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Tumor-Targeted Erythrocyte Membrane Nanoparticles for Theranostics of Triple-Negative Breast Cancer.
Choi, Moon Jung; Lee, Yeon Kyung; Choi, Kang Chan; Lee, Do Hyun; Jeong, Hwa Yeon; Kang, Seong Jae; Kim, Min Woo; You, Young Myoung; Im, Chan Su; Lee, Tae Sup; Park, Yong Serk.
Afiliación
  • Choi MJ; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Lee YK; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Choi KC; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Lee DH; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Jeong HY; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Kang SJ; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Kim MW; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • You YM; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Im CS; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
  • Lee TS; Division of RI Application, Korea Institute of Radiological and Medical Sciences (KIRAMS), Seoul 01812, Republic of Korea.
  • Park YS; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, Republic of Korea.
Pharmaceutics ; 15(2)2023 Jan 20.
Article en En | MEDLINE | ID: mdl-36839675
Triple-negative breast cancer (TNBC) cells do not contain various receptors for targeted treatment, a reason behind the poor prognosis of this disease. In this study, biocompatible theranostic erythrocyte-derived nanoparticles (EDNs) were developed and evaluated for effective early diagnosis and treatment of TNBC. The anti-cancer drug, doxorubicin (DOX), was encapsulated into the EDNs and diagnostic quantum dots (QDs) were incorporated into the lipid bilayers of EDNs for tumor bio-imaging. Then, anti-epidermal growth factor receptor (EGFR) antibody molecules were conjugated to the surface of EDNs for TNBC targeting (iEDNs). According to the confocal microscopic analyses and biodistribution assay, iEDNs showed a higher accumulation in EGFR-positive MDA-MB-231 cancers in vitro as well as in vivo, compared to untargeted EDNs. iEDNs containing doxorubicin (iEDNs-DOX) showed a stronger inhibition of target tumor growth than untargeted ones. The resulting anti-EGFR iEDNs exhibited strong biocompatibility, prolonged blood circulation, and efficient targeting of TNBC in mice. Therefore, iEDNs may be used as potential TNBC-targeted co-delivery systems for therapeutics and diagnostics.
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies / Screening_studies Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies / Screening_studies Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article