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Transdermal Formulation Weight Testing

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The weight test of transdermal formulation is one of the important links to ensure their quality and safety. Therefore, standardized procedures and requirements must be strictly followed when testing to ensure the reliability and accuracy of test results. CD Formulation provides customers with multi-level and comprehensive drug quality analysis services, including weight testing of transdermal formulation.

About Transdermal Formulation Weight Testing

Through weight testing, we can ensure that the weight of transdermal formulation meets the requirements of relevant regulations and standards. During the production process, product weight may fluctuate due to various factors (such as raw material differences, equipment accuracy, etc.). Through weight testing, these errors can be discovered and controlled in time to ensure the stability of product quality and ensure the same performance of each batch of products.

What Can We Offer

CD Formulation can help you develop transdermal formulation weight testing:

Single dose weight testing

Measure the weight of individual transdermal formulations to ensure the dosage of each formulation is accurate.

Average weight testing

Multiple transdermal formulations are measured, and their average weight is calculated to evaluate consistency and stability during formulation production.

Weight change testing

Measure the weight change of the transdermal formulation within a certain period of time to evaluate its stability and durability under different conditions.

Weight change test under environmental conditions

Place the transdermal formulation under different environmental conditions (such as different temperatures and humidity), measure its weight change, and evaluate its sensitivity to environmental conditions.

Our Workflow of Transdermal Formulation Weight Testing

Our experimental process is as follows:

Workflow of transdermal formulation weight testing.Fig.1 Flow chart of transdermal formulation weight testing (CD Formulation)

Our Capabilities for Testing Transdermal Formulation Weight

Features Description
High precision and high reliability It can ensure the accuracy of drug proportioning. It meets the US class 10,000 or GMP class C standards and can be used in GMP clean rooms.
Measuring weight in different environments Place the transdermal formulation under different environmental conditions (such as different temperatures and humidity), measure its weight change, and evaluate its sensitivity to environmental conditions.

Why Choose Us for Transdermal Formulation Weight Testing?

  • Our instruments use precision sensors and data acquisition systems to accurately measure the resistance and damage of materials under bending.
  • Our instruments are not limited to testing folding resistance, but can also perform a variety of tests, such as three-point bending test, four-point bending test, etc., to meet the testing needs of different types of materials.
  • Our instruments have data-saving functions and can automatically measure, count, and print test results. It helps to better analyze and utilize test data.

Published Data

Technology: Methods to transdermal formulation weight testing

Journal: International Journal of Pharmaceutical Investigation

IF: 5.5

Published: 2016

Results: This study is to test and evaluate the thickness, weight change, tensile strength, extensibility, surface pH, water content, moisture absorption rate, drug content, folding endurance, swelling rate, in vitro dissolution and in vitro dermal permeability of transdermal formulation.

Table 1 Physicochemical properties of transdermal films (Garima Thakur, et al., 2016)

CD Formulation offers professional weight testing of transdermal formulation to provide an important basis for the quality, stability and safety of your transdermal formulations, as well as quality control during the production process. If you have any needs, please feel free to contact us and our colleagues will reply to you within three working days.

References

  1. Garima Thakur, Amrinder Singh, et al. Formulation and evaluation of transdermal composite films of chitosan-montmorillonite for the delivery of curcumin. International Journal of Pharmaceutical Investigation. 2019, Vol 6, Issue 1.
How It Works
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We'll email you to provide your quote and confirm order details if applicable.
STEP 3
Execute the project with real-time communication, and deliver the final report promptly.
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