The Effect of the Substitution Level of Some Dextran-methotrexate Conjugates on their Antitumor Activity in Experimental Cancer Models
ANTICANCER RESEARCH • 2006
Publication Information
Authors
DMITRY NEVOZHAY, RENATA BUDZYNSKA, MONIKA JAGIELLO, URSZULA KANSKA,
MOHAMED SALAH OMAR, ADAM OPOLSKI, JOANNA WIETRZYK and JANUSZ BORATYNSKI
Keywords
Dextran, methotrexate conjugates, antitumor activity,
leukemia.
Journal
ANTICANCER RESEARCH
Publisher
Not Available
Volume
26
Issue
Not Available
Pages
2179-2186
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
Methotrexate (MTX) is widely used in the treatment
of a number of oncological and hematological diseases. Due to
its known limitations, MTX is often conjugated with different
carriers to obtain amended forms of the drug. In this study, the
potential influence of the substitution level (loading ratio) of the
dextran T10- and T40-based MTX conjugates
(D-MTX) on their properties were investigated in vitro and in
vivo. The clear dependence of the in vitro antiproliferative effect
on the substitution level was established only in the case of the
dextran T10-based preparations (T10-MTX conjugates).
Conjugates with the higher substitution level had the lower
antiproliferative effect. For the dextran T40-based (T40-MTX
conjugates) set no similar relationship was observed in the tested
range of substitution levels, nor was any dependence observed
between the biological properties of the D-MTX preparations in
vivo and their substitution levels. However, the difference
between the two conjugates was well pronounced in a multipledose
schedule, when the advantage of T40-MTX over T10-MTX
was cumulative during the prolonged course of administration.
of a number of oncological and hematological diseases. Due to
its known limitations, MTX is often conjugated with different
carriers to obtain amended forms of the drug. In this study, the
potential influence of the substitution level (loading ratio) of the
dextran T10- and T40-based MTX conjugates
(D-MTX) on their properties were investigated in vitro and in
vivo. The clear dependence of the in vitro antiproliferative effect
on the substitution level was established only in the case of the
dextran T10-based preparations (T10-MTX conjugates).
Conjugates with the higher substitution level had the lower
antiproliferative effect. For the dextran T40-based (T40-MTX
conjugates) set no similar relationship was observed in the tested
range of substitution levels, nor was any dependence observed
between the biological properties of the D-MTX preparations in
vivo and their substitution levels. However, the difference
between the two conjugates was well pronounced in a multipledose
schedule, when the advantage of T40-MTX over T10-MTX
was cumulative during the prolonged course of administration.
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