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Sample protocol

Currently, high-performance liquid chromatography (HPLC) methods have been widely used in the analysis of tocopherols and tocotrienols in food and nutrition areas. Each form of tocopherol and tocotrienol can be separated and quantified individually using HPLC with either a UV or fluorescence detector. The interferences are largely reduced after separation by HPLC. Therefore, the sensitivity and specificity of HPLC methods are much higher than those obtained with the colorimetric, polarimetric, and GC methods. Also, sample preparation in the HPLC methods is simpler and more efficiently duplicated than in the older methods. Many HPLC methods for the quantification of tocopherols and tocotrienols in various foods and biological samples have been reported. Method number 992.03 of the AOAC International Official Methods of Analysis provides an HPLC method to determine vitamin E in milk-based infant formula. It could probably be said that HPLC methods have become dominant in the analysis of tocopherols and tocotrienols. Therefore, the analytical protocols for tocopherols and tocotrienols in this unit are focused on HPLC methods. Normal and reversed-phase HPLC methods are discussed in the separation and quantification of tocopherols and tocotrienols (see Basic Protocol). Sample... [Pg.479]

Inject extract into the normal- or reversed-phase HPLC system (see Basic Protocol). SAMPLE PREPARATION FROM MEATS... [Pg.483]

Support Protocol Sample Preparation for Anthocyanin Purification FI. 1.4... [Pg.773]

Alternate Protocol Sample Preparation of Acylated Anthocyanins and Their... [Pg.773]

Raw materials, solvents, catalysts, gases, processing aids, processing water, steam, packaging materials and bioburden Process validation protocol Sampling and testing strategy... [Pg.434]

Figure 7.3 A. Human psoriatic tissue (200x). B. Normal human skin (200x). Both samples were immunostained with caspase 14 antibody. Punch biopsies (4 mm) of normal and psoriatic skin samples were obtained from different patients who provided written, informed consent under an IRB-approved protocol. Samples were fixed in 10% neutral-buffered formalin, paraffin embedded, cut to 5-pm sections, and stained with caspase 14 antibody by immunohistochemistry. Figure 7.3 A. Human psoriatic tissue (200x). B. Normal human skin (200x). Both samples were immunostained with caspase 14 antibody. Punch biopsies (4 mm) of normal and psoriatic skin samples were obtained from different patients who provided written, informed consent under an IRB-approved protocol. Samples were fixed in 10% neutral-buffered formalin, paraffin embedded, cut to 5-pm sections, and stained with caspase 14 antibody by immunohistochemistry.
A stability program SOP should define all general aspects of stability studies and serve as the basis for preparation of specific protocols. The SOP should include sections on (or reference other SOPs for) the procedures for the stability protocol, samples, testing, chambers or rooms, and final report. Items to be included in each section of a stability program SOP are outlined in Examples 9-15. [Pg.213]

Analyte MIP format Recognition Protocol Sample Sample modification Washing Elution Detection Referenct... [Pg.359]

Before any sample can be subjected to chromatography, some type of sample preparation is required, which can be as simple as filtration or an involved solid-phase extraction protocol. Sample preparation is that activity or those activities necessary to prepare a sample for analysis. The ultimate goal of sample preparation is to provide the component of interest in solution, free from interferences and at a concentration appropriate for detection. This entry will briefly discuss seven topic areas included in sample preparation standard methods, solid-phase extraction (SPE), matrix solid-phase dispersion (MSPD), solid-phase microextraction (SPME), microdialysis, ultraliltration (UF), and automated systems. [Pg.1391]

In the standard protocol, samples are amplified a total of 30 cycles, this can be varied as needed (see Notes 12 and 13). The negative control, depH20, is allowed to amplify yet another 5-10 sequential cycles for a total number of 35-40 sequential cycles in order to detect contamination. [Pg.74]

Magnetically sedimented DNA (siRNA) (%) = [ l-CPM j / CPM J X100, where CPM. is the radioactivity measured in the reference well A7, if the assay is carried out following the above protocol. Sample results are shown in Figs. 3a and b, for different DNA and siRNA lipoplexes comprising magnetic nanoparticles (see also Note 13). [Pg.500]

Preparation of Soil Sampling Protocols Sampling Techniques and Strategies... [Pg.42]

EPA measurement protocols, sampling methods and guidelines, quality assurance, and EPA s Radon Measurement Proficiency Program. [Pg.193]

Protocol sampling. These are specified plans used for decision purposes in a given situation. Regulations (of the protocol) usually specify the type, size, frequency, and period of sampling in addition to the test methods to be used and other important test issues. A combination of intuitive and statistical considerations may be used, and the above population estimates may be obtained depending on the protocol. Testing for conformance with producer-user specifications for commercial transactions is typical for this approach. [Pg.39]

Statistical Analysis. Analyses were performed for intent-to-treat and per protocol samples with SAS, version 8.0 software (Cary, NC). ANOVA models were generated utilizing the PROC MIXED procedure. Repeated-measures ANOVA was employed to assess effects of treatment, time (week), and treatment X time interactions for the percentage of change from baseline in body weight, fat mass, and lAF area. [Pg.338]

Per Protocol Analyses. Responses to treatment within the per protocol sample were not different from those noted in the intent-to-treat analyses (data not shown). [Pg.338]


See other pages where Sample protocol is mentioned: [Pg.278]    [Pg.493]    [Pg.282]    [Pg.252]    [Pg.147]    [Pg.212]    [Pg.138]    [Pg.157]    [Pg.338]    [Pg.252]    [Pg.493]    [Pg.117]    [Pg.177]    [Pg.244]    [Pg.385]   
See also in sourсe #XX -- [ Pg.133 ]




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