In recent years miscellaneous smart micro/nanosystems that respond to various exogenous/endogenous stimuli including temperature, magnetic/electric field, mechanical force, ultrasound/light irradiation, redox potentials, and biomolecule concentration have been developed for targeted delivery and release of encapsulated therapeutic agents such as drugs, genes, proteins, and metal ions specifically at their required site of action. Owing to physiological differences between malignant and normal cells, or between tumors and normal tissues, pH-sensitive nanosystems represent promising smart delivery vehicles for transport and delivery of anticancer agents. Furthermore, pH-sensitive systems possess applications in delivery of metal ions and biomolecules such as proteins, insulin, etc., as well as co-delivery of cargos, dual pH-sensitive nanocarriers, dual/multi stimuli-responsive nanosystems, and even in the search for new solutions for therapy of diseases such as Alzheimer’s. In order to design an optimized system, it is necessary to understand the various pH-responsive micro/nanoparticles and the different mechanisms of pH-sensitive drug release. This should be accompanied by an assessment of the theoretical and practical challenges in the design and use of these carriers.
Treatment of glioblastoma, the most common and aggressive type of primary brain tumors, is a major medical challenge and the development of new alternatives requires simple yet realistic models for these tumors. In vitro spheroid models offer attractive platforms to mimic the tumor behavior in vivo and have thus, been increasingly applied for assessment of drug efficacy in various tumors. The aim of this study was to produce and characterize size-controlled U251 glioma spheroids towards application in glioma drug evaluation studies. To this end, we fabricated agarose hydrogel microwells with cylindrical shape and diameters of 70–700 μm and applied these wells without any surface modification for glioma spheroid formation. The resultant spheroids were homogeneous in size and shape, exhibited high cell viability (> 90%), and had a similar growth rate to that of natural brain tumors. The final size of spheroids depended on cell seeding density and microwell size. The spheroids’ volume increased linearly with the cell seeding density and the rate of this change increased with the well size. Lastly, we tested the therapeutic effect of an anti-cancer drug, Di-2-pyridylketone-4,4-dimethyl-3-thiosemicarbazone (Dp44mT) on the resultant glioma spheroids and demonstrated the applicability of this spheroid model for drug efficacy studies.
Starch based scaffolds are considered as promising biomaterials for bone tissue engineering. In this study, a highly porous starch/polyvinyl alcohol (PVA) based nanocomposite scaffold with a gradient pore structure was made by incorporating different bio-additives, including citric acid, cellulose nanofibers, and hydroxyapatite (HA) nanoparticles. The scaffold was prepared by employing unidirectional and cryogenic freeze-casting and subsequently freeze-drying methods. Fourier transform infrared (FTIR) spectroscopy confirmed the cross-linking of starch and PVA molecules through multiple esterification phenomenon in presence of citric acid as a cross-linking agent. Field emission scanning electron microscopy (FE-SEM) observations showed formation of aligned lamellar pores with a gradient pore width in the range of 80 to 292 µm, which well meets the pore size requirement for bone regeneration, and also well dispersion of cellulose and HA nanofillers within the scaffold matrix. Based on the mechanical testing results, the cellulose-HA reinforced scaffold possesses sufficient compressive modulus and yield strength for non-load bearing applications in the dry state; and also it presents fast responsive shape recovery in the wet state. According to in-vitro assessments, apatite phase mineralization was extensively induced in the presence of HA nanoparticles as heterogeneous nucleating sites. Also, it was revealed that cellulose and HA nanofillers decelerate and accelerate the scaffold biodegradation rate, respectively. MTT assay proved good cytocompatibility of the nanocomposite scaffold with osteoblast cells. Finally, it was shown that the introduced scaffold provides a suitable platform for the cells adhesion.
Electrochemical devices that transform electrical energy to mechanical energy through an electrochemical process have numerous applications ranging from robotics and micropumps to microlenses and bioelectronics. To date, achievement of large deformation strains and fast responses remains challenging for electrochemical actuators wherein drag forces restrict the device motion and electrode materials/structures limit the ion transportation. Results for electrochemical actuators, electrochemical mass transfers, and electrochemical dynamics made from organic semiconductors (OSNTs) are reported. The OSNTs device exhibits high-performance with fast ion transport and accumulation in liquid and gel-polymer electrolytes. This device demonstrates an impressive performance, including low power consumption/ strain, a large deformation, fast response, and excellent actuation stability. This outstanding performance stems from the enormous effective surface area of nanotubes that facilitates ion transport and accumulation resulting in high electroactivity and durability. Experimental studies of motion and mass transport are utilized along with the theoretical analysis for a variable-mass system to establish the dynamics of the device and to introduce a modified form of Euler-Bernoulli's equation for the OSNTs. Ultimately, a state-of-theart miniaturized device composed of multiple microactuators for potential biomedical applications is demonstrated. This work provides new opportunities for next-generation actuators that can be utilized in artificial muscles and biomedical devices.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.