DOSTALOVA, Simona, Tereza CERNA, David HYNEK, Zuzana KOUDELKOVA, Tomáš VACULOVIČ, Pavel KOPEL, Jan HRABETA, Zbyněk HEGER, Markéta VACULOVICOVA, Tomáš ECKSCHLAGER, Marie STIBOROVA and Vojtěch ADAM. Site-Directed Conjugation of Antibodies to Apoferritin Nanocarrier for Targeted Drug Delivery to Prostate Cancer Cells. ACS APPLIED MATERIALS & INTERFACES. WASHINGTON: AMER CHEMICAL SOC, 2016, vol. 8, No 23, p. 14430-14441. ISSN 1944-8244. Available from: https://dx.doi.org/10.1021/acsami.6b04286.
Other formats:   BibTeX LaTeX RIS
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
Original language English
Type of outcome Article in a journal
Field of Study 10406 Analytical chemistry
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 7.504
RIV identification code RIV/00216224:14310/16:00093826
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1021/acsami.6b04286
UT WoS 000378195000018
Keywords in English antibodies; apoferritin; doxorubicin; nanomedicine; targeted drug delivery
Tags AKR, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 5/3/2020 11:51.
Abstract
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 projectName: CEITEC 2020 (Acronym: CEITEC2020)
Investor: Ministry of Education, Youth and Sports of the CR
PrintDisplayed: 26/4/2024 10:37