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Hypericin albumin nanoparticle-immune globulin G antibody conjugate and preparation method thereof

A technology of albumin nanoparticles and immunoglobulins, which is applied in the direction of antiviral agents, antitumor drugs, drug combinations, etc., to achieve the effects of improving drug efficacy, low energy consumption, and easy storage

Active Publication Date: 2013-04-24
GUANGDONG HINAPHARM PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The above only improves the effective content of hypericin to a certain extent, but if the effective utilization rate of hypericin is further enhanced, there is no relevant record in the prior art

Method used

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  • Hypericin albumin nanoparticle-immune globulin G antibody conjugate and preparation method thereof

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Dissolve 200 μL immunoglobulin G antibody and 200 μL hypericin albumin nanoparticles (mass ratio 1:1) in 4 ml PBS buffer, at room temperature, the stirring condition is 400 rpm / min; at 0.5 ml / min slowly Add 100 μL of fresh glutaraldehyde dropwise (the so-called fresh glutaraldehyde means that it is ready-to-use), stir well for 2 hours to cross-link hypericin albumin nanoparticles with immunoglobulin G antibody, and freeze-dry to obtain Hypericum Albumin Nanoparticles-Immunoglobulin G Antibody Conjugate.

[0031] Oral administration of ordinary hypericin, hypericin albumin nanoparticles and hypericin albumin nanoparticle-immunoglobulin G antibody conjugates to immunosuppressed mice, and the determination of immune organ indexes (including spleen index and thymus index). From the statistical results of the spleen index, it can be seen that the spleen index of the blank control group was (3.60±0.89 mg / g), the spleen index of the immunosuppressive model group was (2.16±0.4...

Embodiment 2

[0033]Dissolve 150 μL immunoglobulin G antibody and 300 μL hypericin albumin nanoparticles (mass ratio 1:2) in 4.5 ml PBS buffer, the pH of the buffer is 7.2. At -10°C, under the stirring condition of 400 rpm / min, slowly add 75 μL of fresh glutaraldehyde dropwise at 0.5 ml / min, stir well for 2 h to cross-link hypericin albumin nanoparticles with immunoglobulin G antibody, freeze After drying, the hypericin albumin nanoparticle-immunoglobulin G antibody conjugate is obtained. Oral administration of ordinary hypericin, hypericin albumin nanoparticles and hypericin albumin nanoparticle-immunoglobulin G antibody conjugates to immunosuppressed mice, and the determination of immune organ indexes (including spleen index and thymus index). From the statistical results of the spleen index, it can be seen that the spleen index of the blank control group was (3.60±0.89 mg / g), the spleen index of the immunosuppressive model group was (2.16±0.45 mg / g), and the normal hypericin group Comp...

Embodiment 3

[0035] Dissolve 100 μL immunoglobulin G antibody and 300 μL hypericin albumin nanoparticles (mass ratio 1:3) in 4 ml PBS buffer, at 10°C, stirring at 700 rpm / min, at 0.5 ml / min Slowly add 50 μL of fresh glutaraldehyde (the so-called fresh glutaraldehyde refers to the ready-to-use), stir well for 2 h to cross-link hypericin albumin nanoparticles with immunoglobulin G antibody, and freeze-dry to obtain gold Sericin albumin nanoparticles-immunoglobulin G antibody conjugate. Oral administration of ordinary hypericin, hypericin albumin nanoparticles and hypericin albumin nanoparticle-immunoglobulin G antibody conjugates to immunosuppressed mice, and the determination of immune organ indexes (including spleen index and thymus index). From the statistical results of the spleen index, it can be seen that the spleen index of the blank control group was (3.60±0.89 mg / g), the spleen index of the immunosuppressive model group was (2.16±0.45 mg / g), and the normal hypericin group Compared...

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Abstract

The invention discloses a hypericin albumin nanoparticle-immune globulin G antibody conjugate, which comprises the following preparing steps: step (1), dissolving the hypericin albumin nanoparticle and the immune globulin G antibody conjugate into phosphate buffer solution (PBF), step (2), adding glutaraldehyde into the solution obtained by the step (1), and obtaining the hypericin albumin nanoparticle-immune globulin G antibody conjugate. The hypericin albumin nanoparticle-immune globulin G antibody conjugate has the advantages of high effective utilization; simultaneously, the preparation method of the hypericin albumin nanoparticle-immune globulin G antibody conjugate has the advantages of being simple in process, easy to operate and specially suitable for industrial production.

Description

technical field [0001] The invention relates to an antiviral natural medicine, in particular to a hypericin albumin nanoparticle-immunoglobulin G antibody conjugate. Background technique [0002] Hypericin (HY) is a naphthalene dianthrone compound extracted from Hypericum perforatum Linn., a plant of the Clusiaceae family. It has photosensitizing activity and photosynthetic activity, and can be applied to the photochemical diagnosis of tumors and treatment. However, due to the instability of hypericin to light and heat, the content of active ingredients of hypericin in the market is extremely low, which is far from meeting the requirements of terminal product development. Nano-drugs refer to the drugs made of nano-scale polymer nanoparticles (nanoparticles, NP), nanospheres (nanospheres, NS), nanocapsules (nanocapsules, NC), etc., combined with drugs in a certain way. Its particle size may exceed 100 nm, but generally should be less than 500 nm. Nano-drugs can also be nano...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/14A61K31/122A61K47/42A61P37/04A61P31/12A61P35/00
Inventor 梁剑平胡小艳陶蕾王学红刘宇尚若峰赫宝成华兰英
Owner GUANGDONG HINAPHARM PHARMA CO LTD
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