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AAPS PharmSciTech

, Volume 19, Issue 5, pp 2103–2117 | Cite as

Thermosensitive Poloxamer 407/Poly(Acrylic Acid) Hydrogels with Potential Application as Injectable Drug Delivery System

  • Wannisa Boonlai
  • Vimon Tantishaiyakul
  • Namon Hirun
  • Tanatchaporn Sangfai
  • Krit Suknuntha
Research Article
  • 176 Downloads

Abstract

Thermosensitive hydrogels are of great interest for in situ gelling drug delivery. The thermosensitive vehicle with a gelation temperature in a range of 30–36°C would be convenient to be injected as liquid and transform into gel after injection. To prepare novel hydrogels gelling near body temperature, the gelation temperature of poloxamer 407 (PX) were tailored by mixing PX with poly(acrylic acid) (PAA). The gelation behaviors of PX/PAA systems as well as the interaction mechanism were investigated by tube inversion, viscoelastic, shear viscosity, DSC, SEM, and FTIR studies. The gelation temperature of the plain PX solutions at high concentration of 18, 20, and 22% (w/w) gelled at temperature below 28°C, which is out of the suitable temperature range. Mixing PX with PAA to obtain 18 and 20% (w/w) PX with 1% (w/w) PAA increased the gelation temperature to the desired temperature range of 30–36°C. The intermolecular entanglements and hydrogen bonds between PX and PAA may be responsible for the modulation of the gelation features of PX. The mixtures behaved low viscosity liquid at room temperature with shear thinning behavior enabling their injectability and rapidly gelled at body temperature. The gel strength increased, while the pore size decreased with increasing PX concentration. Metronidazole, an antibiotic used for periodontitis, was incorporated into the matrices, and the drug did not hinder their gelling ability. The gels showed the sustained drug release characteristic. The thermosensitive PX/PAA hydrogel could be a promising injectable in situ gelling system for periodontal drug delivery.

KEY WORDS

poloxamer 407 poly(acrylic acid) thermosensitive hydrogel gelation temperature 

Notes

Acknowledgements

This work was financially supported by Walailak University through Grant Number WU60309. The authors also acknowledge the support of the Health Science Research Center and the Center for Scientific and Technological Equipments, Walailak University, for research facilities.

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Copyright information

© American Association of Pharmaceutical Scientists 2018

Authors and Affiliations

  • Wannisa Boonlai
    • 1
  • Vimon Tantishaiyakul
    • 2
  • Namon Hirun
    • 1
    • 3
  • Tanatchaporn Sangfai
    • 1
  • Krit Suknuntha
    • 2
  1. 1.School of PharmacyWalailak UniversityNakhon Si ThammaratThailand
  2. 2.Center of Excellence for Drug Delivery System and Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical SciencesPrince of Songkla UniversityHat-YaiThailand
  3. 3.Drug and Cosmetics Excellence CenterWalailak UniversityNakhon Si ThammaratThailand

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