The largest database of trusted experimental protocols

Malvern sizer

Manufactured by Malvern Panalytical
Sourced in United Kingdom

The Malvern sizer is a particle size analyzer that measures the size distribution of particles in a sample. It utilizes laser diffraction technology to determine the particle size distribution accurately and efficiently.

Automatically generated - may contain errors

Lab products found in correlation

3 protocols using malvern sizer

1

Characterization of 4e-loaded PEGylated Bilosomes

Check if the same lab product or an alternative is used in the 5 most similar protocols
The tailored 4e-loaded PEGylated bilosome droplet size, zeta potential and PDI were investigated by utilizing Malvern sizer (Malvern Instruments, Malvern, UK). The amount of 10 mL distilled water was utilized in order to dilute 0.1 mL of 4e-loaded PEGylated bilosomal dispersion within a glass tube that was manipulated, and then it was convulsed manually for 5 min. The manipulated technique was the dynamic laser scattering technique used to determine the distribution size at 25 °C by using 45 mm focus lens and beam lengths of 2.4 mm. The test was performed in triplicate [23 (link)].
+ Open protocol
+ Expand
2

Characterization of tailored PEG-PCL NDs

Check if the same lab product or an alternative is used in the 5 most similar protocols
The mean vesicle size, PDI, and zeta potential of the tailored PEG-PCL modified NDs were adopting the Malvern sizer (Malvern Instruments, Malvern, UK). Before analysis, 0.1 ml of NDs dispersion was diluted with 10 ml distilled water in a glass tube and then convulsed manually for 5 min to acquire the adequate scattering intensity. The test was conducted in triplicate60 (link).
+ Open protocol
+ Expand
3

Niosomal Particle Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The fabricated 2a- or 7-loaded TPGS-modified niosome droplet size, zeta potential and PDI were investigated adopting a Malvern sizer (Malvern Instruments, Malvern, UK). Ten milliliters of distilled water was added in order to dilute 0.1 mL of 2a- or 7-loaded TPGS-modified niosomes dispersion within a glass tube was manipulated and then convulsed manually for 5 min. The manipulated technique was a dynamic laser scattering technique to determine the distribution size at 25 °C using a 45 mm focus lens and a beam length of 2.4 mm. The test was performed in triplicate [54 (link)].
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!