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7D19003

Development of a sublingual mucosal immunization technology platform for needle-free vaccination

Project goals

Development of sublingual delivery module Development of vaccine formulation In vitro testing of vaccine formulation In vivo testing of vaccine formulation Laboratory analysis of immunity Project IP and management

Keywords

nanotechnologysublingualantigenvaccination

Public support

  • Provider

    Ministry of Education, Youth and Sports

  • Programme

    Eurostars

  • Call for proposals

    SMSM20197D001

  • Main participants

    InStar Technologies a.s.

  • Contest type

    VS - Public tender

  • Contract ID

    MŠMT-4048/2019-4

Alternative language

  • Project name in Czech

    Development of a sublingual mucosal immunization technology platform for needle-free vaccination

  • Annotation in Czech

    Development of sublingual delivery module Development of vaccine formulation In vitro testing of vaccine formulation In vivo testing of vaccine formulation Laboratory analysis of immunity Project IP and management

Scientific branches

  • R&D category

    VV - Exeperimental development

  • OECD FORD - main branch

    30401 - Health-related biotechnology

  • OECD FORD - secondary branch

    10700 - Other natural sciences

  • OECD FORD - another secondary branch

    21001 - Nano-materials (production and properties)

  • EI - Biotechnology and bionics
    JJ - Other materials

Completed project evaluation

  • Provider evaluation

    U - Uspěl podle zadání (s publikovanými či patentovanými výsledky atd.)

  • Project results evaluation

    The main goal of the MucoVAC project was the technology development for oromucosal vaccine delivery (needle-free) which should be tested with the model antigen (influenza). The mentioned goal of the project was achieved, the technology was developer and validated. The outputs containing 3 different types of antigen were achieved. Tests on mouse and pig models confirmed that the designed dosing module was able to carry the active substance without damaging the structure, release it, sufficient protection from the surrounding environment and thus allow "safe" transport to the destination. An immune response was elicited in both animal models. SL immunization of pigs activated T and B cells in local tissues that are statistically significantly increased compared to those in pigs receiving the vaccine by the MI route. Here again, SL application appeared to be more effective compared to the IM application, as shown by a significantly increased number of antigen-specific B cells (P < 0.05).

Solution timeline

  • Realization period - beginning

    Jun 1, 2019

  • Realization period - end

    Apr 30, 2022

  • Project status

    U - Finished project

  • Latest support payment

    May 6, 2022

Data delivery to CEP

  • Confidentiality

    C - Předmět řešení projektu podléhá obchodnímu tajemství (§ 504 Občanského zákoníku), ale název projektu, cíle projektu a u ukončeného nebo zastaveného projektu zhodnocení výsledku řešení projektu (údaje P03, P04, P15, P19, P29, PN8) dodané do CEP, jsou upraveny tak, aby byly zveřejnitelné.

  • Data delivery code

    CEP23-MSM-7D-U

  • Data delivery date

    Jun 30, 2023

Finance

  • Total approved costs

    20,110 thou. CZK

  • Public financial support

    8,871 thou. CZK

  • Other public sources

    0 thou. CZK

  • Non public and foreign sources

    8,045 thou. CZK

Recognised costs

20 110 CZK thou.

Public support

8 871 CZK thou.

0%


Provider

Ministry of Education, Youth and Sports

OECD FORD

Health-related biotechnology

Solution period

01. 06. 2019 - 30. 04. 2022