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1.
JAMA Netw Open ; 4(11): e2135452, 2021 11 01.
Article in English | MEDLINE | ID: mdl-34846527

ABSTRACT

Importance: An international expert committee recently revised its recommendations on amino acid intake for very preterm infants, suggesting that more than 3.50 g/kg/d should be administered only to preterm infants in clinical trials. However, the optimal amino acid intake during the first week after birth in these infants is unknown. Objective: To evaluate the association between early amino acid intake and cognitive outcomes at age 5 years. Design, Setting, and Participants: Using the EPIPAGE-2 (Epidemiologic Study on Small-for-Gestational-Age Children-Follow-up at Five and a Half Years) cohort, a nationwide prospective population-based cohort study conducted at 63 neonatal intensive care units in France, a propensity score-matched analysis was performed comparing infants born at less than 30 weeks' gestation who had high amino acid intake (3.51-4.50 g/kg/d) at 7 days after birth with infants who did not. Participants were recruited between April 1 and December 31, 2011, and followed up from September 1, 2016, to December 31, 2017. Full-scale IQ (FSIQ) was assessed at age 5 years. A confirmatory analysis used neonatal intensive care unit preference for high early amino acid intake as an instrumental variable to account for unmeasured confounding. Statistical analysis was performed from January 15 to May 15, 2021. Exposures: Amino acid intake at 7 days after birth. Main Outcomes and Measures: The primary outcome was an FSIQ score greater than -1 SD (ie, ≥93 points) at age 5 years. A complementary analysis was performed to explore the association between amino acid intake at day 7 as a continuous variable and FSIQ score at age 5 years. Data from cerebral magnetic resonance imaging at term were available for a subgroup of preterm infants who participated in the EPIRMEX (Cerebral Abnormalities Detected by MRI, Realized at the Age of Term and the Emergence of Executive Functions) ancillary study. Results: Among 1789 preterm infants (929 boys [51.9%]; mean [SD] gestational age, 27.17 [1.50] weeks) with data available to determine exposure to amino acid intake of 3.51 to 4.50 g/kg/d at 7 days after birth, 938 infants were exposed, and 851 infants were not; 717 infants from each group could be paired. The primary outcome was known in 396 of 646 exposed infants and 379 of 644 nonexposed infants who were alive at age 5 years and was observed more frequently among exposed vs nonexposed infants (243 infants [61.4%] vs 206 infants [54.4%], respectively; odds ratio [OR], 1.33 [95% CI, 1.00-1.71]; absolute risk increase in events [ie, the likelihood of having an FSIQ score >-1 SD at age 5 years] per 100 infants, 7.01 [95% CI, 0.06-13.87]; P = .048). In the matched cohort, correlation was found between amino acid intake per 1.00 g/kg/d at day 7 and FSIQ score at age 5 years (n = 775; ß = 2.43 per 1-point increase in FSIQ; 95% CI, 0.27-4.59; P = .03), white matter area (n = 134; ß = 144 per mm2; 95% CI, 3-285 per mm2; P = .045), anisotropy of the corpus callosum (n = 50; ß = 0.018; 95% CI, 0.016-0.021; P < .001), left superior longitudinal fasciculus (n = 42; ß = 0.018; 95% CI, 0.010-0.025; P < .001), and right superior longitudinal fasciculus (n = 42; ß = 0.014 [95% CI, 0.005-0.024; P = .003) based on magnetic resonance imaging at term. Confirmatory and sensitivity analyses confirmed these results. For example, the adjusted OR for the association between the exposure and the primary outcome was 1.30 (95% CI, 1.16-1.46) using the instrumental variable approach among 978 participants in the overall cohort, and the adjusted OR was 1.35 (95% CI, 1.05-1.75) using multiple imputations among 1290 participants in the matched cohort. Conclusions and Relevance: In this cohort study, high amino acid intake at 7 days after birth was associated with an increased likelihood of an FSIQ score greater than -1 SD at age 5 years. Well-designed randomized studies with long-term follow-up are needed to confirm the benefit of this nutritional approach.


Subject(s)
Amino Acids/standards , Amino Acids/therapeutic use , Child Development/drug effects , Gestational Age , Infant, Premature, Diseases/drug therapy , Intelligence/drug effects , Practice Guidelines as Topic , Child, Preschool , Cohort Studies , Female , France , Humans , Infant , Infant, Newborn , Male , Prospective Studies , Treatment Outcome
2.
J Nutr ; 150(Suppl 1): 2602S-2605S, 2020 10 01.
Article in English | MEDLINE | ID: mdl-33000158

ABSTRACT

We examined international regulatory developments related to the use of proteinogenic amino acids in human nutrition and concluded that the current risk-assessment practices tend to focus exclusively on setting maximum daily limits. In this brief review we argue that controlling the standards of purity and ingredient quality are the key safety issues that should be considered during risk assessment. Moreover, if maximum intake limits on amino acids are implemented, they should be defined using a well-established rationale for the health risks associated with high intakes. This would avoid setting limits that are so low that they render the dietary supplements ineffective and which, therefore, could mislead the consumer. We further suggest that there should be greater regional concordance in how the use of amino acids as ingredients is regulated and use the capacity of industry to oversee pre-competitive issues, such as standards of purity and scientific research on the safety of generic ingredients. Our arguments are based on clinical safety scientific research and oversights of amino acid purity standards conducted in the last decade by the not-for-profit international association, the International Council on Amino Acid Science.


Subject(s)
Amino Acids , Dietary Supplements , Food, Fortified , Policy , Social Control, Formal , Americas , Amino Acids/adverse effects , Amino Acids/standards , Asia , Europe , Humans , Industry/legislation & jurisprudence
3.
Anal Bioanal Chem ; 411(19): 4909-4917, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30923860

ABSTRACT

In this project, we aimed at analyzing native (or free) amino acids with supercritical fluid chromatography coupled to mass spectrometric detection, with modern instruments and methods, and maintaining as simple a mobile phase as possible to ensure applicability of the method. The purpose was twofold: (i) a generic method allowing for satisfactory elution of a wide range of amino acids (acidic, basic, or neutral residue) and (ii) resolution of the enantiomeric pairs. The Chiralpak ZWIX (+) and (-) stationary phases were selected as they are well-known for the enantioresolution of amino acids in liquid chromatographic modes. A wide range elution gradient, starting with a large concentration of carbon dioxide (90%) and finishing at 100% solvent (methanol containing 70 mM ammonium formate and 7% water) allowed the elution of 18 native proteinogenic amino acids out of 19 injected. In these conditions, enantioselectivity was achieved for 16 of them. The basic amino acids (arginine, histidine, and lysine) were the most difficult to elute in these conditions, resulting in rather poor peak shapes. Cysteine was never observed in any of the conditions tested. Sample application was attempted with two food supplements, tablets containing a mixture of 17 proteinogenic amino acids and capsules containing taurine and theanine that were not present in the standards used for the method development. The sample preparation method was very simple, involving dissolution of the tablets and capsules in acidified water, filtration, and dilution with methanol. Mass spectrometric detection (electrospray ionization with single-quadrupole mass detection) allowed for unambiguous identification of most amino acids, except for the leucine and isoleucine isomers that were not separated by the generic gradient. The observation of taurine and theanine also suggests that the method should be generally applicable to other native amino acids than the proteinogenic amino acids selected for the development of this method. As peak shapes and signal-to-noise ratios could still be improved, further developments are wanted to upgrade this method. Due to the wide gradient (10 to 100% co-solvent in carbon dioxide), the method cannot truly be called either supercritical fluid chromatography (SFC) or enhanced-fluidity liquid chromatography (EFLC), but should be related to "unified chromatography" (UC), joining SFC and HPLC. Graphical abstract.


Subject(s)
Amino Acids/analysis , Chromatography, Supercritical Fluid/methods , Spectrometry, Mass, Electrospray Ionization/methods , Amino Acids/standards , Dietary Supplements/analysis , Reference Standards , Stereoisomerism , Tablets
4.
PLoS One ; 13(4): e0195939, 2018.
Article in English | MEDLINE | ID: mdl-29698490

ABSTRACT

Combining different metabolomics platforms can contribute significantly to the discovery of complementary processes expressed under different conditions. However, analysing the fused data might be hampered by the difference in their quality. In metabolomics data, one often observes that measurement errors increase with increasing measurement level and that different platforms have different measurement error variance. In this paper we compare three different approaches to correct for the measurement error heterogeneity, by transformation of the raw data, by weighted filtering before modelling and by a modelling approach using a weighted sum of residuals. For an illustration of these different approaches we analyse data from healthy obese and diabetic obese individuals, obtained from two metabolomics platforms. Concluding, the filtering and modelling approaches that both estimate a model of the measurement error did not outperform the data transformation approaches for this application. This is probably due to the limited difference in measurement error and the fact that estimation of measurement error models is unstable due to the small number of repeats available. A transformation of the data improves the classification of the two groups.


Subject(s)
Metabolomics , Obesity/metabolism , Scientific Experimental Error , Amino Acids/analysis , Amino Acids/standards , Chromatography, High Pressure Liquid/standards , Discriminant Analysis , Humans , Mass Spectrometry/standards , Metabolomics/standards , Obesity/pathology , Principal Component Analysis , Quality Control
5.
Nutrients ; 10(2)2018 Feb 14.
Article in English | MEDLINE | ID: mdl-29443921

ABSTRACT

There are no compatibility studies for neonatal parenteral nutrition solutions without cysteine containing calcium chloride or calcium gluconate using light obscuration as recommended by the United States Pharmacopeia (USP). The purpose of this study was to do compatibility testing for solutions containing calcium chloride and calcium gluconate without cysteine. Solutions of TrophAmine and Premasol (2.5% amino acids), containing calcium chloride or calcium gluconate were compounded without cysteine. Solutions were analyzed for particle counts using light obscuration. Maximum concentrations tested were 15 mmol/L of calcium and 12.5 mmol/L of phosphate. If the average particle count of three replicates exceeded USP guidelines, the solution was determined to be incompatible. This study found that 12.5 and 10 mmol/L of calcium and phosphate, respectively, are compatible in neonatal parenteral nutrition solutions compounded with 2.5% amino acids of either TrophAmine or Premasol. There did not appear to be significant differences in compatibility for solutions containing TrophAmine or Premasol when solutions were compounded with either CaCl2 or CaGlu-Pl. This study presents data in order to evaluate options for adding calcium and phosphate to neonatal parenteral nutrition solutions during shortages of calcium and cysteine.


Subject(s)
Calcium Chloride/analysis , Calcium Gluconate/analysis , Drug Compounding , Drug Incompatibility , Infant Nutritional Physiological Phenomena , Parenteral Nutrition Solutions/chemistry , Amino Acids/chemistry , Amino Acids/standards , Dynamic Light Scattering , Electrolytes/chemistry , Electrolytes/standards , Glucose/chemistry , Glucose/standards , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Lasers , Osmolar Concentration , Parenteral Nutrition Solutions/standards , Pharmacopoeias as Topic , Phosphates/chemistry , Potassium Compounds/chemistry , Solutions/chemistry , Solutions/standards , United States
6.
Molecules ; 22(1)2016 Dec 26.
Article in English | MEDLINE | ID: mdl-28035970

ABSTRACT

Pseudostellariae Radix (PR) is an important traditional Chinese herbal medicine (TCM) with vast clinical consumption because of its positive effects. However, little attention has been devoted to simultaneous analysis of its bioactive components for quality control of PR based on its different harvesting times, different growing habitats, and different processing methods. In this research, the quality of PR was evaluated based on simultaneous determination of multiple bioactive components combined with grey relational analysis (GRA). A reliable method based on ultra-fast liquid chromatography tandem triple quadrupole mass spectrometry (UFLC-QTRAP-MS/MS) was established to simultaneously determine the contents of 30 components in PR, including two cyclopeptides, 12 nucleosides, and 16 amino acids. Furthermore, grey relational analysis was performed to evaluate the quality of PR samples according to the contents of these 30 components. The results showed that the quality of PR harvested in 6 August 2013, cultivated in Jurong, Jiangsu, and treated by oven drying 60 °C was better than that of other PR samples. The proposed method is useful for the overall assessment on the quality of PR, and this study provides valuable information for revealing the dynamic change laws of metabolite accumulation in PR and choosing the most suitable harvesting time and reasonable processing method of PR to obtain the best quality.


Subject(s)
Amino Acids/standards , Caryophyllaceae/chemistry , Drugs, Chinese Herbal/standards , Nucleosides/standards , Peptides, Cyclic/standards , Plant Roots/chemistry , Amino Acids/chemistry , Amino Acids/isolation & purification , China , Chromatography, Liquid , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/isolation & purification , Humans , Nucleosides/chemistry , Nucleosides/isolation & purification , Peptides, Cyclic/chemistry , Peptides, Cyclic/isolation & purification , Quality Control , Seasons , Tandem Mass Spectrometry
7.
Nuklearmedizin ; 50(4): 167-73, 2011.
Article in German | MEDLINE | ID: mdl-21789338

ABSTRACT

For the primary diagnosis of brain tumours, morphological imaging by means of magnetic resonance imaging (MRI) is the current method of choice. The complementary use of functional imaging by positron emitting tomography (PET) and single photon emitting computerized tomography (SPECT) with labelled amino acids can provide significant information on some clinically relevant questions, which are beyond the capacity of MRI. These diagnostic issues affect in particular the improvement of biopsy targeting and tumour delineation for surgery and radiotherapy planning. In addition, amino acid labelled PET and SPECT tracers are helpful for the differentiation between tumour recurrence and non-specific post-therapeutic tissue changes, in predicting prognosis of low grade gliomas, and for metabolic monitoring of treatment response. The application of dynamic PET examination protocols for the assessment of amino acid kinetics has been shown to enable an improved non-invasive tumour grading. The purpose of this guideline is to provide practical assistance for indication, examination procedure and image analysis of brain PET/SPECT with labelled amino acids in order to allow for a high quality standard of the method. After a short introduction on pathobiochemistry and radiopharmacy of amino acid labelled tracers, concrete and detailed information is given on the several indications, patient preparation and examination protocols as well as on data reconstruction, visual and quantitative image analysis and interpretation. In addition, possible pitfalls are described, and the relevant original publications are listed for further information.


Subject(s)
Amino Acids , Brain Neoplasms/diagnostic imaging , Positron-Emission Tomography/standards , Practice Guidelines as Topic , Radiopharmaceuticals/standards , Tomography, Emission-Computed, Single-Photon/standards , Amino Acids/standards , Germany , Humans , Staining and Labeling/standards
8.
AAPS PharmSciTech ; 12(2): 468-75, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21479751

ABSTRACT

A series of amphiphilic ion pairs of erythromycin (ERY) with lipoamino acids (LAAs) were produced. The ion pairs were prepared by evaporation of a water/ethanol co-solution of the drug and LAA bearing an alkyl side chain of 10-16 carbon atoms. For the sake of comparison, equimolar physical mixtures were prepared by triturating ERY and the LAA in the absence of any solvent. FTIR spectroscopy confirmed the structure of ion pairs, while differential scanning calorimetry and powder X-ray diffractometry were used to assess the formation of new saline species. The solubility pattern of the coevaporates in different aqueous and organic solvents confirmed their amphiphilic properties. ERY-LAA ion pairs were submitted to an in vitro microbiological assay against different bacterial strains, both susceptible and resistant to macrolides. The presence of the LAA moiety was shown not altering the antibacterial spectrum of activity of the drug. These results can be the basis for a further evaluation of ERY-LAA ion pairs as a mean to improve the penetration of the drug inside bacterial cells and to optimize the loading of ERY in lipid-based nanocarriers.


Subject(s)
Amino Acids/chemistry , Anti-Bacterial Agents/chemistry , Erythromycin/chemistry , Surface-Active Agents/chemistry , Amino Acids/pharmacology , Amino Acids/standards , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/standards , Drug Evaluation, Preclinical/methods , Drug Evaluation, Preclinical/standards , Erythromycin/pharmacology , Erythromycin/standards , Lipids/chemistry , Lipids/pharmacology , Lipids/standards , Microbial Sensitivity Tests/methods , Microbial Sensitivity Tests/standards , Staphylococcus aureus/drug effects , Surface-Active Agents/pharmacology , Surface-Active Agents/standards
9.
Eur J Pediatr ; 165(8): 512-8, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16622662

ABSTRACT

INTRODUCTION: Parenteral nutrition (PN) plays an important role in the nutritional support of very preterm newborns. It has been suggested that a high proportion of PN orders could be standardized. In 2002, we implemented in our unit the preparation of three standardized formulations for PN adapted to the nutritional requirements of premature infants<32 weeks. Following this change of practice, a retrospective observational study was conducted to evaluate the relevance of the implemented standardized PN regime. Twenty premature inborn infants<32 weeks gestation who had received standardized (STD) PN in 2003 were matched for 20 infants who had received individualized (IND) PN in 2001. Adequacy of nutrition was assessed by comparing daily intravenous nutrient intake and biochemical parameters during the first week. Amino-acid intakes on day 3 were higher in the STD group (1.5+/-0.2 g/kg/d vs. 0.9+/-0.5, p<0.001), and the calcium phosphate intakes were better balanced. The cumulated intake of amino acids for the first week was greater in the STD group (+20% ; p=0.0003). Biochemical parameters were similar in both groups. Insulin infusions were less frequent in the STD group (p<0.06). CONCLUSION: Standardized parenteral formulations provided higher early intakes of amino acid and glucose, a better calcium phosphate ratio, and a greater amount of amino-acid intakes during the first week while maintaining the same biochemical parameters. This strategy forms part of an approach concerning quality control and the respect of good professional practice for the preparation of parenteral nutrition solutions.


Subject(s)
Clinical Protocols , Infant, Premature , Parenteral Nutrition/standards , Amino Acids/administration & dosage , Amino Acids/standards , Calcium Phosphates/administration & dosage , Carbohydrates/administration & dosage , Case-Control Studies , Creatinine/blood , France , Humans , Hypoglycemic Agents/therapeutic use , Infant, Newborn , Insulin/therapeutic use , Nutritional Requirements , Phosphorus/blood , Retrospective Studies , Therapy, Computer-Assisted , Trace Elements/administration & dosage , Trace Elements/standards , Vitamins/administration & dosage , Vitamins/standards , Weight Gain
10.
Poult Sci ; 76(5): 711-20, 1997 May.
Article in English | MEDLINE | ID: mdl-9154624

ABSTRACT

Two trials of identical experimental design were conducted to evaluate the NRC (1994) amino acid requirements for growing turkeys. Diets were formulated for 4-wk age intervals using intact ingredients and amino acid supplements to provide 85, 90, 95, 100, 105, 110, 115, and 120% of the suggested requirements. Formulation was done in a manner to minimize excess levels of as many essential amino acids as possible. Day-old male poults of a commercial Large White strain were grown to 20 wk on the test diets with body weight and feed conversion determined at intervals throughout the test; representative samples of birds were processed to determine carcass composition and parts yield. Results suggested that diets formulated to provide 105% of the suggested NRC requirements were needed to provide maximum body weight gain, feed conversion, and breast meat yield. Ambient temperatures in the present study frequently exceeded 27 C and may have contributed to the need for somewhat greater amino acid needs than the present NRC (1994) suggestions.


Subject(s)
Amino Acids/standards , Animal Nutritional Physiological Phenomena , Diet/veterinary , National Academy of Sciences, U.S. , Nutrition Surveys , Turkeys/physiology , Aging/physiology , Amino Acids/administration & dosage , Animals , Body Composition/physiology , Body Weight/physiology , Diet/standards , Housing, Animal , Male , Nutritional Requirements , Random Allocation , Temperature , Turkeys/growth & development , United States
11.
J Anim Sci ; 73(6): 1746-53, 1995 Jun.
Article in English | MEDLINE | ID: mdl-7673069

ABSTRACT

Three experiments were conducted to evaluate lysine (Lys), threonine (Thr), methionine (Met), tryptophan (Trp), and nonessential N (+N) supplementation of all sorghum grain (S) diets on growth and carcass characteristics of 50- to 100-kg pigs. In Exp. 1, four replicate pens of four pigs each were fed: 1) sorghum-soybean meal positive control (S-SBM); 2) S + Lys + Thr + Met + Trp to equal the amino acid concentrations in S-SBM (LTMT); 3) Diet 2 + N (LTMT+N); and 4) S negative control. Compared with pigs fed S-SBM, pigs fed LTMT or LTMT+N had reduced (P < .05) ADG, ADFI, serum urea N (SUN), pancreas weight, LMA, and percentage of muscling (PM) but higher dressing percentage (DP) and similar 10th rib fat thickness (TRF). Apparent N digestibility was lower (P < .05) in pigs fed LTMT than in pigs fed LTMT+N or S-SBM. In Exp. 2, two replicate pens of four pigs each were fed: 1) S-SBM; 2) S + Lys + Thr (LT); 3) S + Lys + Thr + Met (LTM); 4) S + Lys + Thr + Trp (LTT); 5) LTMT; 6 to 9) as 2 to 5 +N; and 10) S negative control. Compared with pigs fed S-SBM, pigs fed S, LT, LT+N, and LTM+N had lower (P < .05) ADG. Daily gain of pigs fed LTM, LTT, LTMT, LTT+N, or LTMT+N was not different (P > .10) from pigs fed S-SBM.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Amino Acids/standards , Body Weight/physiology , Diet/veterinary , Edible Grain/standards , Swine/growth & development , Animals , Blood Urea Nitrogen , Diet/standards , Eating/physiology , Female , Food, Fortified , Lysine/standards , Male , Meat/standards , Methionine/standards , Muscle, Skeletal/anatomy & histology , Organ Size , Pancreas/anatomy & histology , Swine/physiology , Threonine/standards , Tryptophan/standards
12.
J Anim Sci ; 73(2): 433-40, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7601776

ABSTRACT

An experiment was conducted to evaluate the effect of feeding reduced CP, amino acid (AA)-supplemented diets to pigs from weaning to slaughter weight on growth performance and carcass characteristics. Pigs were fed a 19%-16%-14% CP starter-grower-finisher high-CP sequence of diets, respectively, or a sequence of diets reduced in CP by 4 percentage units (3 percentage units in the finisher period) with or without lysine (LYS), tryptophan (TRP), and threonine (THR) supplementation. Pigs fed the low-CP diets without AA supplementation grew more slowly, were less efficient in feed conversion, and developed carcasses that contained a smaller longissimus muscle, greater, average backfat depths, and a lower percentage of muscle compared with pigs fed the high-CP sequence of diets (P < .01). The reduction in growth performance, feed efficiency, longissimus muscle area, and percentage of muscle in pigs fed the low-CP diets was alleviated by LYS, TRP, and THR supplementation (P > .10). Although pigs fed the low-CP diets supplemented with AA had reduced average and 10th rib backfat depths compared with pigs fed the unsupplemented, low-CP diets (P < .01), these fat depth measures remained greater (P < .05) than those of pigs fed the high-CP diets. Feeding reduced dietary CP, regardless of AA supplementation, resulted in reduced heart (P < .10) and liver weights (P < .01) compared with feeding the high-CP diets.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Amino Acids/standards , Body Composition/physiology , Diet/veterinary , Dietary Proteins/standards , Swine/growth & development , Aging/physiology , Animals , Body Weight/physiology , Female , Food, Fortified , Kidney/anatomy & histology , Lysine/standards , Male , Muscle Development , Muscle, Skeletal/growth & development , Muscle, Skeletal/physiology , Organ Size/physiology , Swine/physiology , Threonine/standards , Trypsin/standards
13.
Arch Latinoam Nutr ; 29(3): 340-53, 1979 Sep.
Article in English | MEDLINE | ID: mdl-543770

ABSTRACT

A screening method for the characterization and differentiation of proteinaceous samples and amino acid mixtures was applied to protein foods (4 protein-rich mixtures, one product sold as dietary supplement, and 3 raw materials of frequent use in the preparation of these products). Graphic profiles which describe the relative amounts of amino acid groups in the samples were obtained and subjected to statistical analysis. According to a previously established criterion of identity or difference, the correlation coefficients showed that at least 90% of the comparisons dealt with different samples. The method is proposed as a valuable tool for the quality control of protein-rich foods and their raw materials.


Subject(s)
Amino Acids/analysis , Dietary Proteins/analysis , Food, Fortified/analysis , Amino Acids/standards , Brazil , Chromatography, Paper , Dietary Proteins/standards , Food, Fortified/standards , Humans , Hydrolysis , Statistics as Topic
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