Formulasi tablet kitosan cangkang kepiting bakau (Scylla serrata) dari co-processed excipient dengan PEG 4000 sebagai meltable binder

Authors

  • Hilya Nur Imtihani Departemen Teknologi Farmasi, Akademi Farmasi Surabaya, Surabaya, Indonesia https://orcid.org/0000-0003-3670-7609
  • Mutia Natarani DIII Farmasi, Akademi Farmasi Surabaya, Surabaya, Indonesia
  • Yessy Kurnia Sandy DIII Farmasi, Akademi Farmasi Surabaya, Surabaya, Indonesia

DOI:

https://doi.org/10.32504/hspj.v6i3.741

Keywords:

Chitosan, co-processed excipient, mangrove crab shells, PEG 4000, tablet

Abstract

Chitosan has many functions in the health sector, one of which can be used as an anti cholesterol supplement. Co-processing is a technique carried out to obtain new additives by combining two or more existing additives, where the combinations of these materials will complement each other, so that new additives with better (superior) properties are obtained. The purpose of this study was to determine the formulation and evaluation of mud crab shell (Scylla serrata) chitosan tablets from co-processed excipients with PEG 4000 as a meltable binder with a ratio of 10% (F1) and 20% (F2). Co-processed excipients are made using the melt granulation method with additional ingredients, namely lactose as a filler and primogel as a disintegrant. Tablets were printed using the direct compression method with the addition of Mg Stearate as a lubricant. The results of the co-processed excipient evaluation showed that each granule met the requirements for the flow rate test, angle of repose test, compressibility test and Hausner's ratio. From the results of statistical tests using the Mann-whitney test method, there is a significant difference between co-processed excipient PEG 4000 10% and PEG 4000 20% as a meltable binder for the parameters of water content with F2 moisture content (1.67%) lower than in F1 (3.33%). In the evaluation of chitosan tablets, they produced tablets that met the test requirements for weight uniformity, tablet friability (F1), tablet hardness, disintegration time (F2) and did not meet the requirements for the tablet size uniformity test. The selected formula for this study was F2 with a PEG 4000 meltable binder of 20% because it produced tablets that met disintegration time with low water content.

References

Maidin AN. Produksi Kitosan Dari Limbah Cangkang Kepiting Rajungan (Portunidae) Secara Enzimatis Dan Aplikasinya Sebagai Penurun Kolesterol. Hasanuddin University; 2017.

Nachaegari SK, Bansal AK. Coprocessed Excipients for Solid Dosage Forms. Pharm Technol. 2004;28(1):52–64.

Gangurde HH. Co- Excipient : Future of Formulation Industry. Acad J Polym Sci. 2019;3(3):54–9.

Patel RP, Bhasvar M. Directly Compressible Materials Via Co-Processing. J Pharm Technol. 2009;1(3):745–53.

Sulaiman TNS, Sulaiman S. Review: Eksipien Untuk Pembuatan Tablet dengan Metode Kempa Langsung. J Pharm Sci. 2020;3(2):64–76.

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.

SNI 01-2891-1992. Cara uji makanan dan minuman. Jakarta: Badan Standarisasi Nasional; 1992.

Salman AD, Hounslow MJ, Seville JPK. Handbook of Powder Technology Granulation. 11th ed. Williams JC, Allen T, editors. Elsevier; 2007.

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.

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.

W S, Hoag, Lim HP. Pharmaceutical Dosage Forms - Tablets. 3rd Editio. CRC Press; 2008.

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.

Chandira MR, Bhowmik D, Yadav R, Jayakar B, Kumar KPS. Formulation and Evaluation The Oral Tablets Ibuprofen. 2012;1(9):32–43.

Lieberman HA, Lachman L. Pharmaceutical Dosage Forms Tablets Volume 1. Second Edi. New York: Marcel Dekker, Inc; 1989.

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.

Departemen Kesehatan Republik Indonesia. Farmakope Indonesia. Edisi V. Jakarta: Departemen Kesehatan Republik Indonesia; 1995.

Kesehatan M (Republik I. Farmakope Indonesia 5 Jilid 2. 2014.

Lachman L, Lieberman HA, Kanig JL. Teori dan praktek farmasi industri 1. III. Jakarta: UI Press; 1994.

Artha S, Intan R. Pengaruh Penerapan Standar Operasional Prosedur dan Kompetensi Terhadap Produktivitas Kerja Karyawan Divisi Ekspor PT. Dua Kuda Indonesia. J Ilm M-Progress. 2021;11(1):38–47.

Suherman H. Pengaruh Penggunaan Variasi Konsentrasi Laktosa Pada Formula Tablet Prednisolone. Viva Med. 2017;1:44–65.

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.

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.

Wade A, Weller PJ. Handbook of pharmaceutical excipients. Second. Washington: The American Pharmaceutical association; 1994.

Sulaiman. Eksipien Untuk Pembuatan Tablet Dengan Metode Kempa Langsung. 2020;3(2):64–76.

Downloads

Published

2023-01-10

Issue

Section

Articles

Citation Check