» Articles » PMID: 36406213

Temperature- and PH-responsive Injectable Chitosan Hydrogels Loaded with Doxorubicin and Curcumin As Long-lasting Release Platforms for the Treatment of Solid Tumors

Overview
Date 2022 Nov 21
PMID 36406213
Authors
Affiliations
Soon will be listed here.
Abstract

The efficacy of treating solid tumors with chemotherapy is primarily hindered by dose-limiting toxicity due to off-target effects and the heterogeneous drug distribution caused by the dense extracellular matrix. The enhanced permeability and retention (EPR) effect within tumors restricts the circulation and diffusion of drugs. To overcome these obstacles, hydrogels formed at the tumor site have been proposed to promote drug accumulation, retention, and long-lasting release. We developed a thiolated chitosan (CSSH) hydrogel with a gelation point of 37°C. Due to the pH-sensitive characteristics of disulfides, the prepared hydrogel facilitated drug release in the acidic tumor environment. A drug release system composed of hydrophilic doxorubicin (Dox) and hydrophobic liposome-encapsulated curcumin (Cur-Lip) was designed to enhance the long-lasting therapeutic impacts and reduce adverse side effects. These composite gels possess a suitable gelation time of approximately 8-12 min under physiological conditions. The cumulative release ratio was higher at pH = 5.5 than at pH = 7.4 over the first 24 h, during which approximately 10% of the Dox was released, and Cur was released slowly over the following 24-120 h. Cell assays indicated that the Cur-Lip/Dox/CSSH gels effectively inhibited the growth of cancer cells. These -formed Cur-Lip/Dox gels with long-term drug release capabilities have potential applications for tumor suppression and tissue regeneration after surgical tumor resection.

Citing Articles

Hydrogel-based platforms for site-specific doxorubicin release in cancer therapy.

Zang C, Tian Y, Tang Y, Tang M, Yang D, Chen F J Transl Med. 2024; 22(1):879.

PMID: 39350207 PMC: 11440768. DOI: 10.1186/s12967-024-05490-3.


Polyphenolic Nanomedicine Regulating Mitochondria REDOX for Innovative Cancer Treatment.

Yang M, He Y, Ni Q, Zhou M, Chen H, Li G Pharmaceutics. 2024; 16(8).

PMID: 39204317 PMC: 11359087. DOI: 10.3390/pharmaceutics16080972.


Biomedical Trends in Stimuli-Responsive Hydrogels with Emphasis on Chitosan-Based Formulations.

Kruczkowska W, Galeziewska J, Grabowska K, Liese G, Buczek P, Klosinski K Gels. 2024; 10(5).

PMID: 38786212 PMC: 11121652. DOI: 10.3390/gels10050295.


Chitosan-Based Composites: Development and Perspective in Food Preservation and Biomedical Applications.

Kumar A, Yadav S, Pramanik J, Sivamaruthi B, Jayeoye T, Prajapati B Polymers (Basel). 2023; 15(15).

PMID: 37571044 PMC: 10421092. DOI: 10.3390/polym15153150.


Recent Development of Functional Chitosan-Based Hydrogels for Pharmaceutical and Biomedical Applications.

Taokaew S, Kaewkong W, Kriangkrai W Gels. 2023; 9(4).

PMID: 37102889 PMC: 10138304. DOI: 10.3390/gels9040277.


References
1.
Cappetta D, Rossi F, Piegari E, Quaini F, Berrino L, Urbanek K . Doxorubicin targets multiple players: A new view of an old problem. Pharmacol Res. 2017; 127:4-14. DOI: 10.1016/j.phrs.2017.03.016. View

2.
Albashari A, He Y, Zhang Y, Ali J, Lin F, Zheng Z . Thermosensitive bFGF-Modified Hydrogel with Dental Pulp Stem Cells on Neuroinflammation of Spinal Cord Injury. ACS Omega. 2020; 5(26):16064-16075. PMC: 7346236. DOI: 10.1021/acsomega.0c01379. View

3.
Raveendran R, Bhuvaneshwar G, Sharma C . Hemocompatible curcumin-dextran micelles as pH sensitive pro-drugs for enhanced therapeutic efficacy in cancer cells. Carbohydr Polym. 2015; 137:497-507. DOI: 10.1016/j.carbpol.2015.11.017. View

4.
Gou M, Men K, Shi H, Xiang M, Zhang J, Song J . Curcumin-loaded biodegradable polymeric micelles for colon cancer therapy in vitro and in vivo. Nanoscale. 2011; 3(4):1558-67. DOI: 10.1039/c0nr00758g. View

5.
Titov A, Valiullina A, Zmievskaya E, Zaikova E, Petukhov A, Miftakhova R . Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment. Cancers (Basel). 2020; 12(1). PMC: 7016531. DOI: 10.3390/cancers12010125. View