Preparation method of CdTe quantum dot nanometer medicine carrying system carrying daunorubicin and gambogic acid
A technology of daunorubicin and nano-drug-loading, which is applied in the directions of pharmaceutical formulations, medical preparations without active ingredients, and medical preparations containing active ingredients, etc., to achieve the effects of prolonged action time, narrow distribution and low immunogenicity
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Embodiment 1
[0037] A preparation method of a co-loaded daunorubicin and gambogic acid CdTe quantum dot nano drug-loading system is characterized in that the method comprises the following steps:
[0038] (1) Functional modification of cadmium telluride (CdTe) with polymer polyethylene glycol (PEG): use 0.23 mmol of Al 2 Te 3 and 15 mL of 0.5M H 2 SO 4 The reaction produces H 2 Te standby; 2.3mmol of Cd (ClO 4 ) 2 ·H 2 O was dissolved in 125 mL of ultrapure water, and 5.5 mmol of cysteamine hydrochloride (Cys) was added dropwise under stirring conditions, then the pH value was adjusted to 5.9, and Ar gas was introduced for 30 minutes, and then the prepared H was added dropwise. 2 Te, the mixture was refluxed for 10 minutes to 9 hours to control the growth of CdTe quantum dots, and finally added 1.84 mmol of high molecular polymer polyethylene glycol (PEG), and reacted for 24 hours to obtain a modified cadmium telluride (CdTe) solution;
[0039] (2) Dissolve daunorubicin (DNR) with a...
Embodiment 2
[0042] A preparation method of a co-loaded daunorubicin and gambogic acid CdTe quantum dot nano drug-loading system is characterized in that the method comprises the following steps:
[0043] (1) Functional modification of cadmium telluride (CdTe) with polymer polyethylene glycol (PEG): use 0.23 mmol of Al 2 Te 3 and 15 mL of 0.5M H 2 SO 4 The reaction produces H 2 Te standby; 2.3mmol of Cd (ClO 4 ) 2 ·H 2 O was dissolved in 125 mL of ultrapure water, and 5.5 mmol of cysteamine hydrochloride (Cys) was added dropwise under stirring conditions, then the pH value was adjusted to 5.9, and Ar gas was introduced for 30 minutes, and then the prepared H was added dropwise. 2 Te, the mixture was refluxed for 10 minutes to 9 hours to control the growth of CdTe quantum dots, and finally added 1.84 mmol of high molecular polymer polyethylene glycol (PEG), and reacted for 24 hours to obtain a modified cadmium telluride (CdTe) solution;
[0044] (2) Dissolve daunorubicin (DNR) with a...
Embodiment 3
[0047] A preparation method of a co-loaded daunorubicin and gambogic acid CdTe quantum dot nano drug-loading system is characterized in that the method comprises the following steps:
[0048] (1) Functional modification of cadmium telluride (CdTe) with polymer polyethylene glycol (PEG): use 0.23 mmol of Al 2 Te 3 and 15 mL of 0.5M H 2 SO 4 The reaction produces H 2 Te standby; 2.3mmol of Cd (ClO 4 ) 2 ·H 2 O was dissolved in 125 mL of ultrapure water, and 5.5 mmol of cysteamine hydrochloride (Cys) was added dropwise under stirring conditions, then the pH value was adjusted to 5.9, and Ar gas was introduced for 30 minutes, and then the prepared H was added dropwise. 2 Te, the mixture was refluxed for 10 minutes to 9 hours to control the growth of CdTe quantum dots, and finally added 1.84 mmol of high molecular polymer polyethylene glycol (PEG), and reacted for 24 hours to obtain a modified cadmium telluride (CdTe) solution;
[0049] (2) Dissolve daunorubicin (DNR) with a...
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