Combined site-specific release retardant mini-matrix tablets (C-SSRRMT) for extended oral delivery of dexketoprofen trometamol: in vitro evaluation and single versus multiple doses pharmacokinetic study in human volunteers

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorSweed N.M.
dc.contributor.authorBasalious E.B.
dc.contributor.authorNour S.A.
dc.contributor.otherPharmaceutics Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherOctober University for Modern Sciences and Arts (MSA)
dc.contributor.otherCairo
dc.contributor.otherEgypt; Department of Pharmaceutics and Industrial Pharmacy
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherCairo University
dc.contributor.otherCairo
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:40:31Z
dc.date.available2020-01-09T20:40:31Z
dc.date.issued2019
dc.descriptionScopus
dc.descriptionMSA Google Scholar
dc.description.abstractDevelopment of extended release oral formulations of dexketoprofen trometamol (DT), a rapidly eliminated drug with high solubility, poses a great challenge especially when a portion of the dose is to be absorbed from the colon. In this study, site-specific release-retardant mini-matrix tablets (SSRRMTs) were developed and functionally coated with pH-responsive materials to achieve a site-specific delivery of DT at the duodenojejunal (DSRRMT) and ileocecal (ISRRMT) regions. Stomach-specific coated mini-tablets (SSCMTs) were manufactured for immediate release of about 16% of the daily dose of DT in the stomach. The SSCMT, DSRRMT, and ISRRMT were combined into a solid dosage form (C-SSRRMT tablets or capsules) to achieve the required linear release profile for once daily administration of DT. The SSRRMT and C-SSRRMT formulations were evaluated for the physical properties, in vitro-disintegration and in vitro dissolution and proved to be consistent with the pharmacopeial specifications. The in vitro release profiles of both C-SSRRMT tablets and capsules showed a constant release rate of about 6 mg/h and were similar to that of the theoretical target linear release profile. The pharmacokinetic study using human volunteers showed the bioequivalence of a single oral dose of C-SSRRMT capsules compared to three-successive oral doses of the immediate release market tablets with less ups and downs in the drug levels. The C-SSRRMT capsules formulation, may therefore, constitute an advance in the extended oral delivery of DT without the lack of efficacy and the adverse events frequently encountered in multiple daily dosing of the immediate release tablets. � 2019, � 2019 Informa UK Limited, trading as Taylor & Francis Group.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=21190&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.1080/03639045.2019.1656737
dc.identifier.doiPubMed ID 31418598
dc.identifier.issn3639045
dc.identifier.otherhttps://doi.org/10.1080/03639045.2019.1656737
dc.identifier.otherPubMed ID 31418598
dc.identifier.urihttps://t.ly/52X1Y
dc.language.isoEnglishen_US
dc.publisherTaylor and Francis Ltd.en_US
dc.relation.ispartofseriesDrug Development and Industrial Pharmacy
dc.relation.ispartofseries45
dc.subjectجامعة أكتوبر للعلوم الحديثة والآداب
dc.subjectMSA University
dc.subjectUniversity for Modern Sciences and Arts
dc.subjectOctober University for Modern Sciences and Arts
dc.subjectDexketoprofenen_US
dc.subjectextended releaseen_US
dc.subjectoralen_US
dc.subjectpH-responsive coatingen_US
dc.subjectrelease retardant mini-matrix tabletsen_US
dc.subjectdexketoprofenen_US
dc.subjecteudragiten_US
dc.subjectplaceboen_US
dc.subjectadulten_US
dc.subjectArticleen_US
dc.subjectAUC (0-24 h)en_US
dc.subjectbioequivalenceen_US
dc.subjectcecumen_US
dc.subjectcontrolled studyen_US
dc.subjectcrossover procedureen_US
dc.subjectdosage schedule comparisonen_US
dc.subjectdrug bioavailabilityen_US
dc.subjectdrug coatingen_US
dc.subjectdrug half lifeen_US
dc.subjectdrug solubilityen_US
dc.subjectduodenumen_US
dc.subjecthumanen_US
dc.subjecthuman experimenten_US
dc.subjectileumen_US
dc.subjectin vitro studyen_US
dc.subjectin vivo studyen_US
dc.subjectjejunumen_US
dc.subjectmaleen_US
dc.subjectmaximum concentrationen_US
dc.subjectmicrocapsuleen_US
dc.subjectnormal humanen_US
dc.subjectpharmacokinetic parametersen_US
dc.subjectplasma concentration-time curveen_US
dc.subjectrandomized controlled trialen_US
dc.subjectsingle drug doseen_US
dc.subjectstomachen_US
dc.subjecttablet compressionen_US
dc.subjecttablet formulationen_US
dc.subjecttablet friabilityen_US
dc.subjecttablet hardnessen_US
dc.subjecttime to maximum plasma concentrationen_US
dc.titleCombined site-specific release retardant mini-matrix tablets (C-SSRRMT) for extended oral delivery of dexketoprofen trometamol: in vitro evaluation and single versus multiple doses pharmacokinetic study in human volunteersen_US
dc.typeArticleen_US
dcterms.isReferencedByMoore, R.A., Barden, J., Systematic review of dexketoprofen in acute and chronic pain (2008) BMC Clin Pharmacol, 8, p. 11; Maule�n, D., Artigas, R., Garc�a, M.L., Preclinical and clinical development of dexketoprofen (1996) Drugs, 52, pp. 24-46; Moffat, A.C., Osselton, M.D., Widdop, B., (2003) Clarke's analysis of drugs and poisons, , 3rd ed, London: Pharmaceutical Press; Barbanoj, M.-J., Antonijoan, R.-M., Gich, I., Clinical pharmacokinetics of dexketoprofen (2001) Clin Pharmacokinet, 40, pp. 245-262; Laporte, J.-R., Ib��ez, L., Vidal, X., Upper gastrointestinal bleeding associated with the use of NSAIDs�newer versus older agents (2004) Drug Saf, 27, pp. 411-420; Gupta, V.K., Beckert, T.E., Price, J.C., A novel pH- and time-based multi-unit potential colonic drug delivery system. I. Development (2001) Int J Pharm, 213, pp. 83-91; Fukui, E., Miyamura, N., Uemura, K., Preparation of enteric coated timed-release press-coated tablets and evaluation of their function by in vitro and in vivo tests for colon targeting (2000) Int J Pharm, 204, pp. 7-15; Chandran, S., Sanjay, K.S., Ali Asghar, L.F., Microspheres with pH modulated release: design and characterization of formulation variables for colonic delivery (2009) J Microencapsul, 26, pp. 420-431; Evans, D., Pye, G., Bramley, R., Measurement of gastrointestinal pH profiles in normal ambulant human subjects (1988) Gut, 29, pp. 1035-1041; Stefanic, M., Vrecer, F., Rizmal, P., Prediction of the in vivo performance of enteric coated pellets in the fasted state under selected biorelevant dissolution conditions (2014) Eur J Pharm Sci, 62, pp. 8-15; Vueba, M., De Carvalho, L.B., Veiga, F., Influence of cellulose ether polymers on ketoprofen release from hydrophilic matrix tablets (2004) Eur J Pharm Sci, 58, pp. 51-59; Petrovic, A., Ibric, S., Trajkovic, S., An investigation into effects of In Vitro Test condition on the release properties of theophylline from HPMC matrices using factorial design (2009) Arch Pharm Res, 32, pp. 1087-1096; Sahoo, J., Murthy, P., Biswal, S., Comparative study of propranolol hydrochloride release from matrix tablets with Kollidon� SR or hydroxy propyl methyl cellulose (2008) AAPS PharmSciTech, 9, pp. 577-582; Al-Tabakha, M.M., Arida, A.I., Fahelelbom, K.M., Performances of new generation of delayed release capsules (2015) J Young Pharm, 7, p. 37; Pandey, S., Mehta, P., Patel, H., Novel time and site specific �tablets in capsule� system for nocturnal asthma treatment (2014) J Pharm Investig, 44, pp. 381-390; Kramar, A., Turk, S., Vre?er, F., Statistical optimisation of diclofenac sustained release pellets coated with polymethacrylic films (2003) Int J Pharm, 256, pp. 43-52; Aleksovski, A., Lu�trik, M., �ibanc, R., Design and evaluation of a specific, bi-phase extended release system based on differently coated mini-tablets (2015) Eur J Pharm Sci, 75, pp. 114-122; Basalious, E.B., Abdullah, A., Ibrahim, M., Utility of mannitol and citric acid for enhancing the solubilizing and taste masking properties of ?-cyclodextrin: development of fast-dissolving tablets containing extremely bitter drug (2014) J Pharm Innov, 9, pp. 309-320; El-Setouhy, D.A., Basalious, E.B., Abdelmalak, N.S., Bioenhanced sublingual tablet of drug with limited permeability using novel surfactant binder and microencapsulated polysorbate: in vitro/in vivo evaluation (2015) Eur J Pharm Biopharm, 94, pp. 386-392; (2014) Appendix XII C. Consistency of formulated preparations, electronic version 18, , UK: TSO; Fouad, S.A., Shamma, R.N., Basalious, E.B., Novel instantly-soluble transmucosal matrix (ISTM) using dual mechanism solubilizer for sublingual and nasal delivery of dapoxetine hydrochloride: in-vitro/in-vivo evaluation (2016) Int J Pharm, 505, pp. 212-222; Costa, P., Lobo, J.S., Influence of dissolution medium agitation on release profiles of sustained-release tablets (2001) Drug Dev Ind Pharm, 27, pp. 811-817; Pai, R., Kohli, K., Jain, G., In vitro and in vivo evaluations of ketoprofen extended release pellets prepared using powder layering technique in a rotary centrifugal granulator (2011) Arch Pharm Res, 34, pp. 1135-1142; El-Kamel, A., Sokar, M., Al Gamal, S., Preparation and evaluation of ketoprofen floating oral delivery system (2001) Int J Pharm, 220, pp. 13-21; Shirsand, S.B., Suresh, S., Jodhana, L.S., Formulation design and optimization of fast disintegrating Lorazepam tablets by effervescent method (2010) Indian J Pharm Sci, 72, pp. 431-436; Liu, F., Merchant, H.A., Kulkarni, R.P., Evolution of a physiological pH6. 8 bicarbonate buffer system: application to the dissolution testing of enteric coated products (2011) Eur J Pharm Biopharm, 78, pp. 151-157; Sahoo, J., Murthy, P., Biswal, S., Formulation of sustained-release dosage form of verapamil hydrochloride by solid dispersion technique using Eudragit RLPO or Kollidon� SR (2009) AAPS PharmSciTech, 10, pp. 27-33; Sakr, W., Alanazi, F., Sakr, A., Effect of Kollidon� SR on the release of albuterol sulphate from matrix tablets (2011) Saudi Pharm J, 19, pp. 19-27; Khan, M.Z.I., �tedul, H.P., Kurjakovi?, N., A pH-dependent colon-targeted oral drug delivery system using methacrylic acid copolymers. II. Manipulation of drug release using Eudragit� L100 and Eudragit S100 combinations (2000) Drug Dev Ind Pharm, 26, pp. 549-554; Hadi, M.A., Rao, N.R., Rao, A.S., Formulation and evaluation of pH-responsive mini-tablets for ileo-colonic targeted drug delivery (2014) Trop J Pharm Res, 13, pp. 1021-1029; Hadi, M.A., Rao, N.R., Rao, A.S., Formulation and evaluation of ileo-colonic targeted matrix-mini-tablets of Naproxen for chronotherapeutic treatment of rheumatoid arthritis (2016) Saudi Pharm J, 24, pp. 64-73; Baviskar, D., Sharma, R., Jain, D., Formulation and in vitro/in vivo evaluation of sustained release diltiazem matrix tablets (2013) Trop J Pharm Res, 12, pp. 679-684; Asghar, L.F.A., Chandran, S., Design and evaluation of matrix base with sigmoidal release profile for colon-specific delivery using a combination of Eudragit and non-ionic cellulose ether polymers (2011) Drug Deliv Transl Res, 1, pp. 132-146; Narendra, C., Srinath, M., Rao, B.P., Development of three layered buccal compact containing metoprolol tartrate by statistical optimization technique (2005) Int J Pharm, 304, pp. 102-114; Vaghani, S., Vasanti, S., Chaturvedi, K., Formulation and evaluation of 5-FU loaded Eudragit microspheres: effect of various eudragit on micromeretic properties of microspheres (2008) J Macromol Sci A, 45, pp. 1015-1027; Mehta, R., Chawla, A., Sharma, P., Formulation and in vitro evaluation of Eudragit S-100 coated naproxen matrix tablets for colon-targeted drug delivery system (2013) J Adv Pharm Tech Res, 4, pp. 31-41; Stefan-van Staden, R.-I., Suzan Nhlapo, N., Frederick van Staden, J., Enantioanalysis of S-ketoprofen using enantioselective, potentiometric membrane electrodes (2009) Anal Lett, 42, pp. 764-774; Vemula, S.K., Formulation and pharmacokinetics of colon-specific double-compression coated mini-tablets: chronopharmaceutical delivery of ketorolac tromethamine (2015) Int J Pharm, 491, pp. 35-41
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