Double-sensitive disintegrating nano-sized vesica medicine carrier preparation and preparation method thereof
A nanovesicle, sensitive technology, applied in drug combinations, pharmaceutical formulations, anti-tumor drugs, etc., can solve the problems of inability to identify tumor sites and normal sites, inability to distinguish between intracellular and extracellular environments, etc. Availability, good biocompatibility, high stability effect
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Embodiment 1
[0035] Preparation of Amphiphilic Block Copolymers
[0036] (1) Preparation of Z-Lys NCA: Suspend 3 g, 23 mmol of benzyloxycarbonyl-protected lysine in 50 mL of anhydrous tetrahydrofuran (THF), dissolve 2.7 g, 9 mmol of triphosgene in 20 mL of anhydrous THF and Add dropwise to the above suspension under air protection, stir and heat to 50°C. Stop the reaction when the solution is clear and cool naturally, recrystallize 2 to 3 times with n-hexane / tetrahydrofuran (5:1, v:v), filter with suction, and dry under vacuum at room temperature to obtain the product Z-LysNCA powder;
[0037] (2)PzLL 5 Preparation: Dissolve 2mmol of ethylamine hydrochloride and 10mmol of Z-Lys NCA in 20mL of anhydrous N,N-dimethylformamide (DMF), carry out ring-opening polymerization reaction under argon protection, first ice React in the bath for 5h, then continue to react for 72h at room temperature, transfer the reaction solution into a dialysis bag (MWCO1KDa) for dialysis, freeze-dry to obtain polyl...
Embodiment 2
[0042] Preparation of Amphiphilic Block Copolymers
[0043] (1) Preparation of Z-Lys NCA: Suspend 3 g, 23 mmol of benzyloxycarbonyl-protected lysine in 50 mL of anhydrous tetrahydrofuran (THF), dissolve 2.7 g, 9 mmol of triphosgene in 20 mL of anhydrous THF and Add dropwise to the above suspension under air protection, stir and heat to 50°C. Stop the reaction when the solution is clear and cool naturally, recrystallize 2 to 3 times with n-hexane / tetrahydrofuran (5:1, v:v), filter with suction, and dry under vacuum at room temperature to obtain the product Z-LysNCA powder;
[0044] (2)PzLL 10 Preparation: Dissolve 2mmol of ethylamine hydrochloride and 20mmol of Z-Lys NCA in 20mL of anhydrous N,N-dimethylformamide (DMF), carry out ring-opening polymerization reaction under argon protection, first ice React in the bath for 5h, then continue to react for 72h at room temperature, transfer the reaction solution into a dialysis bag (MWCO1KDa) for dialysis, freeze-dry to obtain poly...
Embodiment 3
[0049] Preparation of drug carrier formulations with dual-sensitive disintegrable nanovesicles
[0050] Weigh 3 to 10 parts of PzLL 5 - Dissolve SS-NC-mPEG block copolymer in 3-10 parts of THF, use a peristaltic pump to drop 9-30 parts of deionized water into the above solution, weigh 3-10 parts of methotrexate and dissolve in In 1 to 3 parts of THF, weigh 3 to 10 parts of doxorubicin hydrochloride and dissolve in 1 to 3 parts of deionized water, respectively add to the water-oil mixed solution of the above polymer, stir for 5 to 8 hours, and then the above prepared The solution was transferred into a dialysis bag (MWCO3.5KDa) for dialysis in the dark, and the water was changed several times to remove organic solvents and unloaded drugs. After dialysis, freeze-dried to form a drug carrier powder preparation.
[0051] The dynamic mechanical light scattering diagram (particle size and distribution) of the prepared double-sensitive disintegrable nanovesicle drug carrier preparat...
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