Pengaturan Pelepasan Obat dari Tablet dengan Sistem Matriks Karagenan
Abstrak
Sistem matriks merupakan sistem pengaturan pelepasan obat dari tablet yang populer. Matriks tablet yang umum digunakan adalah golongan eter selulosa seperti hidroksi propil metil selulosa (HPMC), hidroksi propil selulosa (HPC) dan natrium karboksi metil selulosa (Na CMC). Golongan eter selulosa sintetik ini banyak digunakan karena memiliki sifat mengembang dan kompresibilitas yang baik. Polimer alam seperti karagenan telah banyak diteliti sebagai komponen penyusun matriks tablet untuk memperoleh pengaturan pelepasan obat dari matriks yang efektif. Karagenan dapat digunakan sebagai penyusun matriks mengingat polimer tersebut memiliki berat molekul yang besar dan mempunyai viskositas dan kemampuan membentuk gel yang tinggi. Dalam upaya pengembangan sistem matriks tablet dari bahan karagenan diperlukan pengetahuan yang baik mengenai karakteristik fisika kimia dari karagenan dan obat yang digunakan.
Kata kunci : sistem matriks, karagenan, pembentukan gel.
Teks Lengkap:
PDFReferensi
Van de Velde, F., Knutsen, S. H., Usov, A. I., Rollema, H. S., & Cerezo, A. S. 2002.1H and13C high resolution NMR spectroscopy of carrageenans: Application in research and industry. Trends in Food Science & Technology, 13(3), 73–92.
K.M. Picker. 1999. The use of carrageenan in mixture with microcrystalline cellulose and its functionality for making tablets. Eur. J. Pharm. Biopharm. 48 27 – 36.
Liang, W., Mao, X., Peng, X., & Tang, S. 2014. Effects of sulfate group in red sea-weed polysaccharides on anticoagulant activity and cytotoxicity. Carbohydrate Polymers, 101, 776–785.
Nerurkar, J., Jun, H. W., Price, J. C., & Park, M. O. 2005. Controlled-release matrix tablets of ibuprofen using cellulose ethers and carrageenans: Effect of formulation factors on dissolution rates. European Journal of Pharmaceutics and Biopharmaceutics, 61, 56–68.
Li, L., Ni, R., Shao, Y., & Mao, S. 2014. Carrageenan and its applications in drug delivery. Carbohydrate Polymers, 103C, 1–11.
Bixler, H. J. 1994. The carrageenan connection IV. British Food Journal, 96(3), 12–17.
Necas, J., & Bartosikova, L. 2013. Carrageenan: A review. Veterinarni Medicina, 58(4),187–205.
Li, L., Wang, L., Shao, Y., Tian, Y., Li, C., Li, Y., et al. 2013. Elucidation of release characteristics of highly soluble drug trimetazidine hydrochloride from chitosan–carrageenan matrix tablets. Journal of Pharmaceutical Sciences, 102(8),2644–2654.
Pavli, M., Vrecer, F., & Baumgartner, S. 2010. Matrix tablets based on carrageenans with dual controlled release of doxazosin mesylate. International Journal of Pharmaceutics, 400(1–2), 15–23.
Campo, V. L., Kawano, D. F., Silva, D. B. d., & Carvalho, I. 2009. Carrageenans: Bio-logical properties, chemical modifications and structural analysis—A review.Carbohydrate Polymers, 77(2), 167–180.
Yuguchi, Y., Urakawa, H., & Kajiwara, K. 2003. Structural characteristics of carrageenan gels: Various types of counter ions. Food Hydrocolloids, 17(4), 481–485.
Pavli, M., Baumgartner, S., Kos, P., & Kogej, K. 2011. Doxazosin-carrageenan interac-tions: A novel approach for studying drug-polymer interactions and relation to controlled drug release. International Journal of Pharmaceutics, 421(1), 110–119.
Miyazaki, S., Ishitani, M., Takahashi, A., Shimoyama, T., Itoh, K., & Attwood, D. 2011. Carrageenan gels for oral sustained delivery of acetaminophen to dysphagic patients. Biological and Pharmaceutical Bulletin, 34(1), 164–166.
Tapia, C., Escobar, Z., Costa, E., Sapag-Hagar, J., Valenzuela, F., Basualto, C., et al. 2004. Comparative studies on polyelectrolyte complexes and mixtures ofchitosan–alginate and chitosan–carrageenan as prolonged diltiazem clorhydrate release systems. European Journal of Pharmaceutics and Biopharmaceutics,57(1), 65–75.
Ghanam, D., & Kleinebudde, P. 2011. Suitability of kappa-carrageenan pellets forthe formulation of multiparticulate tablets with modified release. International Journal of Pharmaceutics, 409(1–2), 9–18.
Kranz, H., Juergens, K., Pinier, M., & Siepmann, J. 2009. Drug release from MCC- andcarrageenan-based pellets: Experiment and theory. European Journal of Pharma-ceutics and Biopharmaceutics, 73, 302–309.
Thommes, M., & Kleinebudde, P. 2006a. Use of kappa-carrageenan as alternative pelletisation aid to microcrystalline cellulose in extrusion/spheronisation.I. Influence of type and fraction of filler. European Journal of Pharmaceutics and Biopharmaceutics, 63, 59–67.
J. Liu et.al. 2015. Review for Carrageenan-Based Pharmaceutical Biomaterials : Favourable Physical Features Versus Adverse Biological Effects. Carbohydrate Polimer 121, 27-36.
Briones, A. V., & Sato, T. 2010. Encapsulation of glucose oxidase (GOD) in polyelec-trolyte complexes of chitosan–carrageenan. Reactive and Functional Polymers,70(1), 19–27.
Hezaveh, H., & Muhamad, I. I. 2012. The effect of nanoparticles on gastrointestinalrelease from modified - carrageenan nanocomposite hydrogels. Carbohydrate Polymers, 89(1), 138–145.
Hezaveh, H., & Muhamad, I. I. 2013a. Controlled drug release via minimization ofburst release in pH-response kappa-carrageenan/polyvinyl alcohol hydrogels. Chemical Engineering Research and Design, 91(3), 508–519.
Hezaveh, H., & Muhamad, I. I. 2013b. Modification and swelling kinetic study of kappa-carrageenan-based hydrogel for controlled release study. Journal of the Taiwan Institute of Chemical Engineers, 44(2), 182–191.
Hezaveh, H., Muhamad, I. I., Noshadi, I., Shu Fen, L., & Ngadi, N. 2012. Swelling behaviour and controlled drug release from cross-linked-carrageenan/NaCMChydrogel by diffusion mechanism. Journal of Microencapsulation, 29(4), 368–379.
Kulkarni, R. V., Boppana, R., Krishna Mohan, G., Mutalik, S., & Kalyane, N. V. 2012.pH-responsive interpenetrating network hydrogel beads of poly(acrylamide)-g-carrageenan and sodium alginate for intestinal targeted drug delivery:Synthesis, in vitro and in vivo evaluation. Journal of Colloid and Interface Science,367(1), 509–517.
Shargel, L. dan Yu. 2005. Biofarmasetika dan Farmakokinetika Terapan. Edisi Kedua. Surabaya: Airlangga University Press.
Manish J. Chauhan, Satish A. Patel. 2012. A concise review on sustained drug delivery system and it’s opportunities. American Journal of PharmTech Research 2012; 2(2) .2249-3387.
Maderuelo, C., Zarzuelo, A., & Lanao, J. M. 2011. Critical factors in the release ofdrugs from sustained release hydrophilic matrices. Journal of Controlled Release,154, 2–19.
Ju, R.T.C., Nixon, P.R., Patel, M.V.1995. Drug release from hydrophilic matrices. 1. New scaling laws for predicting polymer and drug release based on the polymer disentanglement concentration and the diffusion layer. J. Pharm. Sci. 84, 1455-1463.
Bettini, R., Catellani, P.L., Santi, P., Massimo, G., Peppas, N.A., Colombo, P. 2001. Translocation of drug particles in HPMC matrix gel layer : effect of drug solubility and influence on release rate. J. Control. Rel. 70, 383-391.
Hariharan, M., Wheatley, T. A., & Price, J. C. 1997. Controlled-release tablet matrices from carrageenans: Compression and dissolution studies. Pharmaceutical Development and Technology, 2, 383–393.
Picker, K. M. 1999a. The use of carrageenan in mixture with microcrystalline cellulose and its functionality for making tablets. European Journal of Pharmaceuticsand Biopharmaceutics, 48, 27–36.
Rosario, N. L., & Ghaly, E. S. 2002. Matrices of water-soluble drug using natural poly-mer and direct compression method. Drug Development and Industrial Pharmacy,28, 975–988.
Picker, K. M. 1999b. Matrix tablets of carrageenans. II. Release behavior and effectof added cations. Drug Development and Industrial Pharmacy, 25, 339–346.
Bonferoni, M. C., Rossi, S., Tamayo, M., Pedraz, J. L., Dominguez-Gil, A., & Caramella,C. 1994. On the employment of λ-carrageenan in a matrix system. II. λ-Carrageenan and hydroxypropylmethylcellulose mixtures. Journal of Controlled Release, 30, 175–182.
Moreno-Villoslada, I., Oyarzun, F., Miranda, V., Hess, S., & Rivas, B. L. 2005. Binding of chlorpheniramine maleate to pharmacologically important alginic acid,carboxymethylcellulose, kappa-carageenan, and iota-carrageenan as studied by diafiltration. Journal of Applied Polymer Science, 98, 598–602.
Kojima, H., Yoshihara, K., Sawada, T., Kondo, H., & Sako, K. 2008. Extended release of a large amount of highly water-soluble diltiazem hydrochloride by utilizing counter polymer in polyethylene oxides (PEO)/polyethylene glycol (PEG)matrix tablets. European Journal of Pharmaceutics and Biopharmaceutics, 70,556–562.
Bonferoni, M. C., Rossi, S., Tamayo, M., Pedraz, J. L., Dominguez-Gil, A., & Caramella, C. 1993. On the employment of λ-carrageenan in a matrix system. I. Sensitivity to dissolution medium and comparison with Na carboxymethylcellulose and xanthan gum. Journal of Controlled Release, 26, 119–127.
Bonferoni, M. C., Chetoni, P., Giunchedi, P., Rossi, S., Ferrari, F., Burgalassi, S., et al. 2004. Carrageenan–gelatin mucoadhesive systems for ion-exchange based ophthalmic delivery: In vitro and preliminary in vivo studies. European Journal of Pharmaceutics and Biopharmaceutics, 57, 465–472.
Refbacks
- Saat ini tidak ada refbacks.