2019
DOI: 10.1016/j.actbio.2019.02.035
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Synthesis and assessment of drug-eluting microspheres for transcatheter arterial chemoembolization

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Cited by 22 publications
(7 citation statements)
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“…This is because, for the microsphere with the same size, the number and density of binding sites are the same, higher drug concentration accompanying more drug molecules requires more time for completion of drug loading, resulting in a slower encapsulation rate and longer time for equilibrium drug loading. [52] Figure 8 shows the drug elution behavior of PASP-AMA 0.30 microspheres loaded with different amounts (55, 90, and 120 mg g −1 ) of DOX•HCl in saline. The three samples showed similar releasing trends which can be divided into two stages (Figure 8a).…”
Section: Drug-loading Kinetics Of the Microspheresmentioning
confidence: 99%
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“…This is because, for the microsphere with the same size, the number and density of binding sites are the same, higher drug concentration accompanying more drug molecules requires more time for completion of drug loading, resulting in a slower encapsulation rate and longer time for equilibrium drug loading. [52] Figure 8 shows the drug elution behavior of PASP-AMA 0.30 microspheres loaded with different amounts (55, 90, and 120 mg g −1 ) of DOX•HCl in saline. The three samples showed similar releasing trends which can be divided into two stages (Figure 8a).…”
Section: Drug-loading Kinetics Of the Microspheresmentioning
confidence: 99%
“…This can be explained by the fact that the drug release is controlled by the ion exchange mechanism. [52,53] Thus, once the microspheres were exposed to the ion-rich saline solution, the drugs bound on the surface layer of the microspheres were easily replaced by the cations in the medium, and quickly released into the medium, yielding burst release phenomenon. After that, the cations in the medium continuously and slowly penetrated the interior of the microsphere to exchange the bound DOX•HCl, resulting in its slow and continuous diffusion into the medium.…”
Section: Drug-loading Kinetics Of the Microspheresmentioning
confidence: 99%
“…8 Recently, with the increasing demand in clinical, the study of degradable microspheres has become a hot topic. 1 For example, gelatin sponge particles, poly(ethylene glycol) methacrylate (PEGMA) hydrolyzable microspheres, and polysaccharides microspheres combine a Institute of Smart Biomedical Materials, School of Materials Science and with the functions of radiopaque, 9 drug delivery, 10 and on-demand degradable 11 were studied. The size and size distribution of microspheres are critical factors when treating different diseases with embolization.…”
Section: Introductionmentioning
confidence: 99%
“…Over the previous few years, there has been increasing interest in the radiolucent permeability of embolic agents, and the problem of nonvisibility can be addressed to some extent by way of bodily mixing the embolic agent with an iodinated contrast agent and injecting it into the target artery. 4 However, the principal dangers of this approach consist of numerous aspects. First, the contrast agent can effortlessly separate from the embolic agent, leading to blurred imaging and misdiagnosis.…”
mentioning
confidence: 99%
“…The properties of the embolic agent play an important part in the property of TAE treatment. Over the previous few years, there has been increasing interest in the radiolucent permeability of embolic agents, and the problem of nonvisibility can be addressed to some extent by way of bodily mixing the embolic agent with an iodinated contrast agent and injecting it into the target artery . However, the principal dangers of this approach consist of numerous aspects.…”
mentioning
confidence: 99%