Volume : 11, Issue : 10, October – 2024
Title:
FORMULATION AND IN VITRO EVALUATION OF COPOLYMERIZED HYDROGEL BASED EMPAGLIFLOZIN MICROPARTICLES
Authors :
Afshan Sultana*, Sumer Singh, Niranjan Panda, M.S.Ansari
Abstract :
The aim of this work was to enhance the physical and chemical properties of natural polymers while simultaneously reducing production costs by graft copolymerization procedures involving the natural polymer guar gum and the synthetic polymer poly(acrylamide). The optimal hydrogel formulation was developed as microparticles, incorporating Empagliflozin and characterized by various criteria. A graft copolymer of guar gum-g-poly(acrylamide) was synthesized using a free radical polymerization method in a specifically built jacketed reaction vessel under a continuous flow of nitrogen. Ceric ammonium nitrate (CAN) was employed as the initiator for the reaction. The preparation conditions of microparticles were adjusted by evaluating the entrapment effectiveness percentage, particle size, swelling index under varying pH settings, and their release profiles. FTIR measurements support the development of grafted copolymers, whereas DSC experiments indicate a relatively enhanced heat stability of these copolymers. The pAAm-g-GG/sodium alginate microparticles exhibited a nearly spherical morphology, as demonstrated by the SEM analysis. The swelling index was shown to be highest for the formulation that contains more concentration of alginate in phosphate buffer at pH 6.8. The release of Empagliflozin was discovered to be regulated with increasing polyacrylamide and sodium alginate content in the microparticles, with a greater release noted in a pH 6.8 medium compared to pH 1.2. The in vitro kinetics of Empagliflozin release from the polymeric microparticle adhered to the zero-order kinetics model with mechanism of release as anomalous diffusion. Empagliflozin microparticles based on hydrogel were effectively synthesized with optimized batches of Guar gum-g-poly(acrylamide) and sodium alginate through free radical ionization methods. All characterization parameters met the acceptance standards.
Keywords: Empagliflozin, Microparticles, Hydrogel, Guar gum, Acrylamide, Sodium alginate
Cite This Article:
Please cite this article in press Afshan Sultana et al., Formulation And In Vitro Evaluation Of Copolymerized Hydrogel Based Empagliflozin Microparticles..,Indo Am. J. P. Sci, 2024; 11 (10).
Number of Downloads : 10
References:
1. Gwen MJ., Joseph RR., Banker GS and Rhodes CT, (editors). Modern pharmaceutics. 3rd ed., Morcel Dekker. Inc, 1996, 575.
2. Chein YW., Novel drug delivery system. 2nd ed. Morcel Dekker. Inc, 1997, 1-42.
3. Goodman and Gillman’s, The Pharmacological Basis of Therapeutics, 11th ed. Laurence L. Brunton, John S. Lazo, 1635-1638.
4. www. Medicines.org.uk/emc/browsedocuments
5. Aulton ME. Wells TI., Pharmaceutics: The Science of Dosage Form Design, London, England: Churchill Livingstone: 1988: 185-189.
6. X. QU, A. Wirsen, A.C Albertsson, Novel PH-sensitive chitosan hydrogel: swelling behaviour and states of water, polymer 41 (2000) 4589-4598.
7. Narayan B; Jonathan G; Miqin Z; chitosan based hydrogels for controlled localised drug delivery. Adv. Drug Delivery Re 2010, 62, 83-99.
8. Tejraj M. Aminabhavi; et al water transport and drug release study from cross-linked polyacrylamide grafted guar gum hydrogel microsperes for the controlled release application, Euro. Jour. of Ph. And Bioph. 53 (2002) 87-98.
9. P. Sunny Gils, et al; controlled release of Doxofylline from Biopolymer based Hydrogels; Am.Jour. of Biomed. Sc. 2010, 2(4), 373-383.
10. Baljit S., Nirmala, C.; Diatary fiber Psyllium based hydrogels for use insulin delivery. Int. J. Diabet. Melt. 2010, 2, 32-37.
11. T.M Aminavi, G.V. Patil, S.F. Harlapur; R.H. Balundgi; A reviewed on sustained release of cardiovascular drugs through Hydroxy Propyl Methyl Cellulose and sodium carboxymethyl cellulose polymers, Des.Monom. Polym.1(1998) 347-372.
12. B. Gander, V.Beltrami, R. Gurny. et.al, Effects of the method of drug incorporation and the monolith on drug release from cross-linked polymers. Int. J. Pharm. 58(1990) 63-71.
13. Carstensen, J.T.; C.T. Rhodes Drug stability; Principles and practicle; Markel Dekkar: New York; 2000.
14. Hadjioannu T.P.,et.al, Quantitative Calculations in Pharmaceutical Practice and Research, New York: VCH Publishers Inc., 1993, 345-348.
15. Dos Santos, K.S.C.K.; Coelho, et al synthesis and characterization of members obtained by graft copolymerization of 2-Hydroxyethyl methycrylate and acrylic acid onto chitosan. Int. J. Pharm 2006, 310, 37-45.
16. Panda N, Panda KC, Reddy AV, Reddy GV. Process optimization, formulation and evaluation of hydrogel {guargum-g-poly (acrylamide)} based doxofylline microbeads. Asian J Pharm Clin Res. 2014;7(3):60-5.
17. Kumar AR. Aeila AS. Sustained release matrix type drug delivery system: An overview. World J Pharma Pharm Sci. 2019; Oct 24; 8(12): 470-80. DOI: 10.20959/wjpps20201-15241.
18. Saxena AK. Sharma A. Verma N. Microspheres as therapeutically effective multiparticulate drug delivery system: A systemic review. Research Journal of Pharmacy and Technology. 2021; 14(6): 3461-70.
19. Vinod R. Kumar PA. Yadav AS. Rao BS. Kulkarni SV. Formulation and Evaluation of Controlled Release Microspheres of Zidovudine. Research Journal of Pharmaceutical Dosage Forms and Technology. 2010; 2(1): 96-9.
20. Kumbhar DM. Mali KK. Dias RJ. Havaldar VD. Ghorpade VS. Salunkhe NH. Formulation and development of ethyl cellulose coated pectin based capecitabine loaded microspheres for colorectal cancer. Research Journal of Pharmaceutical Dosage Forms and Technology. 2016; 8(4): 261-8.
21. Chandarsekaran N. Balamurugan M. Formulation, Characterization and In-vitro Evaluation of Abacavir Sulphate Loaded Microspheres. Research Journal of Pharmacy and Technology. 2013; 6(7): 731-5.
22. Patel NR. Patel DA. Bharadia PDet al. Microsphere as a novel drug delivery. International Journal of Pharmacy and Life Sciences. 2011; Aug 1; 2(8): 992-997.
23. Patil UK. Sahu R. Yadav SK. Formulation and Evaluation of Controlled Release Microspheres Containing Metformin Hydrochloride. Research Journal of Pharmacy and Technology. 2009; 2(1): 176-9.
24. Ratnaparkhi MP, Gupta jyoti P. Sustained release oral drug delivery systeman overview. International Journal of Pharma Research and Review. 2013; 2(3): 11-21.
25. Bose S. Kaur A. Sharma SK. A review on advances of sustained release drug delivery system. Int. Res. J. Pharm. 2013; 4: 1-5.
26. Gavini V. Murthy MS. Kumar PK. Radhika DL. Formulation and in-vitro evaluation of mucoadhesive microspheres loaded with stavudine using hydrophilic macromolecular polymers. Research Journal of Pharmaceutical Dosage Forms and Technology. 2014; 6(2): 99-104.
27. Talokar SS. Vakhariya RR. Formulation and evaluation of lomefloxacin microspheres. Research Journal of Pharmaceutical Dosage Forms and Technology. 2017; 9(1): 1-5.
28. Nighute AB. Bhise SB. Preparation and evaluation of rifabutin loaded polymeric microspheres. Research Journal of Pharmacy and Technology. 2009; 2(2): 371-4.
29. Ahmed TA. Aljaeid BM. Preparation, characterization, and potential application of chitosan, chitosan derivatives, and chitosan metal nanoparticles in pharmaceutical drug delivery. Drug Design, Development and Therapy. 2016; Jan 28: 483-507.
30. Denkbaş EB. Seyyal M. Pişkin E. Implantable 5-fluorouracil loaded chitosan scaffolds prepared by wet spinning. Journal of Membrane Science. 2000; Jul 1; 172(1-2): 33-8. https://doi.org/10.1016/S0376-7388(00)00314-8.




