In vivo and in vitro taste masking of ofloxacin and sustained release by forming interpenetrating polymer network beads

References

• Gurpreet KM, Inderbir AS. Taste masked microspheres of ofloxacin: formulation and evaluation of orodispersible tablets. Sci Pharm 2011;79:653–672
   PubMedGoogle Scholar
• Nalini CN, Ramachandran S, Kavitha K, Harikrishna. Determination of ofloxoxacin and ornidazole in tablets by spectrophotometry and reverse phase HPLC. Res J Pharm Biol Chem Sci 2011;2:693–708
   Google Scholar
• Park HR, Chung HC, Lee JK, Bark KM. Ionization and divalent cation complexation of quinolones antibiotics in aqueous solution. Bull Korean Chem Soc 2000;21:849–854
   Web of Science ®Google Scholar
• Gellert M. DNA Topoisomerases. Annu Rev Biochem 1981;50:879–910
   PubMed Web of Science ®Google Scholar
• Maniruzzaman M, Boateng JS, Bonnefille M, et al. Taste masking of paracetamol by hot-melt extrusion: an in vitro and in vivo evaluation. Eur J Pharm Biopharm 2012;80:433–442
   PubMed Web of Science ®Google Scholar
• Mennella JA, Spector AC, Reed DR, Coldwell SE. The bad taste of medicines: overview of basic research on bitter taste. Clin Ther 2013;35:1225–1246
   PubMed Web of Science ®Google Scholar
• Al-Omran MF, Al-Suwayeh SA, El-Helw AM, Saleh SI. Taste masking of diclofenac sodium using microencapsulation. J Microencapsul 2002;19:45–52
   PubMed Web of Science ®Google Scholar
• Gowthamarajan K, Kulkarni G, Kumar M. Pop the pills without bitterness. Resonance 2004;9:25–32
   Google Scholar
• Ayenew Z, Puri V, Kumar L, Bansal AK. Trends in pharmaceutical taste masking technologies: a patent review. Recent Pat Drug Deliv Formul 2009;3:26–39
   PubMedGoogle Scholar
• Preis M, Hausler O, Breitkreutz J. Electronic tongues in preformulation studies: application of electronic tongues in preformulation studies to evaluate taste-masking capacities of maltodextrins. Pharm Ind 2014;76:957–962
   Google Scholar
• Arima H, Higashi T, Motoyama K. Improvement of the bitter taste of drugs by complexation with cyclodextrins: applications, evaluations and mechanisms. Ther Deliv 2012;3:633–644
   PubMedGoogle Scholar
• Guo X, Chang R-K, Hussain MA. Ion-exchange resins as drug delivery carriers. J Pharm Sci 2009;98:3886–3902
   PubMed Web of Science ®Google Scholar
• Sivaneswari S, Veena D, Sumana PS, et al. Ion exchange resins as drug delivery carriers. J Chem Pharm Res 2015;7:1436–1445
   Google Scholar
• Tawakkul MA, Shah RB, Zidan A, et al. Complexation of risperidone with a taste-masking resin: novel application of near infra-red and chemical imaging to evaluate complexes. Pharm Dev Technol 2009;14:409–421
   PubMed Web of Science ®Google Scholar
• Shah RB, Tawakkul MA, Sayeed VA, Khan MA. Complexation between risperidone and amberlite resin by various methods of preparation and binding study. Drug Dev Ind Pharm 2009;35:1409–1418
   PubMed Web of Science ®Google Scholar
• Vasiliu S, Bunia I, Racovita S, Neagu V. Adsorption of cefotaxime sodium salt on polymer coated ion exchange resin microparticles: kinetics, equilibrium and thermodynamic studies. Carbohydr Polym 2011;85:376–387
   Web of Science ®Google Scholar
• Kim JI, Cho SM, Cui JH, et al. In vitro and in vivo correlation of disintegration and bitter taste masking using orally disintegrating tablet containing ion exchange resin-drug complex. Int J Pharm 2013;455:31–39
   PubMed Web of Science ®Google Scholar
• Siddiqui A, Shah RB, Khan MA. Oseltamivir phosphate–amberliteTM IRP 64 ionic complex for taste masking: preparation and chemometric evaluation. J Pharm Sci 2013;102:1800–1812
   PubMed Web of Science ®Google Scholar
• Mohite BP, Chafle SA, Somasundaram J, Avari JG. Development and evaluation of ofloxacin orally disintegrating tablets. Braz J Pharm Sci 2012;48:218–225
   Web of Science ®Google Scholar
• Kela SP, Kesharwani D. Formulation, characterization and evaluation of taste masked rapid disintegrating tablet of ofloxacin by ion exchange resin technique. Int J Pharm Sci Rev Res 2013;21:246–253
   Google Scholar
• Goindi S, Kapoor VR. Kamalpreet. Taste masking and formulation of ofloxacin rapid disintegrating tablets and oral suspension. Indian J Pharm Educ Res 2009;43:150–155
   Web of Science ®Google Scholar
• Cantor SL, Khan MA, Gupta A. Development and optimization of taste-masked orally disintegrating tablets (ODTs) of clindamycin hydrochloride. Drug Dev Ind Pharm 2014;1:1156–1164
   Google Scholar
• Ogata T, Tanaka D, Ozeki T. Enhancing the solubility and masking the bitter taste of propiverine using crystalline complex formation. Drug Dev Ind Pharm 2014;40:1084–1091
   PubMed Web of Science ®Google Scholar
• Kosmala JD, Henthorn DB, Peppas LB. Preparation of interpenetrating networks of gelatin and dextran as degradable biomaterials. Biomaterials 2000;21:2019–2023
   PubMed Web of Science ®Google Scholar
• Lei H, Wang W, Chen LL, et al. The preparation and catalytically active characterization of papain immobilized on magnetic composite microspheres. Enzyme Microb Tech 2004;35:15–21
   Web of Science ®Google Scholar
• Eiselt P, Yeh J, Latwala RK, et al. Porous carriers for biomedical applications based on alginate hydrogels. Biomaterials 2000;21:1921–1927
   PubMed Web of Science ®Google Scholar
• Gu F, Amsden B, Neufeld R. Sustained delivery of vascular endothelial growth factor with alginate beads. J Control Rel 2004;96:463–472
   PubMed Web of Science ®Google Scholar
• Hosny EA, Al-Helw RA. Effect of coating of aluminum carboxymethylcellulose beads on the release and bioavailability of diclofenac sodium. Pharm Acta Helv 1998;72:255–261
   PubMedGoogle Scholar
• Rokhade AP, Agnihotr SA, Patil SA, et al. Semi-interpenetrating polymer network microspheres of gelatin and sodium carboxymethyl cellulose for controlled release of ketorolac tromethamine. Carbohydr Polym 2006;65:243–252
   Web of Science ®Google Scholar
• Kim MS, Park SJ, Gu BK, Kim CH. Ionically crosslinked alginate–carboxymethyl cellulose beads for the delivery of protein therapeutics. Appl Surf Sci 2012;262:28–33
   Web of Science ®Google Scholar
• Ramakrishna P, Rao KM, Sekharnath KV, et al. Synthesis and characterization of Interpenetrating polymer network microspheres of acryl amide grafted carboxymethylcellulose and sodium alginate for controlled release of triprolidine hydrochloride monohydrate. J Appl Pharm Sci 2013;3:101–108
   Google Scholar
• Prasad HH, Senger A, Chauhan K, et al. Synthesis of cross-linked methacrylic acid- co-N,N′-methylene bis acrylamide sorbents For recovery of heavy metal ions from dilute solutions. Ind J Chem Tech 2001;8:371–377
   Web of Science ®Google Scholar
• Kevadiya BD, Joshi GV, Mody HM, Bajaj HC. Biopolymer–clay hydrogel composites as drug carrier: Host–guest intercalation and in vitro release study of lidocaine hydrochloride. Appl Clay Sci 2011;52:364–367
   Web of Science ®Google Scholar
• Ritger PL, Peppas NA. A simple equation for description of solute release. II. Fickian and anomalous release from swellable devices. J Control Rel 1987;5:37–42
   Google Scholar
• Gryczke A, Schminke S, Maniruzzaman M, et al. Development and evaluation of orally disintegrating tablets (ODTs) containing ibuprofen granules prepared by hot melt extrusion. Colloids Surf B Biointerfaces 2011;86:275–284
   PubMed Web of Science ®Google Scholar
• Jenquin MR, McGinity JW. Characterization of acrylic resin matrix films and mechanisms of drug–polymer interactions. Int J Pharm 1993;101:23–34
   Web of Science ®Google Scholar
• Kulkarni RV, Mangond BS, Mutalik S, Sa B. Interpenetrating polymer network microcapsules of gellan gum and egg albumin entrapped with diltiazem–resin complex for sustain release application. Carbohydr Polym 2011;83:1001–1007
   Web of Science ®Google Scholar
• Kulkarni AR, Soppimath KS, Aminabhavi TM, Rudzinski WE. In-vitro release kinetics of cefadroxil loaded sodium alginate interpenetrating network beads. Eur J Pharm Biopharm 2001;51:127–133
   PubMed Web of Science ®Google Scholar
• Soppimath KS, Kulkarni AR, Aminabhavi TM. Chemically modified polyacrylamide-g-guar gum-based crosslinked anionic microgels as pH-sensitive drug delivery systems: preparation and characterization. J Control Rel 2001;75:331–345
   PubMed Web of Science ®Google Scholar
• Halder A, Maiti S, Sa B. Entrapment efficiency and release characteristics of polyethyleneimine-treated or untreated calcium alginate beads loaded with propranolol–resin complex. Int J Pharm 2005;290:45–54
   PubMed Web of Science ®Google Scholar
• Mohamadnia Z, Zohuriaan-Mehr MJ, Kabiri K, et al. pH-ensitive IPN hydrogel beads of carrageenan-alginate for controlled drug delivery. J Bioact Com Polym 2007;22:342–356
   Web of Science ®Google Scholar
• Anal AK, Bhopatkar D, Tokura S, et al. Chitosan-alginate multilayer beads for gastric passage and controlled intestinal release of protein. Drug Dev Ind Pharm 2003;29:713–724
   PubMed Web of Science ®Google Scholar
• Agnihotri SA, Aminabhavi TM. Development of novel interpenetrating network gellan gum-poly (vinyl alcohol) hydrogel microspheres for the controlled release of carvedilol. Drug Dev Ind Pharm 2005;31:491–503
   PubMed Web of Science ®Google Scholar