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Hi,
How do we evaluate Pharmacokinetics and biodistribution of
nanoparticulate based vaccines. PLGA microencapsulated antigen is
evaluated as a good vaccine, it has good efficiency of producing
antibodies. I am a new graduate student, I have checked online if
anyone has done Pharmacokinetic study for the nanoparticulate based
vaccines. I would be happy if some one outlines the necessary studies
to be carried out and parameters to be evaluated. Please make some
suggestions even if you some one doesn't know what to do exactly.
Hope to hear some good news soon.
Sincerely,
Vamsi Krishna Karuturi,
Graduate Research Assistant,
Department of Pharmaceutical Sciences,
University of Nebraska Medical Center,
Omaha, Nebraska 68105.
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The following message was posted to: PharmPK
Vamsi: I would think as a model you could use some of the approaches
done
with liposomal carriers.
Edward F. O'Connor, PhD
78 Marbern Drive
Suffield, CT 06078
efoconnor.at.cox.net
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Dear Vamsi,
The disposition kinetics of the carrier may influence the
pharmacokinetics
and distribution of any active (drug/vaccine) as compared to when they
are
given in the naive form (no carrier). The reason for using delivery
systems
(carriers like nanoparticle, liposomes etc) is to make use of the
disposition kinetics of the carrier itself due to either their
long-circulatory nature or else their preferential endolysosomal uptake.
Depending upon the purpose of and selection of carrier (liposome,
nanoparticle etc), the pharmacokinetic profile of the active accrodingly
may vary and can be tailored to the needs to some extent.
For a detailed information on the plan of PK and disposition kinetics of
vaccines/genetic vaccines, books and literature references by Kreuter,
Gregoriadis, Paphadjopoulus, Torchilin and other experts can be
referred.
Hope this will help.
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