Development of camptothecin nano-prodrugs based on trimethyl lock groups toward selective drug release in cancer cells-Reference-Cited by-同舟云学术

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Development of camptothecin nano-prodrugs based on trimethyl lock groups toward selective drug release in cancer cells

Published:2022-08 Issue: Volume:103 Page:153989
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Shibata Aki,Koseki Yoshitaka,Tanita Keita,Suzuki Ryuju,Dao Anh Thi Ngoc,Kasai Hitoshi

Funder

Japan Society for the Promotion of Science

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference31 articles.

1. Evolution of the scientific literature on drug delivery: A 1974–2015 bibliometric study

2. MM-398 (nanoliposomal irinotecan): emergence of a novel therapy for the treatment of advanced pancreatic cancer

3. Tyrosine kinase inhibitor prodrug-loaded liposomes for controlled release at tumor microenvironment

4. Encapsulation of doxorubicin prodrug in heat-triggered liposomes overcomes off-target activation for advanced prostate cancer therapy

5. Tumor targeting via EPR: Strategies to enhance patient responses

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Anticancer nano-prodrugs with drug release triggered by intracellular dissolution and hydrogen peroxide response;Chemical Communications;2024

2. Carrier-free nano-prodrugs for minimally invasive cancer therapy;Nanoscale;2024

3. Recent Advances in Anti-Infective Compounds Produced by Endophytic Fungi;Fungi Bioactive Metabolites;2024

4. Camptothecin-based prodrug nanomedicines for cancer therapy;Nanoscale;2023

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