Ion guiding assisting microneedle patch system and method for delivering biological macromolecular drugs into brain
A bio-macromolecule and micro-needle sticker technology, applied in drug devices, micro-needles, and devices introduced into the body, etc., can solve the problems of low concentration of drugs entering the brain, unguaranteed dosage, and patient discomfort, and achieve self-regulation. Administration time and dose, no adverse reactions and side effects, improved safety and efficacy
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Embodiment 1
[0044] Example 1 Preparation of an ion-assisted microneedle patch system for delivering biomacromolecular drugs into the brain
[0045] According to the experimental group settings set in Table 1, green fluorescent protein-labeled aFGF (acidic fibroblast growth factor) was used as the research object. First, glutamic acid is mixed with propylene glycol (mass ratio 1:1), added to distilled water to prepare an aqueous solution of 1% (mass percentage) glutamic acid, mixed with 10 μM green fluorescent protein-labeled aFGF, dissolved and placed in the weak tank of the delivery device. In the reservoir of the acidic aqueous solution. Arginine is mixed with propylene glycol (mass ratio 1:1), and added to distilled water to prepare a 1% (mass percentage) arginine aqueous solution, which is placed in the liquid reservoir of the weakly alkaline aqueous solution of the delivery device.
[0046] The preparation of the control group was carried out with reference to the experimental group...
Embodiment 2
[0052] Example 2 Application effect of an ion-assisted microneedle patch system for delivering biomacromolecular drugs into the brain
[0053] The second embodiment of the present invention uses the scheme of Example 1 to carry out animal experiments. Several New Zealand white rabbits are taken. After anesthesia, each group of ion-assisted microneedle patch systems is fixed on the upper lip or both sides of the nose of the animal face. The experimental group and control group set up in Table 1 are processed, and the same method is operated every other day, and the same method is administered for a total of 3 times (i.e. 1, 3, 5 days of administration). And on the 10th day, the skull was opened, the brain tissue was separated, and fluorescence imaging was performed to observe the green fluorescence intensity of the brain tissue. The fluorescence intensity was divided into 5 grades, and the experimental group and the control group were compared and analyzed to promote the aFGF la...
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