Drug intelligence / Profile preview

liposomal curcumin + temozolomide

Development stage
Unknown
Lead developer
SignPath Pharma
Modality
Nanoparticles → Drug Delivery Systems, Small Molecules
Administration
Intravenous (liposomal Curcumin), Oral (temozolomide)
01

Overview

**Liposomal curcumin + temozolomide** is a combination therapy under clinical investigation for high-grade gliomas, especially glioblastoma. Liposomal curcumin is a nanoparticle-formulated version of curcumin designed to enhance bioavailability and delivery to tumor tissue, while temozolomide is an oral alkylating chemotherapy agent. Curcumin modulates multiple signaling pathways in cancer cells (e.g., cell proliferation, apoptosis, cell cycle, autophagy, oxidative stress), and has been shown to sensitize glioblastoma cells to temozolomide, promoting synergistic effects. Temozolomide induces cytotoxicity primarily by methylating DNA at the O6 and N7 positions of guanine, leading to DNA damage and apoptosis in tumor cells. Combination in a liposomal (nanoparticle) delivery system improves the pharmacokinetics of both drugs, increasing their solubility, stability, and ability to cross biological barriers, potentially maximizing antitumor efficacy and overcoming resistance [1][2][3][4][5].

Brand names
LipoCurc + temozolomide
Other names
LC + TMZliposomal curcumin + TMZ
02

Targets

AKT1 (Proto-oncogene serine/threonine-protein kinase Akt1)NF-κBSTAT3 (Signal Transducer and Activator of Transcription 3)HDAC (HDAC family)DNMT3B (DNA (cytosine-5)-methyltransferase 3B)AGT (O6-methylguanine-DNA methyltransferase)DNA

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