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Development of thermostable lyophilized inactivated polio vaccine.

Pharmaceutical research (2014-04-25)
Heleen Kraan, Paul van Herpen, Gideon Kersten, Jean-Pierre Amorij
RESUMEN

The aim of current study was to develop a dried inactivated polio vaccine (IPV) formulation with minimal loss during the drying process and improved stability when compared with the conventional liquid IPV. Extensive excipient screening was combined with the use of a Design of Experiment (DoE) approach in order to achieve optimal results with high probability. Although it was shown earlier that the lyophilization of a trivalent IPV while conserving its antigenicity is challenging, we were able to develop a formulation that showed minimal loss of potency during drying and subsequent storage at higher temperatures. This study showed the potential of a highly stable and safe lyophilized polio vaccine, which might be used in developing countries without the need of a cold-chain.

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Fosfato de sodio dibasic, ACS reagent, ≥99.0%
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Sacarosa, for molecular biology, ≥99.5% (GC)
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Glicina, ReagentPlus®, ≥99% (HPLC)
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Cloruro de magnesio hexahydrate, ACS reagent, 99.0-102.0%
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Glicina, suitable for electrophoresis, ≥99%
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Cloruro de sodio, for molecular biology, DNase, RNase, and protease, none detected, ≥99% (titration)
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Fosfato de sodio dibasic, puriss. p.a., ACS reagent, anhydrous, ≥99.0% (T)
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D-Sorbitol, ≥98% (GC)
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Sacarosa, ≥99.5% (GC), BioXtra
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Glicina, BioUltra, for molecular biology, ≥99.0% (NT)
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myo-Inositol, ≥99% (GC), BioReagent
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myo-Inositol, ≥99%
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