The Effect of PEG 4000 in Co-processed Excipient using Melt Granulation Method on the Physical Characteristics of Chitosan Tablets in Mangrove Crab Shells (Scylla serrata)
Pengaruh PEG 4000 dalam Koproses Eksipien dengan Metode Melt Granulation terhadap Karakteristik Fisik Tablet Kitosan Cangkang Kepiting Bakau (Scylla serrata)
DOI:
https://doi.org/10.53342/pharmasci.v9i1.420Keywords:
Co-processed Excipient, Direct Compression, Melt Granulation, PEG 4000, Scylla serrataAbstract
Mangrove Crab (Scylla serrata) is an animal that likes to be consumed but its shell waste is underutilized. The shell contains chitosan which has many benefits, one of which can lower cholesterol levels. The combination of 2 or more excipients is called co-processed excipients which are then continued into tablets by direct compression. The aim of the study was to find out whether chitosan could be formalized into coprocessed tablets (lactose, primogel, and PEG 4000 7.5% & 15%) by direct compression method and the effect of differences in the characteristics of coprocessed and chitosan tablets with a ratio of PEG 4000 7.5% and 15 % as binder. The evaluation results showed that chitosan tablets fulfilled the requirements for the uniformity of weight, hardness, disintegration time (F1) tests, while they did not meet the requirements for the uniformity of tablet size, friability and disintegration times (F2) tests and the results of the coprocessing evaluation met specifications both F1 and F2, namely: particle size distribution, moisture content, flow rate, angle of repose (very good), compressibility index (adequate) and Hausner's ratio (very good). The evaluation results were then processed statistically using the SPSS application using the independent t-test method which showed that there was no significant difference in the effect of PEG 4000 7.5% and 15% as a binder on the characteristics of co-processed and chitosan tablets. Chitosan tablets from mangrove crab shells (Scylla serrata) cannot be formalized by direct compression with co-processing.
References
2. Kusuma SH. Kemampuan Kitin Dari Cangkang Kepiting Bakau (Scylla spp) Dalam Menurunkan Kadar Kolesterol Jeroan Sapi. Vol. 1, Jurnal Ilmiah Mahasiswa Pendidikan Biologi. 2016 Aug.
3. Imtihani HN, Permatasari SN, Prasetya RA. In Vitro Evaluation of Cholesterol-Reducing Ability of Chitosan from Mangrove Crab (Scylla serrata)
Shell Solid Dispersion using PVP K-30 as a Carrier. J Farm Galen (Galenika J Pharmacy). 2021;7(2):99–109.
4. Parikh DM. Handbook of pharmaceutical granulation technology. 2nd ed. Taylor & Francis Group L, editor. Handbook of Pharmaceutical Granulation Technology. Boca Raton: Taylor & Francis Group; 2005. 194 – 198 p.
5. Suherman H. Pengaruh Penggunaan Variasi Konsentrasi Laktosa Pada Formula Tablet Prednisolone. Viva Med. 2017;1:44–65.
6. Agustina. Pengaruh Pemberian Kitosan Terhadap Kadar Kolesterol Total Tikus ( Sprague-dawley ) yang Diberi Pakan Tinggi Asam Lemak Trans. Inst Pertan Bogor. 2014;1–31.
7. Sulaiman. Eksipien Untuk Pembuatan Tablet Dengan Metode Kempa Langsung. 2020;3(2):64–76.
8. Puspita PA., Dewantara IGN., Arisanti CI. Formulasi Tablet Parasetamol Kempa Langsung Menggunakan Eksipien Co-processing dari Amilum Singkong Partially Pregelatinized dan Gom Akasia. Farm Udayana. 2013;2(3):28–34.
9. SNI 01-2891-1992. Cara uji makanan dan minuman. Jakarta: Badan Standarisasi Nasional; 1992.
10. Salman AD, Hounslow MJ, Seville JPK. Handbook of Powder Technology Granulation. 11th ed. Williams JC, Allen T, editors. Elsevier; 2007.
11. Michael E. Aulton KMGT. Aulton’s Pharmaceutics : The Design and Manufacture of Medicines. Fifth. Aulton ME, Taylor KMG, editors. Aulton’s Pharmaceutics The Design and Manufacture of Medicines. Elsevier; 2018.
12. Diyya ASM, Thomas NV. FORMULATION AND EVALUATION OF METRONIDAZOLE EFFERVESCENT GRANULES. Int J Pharm Sci Res. 2018;9(6):2525–9.
13. Kelana AS, Kusuma AP, Indrati O. Formulasi dan Evaluasi Tablet Kaptopril Menggunakan Amilum Umbi Talas dan HPMC yang Dimodifikasi Sebagai Pengisi dan Pengikat Metode Kempa Langsung. J Eksakta. 2018;18(1):8–18.
14. W S, Hoag, Lim HP. Pharmaceutical Dosage Forms - Tablets. 3rd Editio. CRC Press; 2008.
15. Devi LAS, Shodiquna QA, Eni NWSD, Arisanti CIS, Samirana PO. Optimasi Konsentrasi Polivinil Pirolidon ( PVP ) sebagai Bahan Pengikat tehadap Sifat Fisik Tablet Ekstrak Etanol Rimpang Bangle ( Zingiber cassumunar Roxb ). J Farm Udayana. 2018;7(2):45–52.
16. Kalalo T, Yamlean PVY, Citraningtyas G. PENGARUH PENGGUNAAN PATI KULIT NANAS (Ananas comosus (L.) Merr.) SEBAGAI BAHAN PENGIKAT PADA GRANUL CTM. Pharmacon. 2019;8(1):203–13.
17. Permatasari J, Lestari U, Widyastuti R. ISOLASI DAN UJI SIFAT FISIKOKIMIA PATI DARI BIJI KARET (Hevea brasiliensis). Farmasains. 2018;5(1):9–14.
18. Chandira MR, Bhowmik D, Yadav R, Jayakar B, Kumar KPS. Formulation and Evaluation The Oral Tablets Ibuprofen. 2012;1(9):32–43.
19. Lieberman HA, Lachman L. Pharmaceutical Dosage Forms Tablets Volume 1. Second Edi. New York: Marcel Dekker, Inc; 1989.
20. Amaliya S. Pengaruh Penggunaan Gelatin dari Kulit Kambing Etawah sebagai Bahan Pengikat pada Pembuatan Tablet Parasetamol Secara Granulasi Basah. Universitas Islam Negeri Syarif Hidayatullah; 2018.
21. Departemen Kesehatan Republik Indonesia. Farmakope Indonesia. Edisi V. Jakarta: Departemen Kesehatan Republik Indonesia; 1995.
22. Kesehatan M (Republik I. Farmakope Indonesia 5 Jilid 2. 2014.
23. Lachman L, Lieberman HA, Kanig JL. Teori dan praktek farmasi industri 1. III. Jakarta: UI Press; 1994.
24. Siregar S. Statistik Parametrik untuk Penelitian Kuantitatif Dilengkapi dengan Perhitungan Manual dan Aplikasi SPSS Versi 17. Jakarta: Bumi Aksara; 2014.
25. Widiyanto J. SPSS for Windows Untuk Analisis Data Statistik dan Penelitian. Surakarta: BP-FKIP UMS; 2010.
26. Walpole RE, Myers RH. Ilmu peluang dan statistika untuk insiyur dan ilmuwan. 4th ed. Bandung: ITB PRESS; 1995.
27. Supranto J. Statistik Teori Dan Aplikasi. Keenam. Jakarta: Erlangga; 2000.
28. Prasetyo TF, Isdiana AF, Sujadi H. Implementasi Alat Pendeteksi Kadar Air Pada Bahan Pangan Berbasis Internet Of Things. SMARTICS J. 2019;5(2):81–96.
29. Wade A, Weller PJ. Handbook of pharmaceutical excipients. Second. Washington: The American Pharmaceutical association; 1994.
30. Laili N, Komala AM, Maulida H, Suprapto. Optimasi Konsentrasi Amylum Sagu (Metroxylon rumphii) sebagai Co-Processed pada Pembuatan Tablet Teofilin. Pharmacon J Farm Indones. 2017;14(2):72–80.
31. Winarti W, Kartiningsih, Djamil R, Zaidan S, Nugrahaini I. Formulasi Sediaan Tablet Ekstrak Sambung Nyawa ( Gynurae procumbens ( Lour ). Merr ) sebagai Kandidat Antidiabetes. 2016;14(2):240–5.
32. Martin A. Farmasi Fisik (Dasar-Dasar Farmasi Fisik dalam Ilmu Farmasetik 2). II. Jakarta: UI Press; 1993.
33. Ningsi S, Leboe DW, Aeni Q. STUDI KEMAMPUAN PATI BIJI ALPUKAT (Persea americana Mill) PREGELATINASI SEBAGAI BAHAN PENGHANCUR PADA TABLET PARACETAMOL KEMPA LANGSUNG. JF FIK UINAM. 2016;4(3):106–13.
34. Hidayat B, Indriani F, Muliadi. IMPLEMENTASI INDEPENDENT T-TEST PADA APLIKASI PEMBELAJARAN MULTIMEDIA RAGAM DAN GERAK SENI TARI DAERAH KALIMANTAN SELATAN. Kumpul J Ilmu Komput. 2015;02(01):11–21.
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