2013
DOI: 10.1016/j.biomaterials.2013.08.079
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A polyvalent aptamer system for targeted drug delivery

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Cited by 122 publications
(102 citation statements)
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“…Although the sensitivities of some aptamer-based nanosensors for thrombin are superior to that of the H 2 O 2 /AR-TBA 29 -T 30 -CuO/Cu 2 O NP probe [46][47][48][49][50][51][52], our labelfree fluorescence-based assay for thrombin is relatively simple, rapid, and economical. We suspect that bivalent Cu NP-conjugated aptamers may further improve the binding affinity and sensitivity for thrombin [53][54][55][56].…”
Section: Specificity and Sensitivitymentioning
confidence: 99%
“…Although the sensitivities of some aptamer-based nanosensors for thrombin are superior to that of the H 2 O 2 /AR-TBA 29 -T 30 -CuO/Cu 2 O NP probe [46][47][48][49][50][51][52], our labelfree fluorescence-based assay for thrombin is relatively simple, rapid, and economical. We suspect that bivalent Cu NP-conjugated aptamers may further improve the binding affinity and sensitivity for thrombin [53][54][55][56].…”
Section: Specificity and Sensitivitymentioning
confidence: 99%
“…Using the RCA method and the sgc8 aptamer sequence as a circular template, a polyvalent sgc8 aptamer, termed Poly-Aptamer-Drug, was synthesized. 74 It was determined that the Dox payload capacity of the polyvalent sgc8 aptamer increased tenfold, as compared to the monovalent sgc8 aptamer. Moreover, because of their 40-fold greater binding affinity, the Poly-Aptamer-Drug conjugates were more effective than their monovalent counterparts in targeting and killing leukemia cells.…”
Section: Aptamer-mediated Targeted Therapiesmentioning
confidence: 99%
“…Moreover, because of their 40-fold greater binding affinity, the Poly-Aptamer-Drug conjugates were more effective than their monovalent counterparts in targeting and killing leukemia cells. 74 …”
Section: Aptamer-mediated Targeted Therapiesmentioning
confidence: 99%
“…The simple assembly largely relies on the structural property of the drug and its noncovalent association with specific DNA sequences. One classical example is the anthracycline class of anti-cancer drugs, such as doxorubicin (Dox), which prefer to bind to a repetitive sequence (5'-CG-3') in aptamers and to intercalate within the GC pairs to form physical conjugates at certain molar ratios 24. Under these circumstances, the aptamer acts both as a guide and as a cargo for drug delivery (Fig.…”
Section: General Profile Of Aptamers and Relevant Significancementioning
confidence: 99%
“…(H) The biodistribution discrepancy between non-targeted (left) and Muc1-targeted (right) QD-Dox conjugates shows active tumor targeting by preferentially accumulating in subcutaneous ovarian tumors. Adapted from 21, 24, 26.…”
Section: Figurementioning
confidence: 99%