TY - JOUR T1 - Design and optimization of rifaximin macroparticles for colon targeting AU - K Chaturvedi, Ashwani AU - Sara, Uvs AU - Gupta, Ram Dayal PY - 2025 DA - July JF - Journal of Research in Pharmacy JO - J. Res. Pharm. PB - Marmara University WT - DergiPark SN - 2630-6344 SP - 1609 EP - 1618 VL - 28 IS - 5 LA - en AB - This study is focused to design a colon specific pellet formulation of rifaximin based on the combination of time-dependent and pH sensitive delivery system using Quality-by-Design (QbD) approach for better and promising treatment of inflammatory bowel disease (IBD). An extrusion/spheronization process was utilized for the preparation of core macroparticles using ethyl cellulose (EC) as matrix former and microcrystalline cellulose (MCC) as a spheronizing aid. Two critical process parameters (CPPs) i.e., spheronization time and spheronizer speed were taken as independent factors while aspect ratio, sphericity, carr's index, and particle size were taken as dependent responses to optimize the composition of the core macroparticles. To regulate the drug release, core macroparticles were coated with Eudragit NE40D and Eudragit FS30D to impart time-dependent and pH sensitive release of drug. The optimized coated macroparticles were characterized for drug content and in vitrodrug release in different pH media of stomach and intestine. The coating levels of the inner and outer polymers were further optimized for the time required for 10 %, 50 % and 90 % drug release. The result showed that the 90% of drug of P3 and P4 formulation were found to be released in 10.87 and 13.19hrs respectively. When exposed to Scanning Electron Microscopy the images of coated macroparticles suggested a uniform and smooth coat of polymers over the surface of macroparticles. This formulation reduces the dose and the side effects due to its specific targeting at the site of inflammation makes it a better choice over the tablets. The result indicates that the developed formulation may possibly reduce the dosing frequency and side effects associated with the conventional tablet formulation for the site-specific targeting at inflammation site. KW - Macroparticles KW - colon targeted KW - rifaximin KW - Eudragit KW - MCC KW - Optimization CR - [1] Sinha VR, Mittal BR, Bhutani KK, Kumria R. Colonic drug delivery of 5-fluorouracil: An in vitro evaluation. Int J Pharm. 2004;269(1):101–8. https://doi.org/10.1016/j.ijpharm.2003.09.036 CR - [2] Orlu M, Cevher E, Araman A. Design and evaluation of colon specific drug delivery system containing flurbiprofen microsponges. Int J Pharm. 2006;318(1-2):103–17. https://doi.org/10.1016/j.ijpharm.2006.03.025 CR - [3] Zhang F. Melt-extruded Eudragit® FS-based granules for colonic drug delivery. AAPS PharmSciTech. 2016;17:56–67. https://doi.org/10.1208/s12249-015-0357-2 CR - [4] Wei H, Qing D, De-Ying C, Bai X, Li-Fang F. Study on colon-specific pectin/ethylcellulose film-coated 5-fluorouracil macroparticles in rats. Int J Pharm. 2008;348(1-2):35–45. https://doi.org/10.1016/j.ijpharm.2007.07.005 CR - [5] Gupta VK, Beckert TE, Price JC. A novel pH- and time-based multi-unit potential colonic drug delivery system. I. Development. Int J Pharm. 2001;213(1-2):83–91. https://doi.org/10.1016/s0378-5173(00)00649-9 CR - [6] Akhgari A, Sadeghi F, Garekani HA. Combination of time dependent and pH-dependent polymethacrylates as a single coating formulation for colonic delivery of indomethacin macroparticles. Int J Pharm. 2006;320(1):137–42. https://doi.org/10.1016/j.ijpharm.2006.05.011 CR - [7] Kumar J, Newton AMJ. Colon Targeted Rifaximin Nanosuspension for the Treatment of Inflammatory Bowel Disease (IBD). Anti-Inflamm Anti-Allergy Agent Med Chem. 2016;15(2):1–17. https://doi.org/10.2174/1871523015666160720103732 CR - [8] Kumar F, Newton AMJ. Rifaximin - Chitosan nanoparticles for inflammatory bowel disease (IBD). Recent Pat Inflamm Allergy Drug Discov. 2017;11(1):41–52. https://doi.org/10.2174/1872213X10666161230111226 CR - [9] Pinto JF, Buckton G, Newton JM. The influence of four selected processing and formulation factors on the production of spheres by extrusion and spheronisation. Int J Pharm. 1992;83(1-3):187–96. https://doi.org/10.1016/0378-5173(82)90022-9 CR - [10] Krogars K, Heinamaki J, Vesalahti J, Marvola M, Antikainen O, Yliruusi J. Extrusion-spheronization of pH-sensitive polymeric matrix pellets for possible colonic drug delivery. Int J Pharm. 2000;199(2):187–94. https://doi.org/10.1016/s0378-5173(00)00382-3 CR - [11] Lau CLS, Yu Q, Lister VY, Rough SL, Wilson DI, Zhang M. The evolution of pellet size and shape during spheronisation of an extruded microcrystalline cellulose paste. Chem Eng Res Des. 2014;92(11):2413–24. https://doi.org/10.1016/j.cherd.2014.01.018 CR - [12] Newton JM, Chapman SR, Rowe RC. The assessment of the scale-up performance of the extrusion/spheronisation process. Int J Pharm. 1995;120(1):95–9. https://doi.org/10.1016/0378-5173(94)00425-5 CR - [13] Thommes M, Kleinebudde P. Properties of macroparticles manufactured by wet extrusion/spheronization process using kappa-carrageenan: effect of process parameters. AAPS PharmSciTech. 2007;8(4):E1–E8. https://doi.org/10.1208/pt0804095 CR - [14] Rahman NU, Yuen KH. Eudragit NE40-Drug mixed coating system for controlling drug release of core pellets. Drug Dev Ind Pharm. 2005;31:339–47. https://doi.org/10.1081/ddc-54307 CR - [15] Mehta KA, Kislalioglu MS, Phuapradit W, Malick AW, Shah NH. Effect of formulation and process variables on porosity parameters and release rates from a multiunit erosion matrix of a poorly soluble drug. J Control Release. 2000;63(1-2):201–11. https://doi.org/10.1016/s0168-3659(99)00193-5 CR - [16] Korsmeyer RW, Gurny R, Doelker E, Buri P, Peppas NA. Mechanisms of solute release from porous hydrophilic polymers. Int J Pharm. 1983;15:25–35. https://doi.org/10.1016/0378-5173(83)90064-9 CR - [17] Heng PWS, Wong TW, Chan LW. Influence of production variables on the sphericity of melt pellets. Chem Pharm Bull. 2000;48(3):420–4. https://doi.org/10.1248/cpb.48.420 CR - [18] Marvola M, Nykanen P, Rautio S, Isonen N, Autere A. Enteric polymers as binders and coating materials in multiple-unit site-specific drug delivery systems. Eur J Pharm Sci. 1999;7(3):259–67. https://doi.org/10.1016/s0928-0987(98)00032-3 CR - [19] Di Pretoro G, Zema L, Gazzaniga A, Rough SL, Wilson DI. Extrusion-spheronisation of highly loaded 5-ASA multiparticulate dosage forms. Int J Pharm. 2010;402(1-2):153–64. https://doi.org/10.1016/j.ijpharm.2010.10.003 CR - [20] He W, Du Q, Cao DY, Xiang B, Fan LF. Study on colon-specific pectin/ethylcellulose film-coated 5-fluorouracil macroparticles in rats. Int J Pharm. 2008;348(1):35–45. https://doi.org/10.1016/j.ijpharm.2007.07.005 CR - [21] Steckel H, Mindermann-Nogly F. Production of chitosan macroparticles by extrusion/spheronization. Eur J Pharm Biopharm. 2004;57(1):107–14. https://doi.org/10.1016/s0939-6411(03)00156-5 CR - [22] Sriamornsak P, Nunthanid J, Luangtana-Anan M, Weerapol Y, Puttipipatkhachorn S. Alginate-based macroparticles prepared by extrusion/spheronization: Effect of the amount and type of sodium alginate and calcium salts. Eur J Pharm Biopharm. 2008;69(1):274–84. https://doi.org/10.1016/j.ejpb.2007.09.012 CR - [23] Del Curto MD, Palugan L, Foppoli A. Erodible time-dependent colon delivery systems with improved efficiency in delaying the onset of drug release. J Pharm Sci. 2014;103(11):3585–93. https://doi.org/10.1002/jps.24150 CR - [24] Maroni A, Del Curto MD, Cerea M, Zema L, Foppoli A, Gazzaniga A. Polymeric coatings for a multiple-unit pulsatile delivery system: Preliminary study on free and applied films. Int J Pharm. 2013;440:256–63. https://doi.org/10.1016/j.ijpharm.2012.05.075 CR - [25] Liu F, Moreno P, Basit AW. A novel double-coating approach for improved pH-triggered delivery to the ileo-colonic region of the gastrointestinal tract. Eur J Pharm Biopharm. 2010;74(2):311–5. https://doi.org/10.1016/j.ejpb.2009.11.008 CR - [26] Akhgari A, Garekani HA, Sadeghi F. Combination of time-dependent and pH-dependent polymethacrylates as a single coating formulation for colonic delivery of indomethacin pellets. Int J Pharm. 2006;320(1-2):137–42. https://doi.org/10.1016/j.ijpharm.2006.05.011 CR - [27] Sadeghi F, Ford JL, Rubinstein MH, Rajabi Siahboomi AR. Comparative study of drug release from pellets coated with HPMC or Surelease. Drug Dev Ind Pharm. 2000;26(6):651–60. https://doi.org/10.1081/DDC-100101280 CR - [28] Tagizadeh Z, Rakhsahni S, Jahani V, Rajabi O. Preparation and in vitro characterization of carvacrol pellets by combination of liquisolid technique and extrusion-spheronization. J Drug Deliv Sci Technol. 2021;61:102232. https://doi.org/10.1016/j.jddst.2020.102232 CR - [29] Baert L, Remon JP. Influence of amount of granulation liquid on the drug release rate from macroparticles made by extrusion-spheronisation. Int J Pharm. 1993;95(1-3):135–41. https://doi.org/10.1016/0378-5173(93)90400-A CR - [30] Zhao H, Sun D, Tang Y, Yao J, Yuan X, Zhang M. Thermo/pH dual-responsive core–shell particles for apatinib/doxorubicin controlled release: preparation, characterization and biodistribution. J Mater Chem. 2018;6(46):7621–33. https://doi.org/10.1039/C8TB02334D UR - https://dergipark.org.tr/en/pub/jrespharm/issue//1690656 L1 - https://dergipark.org.tr/en/download/article-file/4833787 ER -