• No results found

University of Groningen Paving the way for pulmonary influenza vaccines Tomar, Jasmine

N/A
N/A
Protected

Academic year: 2021

Share "University of Groningen Paving the way for pulmonary influenza vaccines Tomar, Jasmine"

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Paving the way for pulmonary influenza vaccines

Tomar, Jasmine

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from

it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date:

2018

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Tomar, J. (2018). Paving the way for pulmonary influenza vaccines: Exploring formulations, models and

site of deposition. University of Groningen.

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

PROPOSITIONS

Belonging to the PhD thesis

Paving the Way for Pulmonary Influenza Vaccines

Exploring formulations, models and site of deposition

By

Jasmine Tomar

1) Dry influenza vaccines administered via non-parenteral patient friendly dosage forms such as microneedles for administration via the skin, tablets for oral and powders for pulmonary administration are suitable and effective alternatives to parenteral influenza vaccines (Chapter 2 of this thesis).

2) Site of deposition within the respiratory tract holds minor relevance for inhaled vaccines against air-borne infectious diseases such as influenza but deep lung deposition is crucial for inhaled vaccines against non air-borne infectious diseases such as hepatitis B (Chapter 4 of this thesis).

3) Administration of effective influenza vaccine formulations to the lungs of relevant animal models with suitable delivery devices is a step towards clinical application (this thesis). 4) Crystalline delta inulin is a potent mucosal adjuvant (Chapter 5 of this thesis).

5) Passive inhalation is a feasible and effective method of mass vaccination for chickens that has the potential to be translated to field settings and consequently restrict the dissemination of avian influenza (Chapter 6 of this thesis).

6) A PhD thesis involves a long and persistent behavioural output in the absence of immediate reinforcement (James Coyne, ‘’Beating the dissertation blues’’ talk).

7) Hard work combined with a pinch of smartness is the key to success in the 21st century. 8) Success is not final, failure is not fatal: it is the courage to continue that counts (Winston

S. Churchill).

9) The flavour of a good food not only depends upon the right spices but also on the feelings with which the food is cooked.

10) The most challenging yet rewarding work is being a mother, with your child as the center of your universe.

Referenties

GERELATEERDE DOCUMENTEN

a good safety and tolerability record both in animal studies and clinical trials [25–27]. The aim of the current study was to investigate whether passive administration with

In Chapter 3, pulmonary administration of a whole inactivated influenza virus powder vaccine formulation was compared to a liquid formulation in a cotton rat model with respect to

Sproei-vriesdrogen werd gebruikt om een droogpoeder te produceren met een deeltjesgrootte die geschikt is voor inhalatie (1-5 mm). Ondanks het feit dat de poederdeeltjes de

In Chapter 3, pulmonary administration of a whole inactivated influenza virus powder vaccine formulation was compared to a liquid formulation in a cotton rat model with respect to

In order to determine the relative efficacy of WIV vaccines combined with different adjuvants, mice were vaccinated three times via the most suitable route of administration with

To explore the immune mechanisms involved in protection from weight loss and lung virus growth upon challenge, antibody responses induced by sequential infection with PR8 and X-31

Mice were vaccinated twice as described above with modified NC99 (H1N1)-derived virosomes with admixed or attached HK68 NP, with HK68 NP + MPLA or with plain virosomes and

Despite the overt effects of vaccination on lung virus titers several observations indicate that vaccination did not result in sterilizing immunity: (i) the breathing frequency