Related Experiment Video
Updated: May 1, 2026

Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique
Published on: September 20, 2011
Smart nanoconjugates of functionalized cashew gum for targeted co-delivery of curcumin and paclitaxel
Raelle F Gomes1, Álvaro V Vasconcelos1, Maria J M Carneiro1
1Polymer Laboratory, Department of Organic and Inorganic Chemistry, Federal University of Ceará, Fortaleza, Brazil.
Abstract:
Carboxymethylated cashew gum (CMCG) was successfully conjugated with curcumin (CUR) forming an acid-sensitive prodrug. Paclitaxel (PTX) was then encapsulated in CMCG-CUR nanoparticles (CMCG-CUR/PTX) via hydrophobic interaction with CUR. These nanoparticles were designed for co-delivery of CUR and PTX to tumor cells. FTIR and 1H NMR confirmed the structures of the CMCG-CUR and CMCG-CUR/PTX. Self-assembly into nanoparticles, was observed, with fluorescence spectroscopy, dynamic light scattering and atomic force microscopy indicating good dispersion and diameters of 190 nm (CMCG-CUR) and 181 nm (CMCG-CUR/PTX). Drug loading capacity (DLC) values for CUR in CMCG-CUR and CMCG-CUR/PTX nanoparticles were 7.0 and 3.0 % respectively. Nanoparticles promoted the protection of CUR against degradation processes and exhibited a pH-responsive and controlled release of PTX and CUR. Furthermore, the nanoparticles exhibited antitumor activity against the CT-26 (murine colorectal carcinoma) cells and 4T1 (murine breast carcinoma) cells line and reduced cytotoxicity against non-tumor cells (RAW 264.7). The cellular uptake study showed that the nanoparticles were readily taken up by CT-26 cells. Taken together, obtained data suggest that the pH-responsive CMCG-CUR/PTX nanoparticle would be an effective carrier for simultaneous delivery of CUR and PTX to CT-26 tumor cells.
Related Concept Videos
Modified-Release Drug Delivery Systems: Site-Targeted
Site-Targeted Drug Delivery Systems: Polymeric Carriers

