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Cited by 10 publications
(2 citation statements)
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“…The value of the bimolecular quenching constant ( k q ) for C-Fe 3 O 4 NPs@OVA was measured by the relation k q = K sv /τ 0 and is found as 8.94, 7.66, 6.40 and 5.06 × 10 12 dm 3 mol −1 s −1 at 298, 303, 308, and 313 K, respectively. The calculated k q values for the complexation between C-Fe 3 O 4 NPs and OVA at all four temperatures were higher than the maximum diffusion collision rate constant (2.0 × 10 10 L mol −1 s −1 ), 12 revealing a strong complexation between them, probably a static type quenching mechanism. 34 In general, for a dynamic quenching process, the value of K SV increases due to the increase in number of collisions between the protein and NPs.…”
Section: Resultsmentioning
confidence: 71%
See 1 more Smart Citation
“…The value of the bimolecular quenching constant ( k q ) for C-Fe 3 O 4 NPs@OVA was measured by the relation k q = K sv /τ 0 and is found as 8.94, 7.66, 6.40 and 5.06 × 10 12 dm 3 mol −1 s −1 at 298, 303, 308, and 313 K, respectively. The calculated k q values for the complexation between C-Fe 3 O 4 NPs and OVA at all four temperatures were higher than the maximum diffusion collision rate constant (2.0 × 10 10 L mol −1 s −1 ), 12 revealing a strong complexation between them, probably a static type quenching mechanism. 34 In general, for a dynamic quenching process, the value of K SV increases due to the increase in number of collisions between the protein and NPs.…”
Section: Resultsmentioning
confidence: 71%
“…Proteins are generally non-toxic and can be used as delivery vehicles. 12 Proteins can also form coronas on the surface of NPs to enhance the targeting and delivery properties of protein-based NP drug delivery systems. Thus, protein-based NPs hold more advantages such as lower toxicity, reduced drug degradation, increased bioavailability of bioactive substances, and reduced clearance compared with NP-based drug delivery vehicles.…”
Section: Introductionmentioning
confidence: 99%