Sustained Release Multiple Unit Dosage Form for the Oral Day Delivery of Dexketoprofen Trometamol

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorSweed, NM
dc.contributor.authorBasalious, EB
dc.contributor.authorNour, SA
dc.date.accessioned2020-02-26T08:16:37Z
dc.date.available2020-02-26T08:16:37Z
dc.date.issued2017
dc.descriptionMSA Google Scholaren_US
dc.description.abstractThe aim of this study was to prepare sustained release multiple unit dosage form (MUDF) for the oral day delivery of the frequently administered and the highly water soluble drug, dexketoprofen trometamol (DT). The drug was encapsulated into Eudragit RS100 microspheres using emulsification solvent evaporation technique. A D-optimal design was used to determine the effect of amount of polymer (X1), the percentage of hydrophobic plasticizer (X2), the percentage of hydrophilic plasticizer (X3), and stirring rate (X4), on the % entrapment efficiency (Y1), amount of drug released at 1h (Y2), 4h (Y3), and 8 h (Y4). The optimized formulation was prepared using 1.39 g Eudragit, 0.063 g Dibutyl phthalate (DBP), 0.093 g Polyethylene Glycol 400 (PEG 400) and processed using stirring rate of 683 rpm. The optimized microspheres were evaluated by Scanning Electron Microscopy (SEM), Differential Scanning Calorimetry (DSC), and X- ray Diffraction (XRD). Results of the optimized formula showed that the microspheres were spherical with a rough surface and a particle size of 32±1.41 µm, with entrapment efficiency 76.0±1.76%. The amount of drug released was 33.7±0.82%, 60.2±0.05%, and 75.1±1.84%, at 1, 4, and 8 h, respectively. Complete drug release was achieved after 16 h. The sustained release pattern of DT for up to 16 h with an acceptable initial release suggests that the developed MUDF may be useful for oral day delivery of the highly soluble and frequently administered drug such as DTen_US
dc.description.sponsorshipOpen Access Journal of Pharmaceutical Researchen_US
dc.identifier.citationPignatello R, Consoli P, Puglisi G (2000) In vitro release kinetics of Tolmetin from tabletted Eudragit microparticles. J microencapsul 17(3): 373-383. 8. El Say KM, El Helw AR, Ahmed OA, Hosny KM, Ahmed TA, et al. (2015) Statistical optimization of controlled release microspheres containing cetirizine hydrochloride as a model for water soluble drugs. Pharm dev technol 20(6): 738-746. 9. Soppimath K, Kulkarni A, Aminabhavi T (2001) Encapsulation of antihypertensive drugs in cellulose- based matrix microspheres: characterization and release kinetics of microspheres and tableted microspheres. J microencapsul 18(3): 397-409. 10. Basalious EB, Abdullah A, Ibrahim M (2014) Utility of Mannitol and Citric Acid for Enhancing the Solubilizing and Taste Masking Properties of β- Cyclodextrin: Development of Fast-Dissolving Tablets Containing Extremely Bitter Drug. J Pharm Innov 9(4): 309-320. 11. El-Setouhy DA, Basalious EB, Abdelmalak NS (2015) Bioenhanced sublingual tablet of drug with limited permeability using novel surfactant binder and microencapsulated polysorbate: In vitro/in vivo evaluation. European Journal of Pharmaceutics and Biopharmaceutics 94: 386-392. 12. Haznedar S, Dortunc B (2004) Preparation and in vitro evaluation of Eudragit microspheres containing acetazolamide. International journal of pharmaceutics.269(1): 131-140. 13. Martin A (1993) Physical pharmacy: physical chemical principles in the pharmaceutical sciences: BI Waverly. Pvt Ltd. 14. Hausner H (1967) Friction conditions in a mass of metal powder. Polytechnic Inst. of Brooklyn. Univ. of California, Los Angeles. 15. Carr RL (1965) Classifying flow properties of solids. Chem Eng 72: 163-168. 16. Comoglu T, Gonul N, Dogan A, Basci N (2008) Development and in vitro evaluation of pantoprazole- loaded microspheres. Drug delivery 15(5): 295-302. 17. Wagner JG (1969) Interpretation of percent dissolved‐time plots derived from in vitro testing of conventional tablets and capsules. J pharm sci 58(10): 1253-1257. 18. Higuchi T (1963) Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices. J pharm sci 52(12): 1145-1149. 19. Peppas N (1985) Analysis of Fickian and non-Fickian drug release from polymers. Pharmaceutica acta Helvetiae 60(4): 110-111. 20. Pai R, Kohli K, Jain G, Srivastava B (2011) In vitro and in vivo evaluations of ketoprofen extended release pellets prepared using powder layering technique in a rotary centrifugal granulator. Arch Pharm Res 34(7): 1135-1142. 21. El-Kamel A, Sokar M, Al Gamal S, Naggar V (2001) Preparation and evaluation of ketoprofen floating oral delivery system. Int J pharm 220(1-2): 13-21. 22. Sengel Turk CT, Hascicek C, Gonul N (2008) Microsphere-based once-daily modified release matrix tablets for oral administration in angina pectoris. J Microencapsul 25(4): 257-266. 23. Khamanga SM, Walker RB (2012) The use of response surface methodology in the evaluation of captopril microparticles manufactured using an oil in oil solvent evaporation technique. J Microencapsul 29(1): 39-53. 24. Huang YB, Tsai YH, Lee SH, Chang JS, Wu PC (2005) Optimization of pH-independent release of nicardipine hydrochloride extended-release matrix tablets using response surface methodology. Int J pharm 289(1): 87-95. 25. Woitiski CB, Veiga F, Ribeiro A, Neufeld R (2009) Design for optimization of nanoparticles integrating biomaterials for orally dosed insulin. Eur J pharm biopharm 73(1): 25-33. 26. Sadeghi F, Hijazi H, Garekani HA (2011) Production of ibuprofen pellets containing high amount of rate retarding Eudragit RL using PEG400 and investigation of their physicomechanical properties. Iran J of basic med sci 14(4): 383-390. 27. Meier MM, Kanis LA, Soldi V (2004) Characterization and drug-permeation profiles of microporous and dense cellulose acetate membranes: influence of plasticizer and pore forming agent. Int J Pharm 278(1): 99-110. 28. Avachat AM, Bornare PN, Dash RR (2011) Sustained release microspheres of ropinirole hydrochloride:en_US
dc.identifier.doihttps://doi.org/
dc.identifier.otherhttps://doi.org/
dc.identifier.urihttps://cutt.ly/Zr34WPn
dc.language.isoenen_US
dc.publisherMedwin Publishersen_US
dc.relation.ispartofseriesOpen Access Journal of Pharmaceutical Research;Volume 1 Issue 3
dc.subjectMultiple Unit Dosage Formen_US
dc.subjectDifferential Scanning Calorimetryen_US
dc.subjectScanning Electron Microscopyen_US
dc.subjectDexketoprofen Trometamolen_US
dc.subjectX-ray Diffractionen_US
dc.titleSustained Release Multiple Unit Dosage Form for the Oral Day Delivery of Dexketoprofen Trometamolen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 2 of 2
Loading...
Thumbnail Image
Name:
avatar_scholar_128.png
Size:
2.73 KB
Format:
Portable Network Graphics
Description:
Faculty Of Pharmacy Research Paper
Loading...
Thumbnail Image
Name:
OAJPR16000114.pdf
Size:
1.47 MB
Format:
Adobe Portable Document Format
Description:

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
51 B
Format:
Item-specific license agreed upon to submission
Description: