Pharmaceutics 2011, 3(2), 315-325; doi:10.3390/pharmaceutics3020315

In Vitro Dissolution Methods for Hydrophilic and Hydrophobic Porous Silicon Microparticles

1,* email, 2,3email, 1email, 3email, 2email and 1email
Received: 13 April 2011; Accepted: 20 June 2011 / Published: 21 June 2011
(This article belongs to the Special Issue Recent Developments and Future Perspectives in Dissolution Testing)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Porous silicon (PSi) is an innovative inorganic material that has been recently developed for various drug delivery systems. For example, hydrophilic and hydrophobic PSi microparticles have been utilized to improve the dissolution rate of poorly soluble drugs and to sustain peptide delivery. Previously, the well-plate method has been demonstrated to be a suitable in vitro dissolution method for hydrophilic PSi particles but it was not applicable to poorly wetting hydrophobic thermally hydrocarbonized PSi (THCPSi) particles. In this work, three different in vitro dissolution techniques, namely centrifuge, USP Apparatus 1 (basket) and well-plate methods were compared by using hydrophilic thermally carbonized PSi (TCPSi) microparticles loaded with poorly soluble ibuprofen or freely soluble antipyrine. All the methods showed a fast and complete or nearly complete release of both model compounds from the TCPSi microparticles indicating that all methods described in vitro dissolution equally. Based on these results, the centrifuge method was chosen to study the release of a peptide (ghrelin antagonist) from the THCPSi microparticles since it requires small sample amounts and achieves good particle suspendability. Sustained peptide release from the THCPSi microparticles was observed, which is in agreement with an earlier in vivo study. In conclusion, the centrifuge method was demonstrated to be a suitable tool for the evaluation of drug release from hydrophobic THCPSi particles, and the sustained peptide release from THCPSi microparticles was detected.
Keywords: porous silicon; microparticles; drug release; in vitro release methods; peptide
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MDPI and ACS Style

Mönkäre, J.; Riikonen, J.; Rauma, E.; Salonen, J.; Lehto, V.-P.; Järvinen, K. In Vitro Dissolution Methods for Hydrophilic and Hydrophobic Porous Silicon Microparticles. Pharmaceutics 2011, 3, 315-325.

AMA Style

Mönkäre J, Riikonen J, Rauma E, Salonen J, Lehto V-P, Järvinen K. In Vitro Dissolution Methods for Hydrophilic and Hydrophobic Porous Silicon Microparticles. Pharmaceutics. 2011; 3(2):315-325.

Chicago/Turabian Style

Mönkäre, Juha; Riikonen, Joakim; Rauma, Elina; Salonen, Jarno; Lehto, Vesa-Pekka; Järvinen, Kristiina. 2011. "In Vitro Dissolution Methods for Hydrophilic and Hydrophobic Porous Silicon Microparticles." Pharmaceutics 3, no. 2: 315-325.

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