Integration in Shimadzu LabSolutions for HPLC/GC using iPeakFinder by Mehul Pal

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Integration tool iPeakFinder in Shimadzu LabSolutions for HPLC/GC.

Integration is the process of calculating an area that is bounded in part or in whole by a curved line. The goal of chromatographic peak integration is to obtain retention times, heights, and areas of these peaks.

Shimadzu LabSolutions features an innovative operating environment and provides complete data management to ensure secure information in networked laboratories.
#Shimadzu #LabSolutions
LCs and GCs are used extensively in quality control and research and development departments in a wide range of industries, including pharmaceutical, chemical, and food.Recently, an increasing demand for food safety and environmental analysis and measurement has led to a dramatic increase in the number of samples being analyzed which, in turn, has resulted in demands for faster, easier-to-use instruments and software.In the pharmaceutical industry, compliance to regulations and guidelines, such as CSV, Ministry of Health, Labour and Welfare ERIES guidelines and FDA 21 CFR Part 11, and the proper, efficient management of instruments and analytical data is required.With this background, faster, more efficient management of instruments and data is essential. LabSolutions is a network-compatible analysis data system capable of meeting these needs.
Description taken from LabSolutions Brochure.
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Dear sir thank you so much ap a to z videos bna kr appload krein boht achi video apnai bnae hai Jo tamam logon k liye kaffi achi hai..

muhammadazeemuddin
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Thanks for your video, i have a question how to reject negative peak in iPeakFinder method? if in Chromatogram there is feature remove negative peak.

Muksidintaslim
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Make a video on integration and process on complete batch. Also how to execute integration and data processing in real time

fooddelight
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My coloumn shows some unwanted peaks at 2-3 mins even after washing so many times with different solvents i have developed method for my drugs they have RT after 5 mins i have taken linearity for them also only issue is the disturbance at 2-3 mins any way of omitting those unwanted peaks ?

sayuabhishek
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I integrate data in Post run. But same data after integration do not show area in browser window. Can you make full video of data processing in Post run and open it in browser for statistcal result

fooddelight
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Sir aap empower 3 ka bhi video bna digiye please sir aap bahot achha smjhate hai

priyashah
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plz explain in details advanced and program feartures of data integration

mahmadshaikh
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Very good experience, please explain empower software and integration

pachipalamallikarjunarao
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Sir which solvents are used while callibration...and why ...? Please tell me....

mohankundan
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Registered selected option is very useful as automatically RT registered on table 👍
Now pls make video how to do integration in RS by comparing blank and sample peaks simultaneously?
Mean to say suppose in RS run time is 30 min for blank as well as in sample.. After overlaying it was found that on RT at 26 min there is peak observed in Blank as well as in sample also, and on RT at 26 min area in sample run is less compare to Blank RT..
So how to add min area on that perticular RT so that to remove the blank area in sample run.

honeyjarial
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Hello.sir can u please make a vid for how to compile S/N ration of sample in lab Solutions

vallurisoujanya
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Dear Pal Sir... HPLC Calibration ke parameters ko keise integrate karke print lete hain... Vo full video banake upload kijiye... Thanks in advance

chiragbhavsar
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Please explain noise and drift parameters

nishashiriskar
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Sir, How we define a typical peak is hump or peak ?

ajitjadhav
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Hello Sir,
How To Apply ..?
I can Auto Compound name and Report Format To apply All Run.

rakeshmali
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Kindly share LC-2030 PDA peak purity finding procedure...

ShivamChauhan-xucd
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Hi Sir your videos are so helpful, can you please make video on 'how to generate calibration curve using Quant Browser?'

nareshbhadarge
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Dear sir Thanks for this.
Can please explain or share video to online assay or dissolution calculation by using software without excell sheet

rahulgagarevankutekar
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Hello Sir,
Suppose our batch sequence
Blank
Standard-1 - 1 Injection
Standard-2 - 5 Injection
Sample-1 - I Injection
BKT Standard -2 - 1 Injection

When we create a processing method for 1 chromatogram of standard 2 and save it, then how do we apply it for the rest.

sandeepkumar-ozgb
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Can we download this program in personal labtop (for manage the post run data)?

prudlove