http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103224654-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K3-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08L5-08
filingDate 2013-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ce7216fd4955f51c4a7e41ea5c6f54f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c4e9f08b4761facb9c386068c8b6e166
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publicationDate 2015-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103224654-B
titleOfInvention Silver sulfide quantum dot-chitosan nanometer complex preparation method
abstract The present invention relates to a silver sulfide quantum dot-chitosan nanometer complex preparation method, which comprises: 1, dissolving a certain amount of chitosan or a derivative thereof in deionized water at a room temperature to prepare a chitosan aqueous solution with a concentration of 1-20 mg/mL or a chitosan derivative aqueous solution with a concentration of 1-20 mg/mL; 2, under a room temperature stirring condition, sequentially adding a chelating agent and a water soluble silver salt to the chitosan aqueous solution or the chitosan derivative aqueous solution, and carrying out a stirring reaction for 5-20 min; and 3, adding an alkali metal sulfide and a carboxyl compound to the product obtained from the step 2, carrying out a stirring reaction for 5-20 h, carrying out water dialysis and centrifugation on the obtained reaction product, washing sequentially by using absolute methanol and diethyl ether, and carrying out vacuum drying at a room temperature to obtain the silver sulfide quantum dot-chitosan nanometer complex. Compared with the nanometer complex in the prior art, the nanometer complex of the present invention has the following characteristics that: a nanometer complex with a near-infrared fluorescence imaging function is prepared by using a simple and easy-performing method, can be used for biological fluorescence imaging or as a fluorescent probe, and has characteristics of good biocompatibility, no physiological toxicity, and wide application prospects in biomedical fields.
priorityDate 2013-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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