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2000
Volume 3, Issue 1
  • ISSN: 2210-299X
  • E-ISSN: 2210-3007

Abstract

Introduction

Vildagliptin is a dipeptidyl peptidase 4-related inhibitor that is often utilised in the treatment of type-2 diabetes. It is possible that sustained therapeutic levels of vildagliptin for a prolonged length of time might be achieved by controlled release of the drug in the gastrointestinal system, which would result in an improvement in the efficacy of treatment. Due to their high biocompatibility and biodegradability, biopolymers, such as alginate (sodium), pectin, and xanthan gum, are frequently utilized in drug delivery systems. This is because these biopolymers are good alternatives for the development of controlled-release formulations.

Aim

This study aimed to formulate and evaluate the vildagliptin microsphere using pectin and xanthan gum.

Materials and Methods

The delivery of vildagliptin was accomplished by the development of beads that were constituted of sodium alginate-pectin and sodium alginate-xanthan gum. Adjusting the proportions of sodium alginate, pectin, and xanthan gum resulted in the production of pH-sensitive beads throughout the synthesis. This was accomplished through the use of a calcium chloride (CaCl2)-induced ionic gelation approach.

Results

The FTIR revealed the compatibility of medicines and polymers. The synthesized beads were tested for scanning electron microscopy, differential scanning calorimetry, drug content, swelling ratio, and dissolution analysis. The microscopic pictures showed beads of spherical shape and mostly semi-spherical with a broken and rough surface. Swelling was found to be pH-dependent, indicating that water absorption might be minimal in an acid medium and high in an alkaline pH condition. The dissolving study depicted controlled drug release.

Conclusion

This study recorded the successful formulation of vildagliptin microspheres using sodium alginate, pectin, and xanthan beads for the controlled release of vildagliptin.

This is an open access article published under CC BY 4.0 https://creativecommons.org/licenses/by/4.0/legalcode
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2025-01-01
2025-11-12
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References

  1. DeshmukhP.P. BarhateA.N. Formulation and evaluation of microspheres of Glibenclamide by inotropic gelation method.Indo Am J Pharm Res.201779471479
    [Google Scholar]
  2. ManeS. VinchurkarK. KhanM.A. SainyJ. Effect of formulation variables on the characteristics of vildagliptin microspheres.IP Int. J. Comp. Adv. Pharmacol.20227313414010.18231/j.ijcaap.2022.028
    [Google Scholar]
  3. MayC.D. Industrial pectins: Sources, production and applications.Carbohydr. Polym.1990121799910.1016/0144‑8617(90)90105‑2
    [Google Scholar]
  4. MolinaV.E. ContrerasP.E. ReyesA.E.A. PatiñoL.C.A. Pectin and chitosan microsphere preparation via a water/oil emulsion and solvent evaporation method for drug delivery.Int. J. Polym. Mater.202069746747510.1080/00914037.2019.1581199
    [Google Scholar]
  5. BhattacharyaS.S. MazahirF. BanerjeeS. VermaA. GhoshA. Preparation and in vitro evaluation of xanthan gum facilitated superabsorbent polymeric microspheres.Carbohydr. Polym.2013981647210.1016/j.carbpol.2013.05.01123987317
    [Google Scholar]
  6. FuwaM. NakanishiY. MoritakaH. Effect of xanthan gum on blood sugar level of cooked rice.Abstracts of annual congress of the Japan society of home economics 67th annual congress of the Japan society of home economics.The Japan Society of Home Economics2015179
    [Google Scholar]
  7. YahoumMM ToumiS TahraouiH LefnaouiS KebirM AmraneA Formulation and evaluation of xanthan gum microspheres for the sustained release of metformin hydrochloride.Micromachines202314360910.3390/mi14030609
    [Google Scholar]
  8. KumariB. KhansiliA. Analytical method development and validation of UV-visible spectrophotometric method for the estimation of vildagliptin in the gastric medium.Drug Res.202070941742310.1055/a‑1217‑029632746479
    [Google Scholar]
  9. PratleyR. KamelJ.S. GalbreathE. HolmesD. Twelve-week monotherapy with the DPP-4 inhibitor vildagliptin improves glycemic control in subjects with type 2 diabetes.Horm. Metab. Res.200638642342810.1055/s‑2006‑94454616823726
    [Google Scholar]
  10. KumariB. KhansiliA. KumarM. Development and optimization of vildagliptin loaded floating microspheres using central composite design: In vitro and in vivo evaluation.Ann. Rom. Soc. Cell Biol.202125412742127455
    [Google Scholar]
  11. AtaraS.A. SoniwalaM.M. Formulation and evaluation of pectin-calcium chloride beads of azathioprine for colon-targeted drug delivery system.Int. J. Pharm. Pharm. Sci.201810117217710.22159/ijpps.2018v10i1.23175
    [Google Scholar]
  12. Rudhaliliharekfhl Preparation and evaluation of topiramate-loaded microspheres by ionotropic gelation method.World J. Pharm. Pharm. Sci.202091212911313
    [Google Scholar]
  13. KumarK. PantN.C. AhmadS. FatehM.V. RaiA.K. VermaB. ChaurasiaH. Development and evaluation of floating microspheres of curcumin in alloxan-induced diabetic rats.Trop. J. Pharm. Res.20161591819182510.4314/tjpr.v15i9.1
    [Google Scholar]
  14. KawashimaY. NiwaT. TakeuchiH. HinoT. ItohY. Hollow microspheres for use as a floating controlled drug delivery system in the stomach.J. Pharm. Sci.199281213514010.1002/jps.26008102071372046
    [Google Scholar]
  15. AultonM.E. Pharmaceutics - The science of dosage form design.2nd edChurchill Livingstone, Elsevier Science Ltd2002315320
    [Google Scholar]
  16. MullaT.S. SalunkheV.R. BhingeS.D. MohireN. Formulation, design and optimization of antidiabetic drug loaded microspheres.Polym. Bull.20238066171619610.1007/s00289‑022‑04325‑9
    [Google Scholar]
  17. MannaS. AzizA. DasS. BhowmikM. Ionically cross-linked pectin-alginate hydrogel beads for prolonged release of glibenclamide.Int. J. Pharm. Investig.202212447547810.5530/ijpi.2022.4.81
    [Google Scholar]
  18. MohapatraD.K. RoyH. PattanayakD. NandiS. SenapatiP. Design and in vitro evaluation of cefuroxime axetil floating microbeads for the treatment of hospital acquired infection.Int J Pharm Sci Health Care.2012223651
    [Google Scholar]
  19. NaikJ.B. WaghuldeM.R. Development of vildagliptin loaded Eudragit® microspheres by screening design: in vitro evaluation.J. Pharm. Investig.201848662763710.1007/s40005‑017‑0355‑3
    [Google Scholar]
  20. DewanI. IslamS. RanaM.S. Characterization and compatibility studies of different rate retardant polymer loaded microspheres by solvent evaporation technique: in vitro-in vivo study of vildagliptin as a model drug.J. Drug Deliv.2015201511210.1155/2015/49680726640713
    [Google Scholar]
  21. ShindeP.V. PatilS.P. JadhavS.V. Compatibility studies of active pharmaceutical ingredients with excipients using FT-IR spectroscopy.Int. J. Pharm. Sci. Rev. Res.20195534550
    [Google Scholar]
  22. DeshmukhR. ChaudhariP. JadhavV. FT-IR analysis: A versatile tool in pharmaceutical formulations to assess drug-polymer interactions.J. Appl. Pharm. Res.202082102108
    [Google Scholar]
  23. PatelD. KumarR. GuptaP. Structural analysis and compatibility studies of gliptin drugs with excipients using spectroscopic techniques.Spectrochim. Acta A Mol. Biomol. Spectrosc.2018191150157
    [Google Scholar]
  24. KumarS. MishraP. SharmaR. FT-IR spectroscopy in assessing stability and compatibility of vildagliptin-polymer blends.Asian J Pharm Res.2021154234242
    [Google Scholar]
  25. SinghS. KaurG. AroraR. Applications of FT-IR spectroscopy in ensuring stability of pharmaceutical formulations.Int. J. Spectrosc.20202020110
    [Google Scholar]
  26. PeerigaR. BalaganiP.K. RajuG.E. NarayananR. MohammedJ. YarlagaddaL.C. Findings of steroids, coumarins and saponins in ipomeasagittifolia (Burn. f.) leaf extract by HPTLC fingerprints.Int. J. Chem. Biochem. Sci.2023244132140
    [Google Scholar]
  27. PeerigaR. ShaikK. ShaikA. RiazB. RajuG.E. Investigation on ethanolic stem extract of Ipomeasagittifolia to explore the presence of saponins by high performance thin layer chromatography.Int J MembrSci Technol.202310410121020
    [Google Scholar]
  28. PeerigaR. ShaikA. ArabathS.A.M. ChennuruM.L. MarimgantiS.N. Assessment of steroids in ethanolic stem extract of morning glory by high performance thin layer chromatography.Int. J. Chem. Biochem. Sci.2023233361366
    [Google Scholar]
  29. PeerigaR. ArabathS.A.M. AllaN.R. YenireddyA. BangaruG.K.V. Exploring the coumarins from stem extract of IpomeasagittifoliaBurm. f. by high-performance thin layer chromatography.Int. J. Chem. Biochem. Sci.2023233268273
    [Google Scholar]
  30. ManuboluK. PeerigaR. BonthuM.G. VatchavaiB.R. KorukolaN. GopeE.R. Evaluation of anti-inflammatory activity of millingtoniahortensis leaf extract.Int. J. Chem. Biochem. Sci.2023246380385
    [Google Scholar]
  31. ManuboluK. BalaganiP.K. GopeE.R. VaralakshmiJ. PeerigaR. SrideviA.R. Unlocking the potential of aquasomes: A comprehensive review on innovative nanocarriers in drug delivery and beyond.Int. J. Chem. Biochem. Sci.2023246405410
    [Google Scholar]
  32. BonthuM.G. PeerigaR. ManuboluK. VatchavaiB.R. KorukolaN. GopeE.R. A bibliometric analysis of investigations on black pepper published from 1978 to 2023.Int. J. Chem. Biochem. Sci.2023246386394
    [Google Scholar]
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  • Article Type:
    Research Article
Keyword(s): Calcium chloride ion; Pectin; pH-sensitive bead; Sodium alginate; Vildagliptin; Xanthan gum
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