A tumor-targeted drug carrier and its preparation method and application
A tumor-targeting and drug-based technology, applied in anti-tumor drugs, pharmaceutical formulations, drug combinations, etc., can solve the problems of lack of tissue specificity and cell type specificity, large tissue and cell damage, etc., to reduce the number of medications, target The effect of good orientation ability and simple preparation method
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Embodiment 1
[0047] Example 1 Preparation and verification of Pep@BSA@CB[7]
[0048] The preparation method is as follows
[0049] A. Mix 2 μM bovine serum albumin and 40 μM cucurbit[7]uril in PBS solution and incubate at 25°C for 2 hours to form a complex BSA@CB[n] composed of cucurbit[7]uril and bovine serum albumin.
[0050] B. BSA@CB was incubated with 10 μM SPDP protein crosslinker for 2 hours in the dark, then 10 μM cell penetrating peptide Pep was added and the reaction was continued for 4 hours with stirring.
[0051] C. Centrifuge the solution in an ultrafiltration centrifuge tube (MWCO 30K) at a speed of 14,000 for 10 minutes, collect the upper unfiltered part, and dissolve it in PBS, which is Pep@BSA@CB[7].
[0052] The amino acid sequence of the polycation motif of the above cell-penetrating peptide Pep is SEQ ID NO.1, specifically R 9 GGC, the amino acid sequence of the polyanion motif is SEQ ID NO.2, specifically E 9 , the amino acid sequence of the linking motif is SEQ ID...
Embodiment 2
[0060] Example 2 Preparation and pharmacological experiments of Pep@BSA@CB[7]@DOX
[0061] 1. The preparation method is as follows
[0062] A. Mix 2 μM bovine serum albumin and 40 μM cucurbit[7]uril in PBS solution and incubate at 25°C for 2 hours to form a complex BSA@CB[7] composed of cucurbit[7]uril and bovine serum albumin.
[0063] B. Dissolve 2 μM BSA@CB[7] and 10 μM DOX in PBS (pH 7.4) and incubate for 1 hour to form a BSA@CB[7]@DOX complex, then put the solution in an ultrafiltration centrifuge tube at 14000 rpm Centrifuge for 10 minutes, collect the upper unfiltered fraction, and dissolve in PBS.
[0064] C. Incubate 2 μM BSA@CB[7]@DOX complex with 10 μM SPDP protein crosslinker for 2 hours in the dark, then add 10 μM cell penetrating peptide Pep and keep stirring for 4 hours. Centrifuge the solution in an ultrafiltration centrifuge tube at a speed of 14000 for 10 minutes, collect the upper unfiltered part, and dissolve it in PBS to obtain the Pep@BSA@CB[7] DOX comp...
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