Application of tetrahedral framework nucleic acid in medicine for treating pancreatitis
A tetrahedral, pancreatitis technology, which is applied to the tetrahedral framework nucleic acid in the field of drugs for the treatment of pancreatitis, can solve the problems of poor editability, multi-organ damage, large side effects, etc., and achieves the effect of reducing multi-organ damage and good application prospects.
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Embodiment 1
[0029] Embodiment 1, the synthesis of tetrahedral framework nucleic acid
[0030] Dissolve four DNA single strands (S1, S2, S3, S4) in TM Buffer (10mM Tris-HCl, 50mM MgCl 2 ,pH=8.0), the final concentration of the four DNA single strands was 1 μM, mixed thoroughly, rapidly heated to 95°C for 10 minutes, and then rapidly cooled to 4°C and maintained for more than 20 minutes to obtain tetrahedral framework nucleic acid tFNAs.
[0031] The sequences of the four single strands are as follows:
[0032]
[0033] Synthesized tetrahedral framework nucleic acid, PAGE gel electrophoresis ( figure 1 ) and capillary electrophoresis ( figure 2 ) It can be seen that the size of the tetrahedral framework nucleic acid is about 180KD, and it can be considered that the tetrahedral framework nucleic acid has been successfully synthesized. Tetrahedral particle size is about 20.12nm ( image 3 ), the potential is -6.29mV ( Figure 4 ). Using a transmission electron microscope, the tetrah...
experiment example 1
[0035] Experimental example 1. Therapeutic effect of tetrahedral framework nucleic acid on acute pancreatitis model
[0036] 1. Experimental method
[0037] (1) C57BL / 6 mice (male, 6-8 weeks old, 22±2g) were purchased, fed with standard feed and sterile water, and fed under laboratory conditions for 1 week for adaptive feeding.
[0038] (2) Before the start of the experiment, the mice were fasted for 12 hours. In this paper, 2% sodium taurocholate (US Sigma) was injected into the bile-pancreatic duct to induce SAP using a micropump.
[0039] (3) 21 mice were randomly divided into saline (Saline) group, tFNAs group and sham operation (SO) group. In the tFNAs-treated group, mice were injected with tFNAs (125nM, 100ul) twice through the tail vein at 30 minutes and 60 minutes after SAP induction, respectively. At the same time, 30 and 60 minutes after SAP induction, the mice in the normal saline group were also given the same amount of normal saline solution each time. Mice in...
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