Pengembangan Mikrosfer Asiklovir menggunakan Kitosan dan Natrium Tripolifosfat: Faktor Suhu Inlet

  • Cynthia Marisca Muntu Departemen Farmasetika, Fakultas Farmasi, Universitas Surabaya, Surabaya-Indonesia
  • Sadono Departemen Farmasetika, Fakultas Farmasi, Universitas Surabaya, Surabaya-Indonesia
  • Melinda Natalia Suwito Departemen Farmasetika, Fakultas Farmasi, Universitas Surabaya, Surabaya-Indonesia
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Keywords: chitosan, inlet temperature, microspheres, sodium tripolyphosphate, kitosan, mikrosfer, natrium tripolifosfat, suhu inlet

Abstract

AbstractAcyclovir is an antiviral used for the treatment of herpes simplex but it's a short half-life, thereby increasing the administration frequency. To overcome this problem, the acyclovir microsphere system was created with chitosan and sodium tripolyphosphate (NTPP). The formulation used a spray drying method which is influenced by the inlet temperature. Three variations of the inlet temperature are given, i.e. 170 oC (M1), 180 oC (M2), and 190 oC (M3). Physicochemical characterization obtained the same results on the three microspheres. They showed the occurrence of cross-linking between chitosan and NTPP. The average particle sizes of M1, M2, and M3 microspheres were 8.52 µm, 8.92 µm, and 9.83 µm respectively. All microspheres' morphology was spherical with a rough surface. The moisture content of M1, M2, M3 microspheres were 6.63%, 5.49%, 4.63%, respectively. The swelling index of M1, M2, and M3 microspheres obtained from 0.5-4 hours were 143.11-258.86%, 167.26-239.61%, and 152.49-259.60%. The recovery of M1, M2, and M3 microspheres was 33.93%, 47.26%, and 35.09% respectively. The acyclovir encapsulation efficiency of M1, M2, and M3 microspheres were 115.32%, 117.14%, and 111.16% respectively. Dissolution testing showed all three microspheres have the potential for controlled drug delivery systems. The inlet temperature affects the microsphere characteristics and the best inlet temperature was 180 oC.

 

Abstrak—Asiklovir merupakan antivirus yang digunakan untuk terapi herpes simplex karena tingkat selektivitasnya tinggi tetapi waktu paruhnya cepat sehingga meningkatkan frekuensi pemberiannya. Untuk mengatasi masalah ini asiklovir dibuat sistem mikrosfer. Dalam penelitian ini kitosan digunakan sebagai polimer dan natrium tripolifosfat (NTPP) sebagai penyambung silang. Pembuatannya menggunakan metode spray drying yang dipengaruhi oleh suhu inlet, sehingga diberikan tiga variasi suhu inlet yaitu 170 oC (M1), 180 oC (M2), dan 190 oC (M3). Karakteristisasi fisikokimia meliputi identifikasi gugus fungsi, perubahan melting point, dan energi entalpi memperoleh hasil yang sama pada ketiga mikrosfer yaitu terjadinya ikatan sambung silang antara kitosan dengan NTPP. Ukuran partikel rata-rata mikrosfer M1, M2, M3 berturut-turut adalah 8,52 µm, 8,92 µm dan 9,83 µm. Morfologi bentuk ketiga mikrosfer adalah sferis dengan permukaan kasar. Kandungan lembap mikrosfer M1, M2, M3 berturut-turut adalah 6,63%, 5,49%, 4,63%. Indeks pembengkakan mikrosfer M1, M2, M3 yang diperoleh dari 0,5-4 jam berturut-turut adalah 143,11-258,86%, 167,26-239,61% dan 152,49-259,60%. Perolehan kembali mikrosfer M1, M2, M3 berturut-turut adalah 33,93%, 47,26% dan 35,09%. Efisiensi enkapsulasi asiklovir M1, M2, M3 berturut-turut adalah 115,32%, 117,14% dan 111,16%. Pengujian disolusi asiklovir menunjukkan ketiga mikrosfer berpotensi untuk sistem penghantaran obat terkendali. Suhu inlet berpengaruh terhadap karakteristik mikrosfer asiklovir dan suhu terbaik adalah 180 oC.

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References

Handoko & Ronny, P 2010, Ilmu Penyakit Kulit dan Kelamin, edisi keenam, Jakarta: Fakultas Kedokteran Universitas Indonesia, 380-382.

Agnihotri, SA, Mallikarjuna, NN & Aminabhavi, TM 2004, ‘Recent Advances on Chitosan based micro- and nanoparticles in Drug Delivery’, Journal of Controlled Release, Vol. 100, p. 5-28.

Khan, MS, Vishakante, GD, Bathool, A, Kumar, R 2012, ‘Preparation and Evaluation of Spray Dried Microparticles Using Chitosan and Novel Chitosan Derivative for Controlled Release of an Antipsychotic Drug’, International Journal of Biological & Pharmaceutical Research.

Bhavesh, BP, Jayvadan, KP & Subhashis, C 2015, ‘Revealing facts behind spray dried solid dispersion technology used for solubility enhancement’, Saudi Pharmaceutical Journal, Vol. 23, p. 352-365.

Amaro, MI, Tajber, L, Corrigan, OL & Healy, AM 2011, ‘Optimisation of spray drying process conditions for sugar nanoporous microparticles (NPMPs) intended for inhalation’, International Journal of Pharmaceutics, Vol. 421, p. 99-109.

Yuliani, S 2007, ‘Pengaruh Laju Alir Umpan dan Suhu Inlet Spray Drying pada Karakteristik Mikrokapsul Oleoresin Jahe’, Bogor, Fakultas Teknologi Pertanian, Institut Pertanian Bogor.

Mardawati, E, Rialita, T, Anggraini, S 2018, ‘Kajian Pengaruh Suhu Inlet dan Konsentrasi Maltodekstrin terhadap Kadar Air dan Kelarutan Serbuk Xilitol Hasil Spray Dryer’, Prosiding Seminar Nasional Teknologi Pangan, 59-66.

Desai, KG & Park, HJ 2005, ‘Preparation and Characterization of Drug Loaded Chitosan Tripolyphospate by Spray Drying’, Drug Development Research, p. 6114-128.

Bhumkar, DR & Pokharkar, VB 2006, ‘Studies on Effect of ph on Cross-linking of Chitosan With Sodium Tripolyphosphate: A Technical Note’, AAPS PharmSciTech.

Berlianto, AS 2014, ‘Pengaruh Konsentrasi Kitosan terhadap Karakteristik Fisik Mikropartikel Salbutamol-sulfat Menggunakan Penyambung Silang Natrium-Tripolifosfat dengan Metode Spray Drying’, Skripsi tidak dipublikasikan, Surabaya, Fakultas Farmasi Universitas Surabaya.

Garud, A & Garud, DN 2010, ‘Preparation and Evaluation of Chitosan Microcapsules of Metronidazole using Tripolyphosphate Cross-Linking Method’. Dhaka University Journal of Pharmaceutical Science, 9(2), 125-130.

Patel RP, Patel MP, & Suthar AM, 2009, Spray drying technology: an overview. Indian Journal of Science and Technology, 2(10), 44-47.

He P, Davis SS, Illum L, 1999, Chitosan Microspheres Prepared by Spray Drying. International Journal of Pharmaceutics, Vol. 187, p. 53-65.

Maas SG, Schaldach G, Littringer EM, Mescher A, Griesser UJ, Braun DE, Walzel PE, Urbanez, 2011, The impact of spray drying outlet temperature on the particle morphology of mannitol. Powder Technology 213: 27-35.

Mishra, M., dan Mishra B., 2011, Formulation Optimization and Characterization of Spray Dried Microparticles for Inhalation Delivery of Doxycycline Hyclate, India: Banaras Hindu University.

Kissel, T, Maretschek, S, Packhauser, C, Schnieders, J & Seidel, N 2006, ‘Microencapsulation Techniques for Parenteral Depot Systems and Their Application in the Pharmaceutical Industry’, Microencapsulation Method and Industrial Applications, 2nd Ed, New York: CRC Press, p. 99-122.

Sari R, Magda M, Lestari W, Rijal MAS, 2015, Ketoprofen-Carboxymethyl Chitosan Microparticles Prepared By Spray Drying: Optimization And Evaluation, Asian Journal of Pharmaceutical and Clinical Research, Vol. 8.

Departemen Kesehatan RI, 2014, Farmakope Indonesia, edisi V, Jakarta.

Bagdassarian, C, Angelov, T & Atanassova, M 2007, ‘UV-Spectrometric And High Performance Liquid Chromatographic Determination Of Pentoxifylline In Workplace Air’, Journal of the University of Chemical Technology and Metallurgy.

Ibezim, EC, Andrade, CT, Marcia, C, Barretto, B, Odimegwu, DC & Lima, FFD 2011, ‘Ionically Cross-linked Chitosan/Tripolyphosphate Microparticles for the Controlled Delivery of Pyrimethamine’, Department of Pharmaceutics, University of Nigeria, Nsukka, Enugu State, Nigeria.

Published
2022-11-22
How to Cite
Muntu, C. M., Sadono, & Melinda Natalia Suwito. (2022). Pengembangan Mikrosfer Asiklovir menggunakan Kitosan dan Natrium Tripolifosfat: Faktor Suhu Inlet. Keluwih: Jurnal Kesehatan Dan Kedokteran, 4(1), 1-10. https://doi.org/10.24123/kesdok.V4i1.5451