Targeted lipidosome decorated by pH sensitive polypeptide
A technology targeting liposome and polypeptide modification, which is applied in liposome delivery, medical preparations of non-active ingredients, non-active ingredients of polymer compounds, etc., and can solve problems such as strong toxicity and side effects
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Embodiment 1
[0046] Embodiment 1. Preparation of DSPE-PEG2000-A
[0047] In a 25ml round bottom flask, add 10ml chloroform, then add DSPE-PEG2000-Mal 10.0mg, triethylamine 3μL, and then add polypeptide A (sequence is LH L LH H L LH HLL H LL, in the sequence, L is leucine, H is histidine; the underline indicates that the amino acid is a D-type amino acid,) 9.1mg is dissolved in 5ml methanol and added to a round bottom flask, and reacted at room temperature in the dark for 48h, and the reaction solution Spin-dry under reduced pressure to obtain the initial product, add chloroform to dissolve, filter, and then spin-dry under reduced pressure to obtain 15.0 mg (89.3%) of DSPE-PEG2000-A as a colorless oily compound.
[0048]
Embodiment 2
[0049] Example 2. Preparation of liposomes modified by DSPE-PEG2000-A
[0050] Polypeptide A modified targeting liposomes were prepared from soybean phospholipids, cholesterol, DSPE-PEG2000, and DSPE-PEG2000-A. Weigh 1.42 mg of soybean lecithin, 0.40 mg of cholesterol, 0.28 mg of DSPE-PEG2000, and 0.78 mg of DSPE-PEG2000-A, dissolve in an appropriate amount of chloroform, and remove the chloroform by rotary evaporation under reduced pressure in a water bath at 37°C to form a uniform lipid film. Add 1ml of PBS buffer solution for hydration for 1h, and probe sonication (5s, 5s, 15 times). Sequentially extrude through 400nm, 200nm and 100nm polycarbonate membranes to obtain DSPE-PEG2000-A modified liposomes.
[0051]
Embodiment 3
[0052] Example 3. Preparation of liposomes modified by DPPE-PEG-A
[0053] Polypeptide A modified targeting liposomes were prepared from soybean phospholipids, cholesterol, DPPE-PEG3000 and DPPE-PEG3000-A. Weigh soybean lecithin 1.42mg, cholesterol 0.40mg, DPPE-PEG3000 0.26mg, DPPE-PEG3000-A 0.75mg, dissolve in appropriate amount of chloroform, 37 ℃ water bath, vacuum rotary evaporation to remove chloroform, form a uniform lipid film, Add 1ml of PBS buffer solution for hydration for 1h, and probe sonication (5s, 5s, 15 times). Sequentially extrude through 400nm, 200nm and 100nm polycarbonate membranes to obtain DPPE-PEG3000-A modified liposomes.
[0054]
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