Method for raising utilizing degree to oral organism-absorbing of lumbrukinase
A lumbrokinase and lumbrokinase enteric technology, applied in the field of improving or improving the oral absorption bioavailability of lumbrokinase and enteric-coated combination preparations, can solve the problems of in-depth, unsystematic research work, etc., so as to improve the concentration of lumbrokinase and improve the treatment effect, effect of improving bioavailability
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Embodiment 1
[0030] Preparation process of lumbrokinase enteric-coated combination preparation
[0031] 4mg lumbrokinase, 20mg bacitracin, 4mg Na 2 - A 200mg lumbrokinase combination preparation that can be filled into enteric-coated capsules after mixing EDTA and 172mg dextran evenly.
Embodiment 2
[0032] Embodiment 2, lumbrokinase combined with absorption enhancer
[0033] Mix a certain proportion of absorption enhancers (sodium deoxycholate, Na2EDTA, chitosan, sodium lauryl sulfate, sodium octanoate, poloxamer, hydroxypropyl-β-cyclodextrin) with a certain concentration of FITC Fluorescently labeled lumbrokinase was mixed to make a solution. Use lumbrokinase alone as a control. The duodenal administration method was adopted. First, the abdominal cavity was opened by surgery, and a certain volume of drug solution was injected into the intestinal cavity at one time, and blood was collected from the orbit to measure the drug concentration in plasma at each time point.
Embodiment 3
[0034] Embodiment 3, lumbrokinase combined with enzyme inhibitor
[0035] Mix a certain proportion of enzyme inhibitors (bacitracin, casein, betatin, leupeptin, aprotinin, pancreatin inhibitor, sodium glycocholate) with a certain concentration of FITC fluorescently labeled lumbrokinase Prepared as a solution. Use lumbrokinase alone as a control. The duodenal administration method was adopted. First, the abdominal cavity was opened by surgery, and a certain volume of drug solution was injected into the intestinal cavity at one time, and blood was collected from the orbit to measure the drug concentration in plasma at each time point.
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