Development of Injectable Thermosensitive Nanocomposite Hydrogel for Ratiometric Drug Delivery to Treat Drug Resistant Chondrosarcoma In Vivo

Author:

Zhu Jiahui12,Wei Ran3,Hu Guang2,Wang Hui4,Wang Wenbin15,Wang Haiqiang12,Huang Jidan16,Wang Yu12,Li Yujing14ORCID,Meng Huan1ORCID

Affiliation:

1. CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience National Center for Nanoscience and Technology Beijing 100190 China

2. School of Pharmacy and Bioengineering Chongqing University of Technology Chongqing 400054 China

3. Musculoskeletal Tumor Center, Beijing Key Laboratory of Musculoskeletal Tumor Peking University People's Hospital Beijing 100044 China

4. School of Medical Technology Beijing Institute of Technology Beijing 100081 China

5. Academy of Medical Sciences The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan 450052 China

6. USTC Life Sciences and Medicine University of Science and Technology of China Hefei 230000 China

Abstract

AbstractChondrosarcoma(CS), a prevalent primary malignant bone tumor, frequently exhibits chemotherapy resistance attributed to upregulated anti‐apoptosis pathways such as the Bcl‐2 family. In this manuscript, a new strategy is presented to augment chemosensitivity and mitigate systemic toxicity by harnessing a nano‐enabled drug delivery hydrogel platform. The platform utilizes “PLGA‐PEG‐PLGA”, an amphiphilic triblock copolymer combining hydrophilic polyethylene glycol (PEG) and hydrophobic polylactide glycolide (PLGA) blocks, renowned for its properties conducive to crafting a biodegradable, temperature‐sensitive hydrogel. This platform is tailored to encapsulate a ratiometrically designed dual‐loaded liposomes containing a first‐line chemo option for CS, Doxorubicin (Dox), plus a calculated amount of small molecule inhibitor for anti‐apoptotic Bcl‐2 pathway, ABT‐737. In vitro and in vivo evaluations demonstrate successful Bcl‐2 suppression, resulting in the restoration of Dox sensitivity, evident through impeded tumor growth and amplified necrosis rates at the tumor site. This delivery system showcases remarkable thermal responsiveness, injectability, and biodegradability, all finely aligned with the clinical demands of CS treatment. Collectively, this study introduces a transformative avenue for tackling drug resistance in CS chemotherapy, offering significant clinical potential.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Beijing Institute of Technology Research Fund Program for Young Scholars

Chinese Academy of Sciences

Publisher

Wiley

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