2022
DOI: 10.1016/j.bioadv.2022.212851
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PLGA-graphene quantum dot nanocomposites targeted against αvβ3 integrin receptor for sorafenib delivery in angiogenesis

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Cited by 10 publications
(11 citation statements)
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“…The band around 1570 cm −1 in βCD‐PEI‐GQD confirmed secondary amide bond formation between GQD and free amines of βCD‐PEI [51] . The fluorescence spectra (Figure 3) for both GQD and βCD‐PEI‐GQD aqueous dispersions exhibit the excitation at 440 nm that leads to emission at 526 nm, which is consistent with other studies [42,52] . Moreover, the observed peaks were sharp and intense, confirming the size uniformity and homogeneity of these two compounds.…”
Section: Resultssupporting
confidence: 86%
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“…The band around 1570 cm −1 in βCD‐PEI‐GQD confirmed secondary amide bond formation between GQD and free amines of βCD‐PEI [51] . The fluorescence spectra (Figure 3) for both GQD and βCD‐PEI‐GQD aqueous dispersions exhibit the excitation at 440 nm that leads to emission at 526 nm, which is consistent with other studies [42,52] . Moreover, the observed peaks were sharp and intense, confirming the size uniformity and homogeneity of these two compounds.…”
Section: Resultssupporting
confidence: 86%
“…[51] The fluorescence spectra (Figure 3) for both GQD and βCD-PEI-GQD aqueous dispersions exhibit the excitation at 440 nm that leads to emission at 526 nm, which is consistent with other studies. [42,52] Moreover, the observed peaks were sharp and intense, confirming the size uniformity and homogeneity of these two compounds. Furthermore, the higher fluorescence intensity of free GQD when compared to βCD-PEI-GQD nanocarrier indicated that GQD conjugation could reduce the intrinsic fluorescence property.…”
Section: Preparation Of βCd-pei-gqd Nanocarriersupporting
confidence: 52%
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“…The properties and chemical structure of some chemically synthesized anticancer drugs. ○ Poor solubility and bioavailability ○ Systemic toxicity ○ Rapid metabolism by dihydropyramidine dehydrogenase [11][12][13][14] Irinotecan (a topoisomerase I inhibitor) ○ Instability at physiological medium ○ Poor solubility ○ Severe side effects [15][16][17][18] Sorafenib (a multi-kinase inhibitor) ○ Poor solubility and bioavailability ○ Systemic side effects [19][20][21] 10-Hydroxycamptothecin (a member of the enzyme topoisomerase I inhibitor)…”
Section: Introductionmentioning
confidence: 99%