Drug intelligence / Profile preview

gemcitabine-polyacetal conjugate

Development stage
Preclinical
Lead developer
Columbia University
Modality
Small Molecules, Biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Percutaneous, Intratumoral
01

Overview

Gemcitabine-polyacetal conjugate is an experimental polymer-drug conjugate designed for the targeted treatment of pancreatic cancer. Developed by researchers at Columbia University, the therapy consists of the cytotoxic nucleoside analog gemcitabine covalently linked to a temperature-responsive polyacetal polymer. This delivery system is engineered to remain inert at physiological pH but undergoes selective degradation and drug release in the acidic microenvironment characteristic of solid tumors (e.g., pH 6.8). By sequestering gemcitabine in an inactive form until it reaches the tumor site, the conjugate aims to improve drug penetration into stroma-rich hypovascular tumors while minimizing systemic toxicity and off-target effects.

Other names
gemcitabine-polyacetal drug conjugatepolyacetal-gemcitabine conjugate
02

Targets

POLE (DNA polymerase epsilon)DNARNR (Ribonucleotide reductase)

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