Tellurium-containing compound, method for preparing tellurium-gold nanoparticles by using tellurium-containing compound and application of tellurium-gold nanoparticles in preparation of anti-tumor drugs
A tellurium compound, HO-EGY- technology, applied in the field of nano-biomedicine, can solve the problems of complicated synthesis steps, high price, toxic and side effects, etc.
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Embodiment 1
[0053] Embodiment 1: Based on HO-EG 6 -C 6 -Te-C 6 -EG 6 Preparation of gold tellurium nanoparticles of -OH (bis(17-hydroxy-3,6,9,12,15-pentaoxoacetyl) 4,4'-telluryl dihexanoate) and chloroauric acid and its preparation Application in antineoplastic drugs
[0054] (1) 88.7mg HO-EG 6 -C 6 -Te-C 6 -EG 6 -OH was dissolved in 1 mL of deionized water to obtain component A, and 9.6 mg of chloroauric acid was dissolved in 1 mL of deionized water to obtain component B. Fully mix component A and component B in a 5mL reaction bottle to obtain a uniform mixed system. The above mixed system was lyophilized, rinsed three times with 2 mL of dichloromethane, and dried with nitrogen to obtain gold tellurium nanoparticles. where HO-EG 6 -C 6 -Te-C 6 -EG 6 The synthesis process of -OH molecule is as follows:
[0055] Dissolve 5.64g of hexaethylene glycol in a round-bottomed flask containing 100mL of dichloromethane, and add 4.27g of 6-bromohexanoyl chloride dropwise to the round-b...
Embodiment 2
[0065] Embodiment 2: Based on HO-EG 4 -C 6 -Te-C 6 -EG 4 Tellurium of -OH (bis(2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl) 4,4'-telluryl dihexanoate) with chloroauric acid Preparation of gold nanoparticles and its application in the preparation of antitumor drugs
[0066] The difference between this embodiment and Example 1 lies in the preparation of gold tellurium nanoparticles, and all the other steps are the same as in Example 1, specifically:
[0067] 142.0mg HO-EG 4 -C 6 -Te-C 6 -EG 4 -OH was dissolved in 1 mL of ethylene glycol to obtain component A, and 2.6 mg of chloroauric acid was dissolved in 1 mL of dimethyl sulfoxide to obtain component B. Fully mix component A and component B in a 5mL reaction bottle to obtain a uniform mixed system. The above mixed system was dried in a vacuum oven, rinsed three times with 2 mL of tetrahydrofuran, and dried in a vacuum oven to obtain gold tellurium nanoparticles. where HO-EG 4 -C 6 -Te-C 6 -EG 4 The synthesis proce...
Embodiment 3
[0069] Embodiment 3: Based on HO-EG 2 -C 6 -Te-C 6 -EG 2 Preparation of tellurium gold nanoparticles of -OH (bis(2-(2-hydroxyethoxy)ethyl) 6,6'-telluryl dihexanoate) and chloroauric acid and its application in the preparation of antitumor drugs
[0070] The difference between this embodiment and Example 1 lies in the preparation of gold tellurium nanoparticles, and all the other steps are the same as in Example 1, specifically:
[0071] 17.8mg HO-EG 2 -C 6 -Te-C 6 -EG 2 -OH was dissolved in 1 mL of methanol to obtain component A, and 2.0 mg of gold chloride was dissolved in 1 mL of deethylene glycol to obtain component B. Fully mix component A and component B in a 5mL reaction bottle to obtain a uniform mixed system. The above mixed system was dried in a vacuum oven to remove the solvent, rinsed three times with 2 mL of ethyl acetate, and dried with nitrogen to obtain gold tellurium nanoparticles. where HO-EG 2 -C 6 -Te-C 6 -EG 2 The synthesis process of -OH molec...
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