Detailed Information on Publication Record
2016
Site-Directed Conjugation of Antibodies to Apoferritin Nanocarrier for Targeted Drug Delivery to Prostate Cancer Cells
DOSTALOVA, Simona, Tereza CERNA, David HYNEK, Zuzana KOUDELKOVA, Tomáš VACULOVIČ et. al.Basic information
Original name
Site-Directed Conjugation of Antibodies to Apoferritin Nanocarrier for Targeted Drug Delivery to Prostate Cancer Cells
Authors
DOSTALOVA, Simona (203 Czech Republic), Tereza CERNA (203 Czech Republic), David HYNEK (203 Czech Republic), Zuzana KOUDELKOVA (203 Czech Republic), Tomáš VACULOVIČ (203 Czech Republic, belonging to the institution), Pavel KOPEL (203 Czech Republic), Jan HRABETA (203 Czech Republic), Zbyněk HEGER (203 Czech Republic), Markéta VACULOVICOVA (203 Czech Republic), Tomáš ECKSCHLAGER (203 Czech Republic), Marie STIBOROVA (203 Czech Republic) and Vojtěch ADAM (203 Czech Republic, guarantor)
Edition
ACS APPLIED MATERIALS & INTERFACES, WASHINGTON, AMER CHEMICAL SOC, 2016, 1944-8244
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10406 Analytical chemistry
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 7.504
RIV identification code
RIV/00216224:14310/16:00093826
Organization unit
Faculty of Science
UT WoS
000378195000018
Keywords in English
antibodies; apoferritin; doxorubicin; nanomedicine; targeted drug delivery
Tags
International impact, Reviewed
Změněno: 5/3/2020 11:51, Mgr. Marie Šípková, DiS.
Abstract
V originále
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.
Links
LQ1601, research and development project |
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