Three-function peptide-modified gene carrier as well as preparation method and application thereof
A gene carrier and amino acid technology, applied in the fields of genetic engineering and molecular biology, can solve the problems of low transfection efficiency, strong cytotoxicity, easy dissociation, etc., and achieve broad clinical application prospects, low cytotoxicity, and transfection efficiency. high effect
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Embodiment 1
[0044] Example 1 Preparation and functional verification of OTMCS-PEI-R18 (1)
[0045] 1. Preparation of OTMCS-PEI-R18
[0046] (1) Synthesis of amphiphilic chitosan OTMCS
[0047] Add 12 g of chitosan and n-octylaldehyde (34.0 mL, 0.370 mol) into 150 mL of methanol, stir at 30 °C for 12 h, then add KBH three times 4 (a total of 6g / 60 mL), stirred overnight, filtered, washed repeatedly with water and hot methanol, dried under vacuum at 50°C, took 0.96 g of the product, put it in a 100 mL flask, added 15 mL of N-methylpyrrolidone, KI 2.4 g, 5 mL of 15% aqueous NaOH and CH 3 I 5.2 mL, stirred, reacted at 60°C for 1 h, allowed to cool, centrifuged at 1000 r / min for 30 min, discarded the supernatant, dissolved the residue with appropriate amount of water, dialyzed for 5 days, filtered the dialysate, and freeze-dried the filtrate to obtain dilute Yellow OTMCS, molecular weight 2KDa.
[0048] Proton NMR analysis was performed on the final product OTMCS. Depend on figure 1 Vi...
Embodiment 2
[0068] Example 2 Preparation and functional verification of OTMCS-PEI-R18 (2)
[0069] The preparation of OTMCS-PEI-R18 and the in vitro transfection experimental steps are the same as in Example 1, the difference is that in this example, the molecular weight of OTMCS is 1KDa, the molecular weight of PEI is 70KDa, and the molar ratio of OTMCS and PEI used during the synthesis of OTMCS-PEI is 1:1, the molar ratio of R18 and OTMCS-PEI used in the synthesis of OTMCS-PEI-R18 was 15:1; the preparation of OTMCS-PEI-R13 as a control was the same as that of OTMCS-PEI-R18.
[0070] The results of in vitro transfection experiments showed that the expression intensity of OTMCS-PEI-R18 luciferase was much higher than that of OTMCS-PEI-R13, and the expression intensity of OTMCS-PEI-R13 in the heart, liver, spleen, lung, kidney, and tumor was higher than that of OTMCS-PEI-R13. 6.7, 7.2, 7.5, 8.0, 8.6, 8.4 times.
Embodiment 3
[0071] Example 3 Preparation and functional verification of OTMCS-PEI-R18 (3)
[0072]The preparation of OTMCS-PEI-R18 and the experimental steps of in vitro transfection are the same as in Example 1, except that the molecular weight of OTMCS in this example is 20KDa, the molecular weight of PEI is 0.6KDa, and the molar ratio of OTMCS and PEI used in the synthesis of OTMCS-PEI The molar ratio of R18 and OTMCS-PEI used in the synthesis of OTMCS-PEI-R18 was 1:20; the preparation of OTMCS-PEI-R13 as a control was the same as that of OTMCS-PEI-R18.
[0073] The results of in vitro transfection experiments showed that the expression intensity of OTMCS-PEI-R18 luciferase was much higher than that of OTMCS-PEI-R13, and the expression intensity of OTMCS-PEI-R13 in the heart, liver, spleen, lung, kidney, and tumor was higher than that of OTMCS-PEI-R13. 7.3, 7.6, 7.1, 8.2, 8.5, 8.4 times.
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