P., Subudhi, B. B., & Panda, S. (2015). Formulation and optimization of orodispersible tablets of ibuprofen. International Journal of Pharmacy and Pharmaceutical Sciences, 7(2), 441–447.

[17] Rowe, R. C., Sheskey, P. J., & Owen, S. C. (2009). Handbook of Pharmaceutical Excipients (5th ed.).

[18] Ocieczek, A., Mesinger, D., & Toczek, H. (2022). Hygroscopic properties of three cassava (Manihot esculenta Crantz) starch products: Application of BET and GAB models. Foods, 11(13), 1966. https://doi.org/10.3390/foods11131966

[19] Sandoval, A. J., Fernández, A., Leiva, A., Müller, A. J., & Barreiro, J. A. (2012). Moisture adsorption isotherms of amorphous cassava starch at different temperatures determined by a dynamic vapor sorption technique. Journal of Food Process Engineering, 35(2), 218–232.

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Published

2026-10-30

How to Cite

Formulation of Ibuprofen Orally Disintegrating Tablets (ODT) Using a Combination of Cassava Starch (Manihot esculenta Crantz) and Mannitol as a Superdisintegrant. (2026). JURNAL FARMASIMED (JFM), 9(1), 852-860. https://doi.org/10.35451/jfm.v9i1.3998