Skip to content
2000
Volume 18, Issue 3
  • ISSN: 2405-5204
  • E-ISSN: 2405-5212

Abstract

Aims

The aim of this study is to develop mefenamic acid-loaded microspheres using a hydrophilic polymer and a solvent evaporation method for sustained drug release, aiming to reduce the frequency of dosing.

Background

Mefenamic acid is an anti-inflammatory drug commonly used to manage pain, especially menstrual cramps. Microspheres, which are spherical particles ranging from 1 to 1000 micrometres, are effective in enhancing the sustained release of medications. The solvent evaporation method is widely used in the preparation of microspheres to improve drug delivery profiles.

Methods

A UV study of mefenamic acid was conducted to analyze all necessary parameters. Mefenamic acid and ethyl cellulose polymer were dissolved and stirred at 700 rpm using the solvent evaporation method. A surfactant-containing aqueous phase was prepared and maintained under stirring, into which the organic phase was introduced and continuously stirred to form microspheres. The formed microspheres were characterized by loading capacity, drug content, entrapment efficiency, and product yield. Scanning Electron Microscopy was used to confirm the spherical shape of the microspheres. An release study was conducted using a diffusion technique to evaluate the drug release profile.

Result and Discussion

The microspheres were successfully formed with a spherical shape, as observed in SEM images. The evaluation showed favorable loading capacity, entrapment efficiency, and drug content. The release study demonstrated a sustained release profile, indicating the effectiveness of the hydrophilic polymer in prolonging drug release.

Conclusion

The developed mefenamic acid-loaded microspheres using a hydrophilic polymer the solvent evaporation method achieved sustained drug release, potentially reducing the need for frequent dosing. The method and formulation show promise for enhancing the therapeutic efficacy of mefenamic acid.

Loading

Article metrics loading...

/content/journals/rice/10.2174/0124055204375681250513064952
2025-05-15
2026-03-02
Loading full text...

Full text loading...

References

  1. RouholaminiN.A. AsgharianR. TajerzadehH. GilaniK. VatanaraA. DarabiM. The effects of fine lactose as a third component on aerosolization of cefotaxime sodium from dry powder formulations.Daru2006143109115
    [Google Scholar]
  2. AbrahamG.A. GallardoA. San RománJ. Fernández-MayoralasA. ZuritaM. VaqueroJ. Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs.J. Biomed. Mater. Res. A200364A463864710.1002/jbm.a.10297 12601775
    [Google Scholar]
  3. GuptaA.K. NaregalkarR.R. VaidyaV.D. GuptaM. Recent advances on surface engineering of magnetic iron oxide nanoparticles and their biomedical applications.Nanomedicine200721233910.2217/17435889.2.1.23
    [Google Scholar]
  4. GuptaA.K. GuptaM. Synthesis and surface engineering of iron oxide nanoparticles for biomedical applications.Biomaterials200526183995402110.1016/j.biomaterials.2004.10.012
    [Google Scholar]
  5. BinduS. MazumderS. BandyopadhyayU. Non-steroidal anti-inflammatory drugs (NSAIDs) and organ damage: A current perspective.Biochem. Pharmacol.202018011414710.1016/j.bcp.2020.114147 32653589
    [Google Scholar]
  6. HarwoodR.J. Handbook of Pharmaceutical Excipients.5th edLondon, UKPharmaceutical Press2005
    [Google Scholar]
  7. HejaziR. AmijiM. Chitosan-based gastrointestinal delivery systems.J. Control. Release200389215116510.1016/S0168‑3659(03)00126‑3 12711440
    [Google Scholar]
  8. CohenI. LiH. HouglandJ.L. MrksichM. NagelS.R. Using selective withdrawal to coat microparticles.Science2001292551526526710.1126/science.1059175 11303097
    [Google Scholar]
  9. LamprechtA. YamamotoH. TakeuchiH. KawashimaY. pH-sensitive microsphere delivery increases oral bioavailability of calcitonin.J. Control. Release20049811910.1016/j.jconrel.2004.02.001 15245884
    [Google Scholar]
  10. LiuJ. MeisnerD. KwongE. WuX.Y. JohnstonM.R. A novel trans-lymphatic drug delivery system: Implantable gelatin sponge impregnated with PLGA–paclitaxel microspheres.Biomaterials200728213236324410.1016/j.biomaterials.2007.03.022 17434581
    [Google Scholar]
  11. SudhamaniT. ReddyK.N. KumarV.R. RevathiR. GanesanV. Preparation and evaluation of ethyl cellulose microspheres of ibuprofen for sustained drug delivery.Int. J. Pharm. Res. Dev.201028120121
    [Google Scholar]
  12. DattaD. ColacoV. BandiS.P. SharmaH. DhasN. GiramP.S. Classes/types of polymers used in oral delivery (natural, semisynthetic, synthetic), their chemical structure and general functionalities.In: Polymers for Oral Drug Delivery Technologies.Woodhead Publishing202526333310.1016/B978‑0‑443‑13774‑7.00007‑4
    [Google Scholar]
  13. RajputT. MohiteP. GhuleS. VinchurkarK. SinghS. Nanofabrication of losartan potassium sustained release floating microspheres using different grades of ethyl cellulose and its insight on release profiles.Curr. Pharm. Des.202430282257226510.2174/0113816128309675240530060752 38910484
    [Google Scholar]
  14. IbrahimM.A. KoorbanallyN.A. IslamS. Anti-oxidative, (α-glucosidase and α-amylase inhibitory activity of Vitex doniana: Possible exploitation in the management of type 2 diabetes.Acta Pol. Pharm.201673512351247 29638064
    [Google Scholar]
  15. NicoliniM.V.S. Timóteo VieiraW.T. da SilvaM.G.C. de Oliveira NascimentoL. VieiraM.G.A. Mefenamic acid modified-release by encapsulation in a k-carrageenan/sericin blend.J. Ind. Eng. Chem.2023121637610.1016/j.jiec.2023.01.007
    [Google Scholar]
  16. NiefR.A. HusseinA.A. Preparation and evaluation of meloxicam microsponges as transdermal delivery system.Iraqi J. Pharm Sci.2014232627410.31351/vol23iss2pp62‑74
    [Google Scholar]
  17. BonyadiS. GhanbariK. GhiasiM. All-electrochemical synthesis of a three-dimensional mesoporous polymeric g-C3N4/PANI/CdO nanocomposite and its application as a novel sensor for the simultaneous determination of epinephrine, paracetamol, mefenamic acid, and ciprofloxacin.New J. Chem.20204483412342410.1039/C9NJ05954G
    [Google Scholar]
  18. AliH.M.S. Al-KhedairyE.B.H. Formulation and evaluation of prednisolone-loaded alginate beads for taste masking.Egypt. J. Hosp. Med.20239022178218610.21608/ejhm.2023.285683
    [Google Scholar]
  19. AssasN. ElbahriZ. BaiticheM. DjerbouaF. Effects of some process parameters on the niflumic acid controlled release polymeric microspheres: Optimization using designs of experiments.Asia-Pac. J. Chem. Eng.2019142e228310.1002/apj.2283
    [Google Scholar]
  20. DattaD. DasA. GhoshR. Eudragit® RL100 microspheres as delayed-release system for ibuprofen: In vitro evaluation.Int. J. Pharm. Pharm. Sci.20221412610
    [Google Scholar]
  21. ArumugamK.A. BorawakeP.D. ShindeJ.V. Formulation and evaluation of floating microspheres of ciprofloxacin by solvent evaporation method using different polymers.Int. J. Pharm. Pharm. Sci.202113710110810.22159/ijpps.2021v13i7.41204
    [Google Scholar]
  22. AbdelmalakN.S. El-MenshaweS.F. A new topical fluconazole microsponge loaded hydrogel: Preparation and characterization.Int. J. Pharm. Pharm. Sci.201241460468
    [Google Scholar]
  23. PahwaS. TomarM.K. TyagiL.K. GuptaC. MaanP. SethiV.A. Formulation, characterization, and antibacterial study of microsponge-loaded gel of clarithromycin for topical drug delivery.Drug Deliv. Lett.202212212213410.2174/2210303112666220412134241
    [Google Scholar]
  24. PatilP.S. SuryawanshiS.J. PatilS.S. PawarA.P. HME-assisted formulation of taste-masked dispersible tablets of cefpodoxime proxetil and roxithromycin.J. Taibah Univ. Med. Sci.202419225226210.1016/j.jtumed.2023.12.004 38616800
    [Google Scholar]
  25. WannasaritS. MahattanadulS. IssarachotO. PuttarakP. WiwattanapatapeeR. Raft-forming gastro-retentive formulations based on Centella asiatica extract-solid dispersions for gastric ulcer treatment.Eur. J. Pharm. Sci.202014310520410.1016/j.ejps.2019.105204 31870812
    [Google Scholar]
  26. ZhangP. ShadambikarG. AlmutairiM. BandariS. RepkaM.A. Approaches for developing acyclovir gastro-retentive formulations using hot melt extrusion technology.J. Drug Deliv. Sci. Technol.20206010200210.1016/j.jddst.2020.102002
    [Google Scholar]
  27. InamdarA. GurupadayyaB. HalagaliP. Unraveling neurological drug delivery: Polymeric nanocarriers for enhanced blood-brain barrier penetration.Curr. Drug Targets202526424326610.2174/0113894501339455241101065040 39513304
    [Google Scholar]
  28. AnandA. ManjulaS.N. FuloriaN.K. SharmaH. MruthunjayaK. Inulin as a prebiotic and its effect on gut microbiota BT. AkramW. MishraN. HaiderT. Inulin for Pharmaceutical Applications: A Versatile Biopolymer.Springer Nature: Singapore202511313510.1007/978‑981‑97‑9056‑2_6
    [Google Scholar]
  29. HalagaliP. TippavajhalaV.K. RathnanandM. SharmaH. PathakR. Inulin as a natural ingredient in cosmetics and personal care products BT. AkramW. MishraN. HaiderT. Inulin for Pharmaceutical Applications: A Versatile Biopolymer.Springer Nature: Singapore202513714610.1007/978‑981‑97‑9056‑2_7
    [Google Scholar]
  30. SuryawanshiM. KurtkotiS. MullaT. ShahE. SharmaH. BhattH. Edible biopolymers for food applications.In: Green Biopolymers for Packaging Applications.Boca RatonCRC Press202422825410.1201/9781003455356‑10
    [Google Scholar]
  31. SuryawanshiM. MullaT. SuryawanshiI. VinchurkarK. KallawalaU. SharmaH. Modified starch in food packaging.In: Green Biopolymers for Packaging Applications.Boca RatonCRC Press202425527110.1201/9781003455356‑11
    [Google Scholar]
  32. KapoorD.U. SharmaH. MaheshwariR. Konjac glucomannan: A comprehensive review of its extraction, health benefits, and pharmaceutical applications.Carbohydr. Polym.202433912226610.1016/j.carbpol.2024.122266 38823930
    [Google Scholar]
/content/journals/rice/10.2174/0124055204375681250513064952
Loading
/content/journals/rice/10.2174/0124055204375681250513064952
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test