Biomedical Engineering Reference
In-Depth Information
33. Chytil, P., et al.,
N
-(2-Hydroxypropyl)methacrylamide-based polymer
conjugates with pH-controlled activation of doxorubicin for cell-
specific or passive tumour targeting. Synthesis by RAFT polymerisation
and physicochemical characterisation
.
Eur J Pharm Sci
, 2010.
41
(3-4):
p. 473-482.
34. Ulbrich, K., et al.,
Polymeric conjugates of drugs and antibodies for site-
specific drug delivery.
Macromol Symp, 1996.
103
: p. 177-192.
35. Putnam, D. and J. Kopecek,
Polymer conjugates with anticancer activity.
Biopolymers II, 1995.
122
: p. 55-123.
36. Ulbrich, K. and V. Subr,
Polymeric anticancer drugs with pH-controlled
activation.
Adv Drug Deliv Rev, 2004.
56
(7): p. 1023-1050.
37. Kratz, F., U. Beyer, and M.T. Schutte,
Drug-polymer conjugates containing
acid-cleavable bonds.
Crit Rev Ther Drug Carrier Syst, 1999.
16
(3): p.
245-288.
38. Rodrigues, P.C.A., et al., Correlation of the acid-sensitivity of polyethylene
glycol daunorubicin conjugates with their
in vitro
antiproliferative
activity
.
Bioorg Med Chem, 2006.
14
(12): p. 4110-4117.
39. Meng, F.H., W.E. Hennink, and Z. Zhong,
Reduction-sensitive polymers
and bioconjugates for biomedical applications.
Biomaterials, 2009.
30
(12): p. 2180-2198.
40. Kopeček, J., et al.,
Synthetic polymeric drugs
, U.S. Patent, Editor. 1991.
41. Miller, K., et al.,
Targeting bone metastases with a bispecific anticancer
and antiangiogenic polymer-alendronate-taxane conjugate.
Angew
Chem Int Ed Engl, 2009.
48
(16): p. 2949-2954.
42. Dubowchik, G.M., et al.,
Cathepsin B-labile dipeptide linkers for
lysosomal release of doxorubicin from internalizing immunoconjugates:
model studies of enzymatic drug release and antigen-specific in vitro
anticancer activity.
Bioconjug Chem, 2002.
13
(4): p. 855-869.
43. Liu, C., et al.,
Overexpression of legumain in tumors is significant for
invasion/metastasis and a candidate enzymatic target for prodrug
therapy.
Cancer Res, 2003.
63
(11): p. 2957-2964.
44. Stern, L., et al.,
A novel antitumor prodrug platform designed to be
cleaved by the endoprotease legumain.
Bioconjug Chem, 2009.
20
(3):
p. 500-510.
45. Kratz, F., et al.,
Development and in vitro efficacy of novel MMP2 and
MMP9 specific doxorubicin albumin conjugates.
Bioorg Med Chem Lett,
2001.
11
(15): p. 2001-2006.
46. Kratz, F., et al.,
Prodrug strategies in anticancer chemotherapy.
ChemMedChem, 2008.
3
(1): p. 20-53.
Search WWH ::
Custom Search