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Transdermal delivery preparation in three-dimensional netty spatial configuration of agomelatine and preparation method thereof

A three-dimensional network and three-dimensional configuration technology, which can be used in pharmaceutical formulations, medical preparations without active ingredients, and medical preparations containing active ingredients, etc. The shortcomings of bioavailability have not been basically improved, the dissolution testing method has not been disclosed, and the dissolution results are still under discussion, so as to achieve the effect of fast transdermal absorption, avoiding first-pass effect, and reducing the frequency of administration

Active Publication Date: 2014-06-04
SHANGHAI MODERN PHARMA ENG INVESTIGATION CENT
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Both of the above two patents use the direct compression method to prepare orally disintegrating tablets. This orally disintegrating tablet may increase the bioavailability of agomelatine in the human body, but it may be directly disintegrated and released in the oral cavity. Lead to bad taste of the drug and reduce patient compliance
[0010] China CN101919800A and CN101836966A disclose orally disintegrating tablets and dispersible tablets of agomelatine. The above-mentioned patent documents are prepared according to the quality requirements of orally disintegrating tablets or dispersible tablets, but depression is not an emergency and does not need to be used Orally disintegrating or dispersible tablets, an expensive dosage form
Chinese patent CN101048791A discloses agomelatine pharmaceutical composition and its process. In this patent, agomelatine is passed through a 100-mesh sieve and mixed with pharmaceutical excipients to make oral preparations. The study determined the formulation prescription, but did not disclose the dissolution test method, and the dissolution results are open to question
[0013] The shortcomings of agomelatine preparations disclosed in the above patent documents in terms of drug stability, uniformity and bioavailability have not been substantially improved

Method used

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  • Transdermal delivery preparation in three-dimensional netty spatial configuration of agomelatine and preparation method thereof
  • Transdermal delivery preparation in three-dimensional netty spatial configuration of agomelatine and preparation method thereof
  • Transdermal delivery preparation in three-dimensional netty spatial configuration of agomelatine and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0056] prescription:

[0057]

[0058] The nano silica is selected from the VK-SP15E nano silica produced by Xuancheng Jingrui New Material Co., Ltd., with an average particle size of 15nm;

[0059] The dispersant is propylene glycol;

[0060] The pressure-sensitive adhesive is acrylic pressure-sensitive adhesive 87-4098;

[0061] The transdermal penetration enhancer is Azone (Azone)

[0062] (1) Dissolve the drug in absolute ethanol with twice the saturated solubility of the drug, disperse the nano-silica material in the dispersant, mix the above two solutions, sonicate for 0.5 hours, and soak for another 4 hours to obtain a uniformly dispersed three-dimensional network Drug-carrying system with three-dimensional configuration;

[0063] (2) Add a transdermal penetration enhancer to the pressure-sensitive adhesive, add ethyl acetate to adjust the viscosity of the glue to 1500cp at 25°C, and stir at 2000rpm for 2 hours to obtain the glue for use;

[0064] (3) Add the product of step (1) t...

Embodiment 2

[0072] The agomelatine transdermal patch was prepared by the same method as in Example 1. The composition of the prescription is as follows:

[0073]

[0074]

[0075] The nano-silica is selected from the VK-SP20E nano-silica produced by Xuancheng Jingrui New Material Co., Ltd., with an average particle size of 20nm, dispersing agent is PEG200; pressure-sensitive adhesive is silicone pressure-sensitive adhesive 4032; permeation promotion The agent is isopropyl myristate (IPM)

[0076] The agomelatine transdermal patch was prepared by the method of Example 1, and the in vitro transdermal experiment was performed using the same method. The average rate of agomelatine transdermal patch through the skin of nude mice was 4.95ug / cm 2 .h. Uniform rapid release of the drug for 96h, indicating that the in vitro transdermal process conforms to the zero-order release process at 96h, and the controlled release is good. See the cumulative transdermal transport rate of agomelatine transdermal...

Embodiment 3

[0078] The agomelatine transdermal patch was prepared by the same method as in Example 1. The composition of the prescription is as follows:

[0079]

[0080] The nano-silica is selected from the VK-SP25E nano-silica produced by Xuancheng Jingrui New Materials Co., Ltd., with an average particle size of 25nm, and the dispersant is propylene glycol; the pressure-sensitive adhesive is acrylic pressure-sensitive adhesive 87-2287; transdermal The penetration enhancer is glycerol triacetate. The agomelatine transdermal patch was prepared by the method of Example 1, and the in vitro transdermal test was carried out using the same method, then the agomelatine transdermal patch penetrated naked The average velocity of mouse skin is 3.52ug / cm 2 .h. Uniform rapid release of the drug for 96h, indicating that the in vitro transdermal process conforms to the zero-order release process at 96h, and the controlled release is good. See the cumulative transdermal transport rate of agomelatine tra...

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Abstract

The invention discloses a transdermal delivery preparation in three-dimensional netty spatial configuration of agomelatine and a preparation method thereof. The transdermal delivery preparation consists of a backing layer, a medicine-loading system in a three-dimensional netty spatial configuration coated on the backing layer and an anti-sticking layer compounded on the system. The medicine-loading system in the three-dimensional netty spatial configuration comprises the following components in percentage by weight: 1-40% of agomelatine, 0-10% of nano-porous carbon dioxide, 40-90% of a pressure-sensitive adhesive, 1-30% of a transdermal penetration enhancer and 0-20% of a dispersant. The transdermal delivery preparation disclosed by the invention not only can continuously deliver the medicine in a transdermal manner for a longer time to maintain the constant blood concentration, but also is quick in transdermal absorption rate and high in transdermal absorptive amount, so that the preparation has the characteristics of stability and efficiency.

Description

Technical field [0001] The invention relates to a transdermal drug delivery preparation containing agomelatine and a preparation method. Background technique [0002] Depression is a subtype of mood disorder. Patients usually have typical manifestations such as low mood, loss of interest or pleasure, lack of energy or fatigue, and physical symptoms (such as sleep disorders). It can be caused by various reasons, with significant and lasting depression as the main clinical feature, and depression is not commensurate with the situation. In severe cases, suicidal thoughts and behaviors may occur. Most cases have a tendency to recurrent attacks, most of them can be relieved each time, and some may have residual symptoms or become chronic. [0003] At least 10% of patients with depression have episodes of manic symptoms, and bipolar disorder should be diagnosed at this time. In addition, what we often say of depression actually refers to clinical major depression, and 16% of the popula...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/70A61K31/165A61K47/04A61P25/24A61P25/20
Inventor 罗华菲罗静王浩侯惠民
Owner SHANGHAI MODERN PHARMA ENG INVESTIGATION CENT
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