Abstract:Core-shell nanoparticles that exhibit superparamagnetic properties and stability as colloidal suspensions have been widely employed for medical imaging, diagnosis, and targeted drug delivery. These materials are engineered for spatial guidance using an external magnetic field and are capable of transporting therapeutic payloads such as clinical drugs and protein structures. They can be tagged with fluorescent dyes and quantum dots as spectroscopic markers; and can generate an acute influx of heat when exposed … Show more
“…Multiple approaches have been employed to utilize highfrequency magnetic fields in drug delivery and hyperthermia for tumour ablation 7,8,61,62 . One of the most promising designs uses MNPs to release therapeutic cargos from micro/nano hollow capsules (for example, liposomes) [63][64][65] or solid particles (for example, polymer based) [66][67][68] .…”
Section: Static and Low-frequency Magnetic Fields Static And Low-frequency Magnetic Fields Can Be Generated By Magnets Or Electromagnetsmentioning
confidence: 99%
“…Scalability for mass production. There is a rich literature on proof of concepts for various elegant DDSs that are fabricated from complex/long reaction routes and exotic precursors 7,70 . However, their scalability for mass production needs to be studied further.…”
Section: Biocompatibilitymentioning
confidence: 99%
“…On the basis of advances in electronics, actuators and materials engineering, powerful wireless on-demand drug delivery techniques have been created. These approaches exploit exogenous stimuli, including acoustic waves [1][2][3][4] , electric fields 5,6 , magnetic fields 7,8 and electromagnetic radiation [9][10][11] , to trigger the drug carriers. Depending on the material and design of the drug carrier, the physiological characteristics of the target site, and the pharmacokinetics and pharmacodynamics of the cargo, each of these stimuli has particular applications.…”
“…Multiple approaches have been employed to utilize highfrequency magnetic fields in drug delivery and hyperthermia for tumour ablation 7,8,61,62 . One of the most promising designs uses MNPs to release therapeutic cargos from micro/nano hollow capsules (for example, liposomes) [63][64][65] or solid particles (for example, polymer based) [66][67][68] .…”
Section: Static and Low-frequency Magnetic Fields Static And Low-frequency Magnetic Fields Can Be Generated By Magnets Or Electromagnetsmentioning
confidence: 99%
“…Scalability for mass production. There is a rich literature on proof of concepts for various elegant DDSs that are fabricated from complex/long reaction routes and exotic precursors 7,70 . However, their scalability for mass production needs to be studied further.…”
Section: Biocompatibilitymentioning
confidence: 99%
“…On the basis of advances in electronics, actuators and materials engineering, powerful wireless on-demand drug delivery techniques have been created. These approaches exploit exogenous stimuli, including acoustic waves [1][2][3][4] , electric fields 5,6 , magnetic fields 7,8 and electromagnetic radiation [9][10][11] , to trigger the drug carriers. Depending on the material and design of the drug carrier, the physiological characteristics of the target site, and the pharmacokinetics and pharmacodynamics of the cargo, each of these stimuli has particular applications.…”
“…Externally triggerable drug delivery systems show the ability to enhance therapeutic efficacy, while reducing side effects [33,34]. In particular, the unique optical, physical and magnetic properties of inorganic NPs are exploited to reach a selective drug release induced by an external stimulus, such as the application of a magnetic field or light irradiation [35,36]. Light is a versatile and easily tuned external stimulus that can provide spatio-temporal control.…”
Silver (Ag)-grafted PMA (poly-methacrylic acid, sodium salt) nanocomposite loaded with sorafenib tosylate (SFT), an anticancer drug, showed good capability as a drug carrier allowing on-demand control of the dose, timing and duration of the drug release by laser irradiation stimuli. In this study, the preparation of Ag-PMA capsules loaded with SFT by using sacrificial silica microparticles as templates was reported. A high drug loading (DL%) of ∼13% and encapsulation efficiency (EE%) of about 76% were obtained. The photo-release profiles were regulated via the adjustment of light wavelength and power intensity. A significant improvement of SFT release (14% vs. 21%) by comparing SFT-Ag-PMA capsules with Ag-PMA colloids under the same experimental conditions was observed. Moreover, an increase of drug release by up to 35% was reached by tuning the laser irradiation wavelength near to Ag nanoparticles’ surface plasmon resonance (SPR). These experimental results together with more economical use of the active component suggest the potentiality of SFT-Ag-PMA capsules as a smart drug delivery system.
“…Good examples are nanoparticles with a coreshell structure are magnetoliposomes (maghemite nanocrystals enclosed in liposomes). The release of the drug occurs due to the heat generated by the carrier under the influence of an oscillating magnetic field [28]. Heat sensitive media, including micelles, polymers, and hydrogels, change their conformation, solubility, or hydrophilicity at a given temperature, leading to the release of the drug.…”
Titanium oxide nanoparticles modified with D-(+)-mannose were obtained. In the process of their formation, they were conjugated with an active substance (tadalafil). The physicochemical properties of the obtained products were assessed, and the size and electrokinetic potential were determined using a dynamic light scattering technique. X-ray diffractometry was applied in order to define the crystalline properties, and Fourier-transform infrared spectroscopy was used to confirm the formation of the desired products. It was possible to obtain TiO2 coated with D-(+)-mannose. The average size of nanoparticles was between 230 and 268 nm. The release of the active substance from the product over a time period of three hours was assessed against the reference material, which was not modified by D-(+)-mannose. The results indicate that covering titanium oxide nanoparticles with the modifying substance favours a slower rate of release for the active substance, which is the desired effect from a pharmacological point of view. The releasing of active substance from modified products was even 68% slower than that from the reference product. These modified titanium oxides are promising materials that may have found an application as drug carriers.
Graphic Abstract
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