In contrast with traditional chemotherapy, controlled drug delivery systems provide many advantages. Herein, a thermosensitive star polymer pompon with a core-arm structure was synthesized using a grafting-on method as a thermo-responsive controlled release drug carrier. Single-chain cyclized/knotted poly tetra(ethylene glycol) diacrylate (polyTEGDA) was used as the hydrophobic core, and thermosensitive linear poly(-isopropylacrylamide--methylolacrylamide) (poly(NIPAM--NMA)) was selected as the hydrophilic arm. Below or above its lower critical solution temperature (LCST), the linear poly(NIPAM--NMA) grafted onto the polyTEGDA core adopted a stretched or curled status, respectively, then the drug could be loaded in or extruded out. The LCST of star polyTEGDA--poly(NIPAM--NMA) was adjusted to slightly above body temperature (37 °C). The antitumor drug doxorubicin (DOX) was successfully loaded into the pompons with a high loading capacity of 19.45%. The cumulative release of DOX from loaded pompons for 72 hours was 71% and 20.7% at 42 °C and 37 °C, respectively, indicating that the excellent temperature-controlled release characteristics result from the unique thermo-responsive extrusion effect. Moreover, DOX loaded polyTEGDA--poly(NIPAM--NMA) pompons achieved better antitumor ability against ovarian carcinoma SKOV3 cells at 42 °C compared with that at 37 °C. These results suggest that star polyTEGDA--poly(NIPAM--NMA) pompons have considerable promise as thermo-responsive controlled drug delivery carriers.
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http://dx.doi.org/10.1039/c8ra02117a | DOI Listing |
Nat Commun
March 2025
Department of Chemical Engineering, University of California Davis, Davis, CA, 95616, USA.
Granular materials transition between unjammed (deformable) and jammed (rigid) states when adjusting their packing density. Here, we report on experiments demonstrating that the same kind of phase transition can be alternatively achieved through temperature-controlled particle shape change. Using a confined system of randomly-packed rod-like particles made of shape memory alloy (SMA), we exploit that shape recovery of these bent rods with rising temperature at a constant packing density leads to a jammed state.
View Article and Find Full Text PDFDrug Deliv
December 2025
Department of Biomedical Engineering, Stevens Institute of Technology, Hoboken, NJ, USA.
A clinical need exists for more effective intravitreal (IVT) drug delivery systems (DDS). This study tested the hypothesis that a novel biodegradable, injectable microsphere-hydrogel drug delivery system loaded with aflibercept (aflibercept-DDS) would exhibit long-term safety and biocompatibility in a non-human primate (NHP) model. We generated aflibercept-loaded poly (lactic-co-glycolic acid) microparticles with a modified double emulsion technique then embedded them into a biodegradable, thermo-responsive poly (ethylene glycol)-co-(L-lactic-acid) diacrylate/N-isopropylacrylamide hydrogel.
View Article and Find Full Text PDFInt J Biol Macromol
February 2025
Department of Chemical and Biological Engineering, Gachon University, Seongnam 13120, Republic of Korea. Electronic address:
Hydroxypropyl cellulose (HPC) is a nonionic, thermo-responsive polymer with temperature-dependent phase behavior. This behavior can be modified by grafting molecular units and polymer brushes onto the cellulose backbone. However, the thermo-response of such modified celluloses under biological and environmental conditions, such as pH, has been scarcely reported.
View Article and Find Full Text PDFJ Colloid Interface Sci
May 2025
Department of Anesthesiology and Perioperative Medicine, Shanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Clinical Research Center for Anesthesiology and Perioperative Medicine, Translational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People's Hospital, School of Medicine, Tongji University, Shanghai 200434 PR China. Electronic address:
Inorganic nanoparticles serve as versatile nanoplatforms for efficient cancer diagnosis and therapy. However, their limited in vivo degradability and excretion rates may lead to various adverse effects. Furthermore, the cascade-controlled release of drugs remains a challenge.
View Article and Find Full Text PDFMacromol Rapid Commun
February 2025
Department of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, via Mancinelli 7, Milano, 20131, Italy.
Thermo-responsive polymers have emerged as a cutting-edge tool in nanomedicine, paving the way for innovative approaches to targeted drug delivery and advanced therapeutic strategies. These "smart" polymers respond to temperature changes, enabling controlled drug release in pathological environments characterized by high temperatures. By exploiting their unique phase transition, occurring at the lower or upper critical solution temperatures (LCST and UCST), these systems ensure localized therapeutic action, minimizing collateral damage to healthy tissues.
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