Advancing biomedical applications of polyoxometalate-based metal–organic frameworks: from design to therapeutic potential
Lijin Wang,
Pengyu Dai,
Hongli Ma
et al.
Abstract:POMOFs (Polyoxometalate-based Metal-Organic Frameworks) are novel materials composed of POMs (Polyoxometalates) and MOFs (Metal-Organic Frameworks), which are widely used in biomedical research. Synthesis strategies for POMOF materials predominantly utilise liquid-phase...
“…Accordingly, mono-WD POM merits further in vivo research on imaging efficacy and possible toxicity, which may facilitate the development of inexpensive, safe, and innovative CT contrast agents for clinical application. Finally, future research directions could include the latest potential strategies like deep learning to improve novel contrast agents’ effectiveness and potential innovations in imaging and biomaterial technologies [ 49 , 50 , 51 ].…”
Polyoxotungstate nanoclusters have recently emerged as promising contrast agents for computed tomography (CT). In order to evaluate their clinical potential, in this study, we evaluated the in vitro CT imaging properties, potential toxic effects in vivo, and tissue distribution of monolacunary Wells–Dawson polyoxometalate, α2-K10P2W17O61.20H2O (mono-WD POM). Mono-WD POM showed superior X-ray attenuation compared to other tungsten-containing nanoclusters (its parent WD-POM and Keggin POM) and the standard iodine-based contrast agent (iohexol). The calculated X-ray attenuation linear slope for mono-WD POM was significantly higher compared to parent WD-POM, Keggin POM, and iohexol (5.97 ± 0.14 vs. 4.84 ± 0.05, 4.55 ± 0.16, and 4.30 ± 0.09, respectively). Acute oral (maximum-administered dose (MAD) = 960 mg/kg) and intravenous administration (1/10, 1/5, and 1/3 MAD) of mono-WD POM did not induce unexpected changes in rats’ general habits or mortality. Results of blood gas analysis, CO-oximetry status, and the levels of electrolytes, glucose, lactate, creatinine, and BUN demonstrated a dose-dependent tendency 14 days after intravenous administration of mono-WD POM. The most significant differences compared to the control were observed for 1/3 MAD, being approximately seventy times higher than the typically used dose (0.015 mmol W/kg) of tungsten-based contrast agents. The highest tungsten deposition was found in the kidney (1/3 MAD—0.67 ± 0.12; 1/5 MAD—0.59 ± 0.07; 1/10 MAD—0.54 ± 0.05), which corresponded to detected morphological irregularities, electrolyte imbalance, and increased BUN levels.
“…Accordingly, mono-WD POM merits further in vivo research on imaging efficacy and possible toxicity, which may facilitate the development of inexpensive, safe, and innovative CT contrast agents for clinical application. Finally, future research directions could include the latest potential strategies like deep learning to improve novel contrast agents’ effectiveness and potential innovations in imaging and biomaterial technologies [ 49 , 50 , 51 ].…”
Polyoxotungstate nanoclusters have recently emerged as promising contrast agents for computed tomography (CT). In order to evaluate their clinical potential, in this study, we evaluated the in vitro CT imaging properties, potential toxic effects in vivo, and tissue distribution of monolacunary Wells–Dawson polyoxometalate, α2-K10P2W17O61.20H2O (mono-WD POM). Mono-WD POM showed superior X-ray attenuation compared to other tungsten-containing nanoclusters (its parent WD-POM and Keggin POM) and the standard iodine-based contrast agent (iohexol). The calculated X-ray attenuation linear slope for mono-WD POM was significantly higher compared to parent WD-POM, Keggin POM, and iohexol (5.97 ± 0.14 vs. 4.84 ± 0.05, 4.55 ± 0.16, and 4.30 ± 0.09, respectively). Acute oral (maximum-administered dose (MAD) = 960 mg/kg) and intravenous administration (1/10, 1/5, and 1/3 MAD) of mono-WD POM did not induce unexpected changes in rats’ general habits or mortality. Results of blood gas analysis, CO-oximetry status, and the levels of electrolytes, glucose, lactate, creatinine, and BUN demonstrated a dose-dependent tendency 14 days after intravenous administration of mono-WD POM. The most significant differences compared to the control were observed for 1/3 MAD, being approximately seventy times higher than the typically used dose (0.015 mmol W/kg) of tungsten-based contrast agents. The highest tungsten deposition was found in the kidney (1/3 MAD—0.67 ± 0.12; 1/5 MAD—0.59 ± 0.07; 1/10 MAD—0.54 ± 0.05), which corresponded to detected morphological irregularities, electrolyte imbalance, and increased BUN levels.
“…Polyoxometalates (POMs) are a class of nanoscale inorganic polymetallic oxygen clusters that have a wide range of applications in catalysis, assembly, and biomedicine. 14–17 Recently, POMs have shown great potential in biomedical research fields due to their high biocompatibility, versatile structures, adjustable compositions, low cost and easy availability. 18,19 Particularly, the reduction of Mo-based POMs to molybdenum blue produces strong absorption in the NIR region, giving Mo-based POMs great potential as PTAs.…”
Section: Introductionmentioning
confidence: 99%
“…29,30 A variety of POM@MOF materials have been reported in recent years, and the corresponding preparation approaches are well-established. 17,31 POMs residing in the MOF cavity avoid the ineffective encapsulation caused by the surface loading, and maintain a high stability of the POM structure. 32 Notably, MOFs have adjustable inorganic metal centers, which endow them with intrinsic Fenton catalytic activity as a chemodynamic therapy (CDT) agent by tuning the metal center such as Fe and Cu.…”
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