Chemotherapy is the main treatment for cancer therapy. However, its anti-tumor efficiency is always impaired by the poor bioavailability and low tumor accumulation of chemotherapeutic drugs. The variation between the tumor microenvironment and normal tissue has been recognized as an effective tool to improve drug anti-tumor efficiency. Herein, we developed an injectable, pH-responsive, self-assembled drug-peptide hydrogel (MTX-KKFKFEFEF(DA)) for highly efficient local tumor chemotherapy with few side effects. The small molecule drug, methotrexate (MTX), and pH-responsive linker, 2,3-dimethylmaleic anhydride (DA), were facilely conjugated onto the chain of the KKFKFEFEF peptide an amidation reaction. The negatively charged drug-peptide (pH 7.4) can be activated to be positive and achieve a sol-gel phase transition under an acidic microenvironment (pH 6.5) both and , resulting in highly efficient cellular uptake and endocytosis capacities. Moreover, the anti-tumor therapeutic effect revealed that the MTX-KKFKFEFEF(DA) hydrogel exhibits long-term tumor retention time, much better tumor inhibition rate and negligible side effects after intratumoral injection into breast tumor-bearing mice. Therefore, this study reveals a versatile strategy for fabricating a pH-responsive drug-peptide hydrogel to improve the chemotherapeutic efficacy of drugs in cancer treatment.
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http://dx.doi.org/10.1039/d1bm01788h | DOI Listing |
Int J Biol Macromol
January 2025
Department of Microbiology, College of Life Science, Key Laboratory for Agriculture Microbiology, Shandong Agricultural University, Tai'an 271018, PR China; School of Pharmacy, the Key Laboratory of Medical Antibacterial Materials of Shandong Province, Binzhou Medical University, Yantai 264003, PR China. Electronic address:
Chronic wounds caused by microbial infection have emerged as a major challenge on patients and medical health system. Bacterial cellulose (BC) characterized by its excellent biocompatibility and porous network, holds promise for addressing complex wound issues. However, lack of inherent antibacterial activity and cross-linking sites in the molecular network of BC have constrained its efficacy in hydrogel design and treatment of bacterial-infected wounds.
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January 2025
School of Materials Science and Engineering, Henan University of Science and Technology, Luoyang 471023, PR China. Electronic address:
Bacterial infections and inflammation severely impede wound healing. Here, we developed a zwitterionic hydrogel incorporating MOF/GOx for pH-responsive, controlled drug release. The multifunctional hydrogel embedded with MOF/GOx was successfully prepared through the Schiff base reaction between the copolymer poly[(2-methacryloyloxyethyl phosphorylcholine)-co-(4-formylphenyl methacrylate)] (PMF) and the branched polyethylenimine (PEI) modified by the zwitterionic monomer ((4-hydroxyphenyl)sulfonyl)(4-(trimethylammonio)butanoyl)amide (AB), which possessed excellent injectable and self-healing ability, a highly sensitive and reversible responsiveness to pH changes, and good biocompatibility.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Department of Gastroenterology, Changhai Hospital, Naval Medical University, No. 168 Changhai Road, Shanghai 200433, PR China. Electronic address:
In this paper, a pH-sensitive chitosan-grafted phenylboronic acid (CS-BA)/polyvinyl alcohol (PVA) hydrogel was constructed based on dynamic borate bonding for loading chemotherapeutic drug cisplatin (CDDP) and divalent Cu (CS-BA/PVA-Cu-CDDP). The hydrogel can respond and degrade specifically in the simulative acidic tumor microenvironment (TME), and the released Cu can deplete glutathione (GSH) in tumor cells and generate Cu. It is worth noting that, Cu can further catalyze the Fenton-like reaction to generate cancer cell-toxic hydroxyl radicals (OH•).
View Article and Find Full Text PDFColloids Surf B Biointerfaces
December 2024
Department of Pharmacy, The Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan 646000, China. Electronic address:
Breast cancer remains one of the most prevalent and deadly cancers among women worldwide, necessitating the development of more effective and comprehensive treatment strategies. In this study, we successfully synthesized mesoporous polydopamine (MPDA) with photothermal effects for the co-delivery of the chemotherapeutic drug doxorubicin (DOX) and the immune adjuvant imiquimod (R837), resulting in the development of a multifunctional nanoplatforms termed MDR. MDR displayed excellent photothermal conversion efficiency and pH-responsive drug release behavior.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
Marine College, Shandong University, Weihai, Shandong 264209, China. Electronic address:
Managing wounds infected with multi-drug-resistant (MDR) bacteria remains a significant public health challenge in clinical settings. While multifunctional hydrogels are commonly employed to treat skin infections, there is a scarcity of hydrogels that effectively combine cationic guar gum (CG) with both potent antimicrobial and safe therapeutic actions. This study introduces a novel pH responsive, dual-dynamically crosslinked hydrogel (CFC-PDA/Ag), synthesized by crosslinking CG with polydopamine (PDA)-coated silver nanozymes (PDA/PM-AgNPs).
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