纳米载体
LNCaP公司
前列腺癌
阿霉素
靶向给药
药物输送
癌症研究
癌症
抗体
前列腺
癌细胞
脂质体
药品
药理学
材料科学
医学
化疗
免疫学
纳米技术
内科学
作者
Simona Dostálová,Tereza Černá,David Hynek,Zuzana Koudelková,Tomáš Vaculovič,Pavel Kopel,Jan Hraběta,Zbyněk Heger,Markéta Vaculovičová,Tomáš Eckschlager,Marie Stiborová,Vojtěch Adam
标识
DOI:10.1021/acsami.6b04286
摘要
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 μM) 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.
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