2015
DOI: 10.1515/bmt-2015-0052
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Means to increase the therapeutic efficiency of magnetic heating of tumors

Abstract: Abstract:The treatment of tumors via hyperthermia has gained increased attention in the last years. Among the different modalities available so far, magnetic hyperthermia has the particular advantage of offering the possibility of depositing the heating source directly into the tumor. In this study, we summarized the present knowledge we gained on how to improve the therapeutic efficiency of magnetic hyperthermia using magnetic nanoparticles (MNPs), with particular consideration of the intratumoral infiltratio… Show more

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Cited by 11 publications
(9 citation statements)
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“… 18 The better heating efficiency of AFF-3 could be due to larger particle size and higher magnetic response of the SPIOs core to the applied AMFs via (i) enhanced π–π conjugation paths of the surface-attached 34DABA coating molecules due to the intrafunctional group attractions from their close structural orientation (refer Scheme 1 C(i)) (ii) improved anisotropy due to the formation of clusters/linear chains/loops of the SPIOs in the ferrofluids suspension due to the interfunctional group attractions (i.e., −NH 2 and −COOH groups, refer Scheme 1 C(ii)) and interparticle (i.e., particle–particle) interactions among different SPIOs (refer Scheme 1 C(iii)) and their parallel alignment to the applied AMF. 35 , 42 , 43 …”
Section: Resultsmentioning
confidence: 99%
“… 18 The better heating efficiency of AFF-3 could be due to larger particle size and higher magnetic response of the SPIOs core to the applied AMFs via (i) enhanced π–π conjugation paths of the surface-attached 34DABA coating molecules due to the intrafunctional group attractions from their close structural orientation (refer Scheme 1 C(i)) (ii) improved anisotropy due to the formation of clusters/linear chains/loops of the SPIOs in the ferrofluids suspension due to the interfunctional group attractions (i.e., −NH 2 and −COOH groups, refer Scheme 1 C(ii)) and interparticle (i.e., particle–particle) interactions among different SPIOs (refer Scheme 1 C(iii)) and their parallel alignment to the applied AMF. 35 , 42 , 43 …”
Section: Resultsmentioning
confidence: 99%
“…Until now, several attempts have been made for passive and active targeting of anticancer drugs, including self-triggered drug release as a result of a signal specific at the site of treatment (such as presence of specific enzymes or pH changes at the target site) or by externally activated drug release from the carrier (such as the application of light, temperature, magnetic field, and ultrasound) [14,15,16]. Among them, nanoparticle devices designed for hyperthermia treatment seem to gain increased attention in recent years [17,18,19]. Specifically, hyperthermia induced cancer therapy refers to a small temperature rise (from 41 to 45 °C) which leads to cell death through the initiation of a series of pro-apoptotic and apoptotic signaling cascades [20].…”
Section: Introductionmentioning
confidence: 99%
“…On one side it is worth to mention that the size of the synthesized particles falls within the range (200–400 nm) recalled as the suitable dimensions to ease its extravasation into the tumour37, size that has however been discarded as hyperthermia mediators based on their poorer heating efficiency3839. But those studies were based on spherical shape (either single-core or multicore) nanoparticles, and hence it becomes very important to check whether the elongated shape makes a difference.…”
mentioning
confidence: 99%