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Impact of polysorbate 65 on tripalmitin crystal growth and release stability of hot melt coated multiparticulate systems.
Schertel, Sonja; Salar-Behzadi, Sharareh; Karrer, Julia; Laggner, Peter; Zimmer, Andreas.
Afiliación
  • Schertel S; Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology and Biopharmacy, University of Graz, 8010 Graz, Austria; Hermes Arzneimittel GmbH, Division Hermes Pharma, 82049 Pullach, Germany.
  • Salar-Behzadi S; Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology and Biopharmacy, University of Graz, 8010 Graz, Austria; Research Center for Pharmaceutical Engineering GmbH, 8010 Graz, Austria.
  • Karrer J; Research Center for Pharmaceutical Engineering GmbH, 8010 Graz, Austria.
  • Laggner P; Research Center for Pharmaceutical Engineering GmbH, 8010 Graz, Austria.
  • Zimmer A; Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology and Biopharmacy, University of Graz, 8010 Graz, Austria. Electronic address: andreas.zimmer@uni-graz.at.
Int J Pharm ; 607: 120970, 2021 Sep 25.
Article en En | MEDLINE | ID: mdl-34363917
Hydrochlorothiazide (HCT) multiparticulate systems (MPS) were hot melt coated with the binary mixture of tripalmitin (PPP) and polysorbate 65 (PS 65) to gain an immediate release profile. Once, HCT MPS were produced with a constant ratio of PPP/PS 65 (90:10) at three different coating amounts (15, 25, and 60%w/w) and once the PPP/PS 65 ratio was varied on 98:2 and 80:20, by keeping the coating amount at 60%w/w. PS 65 induced the polymorphic transformation of PPP from the α-form to its most stable ß-form right after the hot melt coating (HMC). A release alteration of HCT, either accelerated or decelerated, occurred after the storage under accelerated conditions. The effect of the API core on the lipid lamellar configuration, the thermal behavior of lipid coating, and the effect of PS 65 concentration on the crystal growth of PPP were investigated via X-ray diffraction and DSC. While a low amount of PS 65 was sufficient to promote crystal growth of PPP and resulted in a decelerated release of HCT from the coating, a higher PS 65 concentration favored phase separation of PPP and PS 65 and led to an accelerated release. The increase in PS 65 reinforced the molecular interaction with the lipophilic HCT, reflected in less crystal growth and decelerated release. The knowledge presented in this study supports understanding the instability of binary emulsifier-lipid coating systems, paving the way for developing robust HMC formulations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polisorbatos / Excipientes Idioma: En Revista: Int J Pharm Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polisorbatos / Excipientes Idioma: En Revista: Int J Pharm Año: 2021 Tipo del documento: Article País de afiliación: Alemania