The largest database of trusted experimental protocols

Agilent 1200 series hplc dad

Manufactured by Agilent Technologies
Sourced in United States

The Agilent 1200 Series HPLC/DAD is a high-performance liquid chromatography (HPLC) system with a diode-array detector (DAD). It is designed to provide reliable and accurate separation and detection of a wide range of chemical compounds.

Automatically generated - may contain errors

Lab products found in correlation

3 protocols using agilent 1200 series hplc dad

1

Quantification of Okra Flavonoids

Check if the same lab product or an alternative is used in the 5 most similar protocols
The flavonoids in okra were quantified by external standard method. Quantification of the mixed reference solution was performed by Agilent 1200 Series HPLC/DAD using five point regression curves (R2 > 0.999) (Table 1). Chromatographic analysis refers to HPLC-MS/MS analysis. The working standard mixture was gained by dissolving all of the standard substances in 70% ethanol and diluting with ethanol to a series of appropriate concentrations and used to construct calibration curves. The concentration ranges for six analytes were unfolded in Table 2. All the solutions were injected after being filtered by a 0.22 µm filter.
The accuracy of the above method was verified by a recovery test, which was performed using the above method by six (n = 6) replicate injections of spiked samples with a ratio of 1:1 between the standard content and the sample content and extracted. Precision/injection repeatability test was performed by six (n = 6) replicates injections of the mixed reference solution. The intra-day variations were injected in 1 day; the inter-day variations were injected after a 1 day interval. Variations were expressed as the percentage relative standard deviation (RSD%) of the replicates.
+ Open protocol
+ Expand
2

Standardization of Pinoresinol-4-O-β-D-Glucopyranoside by HPLC

Check if the same lab product or an alternative is used in the 5 most similar protocols
The analysis of the standardization
of EP was done utilizing the Agilent 1200 series HPLC–DAD (Agilent
Technologies, Santa Clara, CA, USA) for analysis. The extract sample
was diluted and injected into a (150 mm, 4.6 mm, 5 μm) C18 reversed-phase
column assembled with a quaternary pump. The mobile phase was composed
of solvent A, water, and solvent B, methanol. Solvent B concentration
was elevated every 3 min by 10% with a 0.2 mL/min flow rate to reach
100% through 30 min to follow a gradient elution system. A λmax of 230 nm was used to detect the chromatographic run where
the EP sample was measured in triplicate. Quantitative determination
of pinoresinol-4-O-β-d-glucopyranoside (PG) was done
by employing HPLC analysis via constructing a calibration curve with
different concentrations of the standard PG solution followed by peak
area calculation.
+ Open protocol
+ Expand
3

HPLC Quantification of Caffeine

Check if the same lab product or an alternative is used in the 5 most similar protocols
After sample dilution, 20 μL were auto-injected into Agilent 1200 series HPLC-DAD (Agilent Technologies, Santa Clara, CA, USA). All chromatographic separations were carried on a C18 reversed-phase column (150 mm, 4.6 mm, 5 μm) equipped with a quaternary pump. Mobile phases consisted of water (Solvent A) and methanol (Solvent B). A gradient elution system was adopted as follows: increasing concentration of solvent B by 10% every 3 min using a flow rate equals to 0.2 mL/min till reaching 40% followed by isocratic elution at 40% B for 15 min then returning back to gradient elution at 90% B till reaching 45 min as total run time. Detection was carried out at 278 nm and each sample was measured 3 times. Caffeine was quantitatively determined in each sample using HPLC via constructing of a calibration curve using standard caffeine solution and calculating the peak area of each sample.
+ 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!