The largest database of trusted experimental protocols

Nano zs equipment

Manufactured by Malvern Panalytical
Sourced in United Kingdom

The Nano ZS is a versatile piece of laboratory equipment designed for particle size and zeta potential analysis. It utilizes dynamic light scattering (DLS) technology to measure the size and size distribution of particles or molecules in suspension. The Nano ZS can be used to characterize a wide range of materials, including nanoparticles, proteins, polymers, and emulsions. The instrument provides accurate and reliable data, making it a valuable tool for researchers and scientists working in various fields.

Automatically generated - may contain errors

4 protocols using nano zs equipment

1

Comprehensive Material Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The molecular arrangement was analyzed by Fourier transform infrared (FTIR) spectroscopy (Jasco 4700 Spectrophotometer, Jasco, Oklahoma City, OK, USA) using the attenuated total reflection (ATR) accessory and determining the main peaks in the 2000–800 cm−1 region. Thermogravimetric analysis (TGA, SDT 650, TA instruments, New Castle, DE, USA) was performed under oxygen flow (50 mL min−1) up to a temperature of 800 K increased in steps of 5 K min−1. Morphological features were examined using scanning electron microscopy (SEM, Quanta FEI 650FEG), also used to observe the atomic distribution of components by energy dispersive spectroscopy (EDS). The BET (Brunauer–Emmet–Teller) surface area (Sa), the BJH (Barrett–Joyner–Halenda), and cumulative adsorption pore volume between 1.7–300 nm (Vp) were determined by collecting N2 adsorption/desorption isotherms at 77 K (ASAP 2020, Micromeritics Inc., Norcross, GA, USA), after degassing the samples at 393 K for 20 h. The zeta potential values of the different bare components and nanocomposite were measured in aqueous suspensions (10 mg L−1) in the 2–8 pH range, adjusted with HNO3, using Malvern Zetasizer Nano ZS equipment (Malvern, UK).
+ Open protocol
+ Expand
2

Characterization and Stability of Liposomes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Liposomal vesicles were diluted in deionized water for evaluation of the average size (nm), polydispersity index (PDI), and zeta potential (mV) by the dynamic light scattering using Nano ZS equipment (Malvern Instruments Ltd., Worcestershire, UK, England) at 25°C in triplicate. To evaluate stability of liposomes, these parameters were monitored during 180 days at 4°C.
+ Open protocol
+ Expand
3

pH Titration of Nanomaterials

Check if the same lab product or an alternative is used in the 5 most similar protocols
The pH titrations were conducted in a Malvern ZetaSizer Nano-ZS equipment (Worcestershire, UK) equipped with an MPT-2 pH titrator. The pH was modified with HCl 1 M and NaOH 1 M solutions. Measurements were carried out in triplicate and at room temperature (~25 °C), using specific folded capillary cells. Data in the corresponding graphs represent the mean of the measurements, with error bars corresponding to the standard error of the mean.
+ Open protocol
+ Expand
4

Characterization and Drug Release of MOF-HMME-RGD

Check if the same lab product or an alternative is used in the 5 most similar protocols
The morphology and structure of MOF-HMME-RGD nanoparticles were examined using transmission electron microscopy (TEM) and X-ray diffraction (XRD) techniques, respectively. The TEM analysis was conducted using a Hitachi instrument from Japan, while the XRD analysis was performed using a MiniFlex 600 instrument, also from Japan. The absorption spectra of nanoparticles (NPs) in phosphate-buffered saline (PBS) were measured using a UV-visible spectrophotometer (Shimadzu, UV-2700, Japan). The average particle size and zeta potential of nanoparticles in a PBS solution were measured using Nano-ZS equipment manufactured by Malvern Panalytical in China. The HMME releasing behaviors from MOF-HMME-RGD were investigated. 200 μg MOF-HMME-RGD was dissolved in 1 mL of PBS buffer and then placed at 37°C with or without ultrasound stimulation under thermostatic shaking. The HMME concentration in the buffer was measured uniformly using a UV spectrophotometer at 0, 10, 30, 60, 120, 180 min, and the drug release rate (Q) was further calculated. Q%=CtV0+i=1t1CiVi/W×100
Ct and Ci in equation represent the concentration of HMME in the tth and ith collected samples, respectively. V0 and Vi represent the original volume in the simulated system and the volume of the ith sampling, respectively (V0 = 1 mL; Vi = 1 mL), and W is the total amount of drug HMME in the simulated system.
+ 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!