Biodegradable subcutaneous implant rod used for long-acting pressure reduction
A biodegradable, long-acting technology, applied in the direction of drug combination, drug delivery, active ingredients of heterocyclic compounds, etc., can solve the problems that the drug release dose is difficult to meet the control standards, the production process is not easy to achieve, and the blood pressure is unstable, etc., to achieve weakening Fluctuation of blood drug concentration, reduction of liver toxicity, and avoidance of direct stimulation
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Embodiment 1
[0025] Example 1 (According to the formula of this example, 110 implant rods can be produced, the diameter of the implant rod is 3mm, and the length is 40mm; the weight of each implant rod is 0.3g, and each rod contains 0.12g of raw material medicine)
[0026] A biodegradable subcutaneous implant rod for long-term antihypertensive treatment, which is made of the following raw materials. The implant rod includes a carrier and a raw material drug. The carrier is modified polyglycerol sebacate, which includes sebacate 15g of acid, 5g of glycerin, 0.1g of pentapentanediol, and the raw materials include 4g of losartan, 6g of lacidipine, 2g of enalapril, and 1g of metoprolol.
[0027] Processing method of the present invention comprises the following steps:
[0028] The first step, the carrier is modified polyglycerol sebacate. The processing method is to put 15g of sebacic acid, 5g of glycerin, and 0.1g of pentapentanediol into the reaction kettle, and stir while heating. The hea...
Embodiment 2
[0031] Example 2 (According to the formula of this example, 200 implant rods can be produced, the diameter of the implant rod is 3mm, and the length is 40mm; the weight of each implant rod is 0.3g, and each rod contains 0.15g of raw material medicine)
[0032] A biodegradable subcutaneous implant stick for long-acting blood pressure reduction, which is made of the following raw materials. The implant stick includes a carrier and a raw material drug. The carrier is a modified polyglycerol sebacate, which includes capric acid 20 g of diacid, 10 g of glycerin, 0.1 g of pentapentanediol; raw materials include 11 g of losartan, 16 g of lacidipine, 2 g of enalapril, and 1 g of metoprolol.
[0033] The processing method of the present embodiment is the same as embodiment 1.
[0034] Implementation steps of the present invention:
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