NOVEL GASTRO-RETENTIVE POLYMERIC MICROSPHERES: AN APPROACH FOR INCREASED BIOAVAILABILITY AND AN ONCE DAILY DOSING OF TERBUTALINE SULPHATE

Authors

  • Shahira F. El-menshawe
  • Amany M. Abdeltwab Department of Pharmaceutics, Faculty of Pharmacy, Beni-Suef University, Beni Suef, Egypt.
  • Ahmed I. Mohamed

Keywords:

Composite microspheres, Ionotropic gelation, CO-Polymer, Chitosan coating, Sustained release, Relative bioavailability

Abstract

Objective: The purpose of this study was to develop multi-unit alginate-copolymer adhesive microspheres to achieve a sustained release of terbutaline sulphate (TBS) and overcome the hepatic first pass effect so as to enhance its bioavailability.

Methods: The microspheres were prepared using inotropic gelation method and different concentration of sodium alginate alone or in combination with other polymers as well as using chitosan as a coating polymer in some formulations. All of the prepared microspheres were evaluated for yield, size, encapsulation efficiency, in vitro release and mucoadhesivity. The selected formulations (F11 and F19) were further subjected to differential scanning calorimetry, Fourier transform infrared spectroscopy, stability and in vivo bioavailability studies.

Results: The prepared microspheres exhibited quite widely varying encapsulation efficiencies from 20 to 74. 8 % and its mean diameter was in range of 963. 3-1. 635 µm. The in vitro release study showed a sustained release profile. The selected formulations were further subjected to differential scanning calorimetry and FTIR which confirm the absence of any incompatibility. X-ray diffraction suggests the amorphous nature of the drug after encapsulation. The selected formulation F11 and F19 showing encapsulation efficiency higher than 55 %, an amount of drug released within 50-60 % after 8 h and a relative bioavailability of 283. 84 % and 202. 04 % respectively compared with the marketed oral Aironyl® tablets.

Conclusion: The prepared microspheres were significantly efficient to achieve a sustained release of terbutaline sulphate with a higher relative bioavailability in comparison with the oral marketed tablet.

Downloads

Download data is not yet available.

References

Abdul M, Rao AS, Martha S, Sirisha Y, Chandrika PU. Development of a floating multiple unit controlled-release beads of zidovudine for the treatment of AIDS. JOPR J Pharm Res 2012;6:78–83.

Biswal I, Dinda A, Das D, Si S, Chowdary KA. Encapsulation protocol for highly hydrophilic drug using non-biodegradable polymer. Int J Pharm Pharm Sci 2011;3:256–9.

Ma N, Xu L, Wang Q, Zhang X, Zhang W, Li Y, et al. Development and evaluation of new sustained-release floating microspheres. Int J Pharm 2008;358:82–90.

Basak SC, Kumar KS, Ramalingam M. Design and release characteristics of sustained release tablet containing metformin HClâ€. Br J Pharm Sci 2008;44 Suppl 3:477–83.

Patel PN, Patel MM, Rathod DM, Patel JN, Modasiya MMK. Sustain release drug delivery: a theoretical prospective. J Pharm Res 2012;5:4165–8.

Raffin RP, Colomé LM, Schapoval EES, Pohlmann AR, Guterres SS. Increasing sodium pantoprazole photostability by microencapsulation: effect of the polymer and the preparation technique. Eur J Pharm Biopharm 2008;69 Suppl 3:1014–8.

O¨ zyazici M, Sevgi F, Ertan G. Micromeritic studies on nicardipine hydrochloride microcapsules. Int J Pharm 1996;138:25–35.

Chambin O, Dupuis G, Champion D, Voilley A, Pourcelot Y. Colonâ€specific drug delivery: influence of solution reticulation properties upon pectin beads performance. Int J Pharm 2006;321:86–93.

Ahmed MM, El-Rasoul SA, Auda SH, Ibrahim MA. Emulsification/internal gelation as a method for preparation of diclofenac sodium-sodium alginate microparticles. Saudi Pharm J Publ Saudi Pharm Soc 2013;21:61–9.

Patil P, Chavanke D, Wagh M. A review on ionotropic gelation method: Novel approach for controlled gastroretentive gelispheres. Int J Pharm Pharm Sci 2012;4 Suppl 4:27–32.

Shu XZ, Zhu KJ. The release behavior of brilliant blue from calcium-alginate gel beads coated by chitosan: the preparation method effect. Eur J Pharm Biopharm 2002;53:193–201.

Josef E, Zilberman M, Bianco-Peled H. Composite alginate hydrogels: an innovative approach for the controlled release of hydrophobic drugs. Acta Biomater 2010;6:4642–9.

SmidsrØd O, Skja G. Alginate as immobilization matrix for cells Trends. Biotechnol 1990;8:71–8.

Elzatahry AA, Eldin MS, Soliman EA, Hassan EA. Evaluation of alginate-chitosan mucoadhesive beads as a drug delivery system for the controlled release of theophylline. J Appl Polym Sci: Appl Polym Symp 2009;111:2452–9.

Patil SB, Sawant KK. Development, optimization and in vitro evaluation of alginate mucoadhesive microspheres of carvedilol for nasal delivery. J Microencapsul 2009;26:432–43.

Gadad AP, Patil MB, Naduvinamani SN, Mastiholimath VS, Dandagi PM, Kulkarni AR, et al. Sodium alginate polymeric floating beads for the delivery of cefpodoxime proxetil. J Appl Polym Sci 2009;114:1921–6.

Sweetman SC. The complete drug references. In: Martindale: Extra-pharmacopoeia. 34th ed; 2005. â€

Tripathi KD. Essentials of medical pharmacology. 5th ed. New Delhi: Jaypee Brothers Medical Publishers; 2004.

Borgstrom L, Nyberg L, Jonsson S, Lindberg C, Paulson J. Pharmacokinetic evaluation in man of terbutaline given as separate enantiomers and as the racemate. Br J Clin Pharmacol 1989;27:49–56.

Rao NR, Panchal H, Hadi MA. Formulation and evaluation of biphasic drug delivery system of Montelukast sodium for chronotherapy. World J Pharm Res 2012;1:757–75.

Multu GM, Moonjelly E, Chan L, Olopade CO. Laryngospasm and paradoxical bronchoconstriction after repeated doses of beta 2-agonists containing edetate disodium. Mayo Clin Proc 2000;75:285–7.

Nagabhushana S. Harmful effects of aerosolized bron-chodilator therapy in broncholitis. Indian Pediatr 2000;37:684–7.

Angadi SC, Manjeshwar LS, Aminabhavi TM. Novel composite blend microbeads of sodium alginate coated with chitosan for controlled release of amoxicillin. Int J Biol Macromol 2012;51:45–55.

Polk A, Amsden B, Yao KD, Peng T, Goosen MFA. Controlled release of albumin from chitosan–alginate microcapsules. J Pharm Sci 1994;83:178–85.

Sezer AD, Akubaga J. Release characteristics of chitosan treated alginate beads: I. Sustained release of a macromolecular drug from chitosan treated alginate beads. J Microencapsul 1999;16:195-203.

Torrado S, Prada P, Paloma M, Torrado S. Chitosan-poly(acrylic) acid polyionic complex: in vivo study to demonstrate prolonged gastric retention. Biomaterials 2004;25:917–23.

Kim CK, Kim MJ, Oh KH. Preparation and evaluation of sustained-release microspheres of terbutaline sulfate. Int J Pharm 1994;106:213–9.

Kotadiya R, Patel V, Patel H, Salaniya B. Evaluation of terbutaline sulphate encapsulated ethylcellulose microspheres : a factorial approach. Int J PharmTech Res 2009;1:1271–8.

Rajgor NB, Patel M, Shah VM, Bhaskar VH, Rajput GC. Preparation and characterization of terbutalin sulphate microsphere. Der Pharm Lett 2010;2:450–9.

Sahin S, Selek H, Ponchel G, Ercan MT, Sargon M, Hincal AA, et al. Preparation, characterization and in vivo distribution of terbutaline sulfate loaded albumin microspheres. J Controlled Release 2002;82:345–58.

Hadi MA, Srinivasa Rao A, Abhinetri V, Rao AHP. Design and in vitro evaluation of multiparticulate drug delivery system of terbutaline sulphate for the treatment of nocturnal asthma. Der Pharm Lett 2012;4:1777–85.

Kota RB, Srikrishna S, Kumar MS, Subrahmanyam KV. Design and characterization of hydrogyl beads of terbutaline sulphate. Int J Innovations Pharm Sci Res 2013;1:383–97.

Prasad S, Mukesh T, Ashok S, Monit S, Ashish S. Preparation and optimization of oral floating alginate gel beads famotidine. J Pharmakin 2011;3:1–15.

López-Cacho JM, González-R PL, Talero B, Rabasco AM, González-Rodríguez ML. Robust optimization of alginate-carbopol 940 bead formulations. Sci World J 2012:1-15. Doi:10. 1100/2012/605610. [Article in Press]

Agarwal T, Narayana SNGH, Pal K, Pramanik K, Giri S, Banerjee I. Calcium alginate-carboxymethyl cellulose beads for colon-targeted drug delivery. Int J Biol Macromol 2015;75:409–17.

Jana S, Samanta A, Nayak AK, Sen KK, Jana S. Novel alginate hydrogel core-shell systems for combination delivery of ranitidine HCl and aceclofenac. Int J Biol Macromol 2015;74:85–92.

Jelvehgari M, Mobaraki V, Montazam SH. Preparation and evaluation of mucoadhesive beads/discs of alginate and algino-pectinate of piroxicam for colon-specific drug delivery via oral route. Jundishapur J Nat Pharm Prod 2014;9:e16576.

Chanda R, Roy A, Bahadur S, Saha S, Das S, Choudhury A. Formulation of terbutaline sulphate mucoadhesive sustained release oral tablets from natural materials and in vitro-in vivo evaluation. Asian J Pharm Sci 2010;5:168–74.

Kumar A, Nanda S. A validated high performance liquid chromatographic method for estimation of bromhexine and terbutaline in bulk and tablet dosage forms. Pharam Methods 2011;2:218–22.

Abd-Ellatif A. A pharmaceutical study on extended release solid dosage forms of certain antidiabetic drugs, "MSc. Thesis", Faculty of pharmacy, Beniseuf University; 2009.

Abou El Ela AESF, Hassan MA, El-Maraghy DA. Ketorolac tromethamine floating beads for oral application: characterization and in vitro/in vivo evaluation. Saudi Pharm J Publ Saudi Pharm Soc 2014;22:349–59.

Rokhade AP, Agnihotri SA, Patil SA, Mallikarjuna NN, Kulkarni PV, Aminabhavi TM. Semiinterpenetrating and, polymer network microspheres of gelatin Ketorolac, sodium carboxymethyl cellulose for controlled release of tromethamine. J Carbohydr Polym 2006;65 Suppl 3:243–52.

Sriamornsak P, Thirawong N, Puttipipatkhachorn S. Emulsion gel beads of calcium pectinate capable of floating on the gastric fluid: effect of some additives, hardening agent or coating on release behavior of metronidazole. Eur J Pharm Sci 2005;24:363–73.

Pandit SS, Hase DP, Bankar MM, Patil AT, Gaikwad NJ. Ketoprofen-loaded Eudragit RSPO microspheres: an influence of sodium carbonate 195on in vitro drug release and surface topology. J Microencapsul 2009;26:195–201.

El-Say KM, El-Helw ARM, Ahmed OA, Hosny KM, Ahmed TA, Kharshoum RM, et al. Statistical optimization of controlled release microspheres containing cetirizine hydrochloride as a model for water soluble drugs. Pharm Dev Technol 2014;20:738–46.

Patel YL, Sher P, Pawar AP. The effect of drug concentration and curing time on processing and properties of calcium alginate beads containing metronidazole by response surface methodology. AAPS PharmSciTech 2006;7 Suppl 4:E24-E30.

Dhankar V, Garima Garg KD, Awasthi R. Preparation, characterization and evaluation of ranitidine hydrochloride-loaded mucoadhesive microspheres. Polim Med 2014;44:75–81.

Hoffman AS. Hydrogels for biomedical applications. Adv Drug Delivery Rev 2012;64:18–23.

Gattani Y, Kawtikwar P, Sakarkar D. Formulation and evaluation of gastro retentive multi particulate drug delivery system of aceclofenac. Int J ChemTech Res 2009;1:1–10.

Lin YH, Liang HF, Chung CK, Chen MC, Sung HW. Physically crosslinked alginate/N,O-carboxymethyl chitosan hydrogels with calcium for oral delivery of protein drugs. Biomaterials 2005;26:2105–13.

Pasparakis G, Bouropoulos N. Swelling studies and in vitro release of verpamil from calcium alginate and calcium alginate–chitosan beads. Int J Pharm 2006;323:34–42.

Kamel S, Ali N, Jahangir K, Shah S, El-Gendy A. Pharmaceutical significance of cellulose: a review. J Express Polym Lett 2008;2 Suppl 11:758–78.

Chun MK, Cho CS, Choi HK. Mucoadhesive microspheres prepared by interpolymer complexation and solvent diffusion method. Int J Pharm 2005;288:295–303.

Silva CM, Ribeiro AJ, Ferreira D, Veiga F. Insulin encapsulation in reinforced alginate microspheres prepared by internal gelation. Eur J Pharm Sci 2006;29:148–59.

Al-Kassas RS, Al-Gohary OMN, Al-Faadhel MM. Controlling of systemic absorption of gliclazide through incorporation into alginate beads. Int J Pharm 2007;341:230–7.

Hua S, Ma H, Li X, Yang H, Wang A. pH-sensitive sodium alginate/poly(vinyl alcohol) hydrogel beads prepared by combined Ca2+crosslinking and freeze-thawing cycles for controlled release of diclofenac sodium. Int J Biol Macromol 2010;46:517–23.

Velasco MV, Ford JL, Rowe P, Rajabi-Siahboomi AR. Influence of drug: hydroxypropylmethylcellulose ratio, drug and polymer particle size and compression force on the release of diclofenac sodium from HPMC tablets. J Controlled Release 1999;57:75–85.

Shaikh R, Singh TRR, Garland MJ, Woolfson AD, Donnelly RF. Mucoadhesive drug delivery systems. J Pharm Bioallied Sci 2011;3:89.

Ahuja A, Khar RK, Ali J. Mucoadhesive drug delivery systems. Drug Dev Ind Pharm 2008;23:489–515.

Suknuntha K, Tantishaiyakul V, Worakul N, Taweepreda W. Characterization of muco-and bioadhesive properties of chitosan, PVP, and chitosan/PVP blends and release of amoxicillin from alginate beads coated with chitosan/PVP. Drug Dev Ind Pharm 2011;37:408–18.

Mahajan AN, Pancholi SS. Formulation and evaluation of timed delayed capsule device for chronotherapeutic delivery of terbutaline sulphate. Ars Pharm 2010;50:215–23.

Bao Y, Ma J, Li N. Synthesis and swelling behaviors of sodium carboxymethyl cellulose-g-poly (AA-co-AM-co-AMPS)/MMT superabsorbent hydrogel. Carbohydr Polym 2011;84:76–82.

Sahoo S, Chakraborti CK, Naik S, Mishra SC, Nanda UN. Structural analysis of ciprofloxacin-carbopol polymeric composites by X-ray diffraction and fourier transform infra-red spectroscopy. Trop J Pharm Res 2011;10:273–80.

Sahoo S, Chakraborti CK, Behera PK. Spectroscopic investigations of a ciprofloxacin/HPMC mucroadhesive suspension. Int J Appl Pharm 2012;4:1–8.

Narkar M, Sher P, Pawar A. Stomach-specific controlled release gellan beads of acid-soluble drug prepared by ionotropic gelation method. AAPS PharmSciTech 2010;11:267–77.

Published

01-08-2016

How to Cite

El-menshawe, S. F., A. M. Abdeltwab, and A. I. Mohamed. “NOVEL GASTRO-RETENTIVE POLYMERIC MICROSPHERES: AN APPROACH FOR INCREASED BIOAVAILABILITY AND AN ONCE DAILY DOSING OF TERBUTALINE SULPHATE”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 8, Aug. 2016, pp. 320-9, https://journals.innovareacademics.in/index.php/ijpps/article/view/12710.

Issue

Section

Original Article(s)