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Site-Directed Conjugation of Antibodies to Apoferritin Nanocarrier for Targeted Drug Delivery to Prostate Cancer Cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62156489%3A43210%2F16%3A43909573" target="_blank" >RIV/62156489:43210/16:43909573 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/16:10324764 RIV/00216208:11130/16:10324764 RIV/00216224:14310/16:00093826 RIV/00216305:26620/16:PU119673 RIV/00064203:_____/16:10324764

  • Result on the web

    <a href="http://dx.doi.org/10.1021/acsami.6b04286" target="_blank" >http://dx.doi.org/10.1021/acsami.6b04286</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acsami.6b04286" target="_blank" >10.1021/acsami.6b04286</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Site-Directed Conjugation of Antibodies to Apoferritin Nanocarrier for Targeted Drug Delivery to Prostate Cancer Cells

  • Original language description

    Herein, we describe a novel approach for targeting of ubiquitous protein apoferritin (APO)-encapsulating doxorubicin (DOX) to prostate cancer using antibodies against prostate specific membrane antigen (PSMA). The conjugation of anti-PSMA antibodies and APO was carried out using HWRGWVC heptapeptide, providing their site-directed orientation. The prostate cancer-targeted and nontargeted nanocarriers were tested using LNCaP and HUVEC cell lines. A total of 90% of LNCaP cells died after treatment with DOX (0.25 mu M) or DOX in nontargeted and prostate-cancer-targeted APO, proving that the encapsulated DOX toxicity for LNCaP cells remained the same. Free DOX showed higher toxicity for nonmalignant cells, whereas the toxicity was lower after treatment with the same dosage of APO-encapsulated DOX (APODOX) and even more in prostate-cancer-targeted APODOX. Hemolytic assay revealed exceptional hemocompatibility of the entire nanocarrier. The APO encapsulation mechanism ensures applicability using a wide variety of chemotherapeutic drugs, and the presented surface modification enables targeting to various tumors.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2016

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    ACS applied materials &amp; interfaces

  • ISSN

    1944-8244

  • e-ISSN

  • Volume of the periodical

    8

  • Issue of the periodical within the volume

    23

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    14430-14441

  • UT code for WoS article

    000378195000018

  • EID of the result in the Scopus database

    2-s2.0-84975299987