Therapeutic Efficacy Evaluation of Pegylated Liposome Encapsulated With Vinorelbine Plus


Journal

Cancer genomics & proteomics
ISSN: 1790-6245
Titre abrégé: Cancer Genomics Proteomics
Pays: Greece
ID NLM: 101188791

Informations de publication

Date de publication:
Historique:
received: 30 09 2019
revised: 04 11 2019
accepted: 05 11 2019
entrez: 29 12 2019
pubmed: 29 12 2019
medline: 3 6 2020
Statut: ppublish

Résumé

In precision therapy, liposomal encapsulated chemotherapeutic drugs have been developed to treat cancers by achieving higher drug accumulation in the tumor compared to normal tissues/organs. We developed a novel chemoradiotherapeutic approach via nanoliposomes conjugated with vinorelbine (VNB) and Pharmacokinetic results showed that the area under the curve (AUC) of PEGylated liposomes was about 17-fold higher than that of the free radioisotope. Tumor growth inhibition by The tumors in NOD/SCID mice bearing HT-29/tk-luc xenografts were significantly suppressed by

Sections du résumé

BACKGROUND/AIM OBJECTIVE
In precision therapy, liposomal encapsulated chemotherapeutic drugs have been developed to treat cancers by achieving higher drug accumulation in the tumor compared to normal tissues/organs.
MATERIALS AND METHODS METHODS
We developed a novel chemoradiotherapeutic approach via nanoliposomes conjugated with vinorelbine (VNB) and
RESULTS RESULTS
Pharmacokinetic results showed that the area under the curve (AUC) of PEGylated liposomes was about 17-fold higher than that of the free radioisotope. Tumor growth inhibition by
CONCLUSION CONCLUSIONS
The tumors in NOD/SCID mice bearing HT-29/tk-luc xenografts were significantly suppressed by

Identifiants

pubmed: 31882552
pii: 17/1/61
doi: 10.21873/cgp.20168
pmc: PMC6937124
doi:

Substances chimiques

Antineoplastic Agents, Phytogenic 0
Indium Radioisotopes 0
Liposomes 0
Polyethylene Glycols 3WJQ0SDW1A
Indium-111 E9NGC49E0T
Vinorelbine Q6C979R91Y

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

61-76

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

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Auteurs

Yi-Chun Chien (YC)

Department of Medical Imaging and Radiological Sciences, I-Shou University, Jiaosu Village, Kaohsiung, Taiwan, R.O.C.
School of Medicine, I-Shou University, Jiaosu Village, Kaohsiung, Taiwan, R.O.C.

Ying-Hsiang Chou (YH)

Department of Radiation Oncology, Chung Shan Medical University Hospital, Taichung, Taiwan, R.O.C.
Department of Medical Imaging and Radiological Sciences, Chung Shan Medical University, Taichung, Taiwan, R.O.C.

Wei-Hsun Wang (WH)

Department of Orthopedic Surgery, Changhua Christian Hospital, Changhua, Taiwan, R.O.C.
Department of Medical Imaging and Radiology, Shu-Zen Junior College of Medicine and Management, Kaohsiung, Taiwan, R.O.C.

John Chun-Hao Chen (JC)

Department of Radiation Oncology, Mackay Memorial Hospital, New Taipei City, Taiwan, R.O.C.

Wen-Shin Chang (WS)

Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.

Chia-Wen Tsai (CW)

Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.

DA-Tian Bau (DT)

Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C. jjhwang@ym.edu.tw johnjjhwang@gmail.com datian@mail.cmuh.org.tw artbau2@gmail.com.
Department of Bioinformatics and Medical Engineering, Asia University, Taichung, Taiwan, R.O.C.

Jeng-Jong Hwang (JJ)

Department of Medical Imaging and Radiological Sciences, Chung Shan Medical University, Taichung, Taiwan, R.O.C. jjhwang@ym.edu.tw johnjjhwang@gmail.com datian@mail.cmuh.org.tw artbau2@gmail.com.
Department of Medical Imaging, Chung Shan Medical University Hospital, Taichung, Taiwan, R.O.C.

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