4.7 Article

Impact of polysorbate 65 on tripalmitin crystal growth and release stability of hot melt coated multiparticulate systems

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 607, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2021.120970

Keywords

Hot melt coating; Solid-state; Phase separation; Lipid crystal growth; Emulsifier concentration; Release instability

Funding

  1. Austrian COMET Program by the Austrian Federal Ministry of Transport, Innovation, and Technology (BMVIT)
  2. Austrian Federal Ministry of Economy, Family, and Youth (BMWFJ)
  3. State of Styria (Styrian Funding Agency SFG)
  4. Harro Hodfliger GmbH (Allmersbach i. T., Germany)
  5. FOSTAG Formenbau AG (Steinen, Switzerland)
  6. Hermes Arzneimittel GmbH (Pullach, Germany)

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This study examined the effect of PS 65 concentration on the crystal growth of PPP, with low concentrations promoting crystal growth and resulting in a slow release of HCT, while high concentrations led to phase separation of PPP and PS 65, accelerating the release. The increase in PS 65 reinforced the molecular interaction with HCT, leading to less crystal growth and a slower release from the coating.
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 alpha-form to its most stable beta-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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