Convenient-type transdermal administration patch apparatus and preparation method thereof
A transdermal drug delivery, convenient technology, applied in the direction of drug devices, drug devices, pharmaceutical formulations, etc., can solve the problems of large volume, inconvenient use for patients, skin epidermal damage, etc., to achieve no skin damage, increase drug Effects of species and bioavailability, convenience of administration
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[0034] A preparation method of a portable transdermal drug delivery patch device, including preparation of a drug-containing patch, preparation of a drug-free patch, electrode installation, docking with a microcontroller b, docking with a communication control system, and delivery The drug initiation step is completed to complete the preparation of the portable transdermal drug delivery patch device; the specific steps are as follows:
[0035] (1) Preparation of drug-containing patch: the prepared drug-containing aqueous solution is injected into the middle part of the medical sand cotton, and the 0.2mm part around the sand cotton is attached to the medical tape, and the middle part of the sand cotton is attached to the protective paper On the top, the preparation of the drug-containing patch is completed;
[0036] (2) Preparation of drug-free patch: inject drug-free water or emulsion, gel, lipid, and microspheres into the middle part of the medical sand cotton, and stick the ...
Embodiment 1
[0046] Simulation experiment of porcine skin membrane transdermal administration in vitro:
[0047] (1) Choose a thickness of 300-500μm and an area of 1.0cm 2 The pigskin is placed between the supply cell of the Franz diffusion cell and the receiving cell of the Franz diffusion cell. The inner side of the pig skin membrane is facing the supply pool. The pool is filled with phosphate buffered saline to simulate blood circulation, and the temperature in the receiving pool is kept at 37°C to simulate human body temperature.
[0048] (2) Set the power: 0.1mA, and the power-on time is 24 hours according to the needs. Press the instrument power switch.
[0049] (3) After 24 hours, take a sample from the receiving pool, conduct drug analysis with a high-pressure liquid phase analyzer, and record.
[0050] Table 1 below shows the comparison information table between the analysis record of the antiemetic drug otansetron hydrochloride and the traditional patch transdermal delivery ...
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