J 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

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
Name: CEITEC 2020 (Acronym: CEITEC2020)
Investor: Ministry of Education, Youth and Sports of the CR