PENGARUH KONSENTRASI CROSPOVIDONE TERHADAP MUTU FISIK SEDIAAN ORAL FAST DISSOLVING TABLETS LORATADINE HCl
Main Article Content
Abstract
Oral Fast Dissolving Tablet (OFDT) is a solid dosage form, containing an active substance which disintegrates rapidly within a few seconds when it is placed on the tongue, and generally will dissolve in less than 60 seconds. The manufacture of OFDT loratadine HCl in this formulation is to find out which results are more optimal from the different concentrations of Crospovidone disintegrants with 2%, 3%, and 4% concentrations. In this study, the method used is wet granulation, which can improve the comparability of loratadine HCl, as medicine formulations. This study aims to determine the effect of the physical quality of the Oral Fast Dissolving Tablet loratadine HCl preparation on the concentration of crospovidone as a disintegrant and to determine concentration of crospovidone that can provide results fulfilling the requirements in the manufacture of Oral Fast Dissolving Tablets. In the first formulation the average disintegration time is 0.34 minute, the second formulation disintegration time is 1.16 minute, the third formulation disintegrated time is 0.50 minute. The results of the three formulations state that only the first and third formulations accomplish the requirements, the second formulation does not accomplish the requirements. In the manufacture of OFDT preparations with different concentrations of Crospovidone, it is very influential on the disintegration time, and in this formulation, the better result is a concentration of 2% because it has a faster disintegration time and physical quality that fulfill the requirements
Downloads
Article Details
References
“Optimasi Sodium Strach Glycolate Dan Crospovidone sebagai superdisentegran dalam Sediaan Orally Disentegrating Tablet Meloksikam (Optimization of Sodium Starch Glycolate and Crospovidone as Superdisetegrant in Orally Disentegranting Meloicam Tablet Dosag”.Pustaka Kesehatan 5. (2017): 399-405.
Abul Kalam Lutful Kabir, Shaikh Mukidur Rahman , Md. Arshad Jahan , Abu Shara Shamsur Rouf, 2009, Formulation Development and Evaluation of Mouth Dissolving Tablets of Loratadine, Department of Pharmacy Jagannath University Bangladesh
Bhowmik, D., Chiranjib, B., & Chandira,
R. M. (2009). Fast Dissolving Tablet : An Overview. 1(1), 163– 177.
Departemen Kesehatan RI 1979. Farmakope Indonesia Edisi III, Jakarta : Depkes RI
Ferri W., Oktavia E. P., Oktavia R. A., Nurus S., (2019)., Teknologi Farmasi Sediaan Solid, Fakultas Kedokteran Universitas Brawijaya
Georgeta PAVALACHE, Vasile DORNEANU and Antoanela POPESCU, 2010, Determination of loratadine by UV molecular absorption spectrometry, Ovidius University Annals of Chemistry
Hadisoewiginyo, L dan Fudloli,A., 2003 .
Sediaan solida, Yogyakarta
Hartesi, B. et al. (2016). Starch as Pharmaceutical Excipient. Int. J. Pharm. Sci. Rev. Res., 41(2), 59-
64
Mariana Raini, Daroham Mutiatikum, Pudji Lastari , Uji Disolusi Dan Penetapan Kadar Tabletloratadin Inovator Dan Generik Bermerek, Media Litbang Kesehatan Volume XX Nomor 2 Tahun 2010.
Nagar., et al. (2011). ‘Orally disintegrating tablets: formulation, preparation techniques and evaluation’. Journal of Applied Pharmaceutical Science. 17 June. Vol. 01 (04).
Nurdianti L., Nudiansyah D dan Aryani R., 2018, Formulasi Fast Disentegrant Tablet (FDT) aspirin sebagai antiplatelet dengan Ac-Di- Sol sebagai superdisentegrant. Tasikmalaya.
Ricky Marthin , Wahyudi Uun Hidayat, 2017, Pengaruh Jenis Dan Konsentrasi Bahan Penghancur, Sodium Starch Glycolate, Crospovidone Coarse Dan Croscarmellose Sodium Terhadap Parameter Fisik Cetirizine Orally
Disintegrating Tablet (Odt) Secara Kempa Langsung, Fakultas Farmasi Universitas 17 Agustus 1945 Jakarta
Surendra Prasad Gupta, Pashupati Bashya and Laxmi Shrestha, 2019, FORMULATION AND EVALUATION OF ORAL DISPERSIBLE TABLETS OF LORATADINE BY DIRECT COMPRESSION METHOD,
Department of Pharmaceutical Sciences, Crimson College of Technology (Affiliated to Pokhara University), Butwal-13, Devinagar, Rupandehi, Nepal.
Trio Adi Saputro. (2016). Optimasi formula fast disintegrating tablet piroksikam dengan kombinasi bahan penghancur crospovidone dan bahan pengisi manitol (doctoral dissertation, universitas muhammadiyah purwokerto).
Yoyo Dodhy Sutikno, Optimasi Formulasi Fast Disentegrating Tablet (FDT)
Chlorpheniramine Maleate Dengan Crospovidone Dan Povidone Dengan Metode, Yogyakarta, Universitas Sanata Dharma, 2018.