2020
DOI: 10.1007/s13204-020-01261-w
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Gram scale synthesis of QD450 core–shell quantum dots for cellular imaging and sorting

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Cited by 14 publications
(12 citation statements)
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“…CdS/ZnS with OA as capping are prepared as described in the established protocol 46 , 47 and labeled as , CdSe/ZnS with DPP as capping agent were prepared as described with minor modifications in the synthesis process 46 , 48 and labeled as ,. The CdSe/ZnS with TOP capped QD’s were prepared as described with minor modifications in the synthesis process 49 51 and labeled as .…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…CdS/ZnS with OA as capping are prepared as described in the established protocol 46 , 47 and labeled as , CdSe/ZnS with DPP as capping agent were prepared as described with minor modifications in the synthesis process 46 , 48 and labeled as ,. The CdSe/ZnS with TOP capped QD’s were prepared as described with minor modifications in the synthesis process 49 51 and labeled as .…”
Section: Methodsmentioning
confidence: 99%
“…QD’s are primarily modified with MPA through biphasic ligand exchange to attain active –COO - group on the surface of QD’s. These QD MPA are allowed for modification with NH 2 -(PEG) 8 -COOH (PEG) and finally conjugated with SA molecules with EDC/NHS coupling chemistry as mentioned in the earlier reports 46 . The conjugation of PEG and SA on the surface of QDs was successfully achieved by adding an equimolar mixture of 1 mM EDC and NHS which was prepared in the MES (2-(N-morpholino) ethane sulfonic acid) buffer at 4 °C (all the reactions are to be worked under the chilling condition to maintain the integrity of the PEG and SA).…”
Section: Methodsmentioning
confidence: 99%
“…CdSe/ZnS/ZnS with OA capping are prepared as described in the established protocoll 28,35 nd labelled as QD 450 , CdSe/ZnS with DPP as capping agent are prepared as described with minor changes in the synthesis process 28,36 and labelled as QD 525 , CdSe/ZnS with TOP capped QDs are prepared as described with minor changes in the synthesis process [37][38][39] and labelled as QD 615 . To make QDs for bio application, the surface of the QDs is modi ed through ligand exchange by MPA following conjugation with nPEGc and SA modi cations with EDC/NHS coupling as mentioned in the previous reports 28 . The QDs with nPEGc-SA are puri ed by dialysis to remove any free/excess nPEGc and SA.…”
Section: Methodsmentioning
confidence: 99%
“…The synthesized nPEGc functionalized quantum dots (QDs) include QD 450 , QD 525 , and QD 615 based on respective uorescence intensities were puri ed and made EDC/NHS coupling to provide an active amide bond between the QDs to the streptavidin 28 . The successful streptavidin conjugation with reference to the uorescence intensities, respective QDs is represented in gure S1, where showed the relative uorescence intensities of blue, green, and red hues.…”
Section: Antibody Conjugation With Quantum Dotsmentioning
confidence: 99%
“…[43] Several reports have raised concerns about the toxicity of cadmium-based QDs in biological applications. [42,[44][45][46][47] The discovery of cadmium ion (Cd 2+ ) presence showed it to be the primary cause of cytotoxicity. To counteract the toxicity of QDs, a coating of inorganic material was utilized to coat the core QDs, preventing oxidation and photobleaching of the core cadmium.…”
Section: =Cysmentioning
confidence: 99%