ACS Macro Letters · 2023 · 12 citations · 28 references
PharmacyPharmaceuticsPharmacologyDrug DeliveryNanoparticle Drug DeliveryPolymer ChemistryNanocarriers For TherapeuticsNanomaterials For Drug DeliveryNanoparticle Delivery SystemsNanoparticle DesignPolymeric Drug Delivery SystemsPolymeric NanoparticlesBlock Copolymer MicellesCyclic Carbonate SynthesisDrug Delivery NanocarriersDrug-loaded MicellesMicellesNanoparticlesPolymeric MicellesPolymeric Nanocarriers
We report the synthesis of block copolymers of monomethoxylated polyethylene glycol and poly(glycerol carbonate) (mPEG- b -PGC) via the ring-opening polymerization of benzyl glycidyl ether, monomethoxylated polyethylene glycol, and carbon dioxide using a cobalt salen catalyst. The resulting block copolymers display high polymer/cyclic carbonate selectivity (>99%) and, if two oxirane monomers are used, random incorporation into the polymer feed. The resulting diblock mPEG- b -PGC polymer shows promise as a nanocarrier for surfactant-free, sustained chemotherapeutic delivery. mPEG- b -PGC, with paclitaxel conjugated to the pendant primary alcohol of the glycerol polymer backbone, readily forms 175 nm diameter particles in solution and contains 4.6 wt % paclitaxel (PTX), which is released over 42 days. The mPEG- b -PGC polymer itself is noncytotoxic, whereas the PTX-loaded nanoparticles are cytotoxic to lung, breast, and ovarian cancer cell lines.
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Cytotoxic studies of paclitaxel (Taxol®) in human tumour cell lines
J. Liebmann, J A Cook, Claudia A. Lipschultz et al. · British Journal of Cancer · 1993 · 424 citations · Full text
Medicine, Oncology, Pharmacology +14