Skip to main content
Log in

Sol–gel one-pot synthesis in soft conditions of mesoporous silica materials ready for drug delivery system

  • Published:
Journal of Sol-Gel Science and Technology Aims and scope Submit manuscript

Abstract

The present work reveals a new and simple strategy, a one-step sol–gel procedure, to encapsulate a low water-soluble drug in silica mesostructured microparticles and to improve its release in physiological media. The synthesis of these new materials is based on the efficient solubilisation of a poorly water-soluble drug in surfactant micelles (Tween 80, a pharmaceutical excipient) which act as template for the silica network. A strict control of the sol–gel process and the parameters procedure in soft conditions (concentration, pH, temperature) was applied to reach the solubilisation limit of the drug in the micellar solution so as to optimise its encapsulation. Even if this one-pot procedure could appear limited by the low drug loading, it could provide an interesting alternative for the formulation of many recent highly active but very poorly soluble drugs.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Hörter D, Dressman JB (2010) Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract. Adv Drug Del Rev 46:75–87

    Article  Google Scholar 

  2. Liu R (2008) Water-insoluble drug formulation. Taylor & Francis, Boca Raton

    Book  Google Scholar 

  3. Aiello R, Cavallaro G, Giammona G, Pasqua L, Pierro P, Testa F (2002) Mesoporous silicate as matrix for drug delivery systems of non-steroidal anti-inflammatory drugs. Stud Surf Sci Catal 142:1165–1172

    Article  Google Scholar 

  4. Anderson J, Rosenholm J, Areva S, Linden M (2004) Influences of material characteristics on ibuprofen drug loading and release profiles from ordered micro- and mesoporous silica matrices. Chem Mater 16:4160–4167

    Article  Google Scholar 

  5. Charnay C, Begu S, Tourne-Peteilh C, Nicole L, Lerner DA, Devoisselle J-M (2004) Inclusion of ibuprofen in mesoporous templated silica: drug loading and release property. Eur J Pharm Biopharm 57:533–540

    Article  CAS  Google Scholar 

  6. Tourne-Peteilh C, Brunel D, Begu S, Chiche B, Fajula F, Lerner DA, Devoisselle J-M (2003) Synthesis and characterisation of ibuprofen-anchored MCM-41 silica and silica gel. New J Chem 3:281–286

    Google Scholar 

  7. Tourne-Peteilh C, Lerner DA, Charnay C, Nicole L, Bégu S, Devoisselle J-M (2003) The potential of ordered mesoporous for the storage of drugs : the example of a pentapeptide encapsulated in a MSU-Tween 80. Chem Phys Chem 3:281–286

    Article  Google Scholar 

  8. Vallet-Regi M, Ramila A, del Real RP, Perez-Pariente J (2001) A new property of MCM-41: drug delivery system. Chem Mater 13:308–311

    Article  CAS  Google Scholar 

  9. Vallet-Regi M, Balas F, Colilla M, Manzano M (2007) Bioceramics and pharmaceuticals: a remarkable synergy. Solid State Sci 9:768–776

    Article  CAS  Google Scholar 

  10. Azaïs T, Tourné-Péteilh C, Aussenac F, Baccile N, Coelho C, Devoisselle J-M, Babonneau F (2006) Solid-state NMR study of ibuprofen confined in MCM-41 material. Chem Mater 18:6382–6390

    Article  Google Scholar 

  11. Heikkilä T, Salonen J, Tuura J, Hamdy MS, Mul G, Kumar N, Salmi T, Murzin DY, Laitinen L, Kaukonen AM, Hirvonen J, Lehto V-P (2007) Mesoporous silica material TUD-1 as a drug delivery system. Int J Pharm 331:133–138

    Article  Google Scholar 

  12. Impurities: guideline for residual solvents (2009) In London–UK, European Medicines Agency, 22

  13. Unger K, Rupprecht H, Valentin B, Kircher W (1983) The use of porous and surface modified silicas as drug delivery and stabilizing agents. Drug Dev Ind Pharm 9:69–91

    Article  CAS  Google Scholar 

  14. Kortesuo P, Ahola M, Karlsson S, Kangasniemi I, Yli-Urpo A, Kiesvaara J (2000) Silica xerogel as an implantable carrier for controlled drug delivery–evaluation of drug distribution and tissue effects after implantation. Biomaterials 21:193–198

    Article  CAS  Google Scholar 

  15. Kortesuo P, Ahola M, Kangas M, Kangasniemi I, Yli-Urpo A, Kiesvaara J (2000) In vitro evaluation of sol–gel processed spray dried sillica gel microsphères as carrier in controlled drug delivery. Int J Pharm 200:223–229

    Article  CAS  Google Scholar 

  16. Ahola M, Säilynoja E, Raitavuo M, Vaahtio M, Salonen J, Yli-Urpo A (2001) In vitro release of heparin from silica xerogels. Biomaterials 22:2163–2170

    Article  CAS  Google Scholar 

  17. Fatnassi M, Tourne-Peteilh C, Cacciaguerra T, Dieudonné P, Devoisselle J-M, Alonso B (2010) Tuning nanophase separation and drug delivery kinetics through spray drying and self-assembly. New J Chem 34:607–610

    Article  CAS  Google Scholar 

  18. Rowe RC, Sheskey PJ, Owen SC (2006) Handbook of pharmaceutical excipients, 5th edn., Pharmaceutical Press, London

  19. Boissière C, Larbot A, Van der Lee A, Kooyman PJ, Prouzet E (2000) A new synthesis of mesoporous MSU-X silica controlled by a two-step pathway. Chem Mater 12:2902–2913

    Article  Google Scholar 

  20. Broekhoff JCP, de Boer JH (1968) Studies on pore systems in catalysts–chap. XIII. J Catal 10:377–390

    Article  CAS  Google Scholar 

  21. Galarneau A, Desplantier D, Dutartre R, Di Renzo F (1999) Micelle-templated silicates as a test bed for methods of mesopore size evaluation. Microporous Mesoporous Mater 27:297–308

    Article  CAS  Google Scholar 

  22. US Pharmacopeia and national formulary (1999)

  23. Costa P, Sousa Lobo JM (2001) Modeling and comparison of dissolution profiles. Eur J Pharm Biopharm 13:123–133

    CAS  Google Scholar 

  24. Gerakis AM, Koupparis MA, Efstathiou CE (1993) Micellar acid-base potentiometric titrations of weak acidic and/or insoluble drugs. J Pharm Biomed Anal 11:33–41

    Article  CAS  Google Scholar 

  25. Schachter DM, Xiong J, Tirol GC (2004) Solid state NMR perspective of drug–polymer solid solutions: a model system based on poly (ethylene oxide). Int J Pharm 281:89–101

    Article  CAS  Google Scholar 

  26. Attwood D, Florence AT (1985) Surfactant systems—their chemistry, pharmacy and biology, 2nd edn. Chapman and Hall, London

    Google Scholar 

  27. Bass JD, Grosso D, Boissiere C, Belamie E, Coradin T, Sanchez C (2007) Stability of mesoporous oxide and mixed metal oxide materials under biologically relevant conditions. Chem Mater 19:4349–4356

    Article  CAS  Google Scholar 

  28. Begu S, Aubert Pouëssel A, Lerner DA, Tourne-Peteilh C, Devoisselle J-M (2007) Liposil, a promising composite material for drug storage and release. J Control Release 118:1–6

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Corine Tourne-Peteilh.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 571 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tourne-Peteilh, C., Begu, S., Lerner, D.A. et al. Sol–gel one-pot synthesis in soft conditions of mesoporous silica materials ready for drug delivery system. J Sol-Gel Sci Technol 61, 455–462 (2012). https://doi.org/10.1007/s10971-011-2646-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10971-011-2646-x

Keywords

Navigation