A new system for targeted delivery of doxorubicin into tumor cells.

Yabbarov N.G., Posypanova G.A., Vorontsov E.A., Obydenny S.I., Severin E.S.
Тип документаJournal Article
Дата публикации2013-06-25
Название журналаJournal of Controlled Release
ИздательElsevier
Квартиль по SCImagoQ1
Квартиль по Web of ScienceQ1
Импакт-фактор 202111.47
ISSN01683659, 18734995
Pharmaceutical Science
Краткое описание
The use of vector molecules for the targeted delivery of antitumor drugs provides their selectivity for cancer cells. The recombinant receptor-binding fragment of alpha-fetoprotein (rAFP3D) was used as a vector molecule. The specific receptor of alpha-fetoprotein is a universal tumor marker, being expressed on the surface of many tumor cells, but not in normal human tissues. And rAFP3D includes the receptor binding cite of AFP. A three-component delivery system including vector protein rAFP3D, PAMAM G2 dendrimer and antitumor antibiotic doxorubicin (Dox) was synthesized. The attachment of two dendrimer molecules to the vector protein did not affect the effectiveness of rAFP3D binding to AFP receptor on the surface of tumor cells nor the effectiveness of receptor-mediated endocytosis. Dox was conjugated with G2 via cis-aconitic anhydride (acid labile linker). The in vitro Dox release study showed that the conjugate was stable at neutral pH but was labile at pH<6. The Dox release was correlated with the intracellular distribution of conjugate in tumor cells. The rAFP3D-G2-Dox conjugate demonstrated a high cytotoxic activity against human ovarian adenocarcinoma cell lines: Dox-sensitive SKOV3 cells and Dox-resistant SKVLB cells and was low-toxic against human peripheral blood lymphocytes. Based on our findings, we may conclude that it is possible to significantly increase the effectiveness of Dox delivery to tumor cells by using the targeted delivery system comprising the recombinant third domain rAFP3D as a vector molecule.
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1. Yabbarov N. G. и др. A new system for targeted delivery of doxorubicin into tumor cells // Journal of Controlled Release. 2013. Т. 168. № 2. С. 135–141.
RIS |
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TY - JOUR

DO - 10.1016/j.jconrel.2013.03.007

UR - http://dx.doi.org/10.1016/j.jconrel.2013.03.007

TI - A new system for targeted delivery of doxorubicin into tumor cells

T2 - Journal of Controlled Release

AU - Yabbarov, N.G.

AU - Posypanova, G.A.

AU - Vorontsov, E.A.

AU - Obydenny, S.I.

AU - Severin, E.S.

PY - 2013

DA - 2013/06

PB - Elsevier BV

SP - 135-141

IS - 2

VL - 168

SN - 0168-3659

ER -

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@article{Yabbarov_2013,

doi = {10.1016/j.jconrel.2013.03.007},

url = {https://doi.org/10.1016%2Fj.jconrel.2013.03.007},

year = 2013,

month = {jun},

publisher = {Elsevier {BV}},

volume = {168},

number = {2},

pages = {135--141},

author = {N.G. Yabbarov and G.A. Posypanova and E.A. Vorontsov and S.I. Obydenny and E.S. Severin},

title = {A new system for targeted delivery of doxorubicin into tumor cells},

journal = {Journal of Controlled Release}

}

MLA
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Yabbarov, N. G., et al. “A New System for Targeted Delivery of Doxorubicin into Tumor Cells.” Journal of Controlled Release, vol. 168, no. 2, June 2013, pp. 135–41. Crossref, https://doi.org/10.1016/j.jconrel.2013.03.007.