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Merck

934607

Sigma-Aldrich

Microneedle template

6x6 array, H 1000 μm, base size 250 μm, 1000µm pitch

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About This Item

分類程式碼代碼:
42142600
NACRES:
NA.21

高度

1000 μm

底座尺寸

250 μm

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一般說明

Microneedles are a platform for transdermal drug delivery. The advantages of microneedles include the delivery of large molecules, painless and less invasive adminsitration of the active pharmaceutical ingredient (API), ease of administration, and improved drug delivery including dose, delivery rate and efficacy. Microneedies are also effective for vaccine delivery due to the abundance of immune cells in the dermis. These microneedle templates can be used to make reproducible and high quality microneedle patches for a variety of therapuetics.

應用

Transdermal delivery of a variety to therapeutics including:

  • Nucleic acid delivery
  • Vaccine delivery
  • Protein or peptide delivery
  • Small molecule delivery

特點和優勢

Microneedle templates are exclusively made for producing dissolvable microneedle patches with excellent qualitty and repeatability. These templates are made of silicone rubber which is extremely durable, and chemical and heat resistant.

物理性質

Microneedle template properties:
  • Silicone Template
  • Material: PDMS
  • Patch Size (D): 10mm x 10mm
  • Array Size: 6 x 6
  • Needle Height (A): 1000 µm
  • Needle Base (B): 250 µm
  • Needle Pitch (C): 1000 µm
  • Length of last microneedle cavity to the edge of the patch (F) can be calculated using the following formula: F = (patch size - [(n-1) x pitch)] / 2 where n = number of microneedles in one array
  • Sterilization: Autoclave (optional)
  • No. of use: repeated use if clean and stored properly

其他說明

Suggested instructions for use:

1. Ensure the microneedle template is clean by washing with mild soap and letting them air dry completely
2. Pipette a small quantity (50-100 µL) of the drug mixture onto the microneedle template
3. Subject the template to cenrifugal force for >60 seconds to ensure that alll microneedle cavities are completely filled. The speed and duration are proportional to the viscosity of the matrix material and the volume of microneedle cavities to fill. Complete filling can be confirmed by observing the microneedle cavities under microscope (20x). No air bubbles are present for complete filling.

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Jie Xu et al.
Molecules (Basel, Switzerland), 26(19), 5912-5912 (2021-10-14)
A microneedle (MN) is a painless and minimally invasive drug delivery device initially developed in 1976. As microneedle technology evolves, microneedles with different shapes (cone and pyramid) and forms (solid, drug-coated, hollow, dissolvable and hydrogel-based microneedles) have been developed. The
Ziad Sartawi et al.
Journal of controlled release : official journal of the Controlled Release Society, 348, 186-205 (2022-06-07)
Microneedles are a rapidly developing method for the transdermal delivery of therapeutic compounds. All types of microneedles, whether solid, hollow, coated, or dissolving function by penetrating the stratum corneum layer of the skin producing a microchannel through which therapeutic agents
Ying Hao et al.
Journal of biomedical nanotechnology, 13(12), 1581-1597 (2018-03-02)
A microneedle (MN) is a micron-sized needle with a height of 10-2000 μm and a width of 10-50 μm, which can penetrate through the epidermis layer to dermal tissue directly without pain. Microneedles are widely used in transdermal drug delivery
Tejashree Waghule et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 109, 1249-1258 (2018-12-16)
The most widely used methods for transdermal administration of the drugs are hypodermic needles, topical creams, and transdermal patches. The effect of most of the therapeutic agents is limited due to the stratum corneum layer of the skin, which serves
Ipshita Menon et al.
Micromachines, 12(4) (2021-05-01)
Transdermal vaccination route using biodegradable microneedles is a rapidly progressing field of research and applications. The fear of painful needles is one of the primary reasons most people avoid getting vaccinated. Therefore, developing an alternative pain-free method of vaccination using

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