Application of apolipoprotein D (ApoD) in preparation of Parkinson's disease medicament, ApoD preparation and preparation method thereof
A Parkinson's disease and drug technology, applied in the field of apolipoprotein D drug research, can solve the problems of less drug development and underutilized medicinal value, etc., to improve the targeting of brain tissue, prolong the circulation time in the body, The effect of improving sustained release properties
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Embodiment 1
[0035] The present embodiment provides a kind of preparation method of the ApoD oral preparation for the treatment of Parkinson's disease, and its steps are as follows:
[0036] 1. Preparation of inner layer liposomes:
[0037] Take 30mmol·L-1 lecithin and 45mmol·L-1 cholesterol ethanol solution, evaporate under reduced pressure in rotary motion, form a phospholipid bilayer film on the inner surface of the container, then add ApoD, protease inhibitor PMSF, ether solution, and conduct ultrasonic Stir for 12 minutes at a temperature of 16° C. to obtain a liposome solution; the dosage of ApoD is 10-500 mg / ml. The concentration of protease inhibitor PMSF is 1-100ug / ml. Then, slowly inject the PEG aqueous solution with a syringe while stirring in the liposome solution, the injection speed is 1ml / min, finally obtain liposome I, carry out freeze-drying process to obtain liposome I freeze-dried powder.
[0038] 2. Immunomodification of inner liposomes:
[0039]The transferrin recep...
Embodiment 2
[0044] The present embodiment provides a kind of preparation method for the oral preparation of ApoD for the treatment of Parkinson's disease, the experimental steps are as follows:
[0045] 1. Preparation of inner layer liposomes:
[0046] Evaporate an equal volume of 35mmol·L-1 lecithin and 40mmol·L-1 cholesterol in ethanol under reduced pressure to form a phospholipid bilayer film on the inner surface of the container, then add an appropriate amount of ApoD, protease inhibitor PMSF, and ether solution , ultrasonically stirred for 15 min at a temperature of 10° C. to obtain a liposome solution. Then, slowly inject the PEG aqueous solution with a syringe while stirring in the liposome solution, the injection speed is 1.5ml / min, finally obtain liposome I, carry out freeze-drying process to obtain liposome I freeze-dried powder.
[0047] 2. Immunomodification of inner liposomes:
[0048] The transferrin receptor antibody OX26 was subjected to thiol treatment, and the method w...
Embodiment 3
[0053] The present embodiment provides a kind of preparation method of the ApoD oral preparation for the treatment of Parkinson's disease, and its steps are as follows:
[0054] 1. Preparation of inner layer liposomes:
[0055] Take 50mmol·L-1 lecithin and 30mmol·L-1 cholesterol ethanol solution, and evaporate under reduced pressure by rotating to form a phospholipid bilayer film on the inner surface of the container; add ApoD, protease inhibitor PMSF, ether solution, and carry out ultrasonic stirring 10min, the temperature is 20 ℃, obtain liposome solution; Next, slowly inject PEG aqueous solution with syringe while stirring into liposome solution, injection speed is 2ml / min, finally obtain liposome I, carry out freeze-drying treatment to obtain Liposome I lyophilized powder. Other conditions are identical with embodiment 1.
[0056] 2. Immunomodification of inner liposomes:
[0057] The transferrin receptor antibody OX26 was subjected to thiol treatment, and the method wa...
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