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Dear all,
We are doing immunogenicity tests for the biological therapeutic drugs,
such as recombinant proteins, peptides and humanized Abs. I would like
to
know what are the in vivo fates of pegylated* or non pegylated
protein/peptide drugs. Are there any
books or published papers discussing details of the processes? If the
fragments of protein/peptide drug are not immunogenic, does the immune
system still process the fragments through APC/T cells?
Thanks a lot,
KC
*. Pegylation is a technology designed to prolong or improve the
effectiveness of pharmaceutical products. Conjugation of protein/peptide
drug to polyethylene glycol (PEG) has shown potential beneficial
effects,
such as increasing biovailability, increasing plasma half-lives,
decreasing immunogenecity, reducing proteolysis, and enhancing
solubility
and stability. Several pegylated-drugs have been on the market.
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This paper may be helpful to you:
Pegylation: a novel process for modifying pharmacokinetics.
Harris JM, Martin NE, Modi M.
Clin Pharmacokinet. 2001;40(7):539-51.
Regards,
Alessandra Milesi-Halle, M.D.
Department of Pharmacology and Toxicology
University of Arkansas for Medical Sciences
4301 West Markham, slot 611
Little Rock, Arkansas 72205
Phone: (501)686-6551
Fax: (501)686-5521
MilesihalleAlessandr.-at-.uams.edu
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Copyright 1995-2010 David W. A. Bourne (david@boomer.org)