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Method for testing suitability of microneedle material suitable for manufacture employing elongation process, and microneedle manufacturing method comprising same

A suitability testing and microneedling technology, applied in microneedles, analysis of materials, measurement of DC flow characteristics, etc., can solve the problems of different molding methods, drug denaturation, insufficient hardness, etc., and achieve the effect of improving efficiency and quality.

Pending Publication Date: 2021-08-06
RAPHAS
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  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since this method uses a method of pulling a heat-fused or viscous substance using a pin structure, it requires a new process of preparing the pin structure according to the desired pattern, making it difficult to overcome the limitations of increased production costs, due to heating It is difficult to load various heat-sensitive biological drugs (hormones, vaccines, other protein drugs, etc.)
[0015] Due to the limitations of the preparation method, the existing solid microneedles are limited to materials such as silicon, polymer, metal, glass, etc., and due to the use of the preparation method using molding technology, the following disadvantages will occur: due to the complexity and time required for the preparation process Long-term drug denaturation, insufficient hardness and drug loss, etc.
[0019] As mentioned above, there is a difference between the blast stretching method and the centrifugal photolithography method in whether or not the blast solidification process is included, but they are the same in that the microneedle shape is prepared by stretching the viscous composition, which is the same as the above molding different ways

Method used

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  • Method for testing suitability of microneedle material suitable for manufacture employing elongation process, and microneedle manufacturing method comprising same
  • Method for testing suitability of microneedle material suitable for manufacture employing elongation process, and microneedle manufacturing method comprising same
  • Method for testing suitability of microneedle material suitable for manufacture employing elongation process, and microneedle manufacturing method comprising same

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Embodiment Construction

[0052] The following detailed description of the invention may refer to the accompanying drawings, which show by way of example specific embodiments in which the invention may be practiced. The detailed description of these embodiments is sufficient to enable those of ordinary skill in the art to which the invention pertains to practice the invention. It should be understood that the various embodiments of the invention differ from each other, but are not necessarily mutually exclusive. For example, it is understood that specific shapes, structures and characteristics described in the specification of the present invention may be changed from one embodiment to another without departing from the spirit and scope of the present invention. Also, it should be understood that the position or arrangement of individual structural elements in each embodiment may be changed without departing from the spirit and scope of the present invention. Therefore, the detailed description to be ...

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Abstract

A microneedle manufacturing method according to one embodiment of the present invention comprises the steps: selecting and providing a microneedle material, wherein a value of the viscosity / elasticity coefficient of the microneedle material, measured for each shear rate by a viscoelasticity measurement apparatus, belongs to a scope between pre-arranged upper and lower limits; and manufacturing the microneedle material having been selected and provided in the previous step into a microneedle by means of an elongation method.

Description

technical field [0001] The present invention relates to a suitability testing method for a microneedle material prepared by a stretching process and a method for preparing a microneedle comprising the same. Background technique [0002] Many drugs and physiologically active substances have been developed for the treatment of diseases, but in the process of delivering drugs and physiologically active substances into the body, biological barriers (biological barriers, such as skin, oral mucosa, and cerebrovascular barrier, etc.) pass through problems And the efficiency of drug delivery still needs to be improved. [0003] Drugs and physiologically active substances are usually administered orally in the form of tablets or capsules, but due to reasons such as being digested or absorbed in the gastrointestinal tract or being lost by hepatic mechanisms, many drugs cannot be effectively delivered by the above-mentioned methods of administration alone . Moreover, some drugs do no...

Claims

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Application Information

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IPC IPC(8): A61L31/14A61L31/04A61M37/00B29C43/02B29C43/00G01N19/04B29L31/00
CPCG01N11/142A61M2037/0053A61M37/0015A61L31/14A61L31/04B29C43/02B29C43/003G01N19/04A61M2205/0244A61M2037/0046B29L2031/7544A61M2205/70B29D99/00G01N11/02
Inventor 陈周永李文洙金泰衡金正东郑道铉
Owner RAPHAS
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