Abstract:Targeted drug delivery with controlled rate is vital for therapeutic purpose especially for cancer therapy. Advanced biomaterials with the aid of nanotechnology have evolved as efficient drug delivery systems (DDS), providing a multi-functional platform for simultaneous therapeutic and diagnostic (theranostic) functions. This review discusses current advances in synthesis and applications of inorganic materials such as quantum dots, carbon nanotubes and graphene oxides for drug delivery. The strategies of surf… Show more
“…[1][2][3][4][5][6] Recent advances in block copolymer-based self-assembly [7][8][9] have led to the development of various magnetic DDS vehicles [1][2][3][4][5][6] such as polymeric nanocarriers into which prodrugs are often co-encapsulated with magnetic nanoparticles (MNPs), and these nanocarriers serve to shield the drug and to enable its magnetically guided imaging and local release in response to an alternating magnetic field (AMF).…”
Section: Introductionmentioning
confidence: 99%
“…However, the synthesis of MNPs with desirable magnetic properties for magnetic DDS platforms requires numerous steps to control the particles' core, diameter, anisotropy, suspension composition and surface coating, [1][2][3][4][5][6][7][8][9] and requires considerable care to avoid adverse effects in vivo. For example, an excessive dose of MNPs can cause oxidative stress-induced cell injury, 10,11 and slow degradation can lead to accumulation in the liver and other organs, 5,12 resulting in potentially fatal effects such as cardiovascular damage, blood clots and hypersensitivity.…”
Section: Introductionmentioning
confidence: 99%
“…Compared with traditional MNP-based methods that require additional co-loading processes of drug reagents, [1][2][3][4][5][6][7][8][9] the Fe(salen)-based system is unprecedented in that a single agent provides both the magnetic properties and anticancer activity. In other words, the Fe(salen) metal complexes, which have been used in the last few decades as asymmetric catalysts [17][18][19][20] and molecular magnets, 21,22 can be employed as magnetically guided anticancer agents.…”
Nanoparticulate agents for magnetic drug delivery systems (DDSs) have extensive applications in targeted drug delivery, contrast imaging and therapeutics. However, no simple synthetic method for magnetic DDS agents has been developed without the need to add magnetic nanoparticles. Here, we describe the one-step fabrication of 'all-in-one' magneto-assemblies using an 'inorganic-metal-salt-free' method, involving spontaneous self-assembly of the water-insoluble prodrug μ-oxo-bis(N,N 0 -ethylenebis (salicylideniminato)iron) [Fe(salen)] (magnetic core) with polypyrrole (PPy)-b-polycaprolactone (PCL) smart diblock copolymers. In the system, PCL serves as a heat-responsive core scaffold, and PPy serves as an electronic core-size controller and pH-responsive shell. This core-shell nanocomposite has a high-loading capacity (~90%), and the core size is tunable by incorporating albumin or gum arabic as bio-coating agents, which also provide colloidal stability, biocompatibility and thermo-stability. Fe(salen), which has intrinsic antitumor activity, also has ubiquitous magnetic properties, which are dramatically enhanced in these molecular assemblies with magnetic coupling. Moreover, these multifunctional nanoassemblies can be delivered magnetically, can serve as magnetic resonance imaging contrast agents, can generate magneto-hyperthermal effects and can enable magnetic field-triggered release of Fe(salen) molecules under acidic conditions.
“…[1][2][3][4][5][6] Recent advances in block copolymer-based self-assembly [7][8][9] have led to the development of various magnetic DDS vehicles [1][2][3][4][5][6] such as polymeric nanocarriers into which prodrugs are often co-encapsulated with magnetic nanoparticles (MNPs), and these nanocarriers serve to shield the drug and to enable its magnetically guided imaging and local release in response to an alternating magnetic field (AMF).…”
Section: Introductionmentioning
confidence: 99%
“…However, the synthesis of MNPs with desirable magnetic properties for magnetic DDS platforms requires numerous steps to control the particles' core, diameter, anisotropy, suspension composition and surface coating, [1][2][3][4][5][6][7][8][9] and requires considerable care to avoid adverse effects in vivo. For example, an excessive dose of MNPs can cause oxidative stress-induced cell injury, 10,11 and slow degradation can lead to accumulation in the liver and other organs, 5,12 resulting in potentially fatal effects such as cardiovascular damage, blood clots and hypersensitivity.…”
Section: Introductionmentioning
confidence: 99%
“…Compared with traditional MNP-based methods that require additional co-loading processes of drug reagents, [1][2][3][4][5][6][7][8][9] the Fe(salen)-based system is unprecedented in that a single agent provides both the magnetic properties and anticancer activity. In other words, the Fe(salen) metal complexes, which have been used in the last few decades as asymmetric catalysts [17][18][19][20] and molecular magnets, 21,22 can be employed as magnetically guided anticancer agents.…”
Nanoparticulate agents for magnetic drug delivery systems (DDSs) have extensive applications in targeted drug delivery, contrast imaging and therapeutics. However, no simple synthetic method for magnetic DDS agents has been developed without the need to add magnetic nanoparticles. Here, we describe the one-step fabrication of 'all-in-one' magneto-assemblies using an 'inorganic-metal-salt-free' method, involving spontaneous self-assembly of the water-insoluble prodrug μ-oxo-bis(N,N 0 -ethylenebis (salicylideniminato)iron) [Fe(salen)] (magnetic core) with polypyrrole (PPy)-b-polycaprolactone (PCL) smart diblock copolymers. In the system, PCL serves as a heat-responsive core scaffold, and PPy serves as an electronic core-size controller and pH-responsive shell. This core-shell nanocomposite has a high-loading capacity (~90%), and the core size is tunable by incorporating albumin or gum arabic as bio-coating agents, which also provide colloidal stability, biocompatibility and thermo-stability. Fe(salen), which has intrinsic antitumor activity, also has ubiquitous magnetic properties, which are dramatically enhanced in these molecular assemblies with magnetic coupling. Moreover, these multifunctional nanoassemblies can be delivered magnetically, can serve as magnetic resonance imaging contrast agents, can generate magneto-hyperthermal effects and can enable magnetic field-triggered release of Fe(salen) molecules under acidic conditions.
“…Various types of NPs have proven effective in numerous applications in medical diagnostics and treatment. 1 Briefly, the functions of nanomedicine include site-directed drug delivery, 2 imaging or tracing, 3 and even immunomodulation. 4 Moreover, the potential of multifunctional theranostic systems is similar to that of photothermal therapy (PTT) 5 or optical imaging applications 6 in addition to that of the direct influence of the NPs.…”
The metastasis of cancer cells is a vital aspect of disease progression and therapy. Although a few nanoparticles (NPs) aimed at controlling metastasis in cancer therapy have been reported, the NPs are normally combined with drugs, yet the direct therapeutic effects of the NPs are not reported. To study the direct influence of NPs on cancer metastasis, the potential suppression capacity of CuS@mSiO
2
-PEG NPs to tumor cell migration, a kind of typical photothermal NPs, was systemically evaluated in this study. Using CuS@mSiO
2
-PEG NP stimulation and a transwell migration assay, we found that the migration of HeLa cells was significantly decreased. This phenomenon may be associated with two classical proteins in metastasis: matrix metalloproteinase 2 (MMP-2) and matrix metalloproteinase 9 (MMP-9). In addition, the mechanism may closely associate with non-receptor tyrosine kinase protein (SRC)/focal adhesion kinase (FAK) signaling pathway which varies in vivo and in vitro. To confirm the differences in the expression of SRC and FAK, related inhibitors were studied for additional comparison. Also, the results indicated that even though the migration inhibition was closely related to SRC and FAK signaling pathway, there may be another unknown regulation mechanism existing and its metastasis inhibition was significant. Confirmed by long-term survival curve study, CuS@mSiO
2
-PEG NPs significantly reduced the metastasis of cancer cells and improved the survival rates of metastasis in a mouse model. Thus, we believe that the direct influence of NPs on cancer cell metastasis is a promising study topic.
“…Diversas propriedades podem ser obtidas mediante a funcionalização, como o uso de epóxido para o melhoramento da termoresistência e resistividade química 9 e o transporte de medicamentos. 10,11 Diversos estudos de funcionalização de nanotubos, através da adsorção de receptores aromáticos, úteis para complexar metais de forma seletiva, têm sido realizados com objetivo de obter materiais adsorventes de íons e catalisadores híbridos. 12 A associação do nanotubo com receptores específicos, mediante adsorção, permite estender ainda a aplicação desta molécula à construção de dispositivos com propriedades catalíticas, redox e fotovoltaicas.…”
Abstract:The adsorption of the N-2-(4-Amine-1,6-dihydro-1-methyl-5-nitroso 6-oxopirimidinil)-tris-(2aminoethyl) amine (AMNTRENH) over the carbon nanotube surface was studied in two different pH values. AMNTRENH was characterized through Langmuir isotherms for adsorption and dissociation. Electronic structure calculations of the interaction between the nanotube and AMNTRENH were carried out using several DFT functionals, including B3LYP, B97XD, B3PW91 and the semi-empirical method PM6.
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