scholarly journals Reliable release testing for nanoparticles with the NanoDis System, an innovative sample and separate technique

Author(s):  
Sonia M. Lombardo ◽  
Nazende Günday Türeli ◽  
Marcus Koch ◽  
Marc Schneider ◽  
Akif E. Türeli
Author(s):  
Michael J. Rathbone ◽  
Jingjian Shen ◽  
Colin R. Ogle ◽  
Shane Burggraaf ◽  
Craig R. Bunt

2018 ◽  
Vol 52 (3) ◽  
pp. 257-265
Author(s):  
Ewelina Gronczewska ◽  
Weronika Worobiec ◽  
Alicja Defort ◽  
Andrzej Jurkowski ◽  
Jacek J. Kozioł

2020 ◽  
Vol 103 (5) ◽  
pp. 1293-1300
Author(s):  
Brendon D Gill ◽  
Harvey E Indyk ◽  
Tadashi Kobayashi ◽  
Iain J McGrail ◽  
David C Woollard

Abstract Background Choline and l-carnitine are classified as pseudo-vitamins because of their conditionally essential status. As they are involved in multiple physiological metabolic pathways in the human body, they are routinely fortified in infant and adult nutritional formulas. Objective The performance of an LC-MS/MS method for the analysis of choline and carnitine, compared with enzymatic methods in routine use for the analysis of total carnitine and total choline, is described. Method Powder samples were reconstituted, with release of carnitine and choline facilitated by both acid and alkaline hydrolysis and the extract analyzed by LC-MS/MS. Quantitation was by internal standard technique using deuterium-labeled carnitine and deuterium-labeled choline. Results Method range, specificity, sensitivity, precision, recovery, accuracy, and ruggedness were assessed for milk powders, infant formulas, and soy- and milk-based nutritional products. Spike recoveries of 94.0–108.4% were obtained for both total carnitine and choline, and no statistical bias (α = 0.05) between measured results and certified values (choline: P = 0.36; free carnitine: P = 0.67) was found for NIST 1849a certified reference material (NIST1849a). Precision, as repeatability relative standard deviation (RSD), was 2.0% RSDr for total carnitine and 1.7% RSDr for total choline. Equivalent results for total choline and total carnitine were obtained by LC-MS/MS and enzymatic methods (n = 30). Conclusions The described LC-MS/MS method is fit for purpose for routine product compliance release testing environments. This validation study has confirmed that alternative enzymatic assays can be used with confidence in laboratories in which LC-MS/MS platforms are unavailable. Highlights An LC-MS/MS method was evaluated and found to be fit-for-purpose for routine product compliance release testing of infant formula. The LC-MS/MS method was compared with enzymatic methods for the analysis of total carnitine and total choline. Alternative enzymatic assays can be used with confidence in laboratories in which LC-MS/MS platforms are unavailable.


Blood ◽  
2019 ◽  
Vol 134 (21) ◽  
pp. 1873-1875 ◽  
Author(s):  
Elise A. Chong ◽  
Bruce L. Levine ◽  
Stephan A. Grupp ◽  
Megan M. Davis ◽  
Don L. Siegel ◽  
...  

Author(s):  
Madhur Kulkarni ◽  
Shrikant Potdar ◽  
Abhijit A. Date ◽  
Aditya Marfatiya

Transfusion ◽  
2018 ◽  
Vol 58 (S3) ◽  
pp. 3084-3089 ◽  
Author(s):  
Maria R. Farcet ◽  
Jens Modrof ◽  
Philip O. Rabel ◽  
Andreas Schirmer ◽  
Andrew J. Macadam ◽  
...  

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